Serotyping versus genotyping in infected sheep and goats with small ruminant lentiviruses


Por: Acevedo Jimenez, Gabriel Eduardo, Tortora Perez, Jorge Luis, Rodriguez Murillo, Cecilia, Arellano Reynoso, Beatriz, Ramirez Alvarez, Hugo

Publicada: 1 ene 2021
Resumen:
Despite SRLV infection being endemic in Mexico, there is little information regarding which genotypes are present. We compared serotyping and PCR-sequencing results from sheep and goats infected with SRLV. We separated plasma and peripheral blood leukocytes (PBL) from 1940 blood samples from sheep and goats from 12 states across Mexico. To detect SRLV infection, we tested plasma samples using two commercial ELISA kits (VMRD and Eradikit SRLV Screening). Then, we semtyped the infecting virus (A/ B) using Eradikit SRLV Genotyping. PBL DNA was used to detect the proviral genome via PCR. Positive amplicons were sequenced to identify viral genotypes using a phylogenetic analysis. Also, we analysed for residues differences in the sequences of a capsid epitope between genotypes. The serological results indicated a higher detection of seropositive animals using the VMRD ELISA compared to Eradikit, with 21 % and 15.3 % more in sheep and goats respectively. Only 25.7 % of the ELISA serotyping results matched those from PCR-sequencing. PCR-sequencing was able to identify genotype A, B and coinfections in animals classified as indeterminate by the ELISA test. This lack of sensitivity may be related to the lack of epitopes from the matrix and transmembrane peptides used by ELISA screening. Sequences analysis revealed that SRLVs found in sheep cluster with genetic subtypes A2 and B1, while those in goats cluster with subtypes A1 and B1. Serotyping did not prove to be an adequate method for predicting the viral genotype (A and / or B) in infections caused by SRLV.

Filiaciones:
Acevedo Jimenez, Gabriel Eduardo:
 Univ Nacl Autonoma Mexico, Fac Higher Educ, Virol Genet & Mol Biol Lab, Cuautitlan,Vet Med, Campus 4,Km 2-5 Ctra Cuautitlan Teoloyucan, San Sebastian Xhala 54714, Cuautitlan Izca, Mexico

Tortora Perez, Jorge Luis:
 Univ Nacl Autonoma Mexico, Fac Higher Educ, Virol Genet & Mol Biol Lab, Cuautitlan,Vet Med, Campus 4,Km 2-5 Ctra Cuautitlan Teoloyucan, San Sebastian Xhala 54714, Cuautitlan Izca, Mexico

Rodriguez Murillo, Cecilia:
 Univ Nacl Autonoma Mexico, Fac Higher Educ, Virol Genet & Mol Biol Lab, Cuautitlan,Vet Med, Campus 4,Km 2-5 Ctra Cuautitlan Teoloyucan, San Sebastian Xhala 54714, Cuautitlan Izca, Mexico

Arellano Reynoso, Beatriz:
 Univ Nacl Auton Mexico, Fac Med Vet & Zootecnia, Dept Microbiol & Inmunol, Ave Univ 3000, Mexico City 04510, DF, Mexico

Ramirez Alvarez, Hugo:
 Univ Nacl Autonoma Mexico, Fac Higher Educ, Virol Genet & Mol Biol Lab, Cuautitlan,Vet Med, Campus 4,Km 2-5 Ctra Cuautitlan Teoloyucan, San Sebastian Xhala 54714, Cuautitlan Izca, Mexico
ISSN: 03781135





VETERINARY MICROBIOLOGY
Editorial
Elsevier, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS, Países Bajos
Tipo de documento: Article
Volumen: 252 Número:
Páginas:
WOS Id: 000604855600008
ID de PubMed: 33271419

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