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Common predators and factors influencing their abundance in Anopheles funestus aquatic habitats in rural south-eastern Tanzania
BACKGROUND: The role of larval predators in regulating the Anopheles funestus population in various malaria-endemic countries remains relatively unknown. This study aimed to investigate the common predators that co-exist with Anopheles funestus group larvae and evaluate factors that influence their...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10292713/ https://www.ncbi.nlm.nih.gov/pubmed/37363899 http://dx.doi.org/10.1371/journal.pone.0287655 |
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author | Mahenge, Herieth H. Muyaga, Letus L. Nkya, Joel D. Kifungo, Khamis S. Kahamba, Najat F. Ngowo, Halfan S. Kaindoa, Emmanuel W. |
author_facet | Mahenge, Herieth H. Muyaga, Letus L. Nkya, Joel D. Kifungo, Khamis S. Kahamba, Najat F. Ngowo, Halfan S. Kaindoa, Emmanuel W. |
author_sort | Mahenge, Herieth H. |
collection | PubMed |
description | BACKGROUND: The role of larval predators in regulating the Anopheles funestus population in various malaria-endemic countries remains relatively unknown. This study aimed to investigate the common predators that co-exist with Anopheles funestus group larvae and evaluate factors that influence their abundance in rural south-eastern Tanzania. METHODS: Mosquito larvae and predators were sampled concurrently using standard dipper (350 ml) or 10 L bucket in previously identified aquatic habitats in selected villages in southern Tanzania. Predators and mosquito larvae were identified using standard identification keys. All positive habitats were geo-located and their physical features characterized. Water physicochemical parameters such as dissolved oxygen (DO), pH, electrical conductivity (EC), total dissolved solids (TDS) and temperature were also recorded. RESULTS: A total of 85 previously identified An. funestus aquatic habitats in nine villages were sampled for larvae and potential predators. A total of 8,295 predators were sampled. Of these Coenagrionidae 57.7% (n = 4785), Corixidae 12.8% (n = 1,060), Notonectidae 9.9% (n = 822), Aeshnidae 4.9% (n = 405), Amphibian 4.5% (n = 370), Dytiscidae 3.8% (n = 313) were common. A total of 5,260 mosquito larvae were sampled, whereby Anopheles funestus group were 60.3% (n = 3,170), Culex spp. 24.3% (n = 1,279), An. gambie s.l. 8.3% (n = 438) and other anophelines 7.1% (n = 373). Permanent and aquatic habitats larger than 100m(2) were positively associated with An. funestus group larvae (P<0.05) and predator abundance (P<0.05). Habitats with submerged vegetation were negatively associated with An. funestus group larvae (P<0.05). Only dissolved oxygen (DO) was positively and significantly affect the abundance of An. funestus group larvae (P<0.05). While predators’ abundance was not impacted by all physicochemical parameters. CONCLUSION: Six potential predator families were common in aquatic habitats of An. funestus group larvae. Additional studies are needed to demonstrate the efficacy of different predators on larval density and adult fitness traits. Interventions leveraging the interaction between mosquitoes and predators can be established to disrupt the transmission potential and survival of the An. funestus mosquitoes. |
format | Online Article Text |
id | pubmed-10292713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-102927132023-06-27 Common predators and factors influencing their abundance in Anopheles funestus aquatic habitats in rural south-eastern Tanzania Mahenge, Herieth H. Muyaga, Letus L. Nkya, Joel D. Kifungo, Khamis S. Kahamba, Najat F. Ngowo, Halfan S. Kaindoa, Emmanuel W. PLoS One Research Article BACKGROUND: The role of larval predators in regulating the Anopheles funestus population in various malaria-endemic countries remains relatively unknown. This study aimed to investigate the common predators that co-exist with Anopheles funestus group larvae and evaluate factors that influence their abundance in rural south-eastern Tanzania. METHODS: Mosquito larvae and predators were sampled concurrently using standard dipper (350 ml) or 10 L bucket in previously identified aquatic habitats in selected villages in southern Tanzania. Predators and mosquito larvae were identified using standard identification keys. All positive habitats were geo-located and their physical features characterized. Water physicochemical parameters such as dissolved oxygen (DO), pH, electrical conductivity (EC), total dissolved solids (TDS) and temperature were also recorded. RESULTS: A total of 85 previously identified An. funestus aquatic habitats in nine villages were sampled for larvae and potential predators. A total of 8,295 predators were sampled. Of these Coenagrionidae 57.7% (n = 4785), Corixidae 12.8% (n = 1,060), Notonectidae 9.9% (n = 822), Aeshnidae 4.9% (n = 405), Amphibian 4.5% (n = 370), Dytiscidae 3.8% (n = 313) were common. A total of 5,260 mosquito larvae were sampled, whereby Anopheles funestus group were 60.3% (n = 3,170), Culex spp. 24.3% (n = 1,279), An. gambie s.l. 8.3% (n = 438) and other anophelines 7.1% (n = 373). Permanent and aquatic habitats larger than 100m(2) were positively associated with An. funestus group larvae (P<0.05) and predator abundance (P<0.05). Habitats with submerged vegetation were negatively associated with An. funestus group larvae (P<0.05). Only dissolved oxygen (DO) was positively and significantly affect the abundance of An. funestus group larvae (P<0.05). While predators’ abundance was not impacted by all physicochemical parameters. CONCLUSION: Six potential predator families were common in aquatic habitats of An. funestus group larvae. Additional studies are needed to demonstrate the efficacy of different predators on larval density and adult fitness traits. Interventions leveraging the interaction between mosquitoes and predators can be established to disrupt the transmission potential and survival of the An. funestus mosquitoes. Public Library of Science 2023-06-26 /pmc/articles/PMC10292713/ /pubmed/37363899 http://dx.doi.org/10.1371/journal.pone.0287655 Text en © 2023 Mahenge et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Mahenge, Herieth H. Muyaga, Letus L. Nkya, Joel D. Kifungo, Khamis S. Kahamba, Najat F. Ngowo, Halfan S. Kaindoa, Emmanuel W. Common predators and factors influencing their abundance in Anopheles funestus aquatic habitats in rural south-eastern Tanzania |
title | Common predators and factors influencing their abundance in Anopheles funestus aquatic habitats in rural south-eastern Tanzania |
title_full | Common predators and factors influencing their abundance in Anopheles funestus aquatic habitats in rural south-eastern Tanzania |
title_fullStr | Common predators and factors influencing their abundance in Anopheles funestus aquatic habitats in rural south-eastern Tanzania |
title_full_unstemmed | Common predators and factors influencing their abundance in Anopheles funestus aquatic habitats in rural south-eastern Tanzania |
title_short | Common predators and factors influencing their abundance in Anopheles funestus aquatic habitats in rural south-eastern Tanzania |
title_sort | common predators and factors influencing their abundance in anopheles funestus aquatic habitats in rural south-eastern tanzania |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10292713/ https://www.ncbi.nlm.nih.gov/pubmed/37363899 http://dx.doi.org/10.1371/journal.pone.0287655 |
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