| Prof. Daniel Munge Mukunya Publications |
| 1 | 2007 | Characterization Of Antibiotic Meta Bolites From Actinomycete Isolates
Click to View Abstract
|
| 2 | 1996 | Mibey, R.K., K.K. Kokwaro And D.M. Mukunya, 1996. A New Species And Four New Records Of Asterina From Kenya. Nova Hedwigia 62: 144
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 3 | 1992 | Some Mechanisms Implicated In The Survival Of Benomyl Tolerant Strains Of Colletotrichum Coffeanum Noack, Casual Agent Of Coffee Berry Disease.
Click to View Abstract
|
| 4 | 1990 | Mutitu, E.W., D.M. Mukunya And S.O. Keya, 1990. Effect Of Moisture On Fusarium Yellows Of Beans Caused By Fusarium Oxysporum F.sp. Phaseoli In Kenya. Accepted For Publication In The Kenya National Academy Journal Series B. For 1990.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 5 | 1990 | Bacterial Black Spot Of Mangoes In Kenya
Click to View Abstract
|
| 6 | 1989 | Mutitu, E.W., D.M. Mukunya And E.M. Gathuru, 1989. Effect Of Organic Amendments On Fusarium Yellow Disease On The Bean Host. Discovery And Innovation Vol 1: 67
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 7 | 1989 | Mukunya, D.M. 1989. Plant Health For Increased Crop Production And A Healthy Nation. A Keynote Address. The 1st Plant Pathology Society Of Kenya Conference Proceedings, 23
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 8 | 1989 | Kihurani, A.W., D.M. Mukunya And R.A. Burucahra, 1989. Evaluation Of Bean Cultivars For Resistance To Rust.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 9 | 1989 | Njiru, J. And D.M. Mukunya, 1989. Variation In Collectotrichum Coffeanum, The Cause Of Coffee Berry Disease As Shown By Eletrophoretic Separation Of Extracellular Proteins Of Different Isolates. Proceedings Of The 1st Plant Pathology Society Of Kenya Conf
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 10 | 1989 | Arama, F.P., D. M. Mukunya And R.A. Buruchara, 1989. The Influence Of Temperature On Infection Of Rhynchosprium Sequels On Susceptible And Resistant Kenya Barley Varieties.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 11 | 1989 | Possible Survival Mechanisms And Control Of Coffee Berry Disease Fungus Strains Resistant To Benzimidazole Fungicides
Click to View Abstract
|
| 12 | 1988 | Mukunya, D.M. And C. Muinamia, 1988. Rational Use Of Pesticides In Horticulture With Special Emphasis On Kenya. ACTA HORT. 218: 261
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 13 | 1988 | Njeru, R.W., D.M. Mukunya And E.M. Gathuru, 1988. Etiology And Chemical Control Of Cercospora Leaf Spot Of The Ornamental Bellies Of Ireland (Molucella Leavis L.) Proceedings Of The 1st Symposium Of The Crop Science Society Of Kenya Held On 4
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 14 | 1988 | Mukunya, D.M. 1988. Safe And Effective Use Of Pesticides. Paper Presented At The PCAK/GIFP Workshop On Responsible And Effective Crop Protection Held In Nairobi, Kenya. 11
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 15 | 1988 | Kedera, C.J., D.M. Mukunya And S.O. Keya, 1988. Survival Of Rhizobium Leguminosarum Bv. Phaseoli In Contact With Captan.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 16 | 1988 | Mwang
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 17 | 1988 | Mutitu, E.W., D.M. Mukunya And S.O. Keya, 1988. Effect Of Antagonistic Bacteria Isolated From Soil Organic Amendments On Fusarium Oxyysporum Schl. In Culture. Abstract 5th International Congress On Plant Pathology, Kyoto, Japan.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 18 | 1988 | Reactions Of Cultivars Of Bean (Phaseolus Vulgaris L.) To Bean Common Mosaic Virus (BCMV)
Click to View Abstract
