Cargando…
Genomic Shifts, Phenotypic Clines, and Fitness Costs Associated With Cold Tolerance in the Asian Tiger Mosquito
Climatic variation is a key driver of genetic differentiation and phenotypic traits evolution, and local adaptation to temperature is expected in widespread species. We investigated phenotypic and genomic changes in the native range of the Asian tiger mosquito, Aedes albopictus. We first refine the...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156037/ https://www.ncbi.nlm.nih.gov/pubmed/35574643 http://dx.doi.org/10.1093/molbev/msac104 |
_version_ | 1784718367416909824 |
---|---|
author | Sherpa, Stéphanie Tutagata, Jordan Gaude, Thierry Laporte, Frédéric Kasai, Shinji Ishak, Intan H. Guo, Xiang Shin, Jiyeong Boyer, Sébastien Marcombe, Sébastien Chareonviriyaphap, Theeraphap David, Jean-Philippe Chen, Xiao-Guang Zhou, Xiaohong Després, Laurence |
author_facet | Sherpa, Stéphanie Tutagata, Jordan Gaude, Thierry Laporte, Frédéric Kasai, Shinji Ishak, Intan H. Guo, Xiang Shin, Jiyeong Boyer, Sébastien Marcombe, Sébastien Chareonviriyaphap, Theeraphap David, Jean-Philippe Chen, Xiao-Guang Zhou, Xiaohong Després, Laurence |
author_sort | Sherpa, Stéphanie |
collection | PubMed |
description | Climatic variation is a key driver of genetic differentiation and phenotypic traits evolution, and local adaptation to temperature is expected in widespread species. We investigated phenotypic and genomic changes in the native range of the Asian tiger mosquito, Aedes albopictus. We first refine the phylogeographic structure based on genome-wide regions (1,901 double-digest restriction-site associated DNA single nucleotide polymophisms [ddRAD SNPs]) from 41 populations. We then explore the patterns of cold adaptation using phenotypic traits measured in common garden (wing size and cold tolerance) and genotype–temperature associations at targeted candidate regions (51,706 exon-capture SNPs) from nine populations. We confirm the existence of three evolutionary lineages including clades A (Malaysia, Thailand, Cambodia, and Laos), B (China and Okinawa), and C (South Korea and Japan). We identified temperature-associated differentiation in 15 out of 221 candidate regions but none in ddRAD regions, supporting the role of directional selection in detected genes. These include genes involved in lipid metabolism and a circadian clock gene. Most outlier SNPs are differently fixed between clades A and C, whereas clade B has an intermediate pattern. Females are larger at higher latitude yet produce no more eggs, which might favor the storage of energetic reserves in colder climate. Nondiapausing eggs from temperate populations survive better to cold exposure than those from tropical populations, suggesting they are protected from freezing damages but this cold tolerance has a fitness cost in terms of egg viability. Altogether, our results provide strong evidence for the thermal adaptation of A. albopictus across its wide temperature range. |
format | Online Article Text |
id | pubmed-9156037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91560372022-06-04 Genomic Shifts, Phenotypic Clines, and Fitness Costs Associated With Cold Tolerance in the Asian Tiger Mosquito Sherpa, Stéphanie Tutagata, Jordan Gaude, Thierry Laporte, Frédéric Kasai, Shinji Ishak, Intan H. Guo, Xiang Shin, Jiyeong Boyer, Sébastien Marcombe, Sébastien Chareonviriyaphap, Theeraphap David, Jean-Philippe Chen, Xiao-Guang Zhou, Xiaohong Després, Laurence Mol Biol Evol Discoveries Climatic variation is a key driver of genetic differentiation and phenotypic traits evolution, and local adaptation to temperature is expected in widespread species. We investigated phenotypic and genomic changes in the native range of the Asian tiger mosquito, Aedes albopictus. We first refine the phylogeographic structure based on genome-wide regions (1,901 double-digest restriction-site associated DNA single nucleotide polymophisms [ddRAD SNPs]) from 41 populations. We then explore the patterns of cold adaptation using phenotypic traits measured in common garden (wing size and cold tolerance) and genotype–temperature associations at targeted candidate regions (51,706 exon-capture SNPs) from nine populations. We confirm the existence of three evolutionary lineages including clades A (Malaysia, Thailand, Cambodia, and Laos), B (China and Okinawa), and C (South Korea and Japan). We identified temperature-associated differentiation in 15 out of 221 candidate regions but none in ddRAD regions, supporting the role of directional selection in detected genes. These include genes involved in lipid metabolism and a circadian clock gene. Most outlier SNPs are differently fixed between clades A and C, whereas clade B has an intermediate pattern. Females are larger at higher latitude yet produce no more eggs, which might favor the storage of energetic reserves in colder climate. Nondiapausing eggs from temperate populations survive better to cold exposure than those from tropical populations, suggesting they are protected from freezing damages but this cold tolerance has a fitness cost in terms of egg viability. Altogether, our results provide strong evidence for the thermal adaptation of A. albopictus across its wide temperature range. Oxford University Press 2022-05-16 /pmc/articles/PMC9156037/ /pubmed/35574643 http://dx.doi.org/10.1093/molbev/msac104 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Discoveries Sherpa, Stéphanie Tutagata, Jordan Gaude, Thierry Laporte, Frédéric Kasai, Shinji Ishak, Intan H. Guo, Xiang Shin, Jiyeong Boyer, Sébastien Marcombe, Sébastien Chareonviriyaphap, Theeraphap David, Jean-Philippe Chen, Xiao-Guang Zhou, Xiaohong Després, Laurence Genomic Shifts, Phenotypic Clines, and Fitness Costs Associated With Cold Tolerance in the Asian Tiger Mosquito |
title | Genomic Shifts, Phenotypic Clines, and Fitness Costs Associated With Cold Tolerance in the Asian Tiger Mosquito |
title_full | Genomic Shifts, Phenotypic Clines, and Fitness Costs Associated With Cold Tolerance in the Asian Tiger Mosquito |
title_fullStr | Genomic Shifts, Phenotypic Clines, and Fitness Costs Associated With Cold Tolerance in the Asian Tiger Mosquito |
title_full_unstemmed | Genomic Shifts, Phenotypic Clines, and Fitness Costs Associated With Cold Tolerance in the Asian Tiger Mosquito |
title_short | Genomic Shifts, Phenotypic Clines, and Fitness Costs Associated With Cold Tolerance in the Asian Tiger Mosquito |
title_sort | genomic shifts, phenotypic clines, and fitness costs associated with cold tolerance in the asian tiger mosquito |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156037/ https://www.ncbi.nlm.nih.gov/pubmed/35574643 http://dx.doi.org/10.1093/molbev/msac104 |
work_keys_str_mv | AT sherpastephanie genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT tutagatajordan genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT gaudethierry genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT laportefrederic genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT kasaishinji genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT ishakintanh genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT guoxiang genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT shinjiyeong genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT boyersebastien genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT marcombesebastien genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT chareonviriyaphaptheeraphap genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT davidjeanphilippe genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT chenxiaoguang genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT zhouxiaohong genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito AT despreslaurence genomicshiftsphenotypicclinesandfitnesscostsassociatedwithcoldtoleranceintheasiantigermosquito |