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Knockdown resistance mutations are common and widely distributed in Xenopsylla cheopis fleas that transmit plague in Madagascar

BACKGROUND: Plague, caused by the bacterium Yersinia pestis, remains an important disease in Madagascar, where the oriental rat flea, Xenopsylla cheopis, is a primary vector. To control fleas, synthetic pyrethroids (SPs) have been used for >20 years, resulting in resistance in many X. cheopis pop...

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Autores principales: Hutton, Shelby M., Miarinjara, Adelaide, Stone, Nathan E., Raharimalala, Fara N., Raveloson, Annick O., Rakotobe Harimanana, Ravo, Harimalala, Mireille, Rahelinirina, Soanandrasana, McDonough, Ryelan F., Ames, Abbe D., Hepp, Crystal, Rajerison, Minoarisoa, Busch, Joseph D., Wagner, David M., Girod, Romain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443838/
https://www.ncbi.nlm.nih.gov/pubmed/37607174
http://dx.doi.org/10.1371/journal.pntd.0011401
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author Hutton, Shelby M.
Miarinjara, Adelaide
Stone, Nathan E.
Raharimalala, Fara N.
Raveloson, Annick O.
Rakotobe Harimanana, Ravo
Harimalala, Mireille
Rahelinirina, Soanandrasana
McDonough, Ryelan F.
Ames, Abbe D.
Hepp, Crystal
Rajerison, Minoarisoa
Busch, Joseph D.
Wagner, David M.
Girod, Romain
author_facet Hutton, Shelby M.
Miarinjara, Adelaide
Stone, Nathan E.
Raharimalala, Fara N.
Raveloson, Annick O.
Rakotobe Harimanana, Ravo
Harimalala, Mireille
Rahelinirina, Soanandrasana
McDonough, Ryelan F.
Ames, Abbe D.
Hepp, Crystal
Rajerison, Minoarisoa
Busch, Joseph D.
Wagner, David M.
Girod, Romain
author_sort Hutton, Shelby M.
collection PubMed
description BACKGROUND: Plague, caused by the bacterium Yersinia pestis, remains an important disease in Madagascar, where the oriental rat flea, Xenopsylla cheopis, is a primary vector. To control fleas, synthetic pyrethroids (SPs) have been used for >20 years, resulting in resistance in many X. cheopis populations. The most common mechanisms of SP resistance are target site mutations in the voltage-gated sodium channel (VGSC) gene. METHODOLOGY/PRINCIPAL FINDINGS: We obtained 25 collections of X. cheopis from 22 locations across Madagascar and performed phenotypic tests to determine resistance to deltamethrin, permethrin, and/or dichlorodiphenyltrichloroethane (DDT). Most populations were resistant to all these insecticides. We sequenced a 535 bp segment of the VGSC gene and identified two different mutations encoding distinct substitutions at amino acid position 1014, which is associated with knockdown resistance (kdr) to SPs in insects. Kdr mutation L1014F occurred in all 25 collections; a rarer mutation, L1014H, was found in 12 collections. There was a significant positive relationship between the frequency of kdr alleles and the proportion of individuals surviving exposure to deltamethrin. Phylogenetic comparisons of 12 VGSC alleles in Madagascar suggested resistant alleles arose from susceptible lineages at least three times. Because genotype can reasonably predict resistance phenotype, we developed a TaqMan PCR assay for the rapid detection of kdr resistance alleles. CONCLUSIONS/SIGNIFICANCE: Our study provides new insights into VGSC mutations in Malagasy populations of X. cheopis and is the first to report a positive correlation between VGSC genotypes and SP resistance phenotypes in fleas. Widespread occurrence of these two SP resistance mutations in X. cheopis populations in Madagascar reduces the viability of these insecticides for flea control. However, the TaqMan assay described here facilitates rapid detection of kdr mutations to inform when use of these insecticides is still warranted to reduce transmission of plague.
