4.7 Article

Development of a multiplex RT-PCR method for the detection of four porcine enteric coronaviruses

期刊

FRONTIERS IN VETERINARY SCIENCE
卷 9, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fvets.2022.1033864

关键词

porcine epidemic diarrhea virus; porcine deltacoronavirus; porcine transmissible gastroenteritis virus; swine acute diarrhea coronavirus; multiplex RT-PCR

资金

  1. Key Laboratory of Zoonosis Prevention and Control of Guangdong Province [P20211154-0302]
  2. Guangdong Province Pig Industrial System Innovation Team [2018LM1103]
  3. Key-Area R&D Program of GuangDong Province [2021B0707010009]
  4. Major Program of Zhaoqing Branch Center of Guangdong Laboratory for Lingnan Modern Agricultural Science and Technology [P20211154-0101]
  5. Guangdong Department of Science and Technology [2020B0202080004]
  6. Guangzhou Science and Technology Bureau [202103000096, 202206010192]
  7. Guangdong Provincial Science and Technology Planning Project [P20211154-030]
  8. Maoming Branch Center of Guangdong Laboratory for Lingnan Modern Agricultural Science and Technology [2021TDQD002]

向作者/读者索取更多资源

This article introduces a quadruplex RT-PCR method that can simultaneously detect four porcine enteric coronaviruses. The method has good specificity and low detection limits, making it suitable for monitoring and researching the prevalence of diseases.
Porcine enteric coronaviruses are pathogens that cause viral diarrhea in pigs and are widely prevalent worldwide. Moreover, studies have shown that some porcine enteric coronaviruses can infect humans and poultry. In order to effectively monitor these viruses, it is necessary to establish a multiple detection method to understand their prevalence and conduct in-depth research. Common porcine enteric coronaviruses include Porcine epidemic diarrhea virus (PEDV), Porcine transmissible gastroenteritis virus (TGEV), Porcine delta coronavirus (PDCoV), and Swine acute diarrhea syndrome coronavirus (SADS-CoV). Pigs infected with these viruses have the common clinical symptoms that are difficult to distinguish. A quadruplex RT-PCR (reverse transcription-polymerase chain reaction) method for the simultaneous detection of PEDV, PDCoV, TGEV and SADS-CoV was developed. Four pairs of specific primers were designed for the PEDV M gene, PDCoV N gene, TGEV S gene and SADS-CoV RdRp gene. Multiplex RT-PCR results showed that the target fragments of PDCoV, SADS-CoV, PEDV and TGEV could be amplified by this method. and the specific fragments with sizes of 250 bp, 368 bp, 616 bp and 801 bp were amplified, respectively. This method cannot amplify any fragment of nucleic acids of Seneca Valley virus (SVV), Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) and Atypical Porcine Pestivirus (APPV), and has good specificity. The lowest detection limits of PDCoV, PEDV, TGEV and SADS-CoV were 5.66 x 10(5) copies/mu L, 6.48 x 10(5) copies/mu L, 8.54 x 10(5) copies/mu L and 7.79 x 10(6) copies/mu L, respectively. A total of 94 samples were collected from pig farms were analyzed using this method. There were 15 positive samples for PEDV, 3 positive samples for mixed infection of PEDV and PDCoV, 2 positive samples for mixed infection of PEDV and TGEV, and 1 positive sample for mixed infection of PEDV, TGEV, and PDCoV. Multiplex RT-PCR method could detect four intestinal coronaviruses (PEDV, PDCoV, TGEV, and SADS-CoV) in pigs efficiently, cheaply and accurately, which can be used for clinical large-scale epidemiological investigation and diagnosis.

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