Literature DB >> 23394800

Isolation and genetic characterization of Toxoplasma gondii from mute swan (Cygnus olor) from the USA.

J P Dubey1, S Choudhary, O C H Kwok, L R Ferreira, S Oliveira, S K Verma, D R Marks, K Pedersen, R M Mickley, A R Randall, D Arsnoe, C Su.   

Abstract

Little is known of the genetic diversity of Toxoplasma gondii circulating in wildlife. In the present study, antibodies to T. gondii were determined in serum samples from 632 mute swans (Cygnus olor) collected from different areas of the USA. Sera were tested by T. gondii modified agglutination test; 54 (8.5%) of 632 samples were seropositive with titers of 25 in 28 sera, 50 in 22 sera, 100 in three samples, and 200 or higher in one swan. Hearts from 14 seropositive swans were bioassayed in mice and viable T. gondii (designated TgSwanUs1-3) were isolated from the hearts of three. These three T. gondii isolates were further propagated in cell culture, and DNA isolated from culture-derived tachyzoites was characterized using 11 PCR-RFLP markers (SAG1, 5'- and 3'-SAG2, alt.SAG2, SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1 and Apico). Results of genotyping revealed that two strains (TgSwanUs1, TgSwanUs2) were Type III (ToxoDB PCR-RFLP genotype #2), and TgSwanUs3 was a new genotype designated here as ToxoDB PCR-RFLP genotype #216. Pathogenicity of oocysts derived from these three strains was determined in Swiss Webster (SW) outbred mice. All mice infected with oocysts and tachyzoites of the atypical isolate (TgSwanUs3) died of acute toxoplasmosis, irrespective of the dose. Oocysts of the remaining two isolates were less pathogenic but differed from each other; 10 oocysts of the TgSwanUs1 killed all inoculated mice whereas 1 million oocysts of the TgSwanUs2 were needed to kill all infected SW mice. Isolation of T. gondii from mute swan indicates that the local waters were contaminated by T. gondii oocysts, and that mouse T. gondii virulent strains are circulating in wildlife. Mute swan is a new host record for T. gondii. Published by Elsevier B.V.

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Year:  2013        PMID: 23394800     DOI: 10.1016/j.vetpar.2012.12.051

Source DB:  PubMed          Journal:  Vet Parasitol        ISSN: 0304-4017            Impact factor:   2.738


  5 in total

1.  Genotyping Toxoplasma gondii from wildlife in Pennsylvania and identification of natural recombinants virulent to mice.

Authors:  J P Dubey; K Van Why; S K Verma; S Choudhary; O C H Kwok; A Khan; M S Behinke; L D Sibley; L R Ferreira; S Oliveira; M Weaver; R Stewart; C Su
Journal:  Vet Parasitol       Date:  2013-11-14       Impact factor: 2.738

2.  Pathogenicity of Five Strains of Toxoplasma gondii from Different Animals to Chickens.

Authors:  Shuai Wang; Guang-Wei Zhao; Wang Wang; Zhen-Chao Zhang; Bo Shen; I A Hassan; Qing Xie; Ruo-Feng Yan; Xiao-Kai Song; Li-Xin Xu; Xiang-Rui Li
Journal:  Korean J Parasitol       Date:  2015-04-22       Impact factor: 1.341

3.  Isolation and characterization of probiotics from dairies.

Authors:  Babak Haghshenas; Yousef Nami; Ali Almasi; Norhafizah Abdullah; Dayang Radiah; Rozita Rosli; Abolfazl Barzegari; Ahmad Yari Khosroushahi
Journal:  Iran J Microbiol       Date:  2017-08

4.  Prevalence of toxoplasmosis and genetic characterization of Toxoplasma gondii strains isolated in wild birds of prey and their relation with previously isolated strains from Turkey.

Authors:  Muhammet Karakavuk; Duygu Aldemir; Aurélien Mercier; Esra Atalay Şahar; Hüseyin Can; Jean-Benjamin Murat; Ömer Döndüren; Şengül Can; Hüseyin Gökhan Özdemir; Aysu Değirmenci Döşkaya; Bayram Pektaş; Marie-Laure Dardé; Adnan Yüksel Gürüz; Mert Döşkaya
Journal:  PLoS One       Date:  2018-04-18       Impact factor: 3.240

5.  First Detection of Cryptosporidium spp. in Migratory Whooper Swans (Cygnus cygnus) in China.

Authors:  Ke Wang; Azhar Gazizova; Yuexin Wang; Kaihui Zhang; Yifan Zhang; Yankai Chang; Yuan Cui; Yuxi Zhang; Sumei Zhang; Longxian Zhang
Journal:  Microorganisms       Date:  2019-12-18
  5 in total

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