Oral susceptibility to ivermectin is over fifty times greater in a wild population of Anopheles albimanus mosquitoes from Belize than the STECLA laboratory reference strain of this mosquito.


Journal

Malaria journal
ISSN: 1475-2875
Titre abrégé: Malar J
Pays: England
ID NLM: 101139802

Informations de publication

Date de publication:
04 Mar 2022
Historique:
received: 26 10 2021
accepted: 16 02 2022
entrez: 5 3 2022
pubmed: 6 3 2022
medline: 9 3 2022
Statut: epublish

Résumé

The STECLA strain of Anopheles albimanus has been in continuous colony for many years and is the reference strain on which genomic studies for the species are based. Recently, the STECLA strain was demonstrated to be much less susceptible to ivermectin ingested in a blood meal (4-day LC To investigate this, host-seeking An. albimanus were captured in northern Belize and used in membrane feeding bioassays of ivermectin, employing the same methods as described earlier with the STECLA strain. Field-collected An. albimanus in Belize were 55 times more susceptible to ingested ivermectin than were the STECLA reference strain. Oral susceptibility to ivermectin in wild An. albimanus from Belize (4-day LC Contrary to initial assessments using a highly inbred strain of mosquito, laboratory studies using a field population indicate that ivermectin treatment of livestock could reduce An. albimanus populations in areas of Central America and the Caribbean where malaria transmission may occur. Toxicity screening of ivermectin and other systemic parasiticides for malaria control should examine wild populations of the vector species being targeted.

Sections du résumé

BACKGROUND BACKGROUND
The STECLA strain of Anopheles albimanus has been in continuous colony for many years and is the reference strain on which genomic studies for the species are based. Recently, the STECLA strain was demonstrated to be much less susceptible to ivermectin ingested in a blood meal (4-day LC
METHODS METHODS
To investigate this, host-seeking An. albimanus were captured in northern Belize and used in membrane feeding bioassays of ivermectin, employing the same methods as described earlier with the STECLA strain.
RESULTS RESULTS
Field-collected An. albimanus in Belize were 55 times more susceptible to ingested ivermectin than were the STECLA reference strain. Oral susceptibility to ivermectin in wild An. albimanus from Belize (4-day LC
CONCLUSIONS CONCLUSIONS
Contrary to initial assessments using a highly inbred strain of mosquito, laboratory studies using a field population indicate that ivermectin treatment of livestock could reduce An. albimanus populations in areas of Central America and the Caribbean where malaria transmission may occur. Toxicity screening of ivermectin and other systemic parasiticides for malaria control should examine wild populations of the vector species being targeted.

Identifiants

pubmed: 35246147
doi: 10.1186/s12936-022-04092-y
pii: 10.1186/s12936-022-04092-y
pmc: PMC8896111
doi:

Substances chimiques

Ivermectin 70288-86-7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

72

Subventions

Organisme : NIAID NIH HHS
ID : R21 AI119771
Pays : United States
Organisme : National Institute of Allergy and Infectious Diseases
ID : R21AI119771

Informations de copyright

© 2022. The Author(s).

Références

J Am Mosq Control Assoc. 1990 Mar;6(1):7-34
pubmed: 2324726
Am J Trop Med Hyg. 2011 Jul;85(1):3-5
pubmed: 21734116
Malar J. 2010 Dec 20;9:365
pubmed: 21171970
Malar J. 2014 Nov 03;13:417
pubmed: 25363349
Malar J. 2019 Aug 29;18(1):296
pubmed: 31464619
Acta Trop. 2010 Nov;116(2):119-26
pubmed: 20540931
Malar J. 2017 Nov 21;16(1):474
pubmed: 29162101
G3 (Bethesda). 2017 Jan 5;7(1):155-164
pubmed: 27821634
Malar J. 2017 Jun 6;16(1):239
pubmed: 28587669
Vet Parasitol. 2004 Jan 30;119(2-3):247-57
pubmed: 14746983
Malar J. 2017 Jul 7;16(1):280
pubmed: 28687086
J Med Entomol. 2012 Mar;49(2):326-31
pubmed: 22493850
J Vet Pharmacol Ther. 1997 Apr;20(2):91-9
pubmed: 9131534
Ann Trop Med Parasitol. 2009 Sep;103(6):539-47
pubmed: 19695159
J Infect Dis. 2010 Jul 1;202(1):113-6
pubmed: 20482251
Malar J. 2016 Sep 22;15(1):491
pubmed: 27660149
Malar J. 2018 Apr 3;17(1):148
pubmed: 29615055
Am J Trop Med Hyg. 2020 Feb;102(2s):3-24
pubmed: 31971144
Vet Parasitol. 2005 Mar 10;128(1-2):169-73
pubmed: 15725548
Malar J. 2015 Sep 17;14:351
pubmed: 26377691
Parasit Vectors. 2018 May 4;11(1):287
pubmed: 29728135

Auteurs

Staci M Dreyer (SM)

University of North Dakota, Grand Forks, ND, 58202, USA.

Kelsey J Morin (KJ)

University of North Dakota, Grand Forks, ND, 58202, USA.

Marla Magaña (M)

Belize Vector and Ecology Center, Orange Walk Town, Belize.

Marie Pott (M)

Belize Vector and Ecology Center, Orange Walk Town, Belize.

Donovan Leiva (D)

Belize Vector and Ecology Center, Orange Walk Town, Belize.

Nicole L Achee (NL)

Belize Vector and Ecology Center, Orange Walk Town, Belize.
University of Notre Dame, South Bend, IN, 46556, USA.

John P Grieco (JP)

Belize Vector and Ecology Center, Orange Walk Town, Belize.
University of Notre Dame, South Bend, IN, 46556, USA.

Jefferson A Vaughan (JA)

University of North Dakota, Grand Forks, ND, 58202, USA. jefferson.vaughan@und.edu.

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Classifications MeSH