Entomological survey of sibling species in the Anopheles funestus group in Tanzania confirms the role of Anopheles parensis as a secondary malaria vector
Background Malaria transmission in Tanzania is driven by mosquitoes of the Anopheles gambiae complex and Anopheles funestus group. The latter includes An . funestus s.s., an anthropophilic vector, which is now strongly resistant to public health insecticides, and several sibling species, which remai...
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| Published in: | Parasites & vectors Vol. 17; no. 1; p. 261 |
|---|---|
| Main Authors: | , , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
London
BioMed Central
17.06.2024
BioMed Central Ltd BMC |
| Subjects: | |
| ISSN: | 1756-3305, 1756-3305 |
| Online Access: | Get full text |
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| Summary: | Background
Malaria transmission in Tanzania is driven by mosquitoes of the
Anopheles gambiae
complex and
Anopheles funestus
group. The latter includes
An
.
funestus
s.s., an anthropophilic vector, which is now strongly resistant to public health insecticides, and several sibling species, which remain largely understudied despite their potential as secondary vectors. This paper provides the initial results of a cross-country study of the species composition, distribution and malaria transmission potential of members of the
Anopheles funestus
group in Tanzania.
Methods
Mosquitoes were collected inside homes in 12 regions across Tanzania between 2018 and 2022 using Centres for Disease Control and Prevention (CDC) light traps and Prokopack aspirators. Polymerase chain reaction (PCR) assays targeting the noncoding internal transcribed spacer 2 (ITS2) and 18S ribosomal DNA (18S rDNA) were used to identify sibling species in the
An
.
funestus
group and presence of
Plasmodium
infections, respectively. Where DNA fragments failed to amplify during PCR, we sequenced the ITS2 region to identify any polymorphisms.
Results
The following sibling species of the
An
.
funestus
group were found across Tanzania:
An
.
funestus
s.s. (50.3%),
An
.
parensis
(11.4%),
An
.
rivulorum
(1.1%),
An
.
leesoni
(0.3%). Sequencing of the ITS2 region in the nonamplified samples showed that polymorphisms at the priming sites of standard species-specific primers obstructed PCR amplification, although the ITS2 sequences closely matched those of
An
.
funestus
s.s., barring these polymorphisms. Of the 914 samples tested for
Plasmodium
infections, 11
An
.
funestus
s.s. (1.2%), and 2
An
.
parensis
(0.2%) individuals were confirmed positive for
P
.
falciparum
. The highest malaria transmission intensities [entomological inoculation rate (EIR)] contributed by the
Funestus
group were in the north-western region [108.3 infectious bites/person/year (ib/p/y)] and the south-eastern region (72.2 ib/p/y).
Conclusions
Whereas
An
.
funestus
s.s. is the dominant malaria vector in the
Funestus
group in Tanzania, this survey confirms the occurrence of
Plasmodium
-infected
An
.
parensis
, an observation previously made in at least two other occasions in the country. The findings indicate the need to better understand the ecology and vectorial capacity of this and other secondary malaria vectors in the region to improve malaria control.
Graphical Abstract |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| ISSN: | 1756-3305 1756-3305 |
| DOI: | 10.1186/s13071-024-06348-9 |