Geographic distribution of the V1016G knockdown resistance mutation in Aedes albopictus: a warning bell for Europe.

Aedes albopictus Arbovirus vector Europe Insecticide resistance Integrated vector management Kdr Mosquito Vector control

Journal

Parasites & vectors
ISSN: 1756-3305
Titre abrégé: Parasit Vectors
Pays: England
ID NLM: 101462774

Informations de publication

Date de publication:
05 Aug 2022
Historique:
received: 18 03 2022
accepted: 14 07 2022
entrez: 5 8 2022
pubmed: 6 8 2022
medline: 10 8 2022
Statut: epublish

Résumé

Colonization of large part of Europe by the Asian tiger mosquito Aedes albopictus is causing autochthonous transmission of chikungunya and dengue exotic arboviruses. While pyrethroids are recommended only to reduce/limit transmission, they are widely implemented to reduce biting nuisance and to control agricultural pests, increasing the risk of insurgence of resistance mechanisms. Worryingly, pyrethroid resistance (with mortality < 70%) was recently reported in Ae. albopictus populations from Italy and Spain and associated with the V1016G point mutation in the voltage-sensitive sodium channel gene conferring knockdown resistance (kdr). Genotyping pyrethroid resistance-associated kdr mutations in field mosquito samples represents a powerful approach to detect early signs of resistance without the need for carrying out phenotypic bioassays which require availability of live mosquitoes, dedicated facilities and appropriate expertise. Here we report results on the PCR-genotyping of the V1016G mutation in 2530 Ae. albopictus specimens from 69 sampling sites in 19 European countries. The mutation was identified in 12 sites from nine countries (with allele frequencies ranging from 1 to 8%), mostly distributed in two geographical clusters. The western cluster includes Mediterranean coastal sites from Italy, France and Malta as well as single sites from both Spain and Switzerland. The eastern cluster includes sites on both sides of the Black Sea in Bulgaria, Turkey and Georgia as well as one site from Romania. These results are consistent with genomic data showing high connectivity and close genetic relationship among West European populations and a major barrier to gene flow between West European and Balkan populations. The results of this first effort to map kdr mutations in Ae. albopictus on a continental scale show a widespread presence of the V1016G allele in Europe, although at lower frequencies than those previously reported from Italy. This represents a wake-up call for mosquito surveillance programs in Europe to include PCR-genotyping of pyrethroid resistance alleles, as well as phenotypic resistance assessments, in their routine activities.

Sections du résumé

BACKGROUND BACKGROUND
Colonization of large part of Europe by the Asian tiger mosquito Aedes albopictus is causing autochthonous transmission of chikungunya and dengue exotic arboviruses. While pyrethroids are recommended only to reduce/limit transmission, they are widely implemented to reduce biting nuisance and to control agricultural pests, increasing the risk of insurgence of resistance mechanisms. Worryingly, pyrethroid resistance (with mortality < 70%) was recently reported in Ae. albopictus populations from Italy and Spain and associated with the V1016G point mutation in the voltage-sensitive sodium channel gene conferring knockdown resistance (kdr). Genotyping pyrethroid resistance-associated kdr mutations in field mosquito samples represents a powerful approach to detect early signs of resistance without the need for carrying out phenotypic bioassays which require availability of live mosquitoes, dedicated facilities and appropriate expertise.
METHODS METHODS
Here we report results on the PCR-genotyping of the V1016G mutation in 2530 Ae. albopictus specimens from 69 sampling sites in 19 European countries.
RESULTS RESULTS
The mutation was identified in 12 sites from nine countries (with allele frequencies ranging from 1 to 8%), mostly distributed in two geographical clusters. The western cluster includes Mediterranean coastal sites from Italy, France and Malta as well as single sites from both Spain and Switzerland. The eastern cluster includes sites on both sides of the Black Sea in Bulgaria, Turkey and Georgia as well as one site from Romania. These results are consistent with genomic data showing high connectivity and close genetic relationship among West European populations and a major barrier to gene flow between West European and Balkan populations.
CONCLUSIONS CONCLUSIONS
The results of this first effort to map kdr mutations in Ae. albopictus on a continental scale show a widespread presence of the V1016G allele in Europe, although at lower frequencies than those previously reported from Italy. This represents a wake-up call for mosquito surveillance programs in Europe to include PCR-genotyping of pyrethroid resistance alleles, as well as phenotypic resistance assessments, in their routine activities.

Identifiants

pubmed: 35932088
doi: 10.1186/s13071-022-05407-3
pii: 10.1186/s13071-022-05407-3
pmc: PMC9356396
doi:

Substances chimiques

Insecticides 0
Pyrethrins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

280

Subventions

Organisme : Junta de Extremadura
ID : IB16135
Organisme : EU Environmental Funding Programme LIFE+ Greek Environment Policy and Governance
ID : LIFE12 ENV/GR/000466
Organisme : Fundacao para a Ciencia e a Tecnologia
ID : UIDP/50017/2020 + UIDB/50017/2020 + LA/P/0094/2020
Organisme : Fundação para a Ciência e a Tecnologia
ID : PTDC/BIA-OUT/29477/2017
Organisme : Ministero dell'Università e della Ricerca
ID : PRIN2020

Informations de copyright

© 2022. The Author(s).

