» Articles » PMID: 16619611

Insecticide Resistance in Anopheles Arabiensis and Anopheles Gambiae from Mozambique

Overview
Journal J Med Entomol
Specialty Biology
Date 2006 Apr 20
PMID 16619611
Citations 43
Authors
Affiliations
Soon will be listed here.
Abstract

Malaria control in the southern part of Mozambique is currently by indoor residual spraying with a carbamate insecticide and by pyrethroid-treated bed-nets distributed to pregnant women and children under five in northern Mozambique. The susceptibility of Anopheles gambiae s.s. and Anopheles arabiensis Patton to pyrethroid, carbamate, organochlorine, and organophosphorus insecticides was determined by World Health Organization adult mosquito susceptibility tests at 17 localities in Mozambique, from March 2000 to July 2002. Biochemical assays were carried out on mosquitoes from the same families to detect shifts in the quantity or activity of enzyme families involved in insecticide detoxification. An. gambiae s.s. from all localities remained fully susceptible to DDT and the organophosphorus insecticide malathion. A low level of pyrethroid resistance was detected in populations in southern Mozambique. Populations outside Maputo province were still susceptible to pyrethroids. Low level resistance to the carbamate propoxur also was detected in An. arabiensis from two localities. Mosquitoes from five of the localities had elevated p450 estimates, compared with the insecticide susceptible Durban strain. The lack of cross-resistance between pyrethroids and DDT in Mozambican populations suggests that a kdr-type target site resistance mechanism has not been selected. Increased frequencies of insecticide insensitive acetylcholinesterase, the target site for carbamates and organophosphates, were found in 16 of the populations tested. Although vector control with bendiocarb is not being compromised by the presence of the acetylcholinesterase mechanism alone, the high level of insensitive acetylcholinesterase unless sensibly managed may have long-term implications for malaria control programs in Mozambique.

Citing Articles

Ace-1 Target Site Status and Metabolic Detoxification Associated with Bendiocarb Resistance in the Field Populations of Main Malaria Vector, in Iran.

Badzohre A, Oshaghi M, Enayati A, Moosa-Kazemi S, Nikookar S, Talebzadeh F J Arthropod Borne Dis. 2024; 17(3):272-286.

PMID: 38860197 PMC: 11162546. DOI: 10.18502/jad.v17i3.14987.


Malaria transmission potential of Anopheles gambiae s.l. in indoor residual spraying areas with clothianidin 50 WG in northern Benin.

Odjo E, Tognidro M, Govoetchan R, Missihoun A, Padonou G, Ahouandjinou J Trop Med Health. 2024; 52(1):18.

PMID: 38336760 PMC: 10854093. DOI: 10.1186/s41182-024-00582-8.


Impact of mass distribution of insecticide-treated nets in Mozambique, 2012 to 2025: Estimates of child lives saved using the Lives Saved Tool.

Wetzler E, Park C, Arroz J, Chande M, Mussambala F, Candrinho B PLOS Glob Public Health. 2023; 2(4):e0000248.

PMID: 36962318 PMC: 10022185. DOI: 10.1371/journal.pgph.0000248.


Six decades of malaria vector control in southern Africa: a review of the entomological evidence-base.

Nkya T, Fillinger U, Sangoro O, Marubu R, Chanda E, Mutero C Malar J. 2022; 21(1):279.

PMID: 36184603 PMC: 9526912. DOI: 10.1186/s12936-022-04292-6.


The mosquito vectors that sustained malaria transmission during the Magude project despite the combined deployment of indoor residual spraying, insecticide-treated nets and mass-drug administration.

Montoya L, Marti-Soler H, Maquina M, Comiche K, Cuamba I, Alafo C PLoS One. 2022; 17(9):e0271427.

PMID: 36084031 PMC: 9462736. DOI: 10.1371/journal.pone.0271427.