3 plants of each cultivar were raised in pots filled with sterile soil, 451 bean cultivars were tested in all. Inoculum was prepared from 30-day-old plants of P. vulgaris. Seedlings of test varieties were inoculated when 2 weeks old, the inoculum consisted of 14 virus isolates ground in 0.01 m phosphate buffer, pH 7.3 and manually inoculated onto primary leaves of seedlings dusted with 500 mesh carborundum. A cultivar was rated resistant if no systemic infection could be detected and susceptible if it became systemically infected or if the presence of the virus in inoculated leaves of plants without systemic symptoms was demonstrated by virus indexing. Only 68 showed some resistance. The other 383 were found susceptible, with 77 of them expressing systemic necrosis, the remainder showing mosaic symptoms
|
| 19 | 1987 | Gathuru, E.M. And D.M. Mukunya And R.A. Buruchara, 1987. Diseases Of Crop Plants In Small Scale Farms Of Embu Agro-ecozone I-IV And Farmers Awareness On Disease Control Methods. In Integrated Crop Protection For Small Scale Farmers In Eastern Africa. Comm
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 20 | 1987 | Kimani, V.W. And D.M. Mukunya, 1987. Control Of Pesticides Residues In Food. Paper Presented At The National Food Control Seminar, Kenya Bureau Of Standards. 6-9th Oct. 1987. Nairobi, Kenya.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 21 | 1987 | Mukunya D.M. 1987. Pesticides In Our Environment. Presented At The Regional Workshop On Environmental Protection For The Greenbelt Movement Held At The College Of Education And External Studies, Kikuyu, University Of Nairobi, Kenya. 11p
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 22 | 1987 | Mukunya D.M. 1987. Pesticides In Our Environment. Presented At The Regional Workshop On Environmental Protection For The Greenbelt Movement Held At The College Of Education And External Studies, Kikuyu, University Of Nairobi, Kenya. 11p
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 23 | 1987 | Omunyin, M.E., E.M. Gathuru And D.M. Mukunya, 1987. Reactions Of Cultivars Of Beans (Phaseolus Vulgaris L.) To Bean Common Mosaic Virus (BCMV). Trop. Agric. (Trinidad) 65 (2): 166
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 24 | 1986 | Bondole Wa Mbula, E.M. Gathuru, 1986. Malakisi Tobacco Necrosis Virus. Proceeding Of The Symposium On Viral Diseases In Africa Held In Nairobi, Kenya. O.A.U. Scientific And Technical Res. Council Publication.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 25 | 1986 | Mathangya, P.M., D.M. Mukunya And E.M. Gathuru, 1986. Aetiology And Sources Of Resistance To Common Blight (Xanthomonas Campestris Pv. Phaseolus (Smith, 1987). Dye,1978, Of Beans (phaseolus Vulgaris L. ) In Kenya. Kenya Jour. Of Science Series B. 7 (2): 2
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 26 | 1986 | Omunyin, M.E. Gathuru And D.M. Mukunya, 1986. Las Cepas, Del BCMCY. Su. Interaction Con Variedades De Frijol Con El Gene 1. Hojas De Frijol 8 (3).
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 27 | 1986 | Strains Of BCMV And Their Interaction With I-gene Bean Varieties
Click to View Abstract
|
| 28 | 1985 | Buruchara, R.A., E.M.Gathuru And D.M. Mukunya, 1985. Disease Progress Of Angular Leaf Spot Caused By Isariopsis Griseola Sacc. And It Implications On Resistance Of Some Bean (Phaseolus Vulgaris L.) Cultivars. ACTA HORTICULATURAE 218: 321
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 29 | 1985 | Buruchara, R.A., E.M.Gathuru And D.M. Mukunya, 1985. Disease Progress Of Angular Leaf Spot Caused By Isariopsis Griseola Sacc. And It Implications On Resistance Of Some Bean (Phaseolus Vulgaris L.) Cultivars. ACTA HORTICULATURAE 218: 321
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 30 | 1985 | Mutitu, E.W., D.M. Mukunya And S.O. Keya, 1985, Biological Control Of Fusarium Yellow On Beans Caused By Fusarium Oxysporum Schl. F.sp Phaseolus Kendrick And Snyder Using Organic Amendments. ACTA HORT. 218:267
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 31 | 1984 | Nyangeri, J.P., E.M. Gathuru And D.M. Mukunya, 1984. Effect Of Latent Infection On The Spread Of Bacterial Wilt Of Potatoes In Kenya. Trop. Pest Management 30 (2): 163
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 32 | 1983 | Current Bean Research Programmes In Kenya.
