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Toxoplasma gondii Comprises Three Clonal Lineages: Correlation of Parasite Genotype with Human Disease

Howe, D. K., Sibley, L. D.·1995·Journal of Infectious Diseases

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.

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Metadata

Authors
Howe, D. K., & Sibley, L. D.
Venue
Journal of Infectious Diseases
Published
1995-12-01
Volume
172
Issue
6
Pages
1561-1566
ISSN
  • 0022-1899 (ISSN-L)
  • 1537-6613
OpenAlex
W2146771667
Cited by
1,445
References
0
FWCI
12.97
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Toxoplasma gondii Comprises Three Clonal Lineages: Correlation of Parasite Genotype with Human Disease. https://app.cochat.ai/papers/10.1093/infdis/172.6.1561
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Howe, D. K., & Sibley, L. D. (1995). Toxoplasma gondii Comprises Three Clonal Lineages: Correlation of Parasite Genotype with Human Disease. Journal of Infectious Diseases. https://doi.org/10.1093/infdis/172.6.1561

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.