College of Veterinary Medicine, University of Agriculture, Makurdi, Benue State, Nigeria; Faculty of Veterinary Medicine, Sumy National Agrarian University, 160 Herasima Kondratieva Street, Sumy 40021, Ukraine.
Department of Veterinary Medicine, University of Ibadan, Oyo State, Nigeria.
Infect Genet Evol. 2021 Oct;94:104996. doi: 10.1016/j.meegid.2021.104996. Epub 2021 Jul 8.
Canine parvovirus (CPV) is a fast-evolving single-stranded DNA virus that causes severe and fatal gastrointestinal disease in dogs. Lately, several mutations affecting viral protein (VP) capsid resulting in highly pathogenic variants with distinctive immunological and clinicopathological characteristics abound. This study involved screening stools of 44 randomly selected clinical cases of canine gastroenteritis from 4 cities (Ibadan, Jos, Makurdi, and Zaria) in Nigeria for CPV antigen using an on-the-spot immunoassay test kit, as well as, molecular detection of viral nucleic acid by polymerase chain reaction. Subsequently, nucleic acid sequencing of 1195-bp amplicons encompassing the VP2 encoding region was done. The resultant 40 high-quality amino acid sequences obtained were analysed for the identification and grouping of the viruses into their discrete variants - CPV-2a, CPV-2b, or CPV-2c, using key amino acids substitutions - Asn, Asp, or Glu respectively at position 426 of the VP2 gene. One-third (11/40; 27.5%) of the analysed sequences were identified as CPV-2a and two-third (29/40; 72.5%) as CPV-2c. The original CPV and CPV-2b were not detected. Also, the "new CPV-2a variant" with mutation S297A identified had two additional mutations (Y324I and T440A) associated with selective pressure and vaccination failure in their sequences. Similarly, unique CPV-2c mutants carrying genetic markers (S297A, Y324I, and Q370R) that are highly related to CPVs of Asian origin were observed. These findings revealed a high level of divergence of existing CPVs in circulation; suggesting that CPV is rapidly evolving in Nigeria lately.
犬细小病毒(CPV)是一种快速进化的单链 DNA 病毒,可导致犬严重且致命的胃肠道疾病。最近,出现了多种影响病毒蛋白(VP)衣壳的突变,导致具有独特免疫和临床病理特征的高致病性变体大量出现。本研究使用现场免疫测定试剂盒对来自尼日利亚 4 个城市(伊巴丹、乔斯、马库尔迪和扎里亚)的 44 例随机选择的犬胃肠炎临床病例的粪便进行 CPV 抗原筛查,并通过聚合酶链反应进行病毒核酸的分子检测。随后,对包含 VP2 编码区的 1195bp 扩增子进行核酸测序。获得的 40 条高质量氨基酸序列用于分析鉴定和分组病毒为其离散变体 - CPV-2a、CPV-2b 或 CPV-2c,使用关键氨基酸取代 - 分别在 VP2 基因的位置 426 处的 Asn、Asp 或 Glu。分析的序列中有三分之一(11/40;27.5%)鉴定为 CPV-2a,三分之二(29/40;72.5%)鉴定为 CPV-2c。未检测到原始 CPV 和 CPV-2b。此外,鉴定出的具有突变 S297A 的“新 CPV-2a 变体”还具有与选择性压力和疫苗接种失败相关的两个额外突变(Y324I 和 T440A)。同样,观察到携带与亚洲来源的 CPV 高度相关的遗传标记(S297A、Y324I 和 Q370R)的独特 CPV-2c 突变体。这些发现显示了循环中现有 CPV 的高度分化;表明 CPV 最近在尼日利亚迅速进化。