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A PCR-RFLP Assay targeting RPS8 gene for the discrimination between bovine Babesia and Theileria species in China

BACKGROUND: Bovine babesiosis and theileriosis is an important hemoprotozoal disease in cattles and yaks in tropical and subtropical regions leading to significant economic losses. In the field, the risk of co-infection between the bovine Babesia and Theileria species is very high. Thus, it is neces...

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Autores principales: Tian, Zhancheng, Du, Junzheng, Yang, Jifei, Liu, Aihong, Liu, Xiaocui, Liu, Guangyuan, Yin, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573672/
https://www.ncbi.nlm.nih.gov/pubmed/26382041
http://dx.doi.org/10.1186/s13071-015-1085-x
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author Tian, Zhancheng
Du, Junzheng
Yang, Jifei
Liu, Aihong
Liu, Xiaocui
Liu, Guangyuan
Yin, Hong
author_facet Tian, Zhancheng
Du, Junzheng
Yang, Jifei
Liu, Aihong
Liu, Xiaocui
Liu, Guangyuan
Yin, Hong
author_sort Tian, Zhancheng
collection PubMed
description BACKGROUND: Bovine babesiosis and theileriosis is an important hemoprotozoal disease in cattles and yaks in tropical and subtropical regions leading to significant economic losses. In the field, the risk of co-infection between the bovine Babesia and Theileria species is very high. Thus, it is necessary to develop a simple, accurate, rapid and cost-effective method for large-scale epidemic investigation, in particular for the detection of co-infection in field. METHODS: In this study, DNA sequences of a ribosomal protein S8 (RPS8) gene from eight species of cattle piroplasms in China were used to develop a species-specific PCR-RFLP diagnostic tool. The eight Theileria and Babesia species could be differentiated by digesting the RPS8 PCR product with Mbo I. RESULTS: The sensitivity of the PCR assays was 0.1 pg DNA for Babesia species but 1 pg DNA for Theileria species. The clearly different size of the PCR-RFLP products allowed for a direct discrimination between eight bovine Theileria and Babesia species (T. annulata, T. sinensis, T. sergenti, B. ovata, B. bovis, B. bigemina, B. major and Babesia species Kashi isolate). CONCLUSION: Our results indicated that the established method based on the RPS8 gene was a reliable molecular diagnostic tool for the simultaneous detection and identification of bovine Babesia and Theileria species in China, which could be applicable for the survey of parasite dynamics, epidemiological studies as well as prevention and control of the disease.
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spelling pubmed-45736722015-09-19 A PCR-RFLP Assay targeting RPS8 gene for the discrimination between bovine Babesia and Theileria species in China Tian, Zhancheng Du, Junzheng Yang, Jifei Liu, Aihong Liu, Xiaocui Liu, Guangyuan Yin, Hong Parasit Vectors Research BACKGROUND: Bovine babesiosis and theileriosis is an important hemoprotozoal disease in cattles and yaks in tropical and subtropical regions leading to significant economic losses. In the field, the risk of co-infection between the bovine Babesia and Theileria species is very high. Thus, it is necessary to develop a simple, accurate, rapid and cost-effective method for large-scale epidemic investigation, in particular for the detection of co-infection in field. METHODS: In this study, DNA sequences of a ribosomal protein S8 (RPS8) gene from eight species of cattle piroplasms in China were used to develop a species-specific PCR-RFLP diagnostic tool. The eight Theileria and Babesia species could be differentiated by digesting the RPS8 PCR product with Mbo I. RESULTS: The sensitivity of the PCR assays was 0.1 pg DNA for Babesia species but 1 pg DNA for Theileria species. The clearly different size of the PCR-RFLP products allowed for a direct discrimination between eight bovine Theileria and Babesia species (T. annulata, T. sinensis, T. sergenti, B. ovata, B. bovis, B. bigemina, B. major and Babesia species Kashi isolate). CONCLUSION: Our results indicated that the established method based on the RPS8 gene was a reliable molecular diagnostic tool for the simultaneous detection and identification of bovine Babesia and Theileria species in China, which could be applicable for the survey of parasite dynamics, epidemiological studies as well as prevention and control of the disease. BioMed Central 2015-09-17 /pmc/articles/PMC4573672/ /pubmed/26382041 http://dx.doi.org/10.1186/s13071-015-1085-x Text en © Tian et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Tian, Zhancheng
Du, Junzheng
Yang, Jifei
Liu, Aihong
Liu, Xiaocui
Liu, Guangyuan
Yin, Hong
A PCR-RFLP Assay targeting RPS8 gene for the discrimination between bovine Babesia and Theileria species in China
title A PCR-RFLP Assay targeting RPS8 gene for the discrimination between bovine Babesia and Theileria species in China
title_full A PCR-RFLP Assay targeting RPS8 gene for the discrimination between bovine Babesia and Theileria species in China
title_fullStr A PCR-RFLP Assay targeting RPS8 gene for the discrimination between bovine Babesia and Theileria species in China
title_full_unstemmed A PCR-RFLP Assay targeting RPS8 gene for the discrimination between bovine Babesia and Theileria species in China
title_short A PCR-RFLP Assay targeting RPS8 gene for the discrimination between bovine Babesia and Theileria species in China
title_sort pcr-rflp assay targeting rps8 gene for the discrimination between bovine babesia and theileria species in china
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573672/
https://www.ncbi.nlm.nih.gov/pubmed/26382041
http://dx.doi.org/10.1186/s13071-015-1085-x
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