Toxoplasma gondii in Captive Wild Felids of Mexico: Its Frequency and Capability to Eliminate Oocysts

被引:7
|
作者
Gomez-Rios, Antonio [1 ,2 ]
Ortega-Pacheco, Antonio [2 ]
Gutierrez-Blanco, Eduardo [2 ]
Acosta-Viana, Karla Y. [1 ]
Guzman-Marin, Eugenia [1 ]
Guiris-Andrade, Marcelino D. [3 ]
Hernandez-Cortazar, Ivonne B. [1 ]
Lopez-Alonso, Ruben [4 ]
Cruz-Aldan, Epigmenio [5 ]
Jimenez-Coello, Matilde [1 ]
机构
[1] Univ Autonomous Yucatan, CIR Dr Hideyo Noguchi, CA Biomed Infect & Parasit Dis, Lab Cell Biol, Ave Rates 490 X Calle 59, Merida 97000, Mexico
[2] Univ Autonomous Yucatan, Fac Vet Med & Zoothecn, Dept Anim Hlth & Prevent Med, Campus Biol & Agropecuary Sci, Merida, Mexico
[3] Univ Autonomous Chiapas, Fac Vet Med, Dept Vet Sci, Acad Grp Biomed & Hlth Studies Fauna Chiapas Mexi, Tuxtla Gutierrez, Mexico
[4] Dept Anim Hlth, Zoofari Zol Pk, Amacuzac, Mexico
[5] Mammals Hlth Sect, Zoomat, Tuxtla Gutierre, Mexico
关键词
Toxoplasma gondii; wild felids; zoo; oocyst; raw meat; nPCR; NEOTROPICAL FELIDS; LEUKEMIA-VIRUS; DURANGO STATE; RISK-FACTORS; SEROPREVALENCE; CATS; ANTIBODIES; PREVALENCE; INFECTION; PRESERVATION;
D O I
10.1089/vbz.2018.2385
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
There is little information about Toxoplasma gondii in wild felids, even when these species have been associated with cases of toxoplasmosis in humans. In this study, samples of serum and whole blood were collected from 42 felids from 10 different species, in 4 Mexican zoos. Stool samples from 36 animals were also collected, corresponding to 82% of the felids included in the study. Stool samples were used for the search of oocysts by light field microscopy and PCR. Serum samples were analyzed by indirect immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) and indirect fluorescent antibody test (IFAT). DNA samples were purified from whole blood and stool for the amplification of a fragment of the SAG1 gene of T. gondii by a nested PCR (nPCR). The seroprevalence of IgG anti-T. gondii-specific antibodies by means of the ELISA was 100% (42/42) and 52.4% (22/42) by IFAT. The titers obtained varied from 1:80 to 1:2560. DNA of T. gondii was detected in 9.5% (4/42) of the blood samples by using nPCR. No oocysts were observed in the stool samples analyzed by light field microscopy. However, the DNA of the parasite was identified in 14.3% (5/35) of the stool samples evaluated. These results indicate a high prevalence of T. gondii in the studied populations of wild felids in captivity, with evidence of parasitemia and elimination of few oocysts even in adult hosts.
引用
收藏
页码:619 / 624
页数:6
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