Universal primer multiplex PCR assay for detection and genotyping of porcine astroviruses

被引:0
|
作者
Zhang, Qiuya [1 ]
Wen, Dan [1 ]
Liu, Qin [1 ]
Opriessnig, Tanja [2 ,3 ]
Yu, Xiaoya [1 ]
Jiang, Yonghou [1 ,4 ]
机构
[1] Zhejiang Sci Tech Univ, Coll Life Sci & Med, Hangzhou, Peoples R China
[2] Moredun Res Inst, Vaccines & Diagnost Dept, Penicuik, Midlothian, Scotland
[3] Iowa State Univ, Coll Vet Med, Dept Vet Diagnost & Prod Anim Med, Ames, IA USA
[4] Zhejiang Sci Tech Univ, Coll Life Sci & Med, 2nd St, Hangzhou 310018, Peoples R China
关键词
Universal primer; Multiplex PCR; Porcine astroviruses; Genotyping; Detection; HIGH PREVALENCE; IDENTIFICATION; PIGS; DISEASE;
D O I
10.1016/j.jviromet.2023.114822
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Porcine astroviruses (PAstV) are members of the family Astroviridae, Mamastravirus genus and have been identified to have five genotypes (PAstV1-5). These viruses are highly prevalent in pigs and can cause enteric disease as well as neurological or respiratory symptoms depending on their genotypes. At present, the epidemiological impacts of some PAstV genotypes on pigs are largely unknown and hence continuously monitoring of these PAstVs may be needed. The purpose of this research was to develop an improved and efficient detection tool for PAstVs and to evaluate the developed method using clinical samples. Initially, a set of five chimeric primers (CP), each comprising genotype specific primer pairs with an identical universal adapter at the 5' end, and a universal primer (UP) that is identical to universal adapter sequence, were designed. With these tools in place, a novel multiplex PCR system with universal primer was established for the simultaneous detection of the five types of PAstV. This method can specifically detect PAstV genotypes, with a limit of detection (LOD) of 5 copies/mu L for each genotype irrespective of single or mixed target template. Using this new assay, 273 pig fecal samples were investigated for further assay evaluation. Among all samples, the positive rate was 70.0% with PAstV4 in 56.8% of the samples, PAstV2 in 38.8%, PAstV1 in 16.8%, and PAstV5 in 11.0%. More than one PAstV in a sample were detected in 39.2% of the samples. The consistency rate between the novel multiplex PCR and singleplex PCRs was 96.4-100%. Given its rapidity, specificity and sensitivity, the novel multiplex PCR is a useful approach for demonstrating single or mixed genotype infections of PAstV.
引用
收藏
页数:6
相关论文
共 50 条
  • [1] Multiplex gel-based PCR assay for the simultaneous detection of 5 genotypes of porcine astroviruses
    Zhang, Qiuya
    Liu, Qin
    Opriessnig, Tanja
    Wen, Dan
    Gu, Keda
    Jiang, Yonghou
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2023, 35 (02) : 132 - 138
  • [2] Multiplex detection and genotyping of pathogenic bacteria on paper-based biosensor with a novel universal primer mediated asymmetric PCR
    Liu, Fang
    Liu, Hongxing
    Liao, Yuhui
    Wei, Jitao
    Zhou, Xiaoming
    Xing, Da
    BIOSENSORS & BIOELECTRONICS, 2015, 74 : 778 - 785
  • [3] Establishment of a Multiplex RT-PCR Method for the Detection of Five Known Genotypes of Porcine Astroviruses
    Liu, Xin
    Zhang, Wenchao
    Wang, Dongjing
    Zhu, Xinyue
    Chen, Ying
    Ouyang, Kang
    Wei, Zuzhang
    Liu, Huan
    Huang, Weijian
    FRONTIERS IN VETERINARY SCIENCE, 2021, 8
  • [4] A multiplex PCR assay with a common primer for the detection of eleven foodborne pathogens
    Tao, Jing
    Liu, Wanwan
    Ding, Wei
    Han, Rong
    Shen, Qiang
    Xia, Yu
    Zhang, Yahan
    Sun, Wanping
    JOURNAL OF FOOD SCIENCE, 2020, 85 (03) : 744 - 754
  • [5] Universal PCR Genotyping Assay that Achieves Single copy Sensitivity with Any Primer Pair
    Jennifer L. Stratman
    Wayne M. Barnes
    Theodore C. Simon
    Transgenic Research, 2003, 12 : 521 - 522
  • [6] Universal PCR genotyping assay that achieves single copy sensitivity with any primer pair
    Stratman, JL
    Barnes, WM
    Simon, TC
    TRANSGENIC RESEARCH, 2003, 12 (04) : 521 - 522
  • [7] Novel multiplex qualitative detection using universal primer-multiplex-PCR combined with pyrosequencing
    Shang, Ying
    Xu, Wentao
    Wang, Yong
    Xu, Yuancong
    Huang, Kunlun
    FOOD CHEMISTRY, 2017, 237 : 773 - 778
  • [8] Multiplex pyrosequencing quantitative detection combined with universal primer-multiplex-PCR for genetically modified organisms
    Shang, Ying
    Xu, Yuancong
    Huang, Kunlun
    Luo, Yunbo
    Xu, Wentao
    FOOD CHEMISTRY, 2020, 320
  • [9] Robust SNP genotyping by multiplex PCR and arrayed primer extension
    Mohua Podder
    Jian Ruan
    Ben W Tripp
    Zane E Chu
    Scott J Tebbutt
    BMC Medical Genomics, 1
  • [10] Robust SNP genotyping by multiplex PCR and arrayed primer extension
    Podder, Mohua
    Ruan, Jian
    Tripp, Ben W.
    Chu, Zane E.
    Tebbutt, Scott J.
    BMC MEDICAL GENOMICS, 2008, 1 (1)