Adaptive Potential of Hybridization among Malaria Vectors: Introgression at the Immune Locus TEP1 between Anopheles coluzzii and A. gambiae in 'Far-West' Africa.

"Far-West" Africa is known to be a secondary contact zone between the two major malaria vectors Anopheles coluzzii and A. gambiae. We investigated gene-flow and potentially adaptive introgression between these species along a west-to-east transect in Guinea Bissau, the putative core of thi...

Full description

Bibliographic Details
Main Authors: Emiliano Mancini, Maria Ida Spinaci, Vasco Gordicho, Beniamino Caputo, Marco Pombi, José Luis Vicente, João Dinis, Amabélia Rodrigues, Vincenzo Petrarca, David Weetman, João Pinto, Alessandra Della Torre
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4457524?pdf=render
_version_ 1828483060314669056
author Emiliano Mancini
Maria Ida Spinaci
Vasco Gordicho
Beniamino Caputo
Marco Pombi
José Luis Vicente
João Dinis
Amabélia Rodrigues
Vincenzo Petrarca
David Weetman
João Pinto
Alessandra Della Torre
author_facet Emiliano Mancini
Maria Ida Spinaci
Vasco Gordicho
Beniamino Caputo
Marco Pombi
José Luis Vicente
João Dinis
Amabélia Rodrigues
Vincenzo Petrarca
David Weetman
João Pinto
Alessandra Della Torre
author_sort Emiliano Mancini
collection DOAJ
description "Far-West" Africa is known to be a secondary contact zone between the two major malaria vectors Anopheles coluzzii and A. gambiae. We investigated gene-flow and potentially adaptive introgression between these species along a west-to-east transect in Guinea Bissau, the putative core of this hybrid zone. To evaluate the extent and direction of gene flow, we genotyped site 702 in Intron-1 of the para Voltage-Gated Sodium Channel gene, a species-diagnostic nucleotide position throughout most of A. coluzzii and A. gambiae sympatric range. We also analyzed polymorphism in the thioester-binding domain (TED) of the innate immunity-linked thioester-containing protein 1 (TEP1) to investigate whether elevated hybridization might facilitate the exchange of variants linked to adaptive immunity and Plasmodium refractoriness. Our results confirm asymmetric introgression of genetic material from A. coluzzii to A. gambiae and disruption of linkage between the centromeric "genomic islands" of inter-specific divergence. We report that A. gambiae from the Guinean hybrid zone possesses an introgressed TEP1 resistant allelic class, found exclusively in A. coluzzii elsewhere and apparently swept to fixation in West Africa (i.e. Mali and Burkina Faso). However, no detectable fixation of this allele was found in Guinea Bissau, which may suggest that ecological pressures driving segregation between the two species in larval habitats in this region may be different from those experienced in northern and more arid parts of the species' range. Finally, our results also suggest a genetic subdivision between coastal and inland A. gambiae Guinean populations and provide clues on the importance of ecological factors in intra-specific differentiation processes.
first_indexed 2024-12-11T08:29:17Z
format Article
id doaj.art-d93e5c41274d4de19e8a021338a2ae42
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-11T08:29:17Z
publishDate 2015-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-d93e5c41274d4de19e8a021338a2ae422022-12-22T01:14:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01106e012780410.1371/journal.pone.0127804Adaptive Potential of Hybridization among Malaria Vectors: Introgression at the Immune Locus TEP1 between Anopheles coluzzii and A. gambiae in 'Far-West' Africa.Emiliano ManciniMaria Ida SpinaciVasco GordichoBeniamino CaputoMarco PombiJosé Luis VicenteJoão DinisAmabélia RodriguesVincenzo PetrarcaDavid WeetmanJoão PintoAlessandra Della Torre"Far-West" Africa is known to be a secondary contact zone between the two major malaria vectors Anopheles coluzzii and A. gambiae. We investigated gene-flow and potentially adaptive introgression between these species along a west-to-east transect in Guinea Bissau, the putative core of this hybrid zone. To evaluate the extent and direction of gene flow, we genotyped site 702 in Intron-1 of the para Voltage-Gated Sodium Channel gene, a species-diagnostic nucleotide position throughout most of A. coluzzii and A. gambiae sympatric range. We also analyzed polymorphism in the thioester-binding domain (TED) of the innate immunity-linked thioester-containing protein 1 (TEP1) to investigate whether elevated hybridization might facilitate the exchange of variants linked to adaptive immunity and Plasmodium refractoriness. Our results confirm asymmetric introgression of genetic material from A. coluzzii to A. gambiae and disruption of linkage between the centromeric "genomic islands" of inter-specific divergence. We report that A. gambiae from the Guinean hybrid zone possesses an introgressed TEP1 resistant allelic class, found exclusively in A. coluzzii elsewhere and apparently swept to fixation in West Africa (i.e. Mali and Burkina Faso). However, no detectable fixation of this allele was found in Guinea Bissau, which may suggest that ecological pressures driving segregation between the two species in larval habitats in this region may be different from those experienced in northern and more arid parts of the species' range. Finally, our results also suggest a genetic subdivision between coastal and inland A. gambiae Guinean populations and provide clues on the importance of ecological factors in intra-specific differentiation processes.http://europepmc.org/articles/PMC4457524?pdf=render
spellingShingle Emiliano Mancini
Maria Ida Spinaci
Vasco Gordicho
Beniamino Caputo
Marco Pombi
José Luis Vicente
João Dinis
Amabélia Rodrigues
Vincenzo Petrarca
David Weetman
João Pinto
Alessandra Della Torre
Adaptive Potential of Hybridization among Malaria Vectors: Introgression at the Immune Locus TEP1 between Anopheles coluzzii and A. gambiae in 'Far-West' Africa.
PLoS ONE
title Adaptive Potential of Hybridization among Malaria Vectors: Introgression at the Immune Locus TEP1 between Anopheles coluzzii and A. gambiae in 'Far-West' Africa.
title_full Adaptive Potential of Hybridization among Malaria Vectors: Introgression at the Immune Locus TEP1 between Anopheles coluzzii and A. gambiae in 'Far-West' Africa.
title_fullStr Adaptive Potential of Hybridization among Malaria Vectors: Introgression at the Immune Locus TEP1 between Anopheles coluzzii and A. gambiae in 'Far-West' Africa.
title_full_unstemmed Adaptive Potential of Hybridization among Malaria Vectors: Introgression at the Immune Locus TEP1 between Anopheles coluzzii and A. gambiae in 'Far-West' Africa.
title_short Adaptive Potential of Hybridization among Malaria Vectors: Introgression at the Immune Locus TEP1 between Anopheles coluzzii and A. gambiae in 'Far-West' Africa.
title_sort adaptive potential of hybridization among malaria vectors introgression at the immune locus tep1 between anopheles coluzzii and a gambiae in far west africa
url http://europepmc.org/articles/PMC4457524?pdf=render
work_keys_str_mv AT emilianomancini adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT mariaidaspinaci adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT vascogordicho adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT beniaminocaputo adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT marcopombi adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT joseluisvicente adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT joaodinis adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT amabeliarodrigues adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT vincenzopetrarca adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT davidweetman adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT joaopinto adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica
AT alessandradellatorre adaptivepotentialofhybridizationamongmalariavectorsintrogressionattheimmunelocustep1betweenanophelescoluzziiandagambiaeinfarwestafrica