Basil Brooke

Prof. Basil Brooke

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

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

Representative Publications

View All Publications
1 June 2000 in Medical and Veterinary Entomology
Verified
Journal Article
Closed access
PDF file
KHK. Hargreaves
K. Hargreaves
LKL. L. Koekemoer
L. L. Koekemoer
BBBasil Brooke
Basil Brooke
RHR. H. Hunt
R. H. Hunt
JMJ. Mthembu
J. Mthembu
MCMaureen Coetzee
Maureen Coetzee

4 August 2010 in Parasites & Vectors
Verified
Journal Article
Open access
PDF file
OWO R Wood
O R Wood
SHS Hanrahan
S Hanrahan
MCMaureen Coetzee
Maureen Coetzee
Lizette Leonie KoekemoerLizette Leonie Koekemoer
Lizette Leonie Koekemoer
BBBasil Brooke
Basil Brooke
Background: Malaria in South Africa is primarily transmitted by Anopheles funestus Giles. Resistance to pyrethroid insecticides in An. funestus in northern Kwazulu/Natal, South Africa, and in neighbouring areas of southern Mozambique enabled populations of this species to increase their ranges into areas where pyrethroids were being exclusively used for malaria control. Pyrethroid resistance in southern African An. funestus is primarily conferred by monooxygenase enzyme metabolism. However, selection for this resistance mechanism is likely to have occurred in conjunction with other factors that improve production of the resistance phenotype. A strong candidate is cuticle thickening. This is because thicker cuticles lead to slower rates of insecticide absorption, which is likely to increase the efficiency of metabolic detoxification. Results: Measures of mean cuticle thickness in laboratory samples of female An. funestus were obtained using scanning electron microscopy (SEM). These females were drawn from a laboratory colony carrying the pyrethroid resistance phenotype at a stable rate, but not fixed. Prior to cuticle thickness measurements, these samples were characterised as either more or less tolerant to permethrin exposure in one experiment, and either permethrin resistant or susceptible in another experiment. There was a significant and positive correlation between mean cuticle thickness and time to knock down during exposure to permethrin. Mean cuticle thickness was significantly greater in those samples characterised either as more tolerant or resistant to permethrin exposure compared to those characterised as either less tolerant or permethrin susceptible. Further, insecticide susceptible female An. funestus have thicker cuticles than their male counterparts. Conclusion: Pyrethroid tolerant or resistant An. funestus females are likely to have thicker cuticles than less tolerant or susceptible females, and females generally have thicker cuticles than males. In pyrethroid resistant An. funestus, this increase in cuticle thickness is likely to have developed as an auxiliary to the primary mode of pyrethroid resistance which is based on enzyme-mediated detoxification.

30 August 2005 in Medical and Veterinary Entomology
Verified
Journal Article
Closed access
PDF file
RHR. H. Hunt
R. H. Hunt
BBBasil Brooke
Basil Brooke
CPC. Pillay
C. Pillay
LKL. L. Koekemoer
L. L. Koekemoer
MCMaureen Coetzee
Maureen Coetzee

1 August 2001 in Bulletin of Entomological Research
Verified
Journal Article
Closed access
PDF file
BBBasil Brooke
Basil Brooke
GKG. Kloke
G. Kloke
RHR.H. Hunt
R.H. Hunt
LKL.L. Koekemoer
L.L. Koekemoer
ETE.A. Tem
E.A. Tem
MCM. Coetzee
M. Coetzee
Anopheles funestus Giles has been implicated as a major malaria vector in sub-Saharan Africa where pyrethroid insecticides are widely used in agriculture and public health. Samples of this species from northern Kwazulu/Natal in South Africa and the Beluluane region of southern Mozambique showed evidence of resistance to pyrethroid insecticides. Insecticide exposure, synergist and biochemical assays conducted on A. funestus suggested that elevated levels of mixed function oxidases were responsible for the detoxification of pyrethroids in resistant mosquitoes in these areas. The data suggested that this mechanism was also conferring cross-resistance to the carbamate insecticide propoxur.

13 October 2009 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
MFMarit Farenhorst
Marit Farenhorst
JMJoel C. Mouatcho
Joel C. Mouatcho
CKChristophe K. Kikankie
Christophe K. Kikankie
BBBasil Brooke
Basil Brooke
RHRichard H. Hunt
Richard H. Hunt
MCMaureen Coetzee
Maureen Coetzee
The evolution of insecticide resistance in mosquitoes is threatening the effectiveness and sustainability of malaria control programs in various parts of the world. Through their unique mode of action, entomopathogenic fungi provide promising alternatives to chemical control. However, potential interactions between fungal infection and insecticide resistance, such as cross-resistance, have not been investigated. We show that insecticide-resistantAnophelesmosquitoes remain susceptible to infection with the fungusBeauveria bassiana. Four different mosquito strains with high resistance levels against pyrethroids, organochlorines, or carbamates were equally susceptible toB. bassianainfection as their baseline counterparts, showing significantly reduced mosquito survival. Moreover, fungal infection reduced the expression of resistance to the key public health insecticides permethrin and dichlorodiphenyltrichloroethane. Mosquitoes preinfected withB. bassianaorMetarhizium anisopliaeshowed a significant increase in mortality after insecticide exposure compared with uninfected control mosquitoes. Our results show a high potential utility of fungal biopesticides for complementing existing vector control measures and provide products for use in resistance management strategies.

4 March 2005 in Insect Molecular Biology
Verified
Journal Article
Closed access
PDF file
WDW. Du
W. Du
TAT. S. Awolola
T. S. Awolola
PHP. Howell
P. Howell
LKL. L. Koekemoer
L. L. Koekemoer
BBBasil Brooke
Basil Brooke
LZL. Zheng
L. Zheng