尼日利亚部分屠宰场猪血液样本中扭力猪瘟病毒及合并感染非洲猪瘟病毒的分子检测

IF 1.1 Q4 VIROLOGY Advances in Virology Pub Date : 2016-10-19 DOI:10.1155/2016/6341015
P. Luka, J. Erume, B. Yakubu, O. Owolodun, D. Shamaki, F. Mwiine
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引用次数: 11

摘要

猪瘟病毒1型(TTSuV1a/TTSuV1b)感染存在于世界各地的猪群中。本研究调查了尼日利亚一些屠宰场家猪中TTSuV1a/TTSuV1b感染的流行情况以及与非洲猪瘟病毒(ASFV)的共感染情况,并描述了与全球菌株相关的系统发育。从4个屠宰场采集181份血液样本,采用PCR方法进行病毒核酸检测。通过比较序列分析来推断系统发育。TTSuV1a/b的总患病率为17.7%。TTSuV1a和TTSuV1b的个体基因型患病率分别为10.5%和7.2%。ASFV/TTSuV1a/b合并感染率为7.7%,TTSuV1a和TTSuV1b合并感染率为1.7%。仅检测到ASFV的样本占总样本的11.91%。尼日利亚TTSuV1a和TTSuV1b的序列同源性分别为91-100%和95-100%。ASFV序列与基因型1的成员完全相同。这是关于TTSuV1a/b在尼日利亚家猪中存在以及与非洲猪瘟合并感染的第一份报告。虽然TTSuV1a/b在尼日利亚的流行率很低,但我们建议进一步研究以确定趋势及其在ASFV发病机制中的可能作用。
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Molecular Detection of Torque Teno Sus Virus and Coinfection with African Swine Fever Virus in Blood Samples of Pigs from Some Slaughterhouses in Nigeria
Torque teno sus virus 1 (TTSuV1a/TTSuV1b) infection is present in pig herds worldwide. This study investigated the prevalence of TTSuV1a/TTSuV1b infections in domestic pigs from some slaughterhouses in Nigeria as well as coinfection with African swine fever virus (ASFV) and described the phylogeny in relation to global strains. One hundred and eighty-one (181) blood samples from four slaughterhouses were used for the study and viral nucleic acid detection was carried out by PCR. Comparative sequence analysis was carried out to infer phylogeny. The overall prevalence of TTSuV1a/b was 17.7%. Prevalence of individual genotypes was 10.5% and 7.2% for TTSuV1a and TTSuV1b, respectively. Coinfection of ASFV/TTSuV1a/b was 7.7% while that of TTSuV1a and TTSuV1b was 1.7%. ASFV alone was detected in 11.91% of the total samples. The Nigerian TTSuV1a and TTSuV1b shared a sequence identity of 91–100% and 95–100%, respectively, among each other. The ASFV sequences were 100% identical to members of genotype 1. This is the first report on the presence of TTSuV1a/b in domestic pigs in Nigeria and coinfection with ASFV. Although the prevalence of TTSuV1a/b in Nigeria was low, we recommend further studies to establish the trend and possible role in the pathogenesis of ASFV.
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23
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22 weeks
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