Abstract
The population genetic structure of Toxoplasma gondii was determined by multilocus restriction fragment length polymorphism analysis at 6 loci in 106 independent isolates from humans and animals. Phylogenetic and statistical analyses indicated a highly unusual population structure consisting of 3 widespread clonal lineages. Extensively mixed genotypes were only apparent in 4 strains, which indicated that, while not separate species, sexual recombination between the 3 lineages is exceedingly rare in natural populations. T. gondii is a major cause of subclinical human infection and an important opportunistic pathogen that causes severe disease in immunocompromised patients. While strains from all 3 lineages were isolated from humans, the majority of human toxoplasmosis cases were associated with strains of a type II genotype. The correlation of specific clonal lineages with human toxoplasmosis has important implications for development of vaccines, drug treatments, and diagnostic protocols.
Original language | English |
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Pages (from-to) | 1561-1566 |
Number of pages | 6 |
Journal | Journal of Infectious Diseases |
Volume | 172 |
Issue number | 6 |
DOIs | |
State | Published - Dec 1995 |
Bibliographical note
Funding Information:Grant support: American Foundation for AIDS Research (02058-15-RGR), National Institutes of Health (AI-36629, AI-07ln), and Burroughs Wellcome Fund.
Funding
Grant support: American Foundation for AIDS Research (02058-15-RGR), National Institutes of Health (AI-36629, AI-07ln), and Burroughs Wellcome Fund.
Funders | Funder number |
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National Institutes of Health (NIH) | AI-07ln |
National Institute of Allergy and Infectious Diseases | R01AI036629 |
Burroughs Wellcome Fund | |
Glenn Foundation/American Federation for Aging Research | 02058-15-RGR |
ASJC Scopus subject areas
- General Medicine