László Ózsvári, Krisztina Bárdos, Agata Moroz-Fik, Kinga Biernacka, Marcin Mickiewicz, Zofia Nowek, Carlos Eduardo Abril, Giuseppe Bertoni, Snorre Stuen, Saulius Petkevičius, Jarosław Kaba, Michał Czopowicz
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PCR products were submitted for Sanger dideoxy sequencing, and phylogenetic and molecular evolutionary analyses were conducted on the 200-250 bp-long proviral DNA sequences from the end of long terminal repeat (LTR) region and beginning of <i>gag</i> gene using the MEGA11 software. Reference strains included strains most identical to Hungarian sequences according to the Standard Nucleotide BLAST and prototypic strains for the relevant genotypes and subtypes. Proviral DNA of SRLV was detected in goats from all ten tested herds. A single SRLV genotype was detected in 6 herds-genotype A in three herds and B also in three herds. In four herds, mixed infection with genotypes A and B was confirmed. In total, 110/135 seropositive goats tested positive in the nRT-PCR (81.5%): 49/110 goats (44.5%) for genotype A, 54/110 goats (49.1%) for genotype B, and 7/110 goats (6.4%) for both genotypes. Hungarian sequences belonged to subtypes A1/A18, A2, and subtype B1. 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引用次数: 0
摘要
2023 年,对匈牙利山羊群体进行了一项分子研究,以确定感染这些羊群的小反刍兽疫病毒(SRLV)的基因型和亚型。根据匈牙利早些时候进行的血清调查,选择了 10 个 SRLV 感染血清阳性的山羊群,并对 135 只成年山羊(1 岁以上)进行了血液采样。采用两阶段巢式实时 PCR(nRT-PCR)检测 SRLV 的前病毒 DNA,并区分两种主要病毒基因型(A 型和 B 型)。PCR 产物被提交给 Sanger 双脱氧测序,并使用 MEGA11 软件对长末端重复(LTR)区末端和 gag 基因起始处的 200-250 bp 长的前病毒 DNA 序列进行了系统发育和分子进化分析。参考菌株包括根据标准核苷酸BLAST与匈牙利序列最相同的菌株,以及相关基因型和亚型的原型菌株。在所有十个检测羊群中都检测到了SRLV的病毒DNA。在 6 个羊群中检测到单一 SRLV 基因型,其中 3 个羊群检测到 A 基因型,3 个羊群检测到 B 基因型。在 4 个牧群中,证实了基因型 A 和 B 的混合感染。共有 110/135 头血清阳性山羊(81.5%)在 nRT-PCR 检测中呈阳性:49/110只山羊(44.5%)为基因型A,54/110只山羊(49.1%)为基因型B,7/110只山羊(6.4%)为两种基因型。匈牙利序列属于 A1/A18、A2 和 B1 亚型。这是首次研究表明匈牙利山羊同时感染了属于 A 和 B 基因型的 SRLV。
First Molecular Characterization of Small Ruminant Lentiviruses in Hungarian Goat Population.
In 2023, a molecular study was conducted on the Hungarian goat population to determine genotypes and subtypes of small ruminant lentiviruses (SRLV) infecting these herds. Ten goat herds seropositive for SRLV infection according to a serosurvey conducted earlier in Hungary were selected, and 135 adult goats (>1 year old) were blood sampled. The two-stage nested real-time PCR (nRT-PCR) was used to detect proviral DNA of SRLV and distinguish between two main viral genotypes (A and B). PCR products were submitted for Sanger dideoxy sequencing, and phylogenetic and molecular evolutionary analyses were conducted on the 200-250 bp-long proviral DNA sequences from the end of long terminal repeat (LTR) region and beginning of gag gene using the MEGA11 software. Reference strains included strains most identical to Hungarian sequences according to the Standard Nucleotide BLAST and prototypic strains for the relevant genotypes and subtypes. Proviral DNA of SRLV was detected in goats from all ten tested herds. A single SRLV genotype was detected in 6 herds-genotype A in three herds and B also in three herds. In four herds, mixed infection with genotypes A and B was confirmed. In total, 110/135 seropositive goats tested positive in the nRT-PCR (81.5%): 49/110 goats (44.5%) for genotype A, 54/110 goats (49.1%) for genotype B, and 7/110 goats (6.4%) for both genotypes. Hungarian sequences belonged to subtypes A1/A18, A2, and subtype B1. This is the first study which shows that Hungarian goats are infected by SRLV belonging to both genotypes A and B.
期刊介绍:
Pathogens (ISSN 2076-0817) publishes reviews, regular research papers and short notes on all aspects of pathogens and pathogen-host interactions. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodical details must be provided for research articles.