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spelling pubmed-104438382023-08-23 Knockdown resistance mutations are common and widely distributed in Xenopsylla cheopis fleas that transmit plague in Madagascar Hutton, Shelby M. Miarinjara, Adelaide Stone, Nathan E. Raharimalala, Fara N. Raveloson, Annick O. Rakotobe Harimanana, Ravo Harimalala, Mireille Rahelinirina, Soanandrasana McDonough, Ryelan F. Ames, Abbe D. Hepp, Crystal Rajerison, Minoarisoa Busch, Joseph D. Wagner, David M. Girod, Romain PLoS Negl Trop Dis Research Article BACKGROUND: Plague, caused by the bacterium Yersinia pestis, remains an important disease in Madagascar, where the oriental rat flea, Xenopsylla cheopis, is a primary vector. To control fleas, synthetic pyrethroids (SPs) have been used for >20 years, resulting in resistance in many X. cheopis populations. The most common mechanisms of SP resistance are target site mutations in the voltage-gated sodium channel (VGSC) gene. METHODOLOGY/PRINCIPAL FINDINGS: We obtained 25 collections of X. cheopis from 22 locations across Madagascar and performed phenotypic tests to determine resistance to deltamethrin, permethrin, and/or dichlorodiphenyltrichloroethane (DDT). Most populations were resistant to all these insecticides. We sequenced a 535 bp segment of the VGSC gene and identified two different mutations encoding distinct substitutions at amino acid position 1014, which is associated with knockdown resistance (kdr) to SPs in insects. Kdr mutation L1014F occurred in all 25 collections; a rarer mutation, L1014H, was found in 12 collections. There was a significant positive relationship between the frequency of kdr alleles and the proportion of individuals surviving exposure to deltamethrin. Phylogenetic comparisons of 12 VGSC alleles in Madagascar suggested resistant alleles arose from susceptible lineages at least three times. Because genotype can reasonably predict resistance phenotype, we developed a TaqMan PCR assay for the rapid detection of kdr resistance alleles. CONCLUSIONS/SIGNIFICANCE: Our study provides new insights into VGSC mutations in Malagasy populations of X. cheopis and is the first to report a positive correlation between VGSC genotypes and SP resistance phenotypes in fleas. Widespread occurrence of these two SP resistance mutations in X. cheopis populations in Madagascar reduces the viability of these insecticides for flea control. However, the TaqMan assay described here facilitates rapid detection of kdr mutations to inform when use of these insecticides is still warranted to reduce transmission of plague. Public Library of Science 2023-08-22 /pmc/articles/PMC10443838/ /pubmed/37607174 http://dx.doi.org/10.1371/journal.pntd.0011401 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Hutton, Shelby M.
Miarinjara, Adelaide
Stone, Nathan E.
Raharimalala, Fara N.
Raveloson, Annick O.
Rakotobe Harimanana, Ravo
Harimalala, Mireille
Rahelinirina, Soanandrasana
McDonough, Ryelan F.
Ames, Abbe D.
Hepp, Crystal
Rajerison, Minoarisoa
Busch, Joseph D.
Wagner, David M.
Girod, Romain
Knockdown resistance mutations are common and widely distributed in Xenopsylla cheopis fleas that transmit plague in Madagascar
title Knockdown resistance mutations are common and widely distributed in Xenopsylla cheopis fleas that transmit plague in Madagascar
title_full Knockdown resistance mutations are common and widely distributed in Xenopsylla cheopis fleas that transmit plague in Madagascar
title_fullStr Knockdown resistance mutations are common and widely distributed in Xenopsylla cheopis fleas that transmit plague in Madagascar
title_full_unstemmed Knockdown resistance mutations are common and widely distributed in Xenopsylla cheopis fleas that transmit plague in Madagascar
title_short Knockdown resistance mutations are common and widely distributed in Xenopsylla cheopis fleas that transmit plague in Madagascar
title_sort knockdown resistance mutations are common and widely distributed in xenopsylla cheopis fleas that transmit plague in madagascar
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443838/
https://www.ncbi.nlm.nih.gov/pubmed/37607174
http://dx.doi.org/10.1371/journal.pntd.0011401
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