Click to View Abstract
|
| 33 | 1982 | Mukunya, D.M. 1982. Development Of Crop Varieties For Disease Resistance.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 34 | 1982 | Onyango, D. And D.M. Mukunya. 1982. Bacterial Blight Of Cassava, Xanthomonas Manihotis In Kenya.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 35 | 1982 | Mukunya, D.M. Et Al. 1982. Citrus Greening Disease In Kenya And Recommendations For Its Control. Ministry Of Agriculture Publication. 128 P.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 36 | 1982 | Mukunya, D.M. 1982. UNDP/FAO Evaluation Study On National Agricultural Research, Kenya 195 +35 Annex Tables, FAO, ROME.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 37 | 1982 | Bacterial Blight Of Cassava, Xanthomonas Manihotis In Kenya.
Click to View Abstract
|
| 38 | 1982 | Improvement Of Beans In The Semi-arid Areas Of Kenya: Report Prepared For The University Of Nairobi And Bean/Cowpea CRSP
Click to View Abstract
|
| 39 | 1982 | Las Cepas, Del BCMCY. Su. Interaction Con Variedades De Frijol Con El Gene 1
Click to View Abstract
|
| 40 | 1982 | Studies On Genetic Resistance Of Beans To Pseudomonas Phaseolicola In Kenya
Click to View Abstract
|
| 41 | 1982 | Undp/fao Evaluation Study On National Agricultural Research, Kenya 195 +35 Annex Tables, Fao, Rome.
Click to View Abstract
|
| 42 | 1981 | Mukunya, D.M., P.M. Muthangya And J.P.E. Esele 1981. Bacterial Blights Of Beans (Phaseolus Vulgaris) In Kenya.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 43 | 1981 | Kinyua, G.K., D.M. Mukunya And E.M. Van Breukelen, 1981. Variability In Isolates Of Pseudomonas Phaseolicola (Burk) Dowson In Kenya And Genetic Studies On Resistance In Dry Food Beans.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 44 | 1981 | Bacterial Blights Of Beans (phaseolus Vulgaris) In Kenya.
Click to View Abstract
|
| 45 | 1981 | Variability In Isolates Of Pseudomonas Phaseolicola (burk) Dowson In Kenya And Genetic Studies On Resistance In Dry Food Beans.
Click to View Abstract
|
| 46 | 1980 | Njuguna, S.K., A.M.M. Ndegwa, H.A. Van Rheenen And D.M. Mukunya, 1980. Bean Production In Kenya. Workshop On Potentials For Bean Production In Eastern Africa, Malawi, March, 1980. In Potentials For Bean Production In Eastern Africa. Published 1981
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 47 | 1980 | Cowpea Research In Kenya
Click to View Abstract
|
| 48 | 1979 | Mukunya, D.M. And S.O. Keya, 1979. Effects Of Seeds Borne Innoculum On Disease Development And Yields Of Canadian Wonder Bean Variety In Kenya.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 49 | 1979 | Keya S.O. And D.M. Mukunya, 1979. The Influence Of Phosphorus And Molybdenum Application On Modulation Of Canadian Wonder Bean Variety.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 50 | 1979 | Mutitu, E.W. And D.M. Mukunya, 1979. Epidemiology And Control Of Bean Scab Caused By Elsinoe Phaseolus Jenkins In Kenya.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 51 | 1979 | Keya, S.O., Ssali, H. Mukunya, D.M., Muruli, B.I. And Onim, J.F. 1979. Legume Research At The University Of Nairobi, In Planning International Network Of Legume Inoculation Trials.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 52 | 1979 | Keya, S.O., Mukunya, D.M., Ngugi, D.N. And Waithaka, K. 1979. Suggestions For Modification Of Curriculum In Agricultural Institutes To Make Them More Effective For Ruraldevelopment. In Seminar Report Of The International Association Of Agriculture Student
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 53 | 1979 | The Influence Of Phosphorus And Molybdenum Applications On Nodulation Of Phaseolus Vulgaris Beans At Kabete.
