P. falciparum msp1 and msp2 genetic diversity in P. falciparum single and mixed infection with P. malariae among the asymptomatic population in Southern Benin
Parasitology International, ISSN: 1383-5769, Vol: 89, Page: 102590
2022
- 6Citations
- 52Captures
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Metrics Details
- Citations6
- Citation Indexes6
- CrossRef6
- Captures52
- Readers52
- 52
Article Description
Plasmodium falciparum and Plasmodium malariae infections are prevalent in malaria-endemic countries. However, very little is known about their interactions especially the effect of P. malariae on P. falciparum genetic diversity. This study aimed to assess P. falciparum genetic diversity in P. falciparum and mixed infection P. falciparum/P. malariae isolates among the asymptomatic populations in Southern Benin. Two hundred and fifty blood samples (125 of P. falciparum and 125 P. falciparum/P. malariae isolates) were analysed by a nested PCR amplification of msp1 and msp2 genes. The R033 allelic family was the most represented for the msp1 gene in mono and mixed infection isolates (99.2% vs 86.4%), while the K1 family had the lowest frequency (38.3% vs 20.4%). However, with the msp2 gene, the two allelic families displayed similar frequencies in P. falciparum isolates while the 3D7 allelic family was more represented in P. falciparum/P. malariae isolates (88.7%). Polyclonal infections were also lower (62.9%) in P. falciparum/P. malariae isolates ( p < 0.05). Overall, 96 individual alleles were identified (47 for msp1 and 49 for msp2 ) in P. falciparum isolates while a total of 50 individual alleles were identified (23 for msp1 and 27 for msp2 ) in P. falciparum/P. malariae isolates. The Multiplicity of Infection (MOI) was lower in P. falciparum/P. malariae isolates ( p < 0.05). This study revealed a lower genetic diversity of P. falciparum in P. falciparum/P. malariae isolates using msp1 and msp2 genes among the asymptomatic population in Southern Benin.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S138357692200054X; http://dx.doi.org/10.1016/j.parint.2022.102590; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85129064462&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/35472441; https://linkinghub.elsevier.com/retrieve/pii/S138357692200054X; https://dx.doi.org/10.1016/j.parint.2022.102590
Elsevier BV
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