First Molecular Characterization of Small Ruminant Lentiviruses in Hungarian Goat Population

被引:0
作者
Ozsvari, Laszlo [1 ,2 ]
Bardos, Krisztina [1 ,2 ]
Moroz-Fik, Agata [3 ]
Biernacka, Kinga [3 ]
Mickiewicz, Marcin [3 ]
Nowek, Zofia [3 ]
Abril, Carlos Eduardo [4 ]
Bertoni, Giuseppe [4 ]
Stuen, Snorre [5 ]
Petkevicius, Saulius [6 ]
Kaba, Jaroslaw [3 ]
Czopowicz, Michal [3 ]
机构
[1] Univ Vet Med Budapest, Dept Vet Forens & Econ, Istvan U 2, H-1078 Budapest, Hungary
[2] Univ Vet Med Budapest, Natl Lab Infect Anim Dis, Antimicrobial Resistance, Vet Publ Hlth & Food Chain Safety, H-1078 Budapest, Hungary
[3] Warsaw Univ Life Sci SGGW, Inst Vet Med, Div Vet Epidemiol & Econ, Nowoursynowska 159C, PL-02776 Warsaw, Poland
[4] Univ Bern, Inst Virol & Immunol, Vetsuisse Fac, Dept Infect Dis & Pathobiol, Laenggass Str 122, CH-3012 Bern, Switzerland
[5] Norwegian Univ Life Sci, Dept Prod Anim Clin Sci, Svebastadveien 112, N-4325 Sandnes, Norway
[6] Lithuanian Univ Hlth Sci, Vet Acad, Dept Vet Pathobiol, Tilzes Str 18, LT-47181 Kaunas, Lithuania
来源
PATHOGENS | 2024年 / 13卷 / 11期
基金
欧盟地平线“2020”;
关键词
CAE; caprine arthritis-encephalitis; real-time PCR; SRLV; CAPRINE-ARTHRITIS-ENCEPHALITIS; PHYLOGENETIC ANALYSIS; VIRUS-INFECTION; NATURAL TRANSMISSION; MILK-PRODUCTION; MIXED FLOCKS; MAEDI-VISNA; SHEEP; HETEROGENEITY; MONOCYTES;
D O I
10.3390/pathogens13110939
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页数:14
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