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Isolation and identification of culturable bacteria from wild Anopheles culicifacies, a first step in a paratransgenesis approach

BACKGROUND: Due to the effect of midgut bacteria on proliferation of parasites and their potential as paratransgenesis tools, their identification in malaria vector mosquitoes is important. Anopheles culicifacies s.l. is one of the main malaria vectors in Asia; however, its midgut microbiota remains...

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Autores principales: Chavshin, Ali Reza, Oshaghi, Mohammad Ali, Vatandoost, Hasan, Pourmand, Mohammad Reza, Raeisi, Ahmad, Terenius, Olle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261757/
https://www.ncbi.nlm.nih.gov/pubmed/25189316
http://dx.doi.org/10.1186/1756-3305-7-419
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author Chavshin, Ali Reza
Oshaghi, Mohammad Ali
Vatandoost, Hasan
Pourmand, Mohammad Reza
Raeisi, Ahmad
Terenius, Olle
author_facet Chavshin, Ali Reza
Oshaghi, Mohammad Ali
Vatandoost, Hasan
Pourmand, Mohammad Reza
Raeisi, Ahmad
Terenius, Olle
author_sort Chavshin, Ali Reza
collection PubMed
description BACKGROUND: Due to the effect of midgut bacteria on proliferation of parasites and their potential as paratransgenesis tools, their identification in malaria vector mosquitoes is important. Anopheles culicifacies s.l. is one of the main malaria vectors in Asia; however, its midgut microbiota remains un-studied. This work was primarily designed to isolate potential candidates for use in a paratransgenesis approach, but also to give a picture of the midgut microbiota of wild-caught An. culicifacies larvae and adults from the southeast corner of Iran, which has the highest malaria endemicity in the country. METHODS: A total of 68 larvae and 34 adult females (newly eclosed and older) from three different biotopes in Iran were analyzed for their midgut microflora. The mosquitoes had their midgut bacterial contents plated on three different culture media (brain heart agar, nutrient agar and blood agar) yielding 57 bacterial isolates. The 16S rRNA genes of the isolates were sequence analyzed for species designation, which then was confirmed by biochemical analysis. RESULTS: A total of twelve bacterial genera were identified: Acinetobacter, Aeromonas, Bacillus, Chryseobacterium, Delftia, Exiguobacterium, Kurthia, Microbacterium, Pseudomonas, Staphylococcus, Thorsellia and Variovorax. In older females, only Gram-negative bacteria were found, whereas larvae and newly-eclosed adults also harbored Gram-positive bacteria. The diversity of isolates also varied between sampling sites and mosquito stages, with the largest number of genera found in the Anguri district and in larvae, respectively. Pseudomonas was the most common genus retrieved from all sampling sites, and in both larvae and adults, suggesting a potential transstadial passage of these bacteria. Interestingly, identical 16S sequences of Pseudomonas were found in mosquitoes originating from different habitats at least 45 km apart, which could suggest that these bacteria have been adapted to the mosquitoes. CONCLUSIONS: The study of vector mosquito microbiota has recently gathered increased interest because of the potential influence on vector competence. By adding data from a hitherto uncharacterized malaria mosquito, a better picture of gut flora in vector mosquitoes was obtained. Furthermore, some species of the predominant genus Pseudomonas will be evaluated for the selection of a paratransgenesis candidate.
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spelling pubmed-42617572014-12-10 Isolation and identification of culturable bacteria from wild Anopheles culicifacies, a first step in a paratransgenesis approach Chavshin, Ali Reza Oshaghi, Mohammad Ali Vatandoost, Hasan Pourmand, Mohammad Reza Raeisi, Ahmad Terenius, Olle Parasit Vectors Research BACKGROUND: Due to the effect of midgut bacteria on proliferation of parasites and their potential as paratransgenesis tools, their identification in malaria vector mosquitoes is important. Anopheles culicifacies s.l. is one of the main malaria vectors in Asia; however, its midgut microbiota remains un-studied. This work was primarily designed to isolate potential candidates for use in a paratransgenesis approach, but also to give a picture of the midgut microbiota of wild-caught An. culicifacies larvae and adults from the southeast corner of Iran, which has the highest malaria endemicity in the country. METHODS: A total of 68 larvae and 34 adult females (newly eclosed and older) from three different biotopes in Iran were analyzed for their midgut microflora. The mosquitoes had their midgut bacterial contents plated on three different culture media (brain heart agar, nutrient agar and blood agar) yielding 57 bacterial isolates. The 16S rRNA genes of the isolates were sequence analyzed for species designation, which then was confirmed by biochemical analysis. RESULTS: A total of twelve bacterial genera were identified: Acinetobacter, Aeromonas, Bacillus, Chryseobacterium, Delftia, Exiguobacterium, Kurthia, Microbacterium, Pseudomonas, Staphylococcus, Thorsellia and Variovorax. In older females, only Gram-negative bacteria were found, whereas larvae and newly-eclosed adults also harbored Gram-positive bacteria. The diversity of isolates also varied between sampling sites and mosquito stages, with the largest number of genera found in the Anguri district and in larvae, respectively. Pseudomonas was the most common genus retrieved from all sampling sites, and in both larvae and adults, suggesting a potential transstadial passage of these bacteria. Interestingly, identical 16S sequences of Pseudomonas were found in mosquitoes originating from different habitats at least 45 km apart, which could suggest that these bacteria have been adapted to the mosquitoes. CONCLUSIONS: The study of vector mosquito microbiota has recently gathered increased interest because of the potential influence on vector competence. By adding data from a hitherto uncharacterized malaria mosquito, a better picture of gut flora in vector mosquitoes was obtained. Furthermore, some species of the predominant genus Pseudomonas will be evaluated for the selection of a paratransgenesis candidate. BioMed Central 2014-09-04 /pmc/articles/PMC4261757/ /pubmed/25189316 http://dx.doi.org/10.1186/1756-3305-7-419 Text en © Chavshin et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Chavshin, Ali Reza
Oshaghi, Mohammad Ali
Vatandoost, Hasan
Pourmand, Mohammad Reza
Raeisi, Ahmad
Terenius, Olle
Isolation and identification of culturable bacteria from wild Anopheles culicifacies, a first step in a paratransgenesis approach
title Isolation and identification of culturable bacteria from wild Anopheles culicifacies, a first step in a paratransgenesis approach
title_full Isolation and identification of culturable bacteria from wild Anopheles culicifacies, a first step in a paratransgenesis approach
title_fullStr Isolation and identification of culturable bacteria from wild Anopheles culicifacies, a first step in a paratransgenesis approach
title_full_unstemmed Isolation and identification of culturable bacteria from wild Anopheles culicifacies, a first step in a paratransgenesis approach
title_short Isolation and identification of culturable bacteria from wild Anopheles culicifacies, a first step in a paratransgenesis approach
title_sort isolation and identification of culturable bacteria from wild anopheles culicifacies, a first step in a paratransgenesis approach
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261757/
https://www.ncbi.nlm.nih.gov/pubmed/25189316
http://dx.doi.org/10.1186/1756-3305-7-419
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