Please wait a minute...
Journal of Integrative Agriculture  2012, Vol. 12 Issue (8): 1347-1353    DOI: 10.1016/S1671-2927(00)8665
ANIMAL SCIENCE · VETERINARY SCIENCE Advanced Online Publication | Current Issue | Archive | Adv Search |
Isolation and Molecular Characterization of Toxoplasma gondii from Chickens in China
 ZHAO Guang-wei, SHEN Bo, XIE Qing, XU Li-xin, YAN Ruo-feng, SONG Xiao-kai, Hassan Ibrahim Adam,  LI Xiang-rui
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, P.R.China
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
摘要  One strain of Toxoplasma gondii was successfully isolated from chickens in China by bioassay in mice. Antibodies and circulating antigens of T. gondii were assayed by the ELISA kits in 100 free range chickens from a rural area surrounding Funing, China. Fifty-three chickens were antibody-positive and 21 chickens were antigen positive. Hearts, brains, spleens, lungs, livers, and kidneys of 21 antibody or antigen-positive chickens were bioassayed in mice. One strain of T. gondii was isolated from 1 of 21 (4.76%) chickens. The isolated T. gondii killed all of the inoculated mice. Genotyping of this isolate using polymorphisms at the loci 5´-SAG2, 3´-SAG2, SAG3, cB21-4, L358, BTUB, and GRA6 revealed that it was Type I. These indicated that it was virulent for mice. This is the first report of isolation of T. gondii from chickens in China.

Abstract  One strain of Toxoplasma gondii was successfully isolated from chickens in China by bioassay in mice. Antibodies and circulating antigens of T. gondii were assayed by the ELISA kits in 100 free range chickens from a rural area surrounding Funing, China. Fifty-three chickens were antibody-positive and 21 chickens were antigen positive. Hearts, brains, spleens, lungs, livers, and kidneys of 21 antibody or antigen-positive chickens were bioassayed in mice. One strain of T. gondii was isolated from 1 of 21 (4.76%) chickens. The isolated T. gondii killed all of the inoculated mice. Genotyping of this isolate using polymorphisms at the loci 5´-SAG2, 3´-SAG2, SAG3, cB21-4, L358, BTUB, and GRA6 revealed that it was Type I. These indicated that it was virulent for mice. This is the first report of isolation of T. gondii from chickens in China.
Keywords:  Toxoplasma gondii      chickens      China      isolation  
Received: 29 March 2011   Accepted:
Fund: 

This work was supported by the Special Fund for Public Welfare Industry of Chinese Ministry of Agriculture (200903036-04).

Corresponding Authors:  Correspondence LI Xiang-rui, Tel: +86-25-84399000, Fax: +86-25-84399000, E-mail:Lixiangrui@njau.edu.cn     E-mail:  Lixiangrui@njau.edu.cn
About author:  ZHAO Guang-wei, Mobile: 18936036162, E-mail: 2009207019@njau.edu.cn

Cite this article: 

ZHAO Guang-wei, SHEN Bo, XIE Qing, XU Li-xin, YAN Ruo-feng, SONG Xiao-kai, Hassan Ibrahim Adam, LI Xiang-rui. 2012. Isolation and Molecular Characterization of Toxoplasma gondii from Chickens in China. Journal of Integrative Agriculture, 12(8): 1347-1353.

[1]de Adriana M F, Ricardo W A V, Ricardo T G, Maria N M. 2006. Genetic analysis of natural recombinant Brazilian Toxoplasma gondii strains by multilocus PCR-RFLP. Infection Genetics and Evolution, 6, 22-31.

[2]Dubey J P. 1998. Refinement of pepsin digestion method for isolation of Toxoplasma gondii from infected tissues. Veterinary Parasitology, 74, 75-77.

[3]Dubey J P, Beattie C P. 1988. Toxoplasmosis of Animals and Man. Boca Raton, CRC Press, USA. p. 220. Dubey J P, Edelhofer R, Marcet P, Vianna M C B, Kwok O C H, Lehmann T. 2005a. Genetic and biologic characteristics of Toxoplasma gondii infections in free range chickens from Austria. Veterinary Parasitology, 133, 299-306.

[4]Dubey J P, Gomez-Marin J E, Bedoya A, Lora F, Vianna M C B, Hill D, Kwok O C H, Shen S K, Marcet P L, Lehmann T. 2005b. Genetic and biologic characteristics of Toxoplasma gondii isolates in free-range chickens from Colombia, South America. Veterinary Parasitology, 134, 67-72.

[5]Dubey J P, Graham D H, Dahl E, Sreekumar C, Lehmann T, Davis M F, Morishita T Y. 2003a. Toxoplasma gondii isolates from free-ranging chickens from the United States. Journal of Parasitology, 89, 1060-1062.

[6]Dubey J P, Huong L T, Lawson B W, Subekti D T, Tassi P, Cabaj W, Sundar N, Velmurugan G V, Kwok O C, Su C. 2008. Seroprevalence and isolation of Toxoplasma gondii from free-range chickens in Ghana, Indonesia, Italy, Poland, and Vietnam. Journal of Parasitology, 94, 68-71.

