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Linked-read sequencing identifies abundant microinversions and introgression in the arboviral vector Aedes aegypti

Abstract:
AbstractBackgroundAedes aegyptiis the principal mosquito vector of Zika, dengue, and yellow fever viruses. Two subspecies ofAe. aegyptiexhibit phenotypic divergence with regard to habitat, host preference, and vectorial capacity. Chromosomal inversions have been shown to play a major role in adaptation and speciation in dipteran insects and would be of great utility for studies ofAe. aegypti.However, the large and highly repetitive genome ofAe. aegyptimakes it difficult to detect inversions with paired-end short-read sequencing data, and polytene chromosome analysis does not provide sufficient resolution to detect chromosome banding patterns indicative of inversions.ResultsTo characterize chromosomal diversity in this species, we have carried out deep Illumina sequencing of linked-read (10X Genomics) libraries in order to discover inversion loci as well as SNPs. We analyzed individuals from colonies representing the geographic limits of each subspecies, one contact zone between subspecies, and a closely related sister species. Despite genome-wide SNP divergence and abundant microinversions, we do not find any inversions occurring as fixed differences between subspecies. Many microinversions are found in regions that have introgressed and have captured genes that could impact behavior, such as a cluster of odorant-binding proteins that may play a role in host feeding preference.ConclusionsOur study shows that inversions are abundant and widely shared among subspecies ofAedes aegyptiand that introgression has occurred in regions of secondary contact. This library of 32 novel chromosomal inversions demonstrates the capacity for linked-read sequencing to identify previously intractable genomic rearrangements and provides a foundation for future population genetics studies in this species.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1186/s12915-020-0757-y

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-2653-760X
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Role:
Author
ORCID:
0000-0001-6299-7553
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Role:
Author
ORCID:
0000-0003-0752-3747
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Role:
Author
ORCID:
0000-0003-4227-3819
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Role:
Author
ORCID:
0000-0002-5790-3548


Publisher:
BioMed Central
Journal:
BMC Biology More from this journal
Volume:
18
Issue:
1
Pages:
26-26
Publication date:
2020-03-12
DOI:
EISSN:
1741-7007
ISSN:
1741-7007


Language:
English
Keywords:
Pubs id:
2410290
Local pid:
pubs:2410290
Source identifiers:
W3012376314
Deposit date:
2026-04-23
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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