Literature DB >> 15893073

Detection of specific antibodies to Neospora caninum and Toxoplasma gondii in naturally infected alpacas (Lama pacos), llamas (Lama glama) and vicunas (Lama vicugna) from Peru and Germany.

D Wolf1, G Schares, O Cardenas, W Huanca, Aida Cordero, Andrea Bärwald, F J Conraths, M Gauly, H Zahner, C Bauer.   

Abstract

Sera of an experimentally Neospora caninum infected llama and a non-infected control llama were used to establish an immunoblot, an ELISA and an IFAT to detect antibodies against N. caninum tachyzoites. Subsequently, serum samples collected from a total of 871 South American Camelids (SAC: Lama glama, Lama pacos, Lama vicugna) of two farms in Peru and from 32 SAC of a farm in central Germany were examined for antibodies against N. caninum and Toxoplasma gondii. Based on the recognition of specific bands in the immunoblot, sera of SAC from Peru were differentiated into N. caninum-positive (n = 18) and T. gondii-positive (n = 30) samples and into samples negative or inconclusive for both parasites. Using the immunoblot results as the reference, a modified version of the p38-ELISA and the IFAT were evaluated for detecting N. caninum antibodies in SAC sera. Applying a cut-off as determined by two graph-receiver operating characteristic analysis both, the ELISA and the IFAT, exhibited a sensitivity and specificity of about 95% in the SAC sera from Peru. Serological testing confirmed that SAC may become infected with N. caninum under field conditions in Peru. In addition to alpacas and llamas also 114 wild living vicunas had been examined for antibodies against N. caninum. However, only the alpacas and llamas but no vicunas were found N. caninum-positive. In contrast, T. gondii-seropositive animals were detected in all three SAC species. The lack of N. caninum-seropositive vicunas indicates that in the study area in Peru wild canids might not serve as definitive hosts of N. caninum while for T. gondii a life cycle including wild felids is likely. On the German farm no N. caninum- but only T. gondii-seropositive SAC (n = 14) were detected. The seroprevalence of T. gondii infection was significantly higher in adult SAC (alpacas in Peru, llamas in Germany) than in crias (i.e. < 12 months old foals) indicating that the predominant route of infection is post natal. Since the present study was restricted to a few farms, the seroprevalences determined are not representative. However, our results confirm natural infections with N. caninum and T. gondii in SAC. Whether these infections are linked to any disease, e.g. reproductive losses, has to be clarified in further studies.

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Year:  2005        PMID: 15893073     DOI: 10.1016/j.vetpar.2005.03.024

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


  9 in total

1.  Toxoplasma gondii and Neospora caninum seroprevalences in domestic South American camelids of the Peruvian Andes.

Authors:  Amanda Chávez-Velásquez; Adriana Aguado-Martínez; Luis M Ortega-Mora; Eva Casas-Astos; Enrique Serrano-Martínez; Gina Casas-Velásquez; Jose A Ruiz-Santa-Quiteria; Gema Alvarez-García
Journal:  Trop Anim Health Prod       Date:  2014-05-25       Impact factor: 1.559

2.  Seroprevalence of Neospora caninum and Toxoplasma gondii in exotic ruminants and camelids in the Czech Republic.

Authors:  Eva Bártová; Kateřina Kobédová; Jiří Lamka; Radim Kotrba; Roman Vodička; Kamil Sedlák
Journal:  Parasitol Res       Date:  2017-05-11       Impact factor: 2.289

3.  Isolation and genetic characterization of Toxoplasma gondii from alpaca (Vicugna pacos) and sheep (Ovis aries).

Authors:  Jitender Prakash Dubey; Sarah Jane Casey; Anne Marie Zajac; Stephen Arthur Wildeus; David Scott Lindsay; Shiv Kumar Verma; Solange Oliveira; Oliver Chun Hung Kwok; Chunlei Su
Journal:  Trop Anim Health Prod       Date:  2014-08-06       Impact factor: 1.559

4.  Health impact evaluation of alternative management systems in vicuña (Vicugna vicugna mensalis) populations in Peru.

Authors:  Veronica Risco-Castillo; Jane Collins Wheeler; Raúl Rosadio; Francisco Javier García-Peña; Ignacio Arnaiz-Seco; Domingo Hoces; Hugo Castillo; Álvaro Veliz; Luis Miguel Ortega-Mora
Journal:  Trop Anim Health Prod       Date:  2014-02-05       Impact factor: 1.559

Review 5.  Epidemiology and control of neosporosis and Neospora caninum.

Authors:  J P Dubey; G Schares; L M Ortega-Mora
Journal:  Clin Microbiol Rev       Date:  2007-04       Impact factor: 26.132

6.  Toxoplasma gondii and Neospora caninum infections in sheep and goats in Switzerland: Seroprevalence and occurrence in aborted foetuses.

Authors:  Walter Basso; Fabienne Holenweger; Gereon Schares; Norbert Müller; Lucía M Campero; Flurin Ardüser; Gaia Moore-Jones; Caroline F Frey; Patrik Zanolari
Journal:  Food Waterborne Parasitol       Date:  2022-08-17

7.  First molecular detection of Neospora caninum from naturally infected slaughtered camels in Tunisia.

Authors:  Yosra Amdouni; Imen Abedennebi; Safa Amairia; Amara Abdelkader; Walid Chandoul; Mohamed Gharbi
Journal:  Vet Med Sci       Date:  2022-08-16

Review 8.  Neospora caninum and Wildlife.

Authors:  Sonia Almería
Journal:  ISRN Parasitol       Date:  2013-06-24

9.  Toxoplasma gondii and Neospora caninum infections in South American camelids in Switzerland and assessment of serological tests for diagnosis.

Authors:  Walter Basso; Elena Sollberger; Gereon Schares; Susanne Küker; Flurin Ardüser; Gaia Moore-Jones; Patrik Zanolari
Journal:  Parasit Vectors       Date:  2020-05-14       Impact factor: 3.876

  9 in total

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