[7]Dubey J P, Jones J L. 2008. Toxoplasma gondii infection in humans and animals in the United States. International Journal for Parasitology, 38, 1257-1278.

[8]Dubey J P, Marcet P L, Lehmann T. 2005c. Characterization of Toxoplasma gondii isolates from free-range chickens in Argentina. Journal of Parasitology, 91, 1335-1339.

[9]Dubey J P, Navarro I T, Graham D H, Dahl E, Freire R L, Prudencio L B, Sreekumar C, Vianna M C, Lehmann T. 2003b. Characterization of Toxoplasma gondii isolates from free range chickens from Paraná, Brazil. Veterinary Parasitology, 117, 229-234.

[10]Dubey J P, Patitucci A N, Su C, Sundar N, Kwok O C H, Shen S K. 2006a. Characterization of Toxoplasma gondii isolates in free-range chickens from Chile, South America. Veterinary Parasitology, 140, 76-82.

[11]Dubey J P, Sundar N, Pineda N, Kyvsgaard N C, Luna L A, Rimbaud E, Oliveira J B, Kwok O C H, Qi Y, Su C. 2006b. Biologic and genetic characteristics of Toxoplasma gondii isolates in free-range chickens from Nicaragua, Central America. Veterinary Parasitology, 142, 47-53.

[12]Frenkel J K, Dubey J P, Miller N L. 1970. Toxoplasma gondii in cats: fecal stages identidied as coccidian oocysts. Science, 167, 893-896.

[13]Grigg M E, Ganatra J, Boothrooyd J C, Margolis T P. 2001. Unusual abundance of atypical strains associated with human ocular toxoplasmosis. Journal of Infectious Diseases, 184, 633-639.

[14]Howe D K, Honore S, Derouin F, Sibley L D. 1997. Determination of genotypes of Toxoplasma gondii strains isolated from patients with toxoplasmosis. Journal of Clinical Microbiology, 35, 1411-1414.

[15]Howe D K, Sibley L D. 1995. Toxoplasma gondii comprises three clonal lineages: correlation of parasite genotype with human disease. Journal of Infectious Diseases, 172, 1561-1566.

[16]Khan A, Su C, German M, Storch G A, Clifford D B, Sibley L D. 2005. Genotyping of Toxoplasma gondii strains from immunocompromised patients reveals high prevalence of type I strains. Journal of Clinical Microbiology, 43, 5881-5887.

[17]Mondragon R, Howe D K, Dubey J P, Sibley L D. 1998. Genotypic analysis of Toxoplasma gondii isolates from pigs. Journal of Parasitology, 84, 639-641.

[18]Pena H F J, Marvulo M F V, Horta M C, Silva M A, Silva J C R, Siqueira D B, Lima P A C P, Vitaliano S N, Gennari S M. 2011. Veterinary Parasitology, 175, 377-381.

[19]Sreekumar C, Graham D H, Dahl E, Lehmann T, Raman M, Bhalerao D P, Vianna M C B, Dubey J P. 2003. Genotyping of Toxoplasma gondii isolates from chickens from India. Veterinary Parasitology, 118, 187-194.

[20]Su C, Howe D K, Dubey J P, Ajioka J W, Sibley L D. 2002. Identification of quantitative trait loci controlling acute virulence in Toxoplasma gondii. Proceedings of the National Academy of Sciences of the United States of America, 99, 10753-10758.

[21]Wang Y H, Li X R, Wang G X, Yin H, Cai X P, Fu B Q, Zhang D L. 2011. Development of an immunochromatographic strip for the rapid detection of Toxoplasma gondii circulating antigens. Parasitology International, 60, 105-107.

[22]Yan C, Yue C L, Yuan Z G, He Y, Yin C C, Lin R Q, Dubey J P, Zhu X Q. 2009. Toxoplasma gondii infection in domestic ducks, free-range and caged chickens in southern China. Veterinary Parasitology, 165, 337-340.

[23]Yan C, Yue C L, Yuan Z G, Lin R Q, He Y, Yin C C, Xu M J, Song H Q, Zhu X Q. 2010. Molecular and serological diagnosis of Toxoplasma gondii infection in experimentally infected chickens. Veterinary Parasitology, 173, 179-183.

[24]Zhu J B, Yin J G, XiaoY, Jiang N, Ankarlev J, Lindh J, Chen Q J. 2008. A sero-epidemiological survey of Toxoplasma gondii infection in free-range and caged chickens in northeast China. Veterinary Parasitology, 158, 360-363.
[1] Libin Liang, Yaning Bai, Wenyan Huang, Pengfei Ren, Xing Li, Dou Wang, Yuhan Yang, Zhen Gao, Jiao Tang, Xingchen Wu, Shimin Gao, Yanna Guo, Mingming Hu, Zhiwei Wang, Zhongbing Wang, Haili Ma, Junping Li. Genetic and biological properties of H9N2 avian influenza viruses isolated in central China from 2020 to 2022[J]. >Journal of Integrative Agriculture, 2024, 23(8): 2778-2791.
[2] Lingzhai Meng, Mengmeng Yu, Suyan Wang, Yuntong Chen, Yuanling Bao, Peng Liu, Xiaoyan Feng, Tana He, Ru Guo, Tao Zhang, Mingxue Hu, Changjun Liu, Xiaole Qi, Kai Li, Li Gao, Yanping Zhang, Hongyu Cui, Yulong Gao.

