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Molecular and physiological analysis of Anopheles funestus swarms in Nchelenge, Zambia
BACKGROUND: Anopheles funestus has been recognized as a major malaria vector in Africa for over 100 years, but knowledge on many aspects of the biology of this species is still lacking. Anopheles funestus, as with most other anophelines, mate through swarming. A key event that is crucial for the An....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785822/ https://www.ncbi.nlm.nih.gov/pubmed/29370805 http://dx.doi.org/10.1186/s12936-018-2196-6 |
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author | Zawada, Jacek W. Dahan-Moss, Yael L. Muleba, Mbanga Dabire, Roch K. Maïga, Hamid Venter, Nelius Davies, Craig Hunt, Richard H. Coetzee, Maureen Koekemoer, Lizette L. |
author_facet | Zawada, Jacek W. Dahan-Moss, Yael L. Muleba, Mbanga Dabire, Roch K. Maïga, Hamid Venter, Nelius Davies, Craig Hunt, Richard H. Coetzee, Maureen Koekemoer, Lizette L. |
author_sort | Zawada, Jacek W. |
collection | PubMed |
description | BACKGROUND: Anopheles funestus has been recognized as a major malaria vector in Africa for over 100 years, but knowledge on many aspects of the biology of this species is still lacking. Anopheles funestus, as with most other anophelines, mate through swarming. A key event that is crucial for the An. funestus male to mate is genitalia rotation. This involves the 135° to 180° rotation of claspers, which are tipped with claws. This physical change then enables the male to grasp the female during copulation. The aim of this investigation was to molecularly characterize wild An. funestus swarms from Zambia and examine the degree of genitalia rotation within the swarm. METHODS: Anopheles funestus swarms were collected from Nchelenge, northern Zambia, during dusk periods in May 2016. All the adults from the swarm were analysed morphologically and identified to species level using a multiplex PCR assay. Anopheles funestus s.s. specimens were molecularly characterized by restriction fragment length polymorphism type and Clade type assays. The different stages of genitalia rotation were examined in the adult males. RESULTS: A total of six swarms were observed during the study period and between 6 and 26 mosquitoes were caught from each swarm. Species analysis revealed that 90% of the males from the swarms were An. funestus s.s. MW-type, with 84% belonging to clade I compared to 14% clade II and 2% failed to amplify. Very few specimens (3.4%) were identified as Anopheles gambiae s.s. Eighty percent of the males from the swarm had complete genitalia rotation. CONCLUSIONS: This is the first time that An. funestus swarms have been molecularly identified to species level. Anopheles funestus swarms appear to be species-specific with no evidence of clade-type differentiation within these swarms. The An. funestus swarms consist mainly of males with fully rotated genitalia, which strongly suggests that swarming behaviour is triggered primarily when males have matured. |
format | Online Article Text |
id | pubmed-5785822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57858222018-02-07 Molecular and physiological analysis of Anopheles funestus swarms in Nchelenge, Zambia Zawada, Jacek W. Dahan-Moss, Yael L. Muleba, Mbanga Dabire, Roch K. Maïga, Hamid Venter, Nelius Davies, Craig Hunt, Richard H. Coetzee, Maureen Koekemoer, Lizette L. Malar J Research BACKGROUND: Anopheles funestus has been recognized as a major malaria vector in Africa for over 100 years, but knowledge on many aspects of the biology of this species is still lacking. Anopheles funestus, as with most other anophelines, mate through swarming. A key event that is crucial for the An. funestus male to mate is genitalia rotation. This involves the 135° to 180° rotation of claspers, which are tipped with claws. This physical change then enables the male to grasp the female during copulation. The aim of this investigation was to molecularly characterize wild An. funestus swarms from Zambia and examine the degree of genitalia rotation within the swarm. METHODS: Anopheles funestus swarms were collected from Nchelenge, northern Zambia, during dusk periods in May 2016. All the adults from the swarm were analysed morphologically and identified to species level using a multiplex PCR assay. Anopheles funestus s.s. specimens were molecularly characterized by restriction fragment length polymorphism type and Clade type assays. The different stages of genitalia rotation were examined in the adult males. RESULTS: A total of six swarms were observed during the study period and between 6 and 26 mosquitoes were caught from each swarm. Species analysis revealed that 90% of the males from the swarms were An. funestus s.s. MW-type, with 84% belonging to clade I compared to 14% clade II and 2% failed to amplify. Very few specimens (3.4%) were identified as Anopheles gambiae s.s. Eighty percent of the males from the swarm had complete genitalia rotation. CONCLUSIONS: This is the first time that An. funestus swarms have been molecularly identified to species level. Anopheles funestus swarms appear to be species-specific with no evidence of clade-type differentiation within these swarms. The An. funestus swarms consist mainly of males with fully rotated genitalia, which strongly suggests that swarming behaviour is triggered primarily when males have matured. BioMed Central 2018-01-25 /pmc/articles/PMC5785822/ /pubmed/29370805 http://dx.doi.org/10.1186/s12936-018-2196-6 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zawada, Jacek W. Dahan-Moss, Yael L. Muleba, Mbanga Dabire, Roch K. Maïga, Hamid Venter, Nelius Davies, Craig Hunt, Richard H. Coetzee, Maureen Koekemoer, Lizette L. Molecular and physiological analysis of Anopheles funestus swarms in Nchelenge, Zambia |
title | Molecular and physiological analysis of Anopheles funestus swarms in Nchelenge, Zambia |
title_full | Molecular and physiological analysis of Anopheles funestus swarms in Nchelenge, Zambia |
title_fullStr | Molecular and physiological analysis of Anopheles funestus swarms in Nchelenge, Zambia |
title_full_unstemmed | Molecular and physiological analysis of Anopheles funestus swarms in Nchelenge, Zambia |
title_short | Molecular and physiological analysis of Anopheles funestus swarms in Nchelenge, Zambia |
title_sort | molecular and physiological analysis of anopheles funestus swarms in nchelenge, zambia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785822/ https://www.ncbi.nlm.nih.gov/pubmed/29370805 http://dx.doi.org/10.1186/s12936-018-2196-6 |
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