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
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.
引用
收藏
页数:9
相关论文
共 50 条
  • [21] Exposure to deltamethrin affects development of Plasmodium falciparum inside wild pyrethroid resistant Anopheles gambiae s.s. mosquitoes in Uganda
    Mojca Kristan
    Jo Lines
    Anthony Nuwa
    Charles Ntege
    Sylvia R. Meek
    Tarekegn A. Abeku
    Parasites & Vectors, 9
  • [22] Exposure to deltamethrin affects development of Plasmodium falciparum inside wild pyrethroid resistant Anopheles gambiae s.s. mosquitoes in Uganda
    Kristan, Mojca
    Lines, Jo
    Nuwa, Anthony
    Ntege, Charles
    Meek, Sylvia R.
    Abeku, Tarekegn A.
    PARASITES & VECTORS, 2016, 9
  • [23] Contrasting patterns of differentiation between the M and S molecular forms of Anopheles gambiae in mali and Cameroon
    Slotman, Michel A.
    Tripet, Frederic
    Reimer, Lisa
    Thiemann, Tara
    Meneses, Claudio
    Fofana, Abdrahamane
    McAbee, Rory
    CorneJ, Anton
    Fondjo, Etienne
    Dolo, Giumogo
    Traore, Sekou
    Lanzaro, Gregory C.
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2005, 73 (06): : 195 - 195
  • [24] Genetic differentiation of Anopheles gambiae s.s. populations in Mali, West Africa, using microsatellite loci
    Carnahan, J
    Zheng, L
    Taylor, CE
    Touré, YT
    Norris, DE
    Dolo, G
    Diuk-Wasser, M
    Lanzaro, GC
    JOURNAL OF HEREDITY, 2002, 93 (04) : 249 - 253
  • [25] The circadian clock modulates Anopheles gambiae infection with Plasmodium falciparum
    Habtewold, Tibebu
    Tapanelli, Sofia
    Masters, Ellen K. G.
    Windbichler, Nikolai
    Christophides, George K.
    PLOS ONE, 2022, 17 (12):
  • [26] Chromatin changes in Anopheles gambiae induced by Plasmodium falciparum infection
    Ruiz, Jose L.
    Yerbanga, Rakiswende S.
    Lefevre, Thierry
    Ouedraogo, Jean B.
    Corces, Victor G.
    Gomez-Diaz, Elena
    EPIGENETICS & CHROMATIN, 2019, 12 (1)
  • [27] Chromatin changes in Anopheles gambiae induced by Plasmodium falciparum infection
    José L. Ruiz
    Rakiswendé S. Yerbanga
    Thierry Lefèvre
    Jean B. Ouedraogo
    Victor G. Corces
    Elena Gómez-Díaz
    Epigenetics & Chromatin, 12
  • [28] Reduced recombination rate and genetic differentiation between the M and S forms of Anopheles gambiae s.s.
    Slotman, Michel A.
    Reimer, Lisa J.
    Thiemann, Tara
    Dolo, Guimogo
    Fondjo, Etienne
    Lanzaro, Gregory C.
    GENETICS, 2006, 174 (04) : 2081 - 2093
  • [29] Differences in timing of mating swarms in sympatric populations of Anopheles coluzzii and Anopheles gambiae s.s. (formerly An. gambiae M and S molecular forms) in Burkina Faso, West Africa
    Simon P Sawadogo
    Carlo Costantini
    Cédric Pennetier
    Abdoulaye Diabaté
    Gabriella Gibson
    Roch K Dabiré
    Parasites & Vectors, 6
  • [30] Distribution of genetic variation among chromosomal forms of Anopheles gambiae s.s.:: introgressive hybridization, adaptive inversions, or recent reproductive isolation?
    Black, WC
    Lanzaro, GC
    INSECT MOLECULAR BIOLOGY, 2001, 10 (01) : 3 - 7