Charles Nguli Kimwele

Charles Nguli Kimwele


Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2014 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
DODominic O. Ochwang’i
Dominic O. Ochwang’i
CKCharles Nguli Kimwele
Charles Nguli Kimwele
JOJemimah A. Oduma
Jemimah A. Oduma
PGPeter K. Gathumbi
Peter K. Gathumbi
JMJames M. Mbaria
James M. Mbaria
SKStephen G. Kiama
Stephen G. Kiama

19 December 2002 in Molecular Ecology
Verified
Journal Article
Closed access
PDF file
CKCharles Nguli Kimwele
Charles Nguli Kimwele
JGJ. A. Graves
J. A. Graves

1 April 2018 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
DODominic O. Ochwang’i
Dominic O. Ochwang’i
CKCharles Nguli Kimwele
Charles Nguli Kimwele
JOJemimah A. Oduma
Jemimah A. Oduma
PGPeter K. Gathumbi
Peter K. Gathumbi
SKStephen G. Kiama
Stephen G. Kiama
Thomas EfferthThomas Efferth
Thomas Efferth

1 January 2012 in BMC Genetics
Verified
Journal Article
Open access
PDF file
COCaleb O Orenge
Caleb O Orenge
LMLeonard Munga
Leonard Munga
CKCharles Nguli Kimwele
Charles Nguli Kimwele
SKSteve Kemp
Steve Kemp
AKAbraham Korol
Abraham Korol
MSMorris Soller
Morris Soller
Trypanosomosis, a protozoal disease affecting livestock, transmitted by Glossina (tsetse) flies is a major constraint to agricultural production in Sub-Saharan Africa. It is accepted that utilization of the native trypanotolerance exhibited in some of the African cattle breeds to improve trypanotolerance of more productive but susceptible breeds, will offer a cost effective and sustainable solution to the problem. The success of this approach is based on the premise that quantitative trait loci previously identified under relatively controlled situations confer useful trypanotolerance under natural field situations. As part of a study to authenticate this hypothesis, a population of 192 cattle, consisting of six batches of N’Dama and Kenya-Boran backcross animals [(N’Dama x Kenya-Boran) x Kenya-Boran] born over the period 2002 to 2006 was constructed. Some of the batches also included pure Kenya-Boran cattle, or N’Dama x Kenya- Boran F1 animals. Each batch was exposed as yearlings to natural field trypanosomosis challenge over a period of about one year; the entire challenge period extending from December 2003 to June 2007. Performance of the animals was evaluated by weekly or biweekly measurements of body weight, packed blood cell volume (PCV), parasitemia score, and number of trypanocide treatments. From these basic data, 49 phenotypes were constructed reflecting dynamics of body weight, packed cell volume (PCV) and parasitemia under challenge.

3 June 2011 in BMC Proceedings
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Journal Article
Open access
PDF file
COCaleb Orenge
Caleb Orenge
LMLeonard Munga
Leonard Munga
CKCharles Nguli Kimwele
Charles Nguli Kimwele
SKSteve Kemp
Steve Kemp
AKAbraham Korol
Abraham Korol
MSMorris Soller
Morris Soller
Background: Animal trypanosomosis in sub-Saharan Africa is a major obstacle to livestock based agriculture. Control relies on drugs with increasing incidence of multiple-drug resistance. A previous mapping experiment in an F2 population derived from the indigenous trypanotolerant N’Dama cattle crossed to susceptible (Kenya)-Boran cattle under controlled challenge, uncovered a number of trypanotolerance QTL (T-QTL). The present study was to determine expression of N’Dama trypanotolerance in a backcross to the Boran under conditions of field challenge, and whether chromosomal regions associated with trypanotolerance in the F2 experiment showed similar effects in the BC population. Methods: 192 backcross animals to the Boran were produced in six batches from June 2001 to December 2006. At one year of age animals were moved to the field and exposed to natural challenge over about one year in Southwest Kenya (Narok). The animals were individually recorded weekly for body weight, packed cell volume, parasitaemia score, and drug treatments, and were genotyped using 35 microsatellite markers spanning 5 chromosomes found in the F2 study to harbour T-QTL. Results: The F1 were most trypanotolerant, Boran least, and BC intermediate. Females showed distinctly higher trypanotolerance than males. There was a positive correlation in the BC population between trypanotolerance and number of N’Dama origin marker alleles. QTL mapping revealed T-QTL distributed among all five targeted chromosomes, corresponding in part to the results obtained in the F2 experiment. Conclusions: N’Dama origin trypanotolerance is expressed in a BC population under field conditions in proportion to N’Dama origin marker alleles. Consequently, marker assisted selection in such populations may be a means of increasing trypanotolerance, while retaining the desirable productive qualities of the recurrent parent.

1 February 1998
Verified
Journal Article
Closed access
CKCharles Nguli Kimwele
Charles Nguli Kimwele
JGJ A Graves
J A Graves
TBT Burke
T Burke
OHOlivier Hanotte
Olivier Hanotte