Madadgar Omid, Nazaktabar Ahmad, Keivanfar Hadi, Zahraei Salehi Taghi, Lotfollah Zadeh Samad
Faculty of Veterinary Medicine, University of Tehran, Department of Microbiology, Tehran, Iran.
Faculty of Veterinary Medicine, Amol University of Special Modern Technology, Amol, Iran.
Vet Microbiol. 2015 Sep 30;179(3-4):190-6. doi: 10.1016/j.vetmic.2015.04.024. Epub 2015 May 2.
Determination and distribution of the G and P genotypes of group A bovine rotavirus was investigated on 386 fecal samples collected from calves with diarrhea using a semi-nested RT-PCR typing assay. Samples were collected from 11 provinces of Iran during 2010-2012. The provinces divided into 5 different groups based on geographical distance and climates. One hundred and nine samples (28.2%) were confirmed positive for rotavirus group A using ELISA. 75 positive samples were selected randomly and subjected to typing assay. G10 (50.6%) and P[11] (64%) were detected more than G6 (21.3%) and P[5] (9.3%). No any G8 and P[1] were observed. Of the 75 samples analyzed by RT-PCR in each geographical areas named as the south of Alborz mountain ranges area, the north-east area, the central area, the north-west area and the south-east area, number of samples with G10 genotype were 19, 9, 9, 0 and 1; G6 were 8, 0, 3, 5 and 0; P[11] were 25, 7, 11, 5 and 0 and finally P[5] were 5, 0, 2, 0 and 0 in each area, respectively. The most common VP7/VP4 combinations were G10P[11] (40%), G6P[11] (12%), G6P[5] (5.3%) and G10P[5] (2.6%). Phylogenetic analysis of one strain showed high identity with strain B223. Since the identification of G and P genotypes and their diversity is fundamental to development and use of effective vaccines, we determined the most prevalence G and P genotypes of bovine rotavirus group A (BRVA) in a broad area of Iran.
采用半巢式逆转录聚合酶链反应(RT-PCR)分型检测法,对从腹泻犊牛采集的386份粪便样本进行了A组牛轮状病毒G和P基因型的测定及分布研究。样本于2010年至2012年期间从伊朗的11个省份采集。这些省份根据地理距离和气候分为5个不同的组。使用酶联免疫吸附测定(ELISA)法确认109份样本(28.2%)为A组轮状病毒阳性。随机选择75份阳性样本进行分型检测。检测到G10(50.6%)和P[11](64%)的比例高于G6(21.3%)和P[5](9.3%)。未观察到任何G8和P[1]。在每个地理区域(分别命名为阿尔伯兹山脉以南地区、东北地区、中部地区、西北地区和东南部地区)通过RT-PCR分析的75份样本中,G10基因型样本数量在每个区域分别为19、9、9、0和1;G6分别为8、0、3、5和0;P[11]分别为25、7、11、5和0;最后P[5]分别为5、0、2、0和0。最常见的VP7/VP4组合为G10P[11](40%)、G6P[11](12%)、G6P[5](5.3%)和G10P[5](2.6%)。对一株病毒的系统发育分析显示与B223毒株具有高度同源性。由于G和P基因型的鉴定及其多样性对于有效疫苗的开发和使用至关重要,我们确定了伊朗广大地区A组牛轮状病毒(BRVA)最流行的G和P基因型。