Literature DB >> 33522944

Geographically extensive larval surveys reveal an unexpected scarcity of primary vector mosquitoes in a region of persistent malaria transmission in western Zambia.

Dónall Eoin Cross1, Chris Thomas2, Niall McKeown1, Vincent Siaziyu3, Amy Healey4, Tom Willis5, Douglas Singini6,7, Francis Liywalii6, Andrew Silumesii8, Jacob Sakala6, Mark Smith5, Mark Macklin4, Andy J Hardy9, Paul W Shaw1,10.   

Abstract

BACKGROUND: The Barotse floodplains of the upper Zambezi River and its tributaries are a highly dynamic environment, with seasonal flooding and transhumance presenting a shifting mosaic of potential larval habitat and human and livestock blood meals for malaria vector mosquitoes. However, limited entomological surveillance has been undertaken to characterize the vector community in these floodplains and their environs. Such information is necessary as, despite substantial deployment of insecticide-treated nets (ITNs) and indoor residual spraying (IRS) against Anopheles vectors, malaria transmission persists across Barotseland in Zambia's Western Province.
METHODS: Geographically extensive larval surveys were undertaken in two health districts along 102 km of transects, at fine spatial resolution, during a dry season and following the peak of the successive wet season. Larvae were sampled within typical Anopheles flight range of human settlements and identified through genetic sequencing of cytochrome c oxidase I and internal transcribed spacer two regions of mitochondrial and nuclear DNA. This facilitated detailed comparison of taxon-specific abundance patterns between ecological zones differentiated by hydrological controls.
RESULTS: An unexpected paucity of primary vectors was revealed, with An. gambiae s.l. and An. funestus representing < 2% of 995 sequenced anophelines. Potential secondary vectors predominated in the vector community, primarily An. coustani group species and An. squamosus. While the distribution of An. gambiae s.l. in the study area was highly clustered, secondary vector species were ubiquitous across the landscape in both dry and wet seasons, with some taxon-specific relationships between abundance and ecological zones by season.
CONCLUSIONS: The diversity of candidate vector species and their high relative abundance observed across diverse hydro-ecosystems indicate a highly adaptable transmission system, resilient to environmental variation and, potentially, interventions that target only part of the vector community. Larval survey results imply that residual transmission of malaria in Barotseland is being mediated predominantly by secondary vector species, whose known tendencies for crepuscular and outdoor biting renders them largely insensitive to prevalent vector control methods.

Entities:  

Keywords:  Anopheles; COI; Exophagy; ITS2; Larvae; Malaria; Primary vector; Residual transmission; Secondary vector

Year:  2021        PMID: 33522944      PMCID: PMC7849156          DOI: 10.1186/s13071-020-04540-1

Source DB:  PubMed          Journal:  Parasit Vectors        ISSN: 1756-3305            Impact factor:   3.876


  39 in total

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Journal:  PLoS Med       Date:  2010-08-03       Impact factor: 11.069

4.  Impact of promoting longer-lasting insecticide treatment of bed nets upon malaria transmission in a rural Tanzanian setting with pre-existing high coverage of untreated nets.

Authors:  Tanya L Russell; Dickson W Lwetoijera; Deodatus Maliti; Beatrice Chipwaza; Japhet Kihonda; J Derek Charlwood; Thomas A Smith; Christian Lengeler; Mathew A Mwanyangala; Rose Nathan; Bart Gj Knols; Willem Takken; Gerry F Killeen
Journal:  Malar J       Date:  2010-06-28       Impact factor: 2.979

5.  Identification of single specimens of the Anopheles gambiae complex by the polymerase chain reaction.

Authors:  J A Scott; W G Brogdon; F H Collins
Journal:  Am J Trop Med Hyg       Date:  1993-10       Impact factor: 2.345

6.  A new species concealed by Anopheles funestus Giles, a major malaria vector in Africa.

Authors:  Belinda L Spillings; Basil D Brooke; Lizette L Koekemoer; John Chiphwanya; Maureen Coetzee; Richard H Hunt
Journal:  Am J Trop Med Hyg       Date:  2009-09       Impact factor: 2.345

7.  The effect of malaria control on Plasmodium falciparum in Africa between 2000 and 2015.

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Journal:  Nature       Date:  2015-09-16       Impact factor: 49.962

Review 8.  The need for new vector control approaches targeting outdoor biting Anopheline malaria vector communities.

Authors:  Seynabou Sougoufara; Emmanuel Chinweuba Ottih; Frederic Tripet
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9.  A new species in the major malaria vector complex sheds light on reticulated species evolution.

Authors:  Maite G Barrón; Christophe Paupy; Nil Rahola; Ousman Akone-Ella; Marc F Ngangue; Theodel A Wilson-Bahun; Marco Pombi; Pierre Kengne; Carlo Costantini; Frédéric Simard; Josefa González; Diego Ayala
Journal:  Sci Rep       Date:  2019-10-14       Impact factor: 4.379

10.  Unexpected diversity of Anopheles species in Eastern Zambia: implications for evaluating vector behavior and interventions using molecular tools.

Authors:  Neil F Lobo; Brandyce St Laurent; Chadwick H Sikaala; Busiku Hamainza; Javan Chanda; Dingani Chinula; Sindhu M Krishnankutty; Jonathan D Mueller; Nicholas A Deason; Quynh T Hoang; Heather L Boldt; Julie Thumloup; Jennifer Stevenson; Aklilu Seyoum; Frank H Collins
Journal:  Sci Rep       Date:  2015-12-09       Impact factor: 4.379

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  4 in total

1.  Temporally consistent predominance and distribution of secondary malaria vectors in the Anopheles community of the upper Zambezi floodplain.

Authors:  Dónall Eoin Cross; Amy J E Healey; Niall J McKeown; Christopher James Thomas; Nicolae Adrian Macarie; Vincent Siaziyu; Douglas Singini; Francis Liywalii; Jacob Sakala; Andrew Silumesii; Paul W Shaw
Journal:  Sci Rep       Date:  2022-01-07       Impact factor: 4.379

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Journal:  Front Trop Dis       Date:  2021-12-09

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Review 4.  Six decades of malaria vector control in southern Africa: a review of the entomological evidence-base.

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