Molecular evidence supports an African affinity of the Neotropical freshwater gastropod, Biomphalaria glabrata, Say 1818, an intermediate host for Schistosoma mansoni

被引:57
作者
Campbell, G
Jones, CS
Lockyer, AE
Hughes, S
Brown, D
Noble, LR
Rollinson, D
机构
[1] Univ Aberdeen, Dept Zool, Aberdeen AB24 2TZ, Scotland
[2] Nat Hist Museum, Dept Zool, London SW7 5BD, England
关键词
Biomphalaria glabrata; African and Neotropical snails; mitochondrial DNA; nuclear ribosomal DNA; phylogeny; Pleistocene;
D O I
10.1098/rspb.2000.1291
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Freshwater snails of the genus Biomphalaria, Preston 1910, are the most important and widely distributed intermediate hosts of Schistosoma mansoni, the blood fluke responsible for human intestinal schistosomiasis, in Africa and the Neotropics. S. mansoni is thought to have been imported repeatedly into the Americas during the last 500 years with the African slave trade. Surprisingly, considering that the New and Old World separated 95-106 million years (Myr) ago, the disease rapidly became established due to the presence of endemic susceptible hosts. Reconstructing the phylogenetic relationships within Biomphalaria may provide insights into the successful intercontinental spread of S. mansoni. Parsimony and distance analyses of mitochondrial and nuclear sequences show African taxa to be monophyletic and Neotropical species paraphyletic, with Biomphalaria glabrata forming a separate clade from other Neotropical Biomphalaria, and ancestral to the African taxa. A west to east trans-Atlantic dispersal of a B. glabrata-like taxon, possibly as recently as the Plio-Pleistocene (1.8-3.6 Myr ago) according to a general mitochondrial clock, would fit these observations. Vicariance or an African origin for B. glabrata followed by multiple introductions to South America over the past 500 years with the African slave trade seem unlikely explanations. Knowledge of the phylogenetic relationships among important intermediate host species may prove useful in furthering control measures which exploit genetic differences in susceptibility to parasites, and in elucidating the evolution of schistosome resistance.
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页码:2351 / 2358
页数:8
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