Contrasting patterns of gene expression indicate differing pyrethroid resistance mechanisms across the range of the New World malaria vector Anopheles albimanus.


Journal

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

Informations de publication

Date de publication:
2019
Historique:
received: 22 10 2018
accepted: 25 12 2018
entrez: 31 1 2019
pubmed: 31 1 2019
medline: 17 10 2019
Statut: epublish

Résumé

Decades of unmanaged insecticide use and routine exposure to agrochemicals have left many populations of malaria vectors in the Americas resistant to multiple classes of insecticides, including pyrethroids. The molecular basis of pyrethroid resistance is relatively uncharacterised in American malaria vectors, preventing the design of suitable resistance management strategies. Using whole transcriptome sequencing, we characterized the mechanisms of pyrethroid resistance in Anopheles albimanus from Peru and Guatemala. An. albimanus were phenotyped as either deltamethrin or alpha-cypermethrin resistant. RNA from 1) resistant, 2) unexposed, and 3) a susceptible laboratory strain of An. albimanus was sequenced and analyzed using RNA-Seq. Expression profiles of the three groups were compared based on the current annotation of the An. albimanus reference genome. Several candidate genes associated with pyrethroid resistance in other malaria vectors were found to be overexpressed in resistant An. albimanus. In addition, gene ontology terms related to serine-type endopeptidase activity, extracellular activity and chitin metabolic process were also commonly overexpressed in the field caught resistant and unexposed samples from both Peru and Guatemala when compared to the susceptible strain. The cytochrome P450 CYP9K1 was overexpressed 14x in deltamethrin and 8x in alpha-cypermethrin-resistant samples from Peru and 2x in deltamethrin-resistant samples from Guatemala, relative to the susceptible laboratory strain. CYP6P5 was overexpressed 68x in deltamethrin-resistant samples from Peru but not in deltamethrin-resistant samples from Guatemala. When comparing overexpressed genes between deltamethrin-resistant and alpha-cypermethrin-resistant samples from Peru, a single P450 gene, CYP4C26, was overexpressed 9.8x (p<0.05) in alpha-cypermethrin-resistant samples. In Peruvian deltamethrin-resistant samples, the knockdown resistance mutation (kdr) variant alleles at position 1014 were rare, with approximately 5% frequency, but in the alpha-cypermethrin-resistant samples, the frequency of these alleles was approximately 15-30%. Functional validation of the candidate genes and the kdr mutation as a resistance marker for alpha-cypermethrin will confirm the role of these mechanisms in conferring pyrethroid resistance.

Identifiants

pubmed: 30699158
doi: 10.1371/journal.pone.0210586
pii: PONE-D-18-30552
pmc: PMC6353143
doi:

Substances chimiques

Codon 0
Nitriles 0
Pyrethrins 0
cypermethrin 1TR49121NP
decamethrin 2JTS8R821G
Electron Transport Complex IV EC 1.9.3.1

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0210586

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Lucy Mackenzie-Impoinvil (L)

Entomology Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Gareth D Weedall (GD)

Vector Biology Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
School of Natural Sciences and Psychology, Liverpool John Moores University, Liverpool, United Kingdom.

Juan C Lol (JC)

Centro de Estudios en Salud, Universidad del Valle de Guatemala, Guatemala.

Jesús Pinto (J)

Instituto Nacional de Salud Lima, Lima, Peru.

Lucrecia Vizcaino (L)

Entomology Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Nicole Dzuris (N)

Entomology Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Jacob Riveron (J)

Vector Biology Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Centre for Research in Infectious Diseases (CRID), Yaoundé, Cameroon.

Norma Padilla (N)

Centro de Estudios en Salud, Universidad del Valle de Guatemala, Guatemala.

Charles Wondji (C)

Vector Biology Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Centre for Research in Infectious Diseases (CRID), Yaoundé, Cameroon.

Audrey Lenhart (A)

Entomology Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

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