A novel live attenuated vaccine candidate protects chickens against subtype B avian metapneumovirus [J]. >Journal of Integrative Agriculture, 2024, 23(5): 1658-1670.

[3] Xuan Li, Shaowen Wang, Yifan Chen, Danwen Zhang, Shanshan Yang, Jingwen Wang, Jiahua Zhang, Yun Bai, Sha Zhang.

Improved simulation of winter wheat yield in North China Plain by using PRYM-Wheat integrated dry matter distribution coefficient [J]. >Journal of Integrative Agriculture, 2024, 23(4): 1381-1392.

[4] Dian Chen, Xiangming Fang, Yu Chen, Xiaodong Zheng, Zhuo Chen, Rodney B.W. Smith.

The impact of the Rural Minimum Living Standard Guarantee (Rural Dibao) Program on child nutrition outcomes [J]. >Journal of Integrative Agriculture, 2024, 23(2): 444-456.

[5] Yi Cui, Qiran Zhao, Thomas Glauben, Wei Si. The impact of Internet access on household dietary quality: Evidence from rural China[J]. >Journal of Integrative Agriculture, 2024, 23(2): 374-383.
[6] Xiao Han, Kaiyu Lyu, Fengying Nie, Yuquan Chen.

Resilience effects for household food expenditure and dietary diversity in rural western China [J]. >Journal of Integrative Agriculture, 2024, 23(2): 384-396.

[7] Jie Xue, Xianglin Zhang, Songchao Chen, Bifeng Hu, Nan Wang, Zhou Shi.

Quantifying the agreement and accuracy characteristics of four satellite-based LULC products for cropland classification in China [J]. >Journal of Integrative Agriculture, 2024, 23(1): 283-297.

[8] ZHANG Sha, YANG Shan-shan, WANG Jing-wen, WU Xi-fang, Malak HENCHIRI, Tehseen JAVED, ZHANG Jia-hua, BAI Yun. Integrating a novel irrigation approximation method with a process-based remote sensing model to estimate multi-years' winter wheat yield over the North China Plain[J]. >Journal of Integrative Agriculture, 2023, 22(9): 2865-2881.
[9] YU Wen-jia, LI Hai-gang, Peteh M. NKEBIWE, YANG Xue-yun, GUO Da-yong, LI Cui-lan, ZHU Yi-yong, XIAO Jing-xiu, LI Guo-hua, SUN Zhi, Torsten MÜLLER, SHEN Jian-bo. Combining rhizosphere and soil-based P management decreased the P fertilizer demand of China by more than half based on LePA model simulations[J]. >Journal of Integrative Agriculture, 2023, 22(8): 2509-2520.
[10] LI Dong-qing, ZHANG Ming-xue, LÜ Xin-xin, HOU Ling-ling. Does nature-based solution sustain grassland quality? Evidence from rotational grazing practice in China[J]. >Journal of Integrative Agriculture, 2023, 22(8): 2567-2576.
[11] YANG Rui, XU Hang. Water diversion and agricultural production: Evidence from China[J]. >Journal of Integrative Agriculture, 2023, 22(4): 1244-1257.
[12] HOU Jing, ZHOU Li, Jennifer IFFT, YING Rui-yao. The role of time preferences in contract breach: Evidence from Chinese poultry farmers participating in contract farming[J]. >Journal of Integrative Agriculture, 2023, 22(2): 623-641.
[13] SHI Peng-fei, HUANG Ji-kun. Rural transformation, income growth, and poverty reduction by region in China in the past four decades[J]. >Journal of Integrative Agriculture, 2023, 22(12): 3582-3595.
[14] YANG Xu, ZHANG Jia-hua, YANG Shan-shan, WANG Jing-wen, BAI Yun, ZHANG Sha. Modelling the crop yield gap with a remote sensing-based process model: A case study of winter wheat in the North China Plain[J]. >Journal of Integrative Agriculture, 2023, 22(10): 2993-3005.
[15] ZENG Xian-ying, HE Xin-wen, MENG Fei, MA Qi, WANG Yan, BAO Hong-mei, LIU Yan-jing, DENG Guo-hua, SHI Jian-zhong, LI Yan-bing, TIAN Guo-bin, CHEN Hua-lan. Protective efficacy of an H5/H7 trivalent inactivated vaccine (H5-Re13, H5-Re14, and H7-Re4 strains) in chickens, ducks, and geese against newly detected H5N1, H5N6, H5N8, and H7N9 viruses[J]. >Journal of Integrative Agriculture, 2022, 21(7): 2086-2094.
No Suggested Reading articles found!