A novel one-step amplification refractory mutation system PCR (ARMS-PCR) for differentiation of canine parvovirus-2 variants

被引:6
|
作者
Dema, Anusha [1 ]
Ganji, Vishweshwar Kumar [1 ]
Yella, Narasimha Reddy [2 ]
Putty, Kalyani [1 ]
机构
[1] PVNRTVU, Coll Vet Sci, Dept Vet Biotechnol, Hyderabad 500030, India
[2] PVNRTVU, Coll Vet Sci, Dept Vet Microbiol, Hyderabad 500030, India
关键词
CPV-2; ARMS-PCR; Antigenic typing; Phylogenetic analysis; POLYMERASE-CHAIN-REACTION; PARTIAL VP2 GENE; PHYLOGENETIC ANALYSIS; MOLECULAR CHARACTERIZATION; TYPE-2; EPIDEMIOLOGY; REPLACEMENT; EVOLUTION; DIAGNOSIS; SEQUENCE;
D O I
10.1007/s11262-021-01861-w
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Enteritis caused by CPV-2 antigenic variants (CPV-2a, 2b, and 2c) is frequently reported in dogs worldwide leading to significant morbidity and mortality. Here, we describe about a simple, single-step, ARMS-PCR strategy targeting the mutant 426 amino acid of VP2 to differentiate CPV-2 antigenic types. A total of 150 fecal samples were subjected to ARMS-PCR of which 18 were typed as CPV-2a, 79 were typed as CPV-2b, and 6 were typed as CPV-2c. The ARMS-PCR results were validated by randomly sequencing partial VP2 gene of 14 samples. Phylogenetic analysis of partial VP2 gene sequencing of each of the CPV-2 variants revealed that CPV-2a and CPV-2b isolates formed a separate clade of Indian lineage, while CPV-2c shared common evolutionary origin with Asian lineage. The developed technique is first of its kind, one-step, rapid, sequencing independent method for typing of CPV-2 antigenic variants.
引用
收藏
页码:426 / 433
页数:8
相关论文
共 50 条
  • [41] A novel one-step quantitative reverse transcription PCR assay for selective amplification of hepatitis B virus pregenomic RNA from a mixture of HBV DNA and RNA in serum
    Ming Gao
    Chengqian Feng
    Ruosu Ying
    Yuan Nie
    Xizi Deng
    Ying Zhu
    Xiaoping Tang
    Yujuan Guan
    Fengyu Hu
    Feng Li
    Archives of Virology, 2019, 164 : 2683 - 2690
  • [42] A novel one-step quantitative reverse transcription PCR assay for selective amplification of hepatitis B virus pregenomic RNA from a mixture of HBV DNA and RNA in serum
    Gao, Ming
    Feng, Chengqian
    Ying, Ruosu
    Nie, Yuan
    Deng, Xizi
    Zhu, Ying
    Tang, Xiaoping
    Guan, Yujuan
    Hu, Fengyu
    Li, Feng
    ARCHIVES OF VIROLOGY, 2019, 164 (11) : 2683 - 2690
  • [43] Development of a Quantitative One-Step RT-PCR Method for the Detection of Sabin 2 Virus Contamination in a Novel Oral Poliovirus Vaccine Type 2
    Manukyan, Hasmik
    Tritama, Erman
    Wahid, Rahnuma
    Ansari, Azeem
    Konz, John
    Chumakov, Konstantin
    Laassri, Majid
    VACCINES, 2021, 9 (07)
  • [44] Quantitative Detection of the M204V Hepatitis B Virus Minor Variants by Amplification Refractory Mutation System Real-Time PCR Combined with Molecular Beacon Technology
    Ntziora, F.
    Paraskevis, D.
    Haida, C.
    Magiorkinis, E.
    Manesis, E.
    Papatheodoridis, G.
    Manolakopoulos, S.
    Beloukas, A.
    Chryssoy, S.
    Magiorkinis, G.
    Sypsa, V.
    Hatzakis, A.
    JOURNAL OF CLINICAL MICROBIOLOGY, 2009, 47 (08) : 2544 - 2550
  • [45] A broad spectrum, one-step RT-PCR to detect Satsuma dwarf virus variants using universal primers targeting both segmented RNAs 1 and 2
    Shimizu, Shin-ichi
    Ito, Takao
    Miyoshi, Takanori
    Tachibana, Yasunobu
    Ito, Tsutae
    JOURNAL OF GENERAL PLANT PATHOLOGY, 2011, 77 (06) : 326 - 330
  • [46] A broad spectrum, one-step RT-PCR to detect Satsuma dwarf virus variants using universal primers targeting both segmented RNAs 1 and 2
    Shin-ichi Shimizu
    Takao Ito
    Takanori Miyoshi
    Yasunobu Tachibana
    Tsutae Ito
    Journal of General Plant Pathology, 2011, 77 : 326 - 330
  • [47] Comparison of different molecular methods for assessment of equine arteritis virus (EAV) infection: A novel one-step MGB real-time RT-PCR assay, PCR-ELISA and classical RT-PCR for detection of highly diverse sequences of Slovenian EAV variants
    Mankoc, S.
    Hostnik, P.
    Grom, J.
    Toplak, I.
    Klobucar, I.
    Kosec, M.
    Barlic-Maganja, D.
    JOURNAL OF VIROLOGICAL METHODS, 2007, 146 (1-2) : 341 - 354
  • [48] Polymerase chain reaction-restriction fragment length polymorphism (PCR-RELP) and Amplification Refractory Mutation System (ARMS) analyses of medicinally used Rheum species and their application for identification of Rhei rhizoma
    Yang, DY
    Fushimi, H
    Cai, SQ
    Komatsu, K
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2004, 27 (05) : 661 - 669
  • [49] Novel One-Step Single-Tube Nested Quantitative Real-Time PCR Assay for Highly Sensitive Detection of SARS-CoV-2
    Wang, Ji
    Cai, Kun
    Zhang, Ruiqing
    He, Xiaozhou
    Shen, Xinxin
    Liu, Jun
    Xu, Junqiang
    Qiu, Feng
    Lei, Wenwen
    Wang, Jinrong
    Li, Xinna
    Gao, Yuan
    Jiang, Yongzhong
    Xu, Wenbo
    Ma, Xuejun
    ANALYTICAL CHEMISTRY, 2020, 92 (13) : 9399 - 9404
  • [50] Genotyping the CRHR1 rs242939 (A > G) Polymorphism by a One-Step Tetra Primer-Amplification Refractory Mutation System-Polymerase Chain Reaction
    Sharma, Neeraj
    Awasthi, Shally
    Phadke, Subha R.
    Gupta, Sarika
    GENETIC TESTING AND MOLECULAR BIOMARKERS, 2012, 16 (07) : 794 - 797