Malaria Journal | |
Differential Plasmodium falciparum infection of Anopheles gambiae s.s. molecular and chromosomal forms in Mali | |
Research | |
Rebecca T Trout Fryxell1  Anthony J Cornel2  Shirley Luckhart3  Abdrahamane Fofana4  Sekou F Traoré4  Catelyn C Nieman5  Yoosook Lee5  Gregory C Lanzaro5  | |
[1] Department of Entomology and Plant Pathology, University of Tennessee, 37996, Knoxville, TN, USA;Department of Entomology, Mosquito Control Research Laboratory, University of California – Davis, 95616, Davis, CA, USA;Department of Medical Microbiology and Immunology, School of Medicine, University of California – Davis, 95616, Davis, CA, USA;Malaria Research and Training Center, University of Bamako, Bamako, Mali;Vector Genetics Laboratory, Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California – Davis, 95616, Davis, CA, USA; | |
关键词: Anopheles gambiae; Mali; Malaria; Plasmodium falciparum; Molecular form; Chromosomal form; | |
DOI : 10.1186/1475-2875-11-133 | |
received in 2012-01-25, accepted in 2012-04-27, 发布年份 2012 | |
来源: Springer | |
【 摘 要 】
BackgroundAnopheles gambiae sensu stricto (s.s.) is a primary vector of Plasmodium falciparum in sub-Saharan Africa. Although some physiological differences among molecular and chromosomal forms of this species have been demonstrated, the relative susceptibility to malaria parasite infection among them has not been unequivocally shown. The objective of this study was to investigate P. falciparum circumsporozoite protein infection (CSP) positivity among An. gambiae s.s. chromosomal and molecular forms.MethodsWild An. gambiae from two sites Kela (n = 464) and Sidarebougou (n = 266) in Mali were screened for the presence of P. falciparum CSP using an enzyme-linked immunosorbent assay (ELISA). Samples were then identified to molecular form using multiple PCR diagnostics (n = 713) and chromosomal form using chromosomal karyotyping (n = 419).ResultsOf 730 An. gambiae sensu lato (s.l.) mosquitoes, 89 (12.2%) were CSP ELISA positive. The percentage of positive mosquitoes varied by site: 52 (11.2%) in Kela and 37 (13.9%) in Sidarebougou. Eighty-seven of the positive mosquitoes were identified to molecular form and they consisted of nine Anopheles arabiensis (21.4%), 46 S (10.9%), 31 M (12.8%), and one MS hybrid (14.3%). Sixty of the positive mosquitoes were identified to chromosomal form and they consisted of five An. arabiensis (20.0%), 21 Savanna (15.1%), 21 Mopti (30.4%), 11 Bamako (9.2%), and two hybrids (20.0%).DiscussionIn this collection, the prevalence of P. falciparum infection in the M form was equivalent to infection in the S form (no molecular form differential infection). There was a significant differential infection by chromosomal form such that, P. falciparum infection was more prevalent in the Mopti chromosomal forms than in the Bamako or Savanna forms; the Mopti form was also the most underrepresented in the collection. Continued research on the differential P. falciparum infection of An. gambiae s.s. chromosomal and molecular forms may suggest that Plasmodium – An. gambiae interactions play a role in malaria transmission.
【 授权许可】
CC BY
© Trout Fryxell et al.; licensee BioMed Central Ltd. 2012
【 预 览 】
Files | Size | Format | View |
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RO202311102390561ZK.pdf | 1990KB | download |
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