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Auteurs

Verena Pichler (V)

Dipartimento di Sanità Pubblica & Malattie Infettive, Università di Roma Sapienza, Rome, Italy.

Beniamino Caputo (B)

Dipartimento di Sanità Pubblica & Malattie Infettive, Università di Roma Sapienza, Rome, Italy.

Vera Valadas (V)

Global Health and Tropical Medicine, Instituto De Higiene E Medicina Tropical, Universidade Nova De Lisboa, Lisbon, Portugal.

Martina Micocci (M)

Dipartimento di Sanità Pubblica & Malattie Infettive, Università di Roma Sapienza, Rome, Italy.

Cintia Horvath (C)

University of Agricultural Sciences and Veterinary Medicine, Cluj-Napoca, Romania.

Chiara Virgillito (C)

Dipartimento di Sanità Pubblica & Malattie Infettive, Università di Roma Sapienza, Rome, Italy.

Mustafa Akiner (M)

Recep Tayyip Erdoğan Üniversitesi, Rize, Turkey.

Georgios Balatsos (G)

Laboratory of Insects & Parasites of Medical Importance, Benaki Phytopathological Institute, Kifisia, Greece.

Christelle Bender (C)

Syndicat de Lutte Contre Les Moustiques du Bas-Rhin, Strasbourg, France.

Gilles Besnard (G)

Entente Interdépartementale Rhône-Alpes pour la Démoustication, Chindrieux, France.

Daniel Bravo-Barriga (D)

Animal Health Department, Veterinary Faculty, University of Extremadura (UEx), Cáceres, Spain.

Rubén Bueno-Mari (R)

Lokimica Laboratorios, Valencia, Spain.

Francisco Collantes (F)

University of Murcia, Murcia, Spain.

Sarah Delacour-Estrella (S)

University of Zaragoza, Saragossa, Spain.

Enkelejda Dikolli (E)

Institute of Public Health, Tiranë, Albania.

Elena Falcuta (E)

Cantacuzino, National Military-Medical Institute of Research and Development, Bucharest, Romania.

Eleonora Flacio (E)

University of Applied Sciences of Southern Switzerland, Manno, Switzerland.

Ana L García-Pérez (AL)

Neiker-Basque Institute for Agricultural Research and Development, Derio, Spain.

Katja Kalan (K)

University of Primorska, Koper, Slovenia.

Mihaela Kavran (M)

University of Novi Sad, Novi Sad, Serbia.

Gregory L'Ambert (G)

Entente Interdépartementale Rhône-Alpes pour la Démoustication, Chindrieux, France.

Riccardo P Lia (RP)

Università degli Studi di Bari Aldo Moro, Bari, Italy.

Eduardo Marabuto (E)

Museum of Zoology, Senckenberg Natural History Collections Dresden, Dresden, Germany.

Raquel Medialdea (R)

Ministry for Health of Malta, Valetta, Malta.

Rosario Melero-Alcibar (R)

Facultad de Ciencias Biológicas, Universidad Complutense de Madrid, Madrid, Spain.

Antonios Michaelakis (A)

Laboratory of Insects & Parasites of Medical Importance, Benaki Phytopathological Institute, Kifisia, Greece.

Andrei Mihalca (A)

University of Agricultural Sciences and Veterinary Medicine, Cluj-Napoca, Romania.

Ognyan Mikov (O)

National Centre of Infectious and Parasitic Diseases, Sofia, Bulgaria.

Miguel A Miranda (MA)

Applied Zoology and Animal Conservation, University of the Balearic Islands, Palma, Spain.

Pie Müller (P)

Swiss Tropical and Public Health Institute, Allschwil, Switzerland.
University of Basel, Basel, Switzerland.

Domenico Otranto (D)

Università degli Studi di Bari Aldo Moro, Bari, Italy.

Igor Pajovic (I)

University of Montenegro, Podgorica, Montenegro.

Dusan Petric (D)

University of Novi Sad, Novi Sad, Serbia.

Maria Teresa Rebelo (MT)

CESAM-Ciências, Faculdade de Ciências da Universidade de Lisboa, , Lisbon, Portugal.

Vincent Robert (V)

Mivegec Laboratory, Institut de Recherche pour le Développement, Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, France.

Elton Rogozi (E)

Institute of Public Health, Tiranë, Albania.

Ana Tello (A)

Facultad de Ciencias Biológicas, Universidad Complutense de Madrid, Madrid, Spain.

Toni Zitko (T)

Institute of Public Health of Split-Dalmatia County, Split, Croatia.

Francis Schaffner (F)

Francis Schaffner Consultancy, Riehen, Switzerland.

Joao Pinto (J)

Global Health and Tropical Medicine, Instituto De Higiene E Medicina Tropical, Universidade Nova De Lisboa, Lisbon, Portugal.

Alessandra Della Torre (A)

Dipartimento di Sanità Pubblica & Malattie Infettive, Università di Roma Sapienza, Rome, Italy. alessandra.dellatorre@uniroma1.it.

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