Which indoor residual spraying insecticide best complements standard pyrethroid long-lasting insecticidal nets for improved control of pyrethroid resistant malaria vectors?


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 20 10 2020
accepted: 07 01 2021
entrez: 28 1 2021
pubmed: 29 1 2021
medline: 7 9 2021
Statut: epublish

Résumé

Where resources are available, non-pyrethroid IRS can be deployed to complement standard pyrethroid LLINs with the aim of achieving improved vector control and managing insecticide resistance. The impact of the combination may however depend on the type of IRS insecticide deployed. Studies comparing combinations of pyrethroid LLINs with different types of non-pyrethroid IRS products will be necessary for decision making. The efficacy of combining a standard pyrethroid LLIN (DuraNet®) with IRS insecticides from three chemical classes (bendiocarb, chlorfenapyr and pirimiphos-methyl CS) was evaluated in an experimental hut trial against wild pyrethroid-resistant Anopheles gambiae s.l. in Cové, Benin. The combinations were also compared to each intervention alone. WHO cylinder and CDC bottle bioassays were performed to assess susceptibility of the local An. gambiae s.l. vector population at the Cové hut site to insecticides used in the combinations. Susceptibility bioassays revealed that the vector population at Cové, was resistant to pyrethroids (<20% mortality) but susceptible to carbamates, chlorfenapyr and organophosphates (≥98% mortality). Mortality of wild free-flying pyrethroid resistant An. gambiae s.l. entering the hut with the untreated net control (4%) did not differ significantly from DuraNet® alone (8%, p = 0.169). Pirimiphos-methyl CS IRS induced the highest mortality both on its own (85%) and in combination with DuraNet® (81%). Mortality with the DuraNet® + chlorfenapyr IRS combination was significantly higher than each intervention alone (46% vs. 33% and 8%, p<0.05) demonstrating an additive effect. The DuraNet® + bendiocarb IRS combination induced significantly lower mortality compared to the other combinations (32%, p<0.05). Blood-feeding inhibition was very low with the IRS treatments alone (3-5%) but increased significantly when they were combined with DuraNet® (61% - 71%, p<0.05). Blood-feeding rates in the combinations were similar to the net alone. Adding bendiocarb IRS to DuraNet® induced significantly lower levels of mosquito feeding compared to adding chlorfenapyr IRS (28% vs. 37%, p = 0.015). Adding non-pyrethroid IRS to standard pyrethroid-only LLINs against a pyrethroid-resistant vector population which is susceptible to the IRS insecticide, can provide higher levels of vector mosquito control compared to the pyrethroid net alone or IRS alone. Adding pirimiphos-methyl CS IRS may provide substantial improvements in vector control while adding chlorfenapyr IRS can demonstrate an additive effect relative to both interventions alone. Adding bendiocarb IRS may show limited enhancements in vector control owing to its short residual effect.

