Natural Variation in Physicochemical Profiles and Bacterial Communities Associated with Aedes aegypti Breeding Sites and Larvae on Guadeloupe and French Guiana.


Journal

Microbial ecology
ISSN: 1432-184X
Titre abrégé: Microb Ecol
Pays: United States
ID NLM: 7500663

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 28 02 2020
accepted: 15 06 2020
pubmed: 6 7 2020
medline: 17 7 2021
entrez: 5 7 2020
Statut: ppublish

Résumé

Aedes aegypti develop in aquatic habitats in which mosquito larvae are exposed to physicochemical elements and microorganisms that may influence their life cycle and their ability to transmit arboviruses. Little is known about the natural bacterial communities associated with A. aegypti or their relation to the biotic and abiotic characteristics of their aquatic habitats. We characterized the physicochemical properties and bacterial microbiota of A. aegypti breeding sites and larvae on Guadeloupe and in French Guiana. In addition, we explored whether geographic location, the type of breeding site and physicochemical parameters influenced the microbiota associated with this mosquito species. We used large-scale 16S rRNA gene sequencing of 160 breeding sites and 147 pools of A. aegypti larvae and recorded 12 physicochemical parameters at the sampled breeding sites. Ordination plots and multiple linear regression were used to assess the influence of environmental factors on the bacterial microbiota of water and larvae. We found territory-specific differences in physicochemical properties (dissolved oxygen, conductivity) and the composition of bacterial communities in A. aegypti breeding sites that influenced the relative abundance of several bacteria genera (e.g., Methylobacterium, Roseoccocus) on the corresponding larvae. A significant fraction of the bacterial communities identified on larvae, dominated by Herbiconiux and Microvirga genera, were consistently enriched in mosquitoes regardless the location. In conclusion, territory-specific differences observed in the biotic and abiotic properties of A. aegypti breeding sites raise concern about the impact of these changes on pathogen transmission by different A. aegypti populations.

Identifiants

pubmed: 32621210
doi: 10.1007/s00248-020-01544-3
pii: 10.1007/s00248-020-01544-3
pmc: PMC7794107
doi:

Substances chimiques

RNA, Ribosomal, 16S 0
Water 059QF0KO0R

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

93-109

Subventions

Organisme : Action Concertées Inter Pasteuriennes
ID : Grant ACIP 01-2016
Organisme : Programme Opérationnel FEDER-Guadeloupe-Conseil Régional 2014-2020
ID : grant 2015-FED-192
Organisme : Calmette & Yersin
ID : Stage-2018
Organisme : La Région Guadeloupe
ID : 2017-2020

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Auteurs

Lyza Hery (L)

Laboratory of Vector Control Research, Transmission Reservoir and Pathogens Diversity Unit, Institut Pasteur of Guadeloupe, Morne Jolivière, Guadeloupe, France.

Amandine Guidez (A)

Vector Control and Adaptation Unit, Cayenne, Institut Pasteur of French Guiana, Vectopôle Amazonien Emile Abonnenc, Cayenne, French Guiana, France.

Audrey-Anne Durand (AA)

INRS-Centre Armand-Frappier Santé Biotechnologie, Laval, Québec, Canada.

Christelle Delannay (C)

Laboratory of Vector Control Research, Transmission Reservoir and Pathogens Diversity Unit, Institut Pasteur of Guadeloupe, Morne Jolivière, Guadeloupe, France.

Josiann Normandeau-Guimond (J)

INRS-Centre Armand-Frappier Santé Biotechnologie, Laval, Québec, Canada.

Yann Reynaud (Y)

Laboratory of Vector Control Research, Transmission Reservoir and Pathogens Diversity Unit, Institut Pasteur of Guadeloupe, Morne Jolivière, Guadeloupe, France.

Jean Issaly (J)

Vector Control and Adaptation Unit, Cayenne, Institut Pasteur of French Guiana, Vectopôle Amazonien Emile Abonnenc, Cayenne, French Guiana, France.

Daniella Goindin (D)

Laboratory of Vector Control Research, Transmission Reservoir and Pathogens Diversity Unit, Institut Pasteur of Guadeloupe, Morne Jolivière, Guadeloupe, France.

Grégory Legrave (G)

Laboratory of Environment and Food Hygiene, Institut Pasteur of Guadeloupe, Morne Jolivière, Guadeloupe, France.

Joel Gustave (J)

Regional Health Agency of Guadeloupe, Gourbeyre, Guadeloupe, France.

Stéphanie Raffestin (S)

Laboratory of Environment and Hygiene, Institut Pasteur of French Guiana, Cayenne, French Guiana, France.

Sebastien Breurec (S)

Transmission, Reservoir and Diversity of Pathogens Unit, Institut Pasteur of Guadeloupe, Pointe-à-Pitre, France.
Hyacinthe Bastaraud Faculty of Medicine, University of Antilles, Pointe-à-Pitre, France.
INSERM Centre for Clinical Investigation 1424, Pointe-à-Pitre, Les Abymes, France.

Philippe Constant (P)

INRS-Centre Armand-Frappier Santé Biotechnologie, Laval, Québec, Canada.

Isabelle Dusfour (I)

Vector Control and Adaptation Unit, Cayenne, Institut Pasteur of French Guiana, Vectopôle Amazonien Emile Abonnenc, Cayenne, French Guiana, France.

Claude Guertin (C)

INRS-Centre Armand-Frappier Santé Biotechnologie, Laval, Québec, Canada.

Anubis Vega-Rúa (A)

Laboratory of Vector Control Research, Transmission Reservoir and Pathogens Diversity Unit, Institut Pasteur of Guadeloupe, Morne Jolivière, Guadeloupe, France. avega@pasteur.fr.

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