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Differential Plasmodium falciparum infection of Anopheles gambiae s.s. molecular and chromosomal forms in Mali
被引:20
|作者:
Fryxell, Rebecca T. Trout
[1
]
Nieman, Catelyn C.
[2
]
Fofana, Abdrahamane
[3
]
Lee, Yoosook
[2
]
Traore, Sekou F.
[3
]
Cornel, Anthony J.
[4
]
Luckhart, Shirley
[5
]
Lanzaro, Gregory C.
[2
]
机构:
[1] Univ Tennessee, Dept Entomol & Plant Pathol, Knoxville, TN 37996 USA
[2] Univ Calif Davis, Vector Genet Lab, Dept Pathol Microbiol & Immunol, Sch Vet Med, Davis, CA 95616 USA
[3] Univ Bamako, Malaria Res & Training Ctr, Bamako, Mali
[4] Univ Calif Davis, Dept Entomol, Mosquito Control Res Lab, Davis, CA 95616 USA
[5] Univ Calif Davis, Dept Med Microbiol & Immunol, Sch Med, Davis, CA 95616 USA
来源:
关键词:
Anopheles gambiae;
Mali;
Malaria;
Plasmodium falciparum;
Molecular form;
Chromosomal form;
GENOME-WIDE ANALYSIS;
MALARIA TRANSMISSION;
WEST-AFRICA;
GENE FLOW;
IDENTIFICATION;
POPULATIONS;
COMPLEX;
VECTOR;
POLYMORPHISMS;
DIVERGENCE;
D O I:
10.1186/1475-2875-11-133
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Background: Anopheles 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. Methods: Wild 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). Results: Of 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%). Discussion: In 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.
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