Sections du résumé

BACKGROUND
Where resources are available, non-pyrethroid IRS can be deployed to complement standard pyrethroid LLINs with the aim of achieving improved vector control and managing insecticide resistance. The impact of the combination may however depend on the type of IRS insecticide deployed. Studies comparing combinations of pyrethroid LLINs with different types of non-pyrethroid IRS products will be necessary for decision making.
METHODS
The efficacy of combining a standard pyrethroid LLIN (DuraNet®) with IRS insecticides from three chemical classes (bendiocarb, chlorfenapyr and pirimiphos-methyl CS) was evaluated in an experimental hut trial against wild pyrethroid-resistant Anopheles gambiae s.l. in Cové, Benin. The combinations were also compared to each intervention alone. WHO cylinder and CDC bottle bioassays were performed to assess susceptibility of the local An. gambiae s.l. vector population at the Cové hut site to insecticides used in the combinations.
RESULTS
Susceptibility bioassays revealed that the vector population at Cové, was resistant to pyrethroids (<20% mortality) but susceptible to carbamates, chlorfenapyr and organophosphates (≥98% mortality). Mortality of wild free-flying pyrethroid resistant An. gambiae s.l. entering the hut with the untreated net control (4%) did not differ significantly from DuraNet® alone (8%, p = 0.169). Pirimiphos-methyl CS IRS induced the highest mortality both on its own (85%) and in combination with DuraNet® (81%). Mortality with the DuraNet® + chlorfenapyr IRS combination was significantly higher than each intervention alone (46% vs. 33% and 8%, p<0.05) demonstrating an additive effect. The DuraNet® + bendiocarb IRS combination induced significantly lower mortality compared to the other combinations (32%, p<0.05). Blood-feeding inhibition was very low with the IRS treatments alone (3-5%) but increased significantly when they were combined with DuraNet® (61% - 71%, p<0.05). Blood-feeding rates in the combinations were similar to the net alone. Adding bendiocarb IRS to DuraNet® induced significantly lower levels of mosquito feeding compared to adding chlorfenapyr IRS (28% vs. 37%, p = 0.015).
CONCLUSIONS
Adding non-pyrethroid IRS to standard pyrethroid-only LLINs against a pyrethroid-resistant vector population which is susceptible to the IRS insecticide, can provide higher levels of vector mosquito control compared to the pyrethroid net alone or IRS alone. Adding pirimiphos-methyl CS IRS may provide substantial improvements in vector control while adding chlorfenapyr IRS can demonstrate an additive effect relative to both interventions alone. Adding bendiocarb IRS may show limited enhancements in vector control owing to its short residual effect.

Identifiants

pubmed: 33507978
doi: 10.1371/journal.pone.0245804
pii: PONE-D-20-32956
pmc: PMC7842967
doi:

Substances chimiques

Insecticides 0
Pyrethrins 0

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0245804

Subventions

Organisme : Medical Research Council
ID : MR/L004437/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R006040/1
Pays : United Kingdom

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Thomas Syme (T)

London School of Hygiene and Tropical Medicine (LSHTM), London, United Kingdom.
Centre de Recherches Entomologiques de Cotonou (CREC), Benin, West Africa.
Panafrican Malaria Vector Research Consortium (PAMVERC), Benin, West Africa.

Augustin Fongnikin (A)

Centre de Recherches Entomologiques de Cotonou (CREC), Benin, West Africa.
Panafrican Malaria Vector Research Consortium (PAMVERC), Benin, West Africa.

Damien Todjinou (D)

Centre de Recherches Entomologiques de Cotonou (CREC), Benin, West Africa.
Panafrican Malaria Vector Research Consortium (PAMVERC), Benin, West Africa.

Renaud Govoetchan (R)

London School of Hygiene and Tropical Medicine (LSHTM), London, United Kingdom.
Centre de Recherches Entomologiques de Cotonou (CREC), Benin, West Africa.
Panafrican Malaria Vector Research Consortium (PAMVERC), Benin, West Africa.

Martial Gbegbo (M)

Centre de Recherches Entomologiques de Cotonou (CREC), Benin, West Africa.
Panafrican Malaria Vector Research Consortium (PAMVERC), Benin, West Africa.

Mark Rowland (M)

London School of Hygiene and Tropical Medicine (LSHTM), London, United Kingdom.
Panafrican Malaria Vector Research Consortium (PAMVERC), Benin, West Africa.

Martin Akogbeto (M)

Centre de Recherches Entomologiques de Cotonou (CREC), Benin, West Africa.
Panafrican Malaria Vector Research Consortium (PAMVERC), Benin, West Africa.

Corine Ngufor (C)

London School of Hygiene and Tropical Medicine (LSHTM), London, United Kingdom.
Centre de Recherches Entomologiques de Cotonou (CREC), Benin, West Africa.
Panafrican Malaria Vector Research Consortium (PAMVERC), Benin, West Africa.

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