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Updated: Jun 23, 2026

QTL Mapping and CRISPR/Cas9 Editing to Identify a Drug Resistance Gene in Toxoplasma gondii
Published on: June 22, 2017
Population genetic structure of zoonotic Toxoplasma gondii in China revealed using multilocus sequence typing
Yi-Tian Fu1, Yu-Na Xiao1, Xi-Long Yi1
1Research Center for Parasites & Vectors, College of Veterinary Medicine, Hunan Agricultural University, Changsha 410128, Hunan, China.
Background:
The zoonotic pathogen Toxoplasma gondii exhibits a diverse global population structure, with a few dominant lineages primarily in the Northern Hemisphere. However, reliance on low-resolution, restriction-based genotyping methods has created a "resolution ceiling," potentially masking hidden genetic diversity and complex transmission dynamics.
Methods:
In this study, we combined conventional PCR-restriction fragment length polymorphism (RFLP) screening with high-resolution Sanger sequencing targeting 16 genetic markers to unravel the fine-scale epidemiology of 96 T. gondii DNA samples collected from various hosts (including pigs, cats, sheep, birds, bats, and captive wildlife) across 12 provinces and regions in China.
Results:
Our analysis identifies ToxoDB#9 as the dominant lineage (41/96 samples), revealing substantial intra-clonal diversity within this lineage. We report the North American sylvatic ToxoDB#5 (Haplogroup 12) lineage in a captive caracal in China, documenting the presence of this rare lineage outside its previously recognized range, although its public health significance remains uncertain. Population genetic analyses show high haplotype diversity consistent with clonal diversification with limited geographic structuring.
Conclusion:
Our study provides an updated baseline for T. gondii genetic diversity in China and supports the value of systematic molecular monitoring within a One Health framework, with whole-genome sequencing required to confirm introduction scenarios, resolve transmission routes, and assess recombination.
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