Click to View Abstract
|
| 54 | 1979 | The Influence Of Seed‐bone Anthracnose And Halo Blight Inocula On Yield And Disease Development In A Canadian Wonder Bean Selection At Kabete
Click to View Abstract
|
| 55 | 1978 | Mukunya, D.M. And S.O. Keya, 1978. Yield Performance And Selection Of Resistance In Beans (Phaseolus Vulgaris L.) To Common Disease In Kenya. In E.A. Agric. For. J. 43:4-8.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 56 | 1978 | Mukunya, D.M. 1978. Diseases Affecting Cowpeas In Kenya. Cowpeas Improvement Programme In Kenya. First Annual Report 61
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 57 | 1977 | Mukunya, D.M. 1977. Development Of Horizontal Resistance In Beans.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 58 | 1976 | Mukunya, D.M. And S.O. Keya, 1976. Phaseolus Bean Production In East Africa. A Review Paper Prepared For Publication In The Handbook Of Agriculture In East Africa Publishing House, Nairobi 81 P.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 59 | 1976 | Mukunya, D.M. 1976. Grain Storage, A Chapter In D. Ngugi Et Al. East Africa Agriculture. A Text Book For Schools. Macmillan Publishers Ltd. P. 76
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 60 | 1976 | Mukunya, D.M. 1976. Agriculture
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 61 | 1976 | Mukunya, D. M. 1976. Development Disease Resistance In Local Beans (Phaseolus Vulgaris L.) In Kenya.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 62 | 1976 | Agriculture
Click to View Abstract
|
| 63 | 1976 | Grain Storage
Click to View Abstract
|
| 64 | 1975 | Mukunya, D.M. 1975. The Occurrence In Kenya Of A Maize Leaf Blight Caused By Phyllosticta Maydis. Plant Disease Rept. 59:164-168.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 65 | 1975 | Mukunya, D.M., C.W. Boothroyd And C.O. Grogan 1975. Genetic Nature Of Resistance In Corn To Yellow Leaf Blight. Crop Science 15:495-501.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 66 | 1975 | Mukunya, D.M. 1975. Sources Of Resistance To Bean Anthracnose And Bean Rust In Kenya Local Dry Beans. Ann. Rept. Improvement Co-op.18:49-51.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 67 | 1975 | Sources Of Resistance To Bean Anthracnose And Bean Rust In Kenya Local Dry Beans
Click to View Abstract
|
| 68 | 1974 | Mukunya, D.M. 1974. Bean Diseases In Kenya. Ann. Rept. Bean Improvement Coop. 17; 57-59.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 69 | 1974 | Bean Diseases In Kenya.
Click to View Abstract
|
| 70 | 1973 | Mukunya, D.M. And C.W. Boothroyd 1973. Survival And Spore Dissertation Of Mycosphaerella Zeamaydis. Phytopathology 63:568.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 71 | 1973 | Mukunya, D.M. And C.W. Boothroyd 1973. Mycosphaerella Zea-mays Sp.n, The Sexual Of Phyllostica Maydis. Phytopathology 63:529-532.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 72 | 1973 | Yellow Leaf Blight Of Corn (Zea Mays L.): Etiology, Epidemiology And Development Of Resistance
Click to View Abstract
|
| 73 | 1973 | Survival And Spore Dissertation Of Mycosphaerella Zeamaydis
Click to View Abstract
|
| 74 | 1972 | Yoder, O And D.M.Mukunya, 1972. A Host Specific Toxin Metabolite Produced By Phyllostica Maydis. Phytopathology 62:799.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 75 | 1970 | Mukunya, D.M. And C.W. Boothroyd, 1970. Phyllosticta Leaf Spot And Tests For Resistance To This Disease. Phytopathology 60:577.
Click to View Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on
tissue culture facilities.
Keywords: Carpripox, latex agglutination test, attachment gene
J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43 |
| 76 | 1970 | Phyllosticta Yellow Leaf Blight Of Corn
Click to View Abstract
|
