Biogeographic range expansion into South America byCoccidioides immitismirrors New World patterns of human migration

Matthew C. Fisher1, Gina L. Koenig1, Thomas J. White1, Gioconda San-Blas1, Ricardo Negroni1, Isidro Gutiérrez Alvarez1, Bodo Wanke1, John W. Taylor1
1Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720; Roche Molecular Systems, 1145 Atlantic Avenue, Alameda, CA 94501; Venezuelan Institute for Scientific Research, Center of Microbiology and Cell Biology, P.O. Box 21827, Caracas 1020A, Venezuela; Facultad de Medicina, Centro de Micologia, Departmento de Microbiologia, Buenos Aires, Argentina; Health Sciences Department, Universidad de Valle de México, C.P. 76100, Querétaro, Mexico; Laboratório de...

Tóm tắt

Long-distance population dispersal leaves its characteristic signature in genomes, namely, reduced diversity and increased linkage between genetic markers. This signature enables historical patterns of range expansion to be traced. Herein, we use microsatellite loci from the human pathogenCoccidioides immitisto show that genetic diversity in this fungus is geographically partitioned throughout North America. In contrast, analyses of South AmericanC. immitisshow that this population is genetically depauperate and was founded from a single North American population centered in Texas. Variances of allele distributions show that South AmericanC. immitishave undergone rapid population growth, consistent with an epidemic increase in postcolonization population size. Herein, we estimate the introduction into South America to have occurred within the last 9,000–140,000 years. This range increase parallels that ofHomo sapiens. Because of known associations between Amerindians and this fungus, we suggest that the colonization of South America byC. immitisrepresents a relatively recent and rapid codispersal of a host and its pathogen.

Từ khóa


Tài liệu tham khảo

10.1073/pnas.91.24.11591

10.1094/Phyto-85-155

10.1146/annurev.phyto.36.1.249

10.1146/annurev.phyto.37.1.197

10.1038/35016000

J W Rippon Medical Mycology (Saunders, Philadelphia, 1988).

M Saubolle Coccidioidomycosis, eds H E Einstein, A Catenzaro (Natl. Found. Infect. Dis., Washington, DC), pp. 1–8 (1996).

K T Maddy, T Crecelius Coccidioidomycosis, ed L Ajello (Univ. of Arizona Press, Tucson, AZ), pp. 309–312 (1967).

61 Federal Register 207 (1996) p. 55190.

10.4148/1941-4765.1335

10.1046/j.1365-294X.1999.00655_5.x

J C Stephens, D A Gilbert, N Yuhki, S J O'Brien Mol Biol Evol 9, 729–743 (1992).

10.1038/368455a0

10.1073/pnas.92.15.6723

10.1093/genetics/139.1.463

J C Garza, M Slatkin, N B Freimer Mol Biol Evol 12, 594–603 (1995).

10.1093/genetics/144.3.1155

10.1093/oxfordjournals.molbev.a026399

E Minch, A Ruiz-Linares, D Goldstein, M Feldman, L L Cavalli-Sforza microsat, The Microsatellite Distance Program (Stanford Univ. Press, Stanford, CA, 1995).

D L Hartl, A G Clark Principles of Population Genetics (Sinauer, Sunderland, MA, 1997).

10.1073/pnas.95.14.8119

10.1093/oxfordjournals.molbev.a026127

10.1073/pnas.94.10.5478

D G Higgins, A J Bleasby, R Fuchs Comput Appl Biosci 8, 189–191 (1992).

D L Swofford paup*, Phylogenetic Analysis Using Parsimony (* and Other Methods) (Sinauer, Sunderland, MA, , Version 4. (1998).

V Koufopanou, A Burt, J W Taylor Proc Natl Acad Sci USA 95, 8414–8414 (1998).

D Pappagianis, H Einstein West J Med 129, 527–530 (1978).

10.1086/282771

N Mantel Cancer Res 27, 209–220 (1967).

10.1038/hdy.1996.142

10.1038/ng0795-337

10.1016/0888-7543(92)90370-8

10.1128/mcb.12.6.2749-2757.1992

10.1126/science.3576198

10.1007/BF02447922

10.1126/science.215.4538.1351

10.1128/am.27.2.379-388.1974

10.1126/science.276.5313.754

T Dillehay Monte Verde: A Late Pleistocene Settlement in Chile: The Archaeological Context and Interpretation (Smithisonian, Washington, DC) 2 (1997).

D Pappagianis Current Topics in Medical Mycology (Springer, Berlin), pp. 199–238 (1988).

10.1073/pnas.93.1.181

10.1046/j.1365-294X.1997.00245.x