» Articles » PMID: 37375517

Low Prevalence of in Sheep and Isolation of a Viable Strain from Edible Mutton from Central China

Overview
Journal Pathogens
Date 2023 Jun 28
PMID 37375517
Authors
Affiliations
Soon will be listed here.
Abstract

Sheep are highly susceptible to , and miscarriage is the main clinical feature. This study investigated 227 sheep samples (210 myocardial tissues from slaughterhouses, 6 ewe serum samples, 3 aborted fetuses, and 8 dead lambs from veterinary clinics) from central China for infection. Antibodies against were detected using the modified agglutination test (MAT). PCR was performed to detect DNA in the tissue samples. The results showed that four samples were seropositive (MAT titer ≥ 1:100), with a seroprevalence of 1.8% (4/227). The seropositive samples included two myocardial samples from a slaughterhouse, one ewe and its aborted fetus from a veterinary clinic. The results revealed that 7 out of 207 (3.4%) sheep tissue samples were PCR-positive, including two myocardial tissue samples from slaughterhouses, three aborted fetuses, and two lambs from veterinary clinics. vertical transmission had occurred in two of three pairs of ewes and her pups. One viable strain (TgSheepCHn14) was isolated from the myocardial tissues of sheep from a slaughterhouse. Tachyzoites were obtained from cell cultures at 70 days following seeding in the brains and lungs of mice. This strain was non-lethal to Swiss mice. The number of parasite brain cysts in mice decreased with time post-infection ( < 0.05). Overall, the prevalence of in the sheep samples was low. Although the samples were scattered, and not from planned collections, the current study detected antibodies and DNA in aborted fetuses, indicating that vertical transmission could occur and maintain the parasites in sheep herds without exogenous infection.

Citing Articles

Gut commensal bacteria exacerbate toxoplasmosis associated with TgSheepCHn5 (ToxoDB#2) and TgRedpandaCHn1 (ToxoDB#20) through Th1 immune response.

Su R, Yang Y Parasitol Res. 2023; 122(12):2795-2806.

PMID: 37782335 DOI: 10.1007/s00436-023-07962-9.


Isolation and Genetic Characterization of from a Patas Monkey () in China.

Yang L, Ren H, Zhu N, Xin S, Mao G, Ma Y Genes (Basel). 2023; 14(8).

PMID: 37628657 PMC: 10454590. DOI: 10.3390/genes14081606.

References
1.
Dubey J, Thulliez P, Weigel R, Andrews C, Lind P, Powell E . Sensitivity and specificity of various serologic tests for detection of Toxoplasma gondii infection in naturally infected sows. Am J Vet Res. 1995; 56(8):1030-6. View

2.
Nounnagnon Tonouhewa A, Akpo Y, Sessou P, Adoligbe C, Yessinou E, Hounmanou Y . infection in meat animals from Africa: Systematic review and meta-analysis of sero-epidemiological studies. Vet World. 2017; 10(2):194-208. PMC: 5352845. DOI: 10.14202/vetworld.2017.194-208. View

3.
Costa F, Nogueira D, Oliveira M, Silva S, Silva R, Sarmento W . Vertical transmission of Toxoplasma gondii in naturally infected ewes in the semiarid region of Brazil. Comp Immunol Microbiol Infect Dis. 2020; 74:101595. DOI: 10.1016/j.cimid.2020.101595. View

4.
Huang S, Cong W, Zhou P, Zhou D, Wu S, Xu M . First report of genotyping of Toxoplasma gondii isolates from wild birds in China. J Parasitol. 2012; 98(3):681-2. DOI: 10.1645/GE-3038.1. View

5.
Dubey J, Ferreira L, Martins J, McLeod R . Oral oocyst-induced mouse model of toxoplasmosis: effect of infection with Toxoplasma gondii strains of different genotypes, dose, and mouse strains (transgenic, out-bred, in-bred) on pathogenesis and mortality. Parasitology. 2011; 139(1):1-13. PMC: 3683600. DOI: 10.1017/S0031182011001673. View