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Genotyping Based on the LTR Region of Small Ruminant Lentiviruses from Naturally Infected Sheep and Goats from Mexico

Small ruminant lentiviruses (SRLVs) belong to the genus Lentivirus in the Retroviridae family. There are five genotypes (A, B, C, D, and E), where genotypes A and B have a global distribution and genotypes C, D, and E are limited to Europe. The presence of SRLV has been confirmed in Mexico, with gen...

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Autores principales: Mendiola, Wolfang P. S., Tórtora, Jorge L., Martínez, Humberto A., García, María M., Cuevas-Romero, Sandra, Cerriteño, José L., Ramírez, Hugo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535881/
https://www.ncbi.nlm.nih.gov/pubmed/31214614
http://dx.doi.org/10.1155/2019/4279573
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author Mendiola, Wolfang P. S.
Tórtora, Jorge L.
Martínez, Humberto A.
García, María M.
Cuevas-Romero, Sandra
Cerriteño, José L.
Ramírez, Hugo
author_facet Mendiola, Wolfang P. S.
Tórtora, Jorge L.
Martínez, Humberto A.
García, María M.
Cuevas-Romero, Sandra
Cerriteño, José L.
Ramírez, Hugo
author_sort Mendiola, Wolfang P. S.
collection PubMed
description Small ruminant lentiviruses (SRLVs) belong to the genus Lentivirus in the Retroviridae family. There are five genotypes (A, B, C, D, and E), where genotypes A and B have a global distribution and genotypes C, D, and E are limited to Europe. The presence of SRLV has been confirmed in Mexico, with genotype B detected in the central region of the country. We examined the presence of SRLVs and genotype prevalence in 1014 sheep and 1383 goats from 12 Mexican states. Using a commercial competitive ELISA (cELISA) test, we detected SRLV antibodies in 107 sheep (10.55%) and 466 goats (33.69%). We used an endpoint PCR to amplify the LTR region on seropositive animals. A total of 50 sheep and 75 goats tested positive via PCR. Positive amplicons from 11 sheep and 17 goats from ten Mexican States were cloned and sequenced. With the LTR sequence data obtained in this study, a phylogenetic analysis was performed; we also constructed a phylogenetic tree using the obtained sequences and GenBank's available sequences. All studied sequences were associated with genotype B, specifically with the FESC-752 isolate previously identified in Mexico. Highly conserved transcription factor binding sites were observed in analyzed alignments, such as AML (vis), AP-4, and TATA box. However, we identified nucleotide differences at site AP-1 that suggest function loss. Our study found that ovine and caprine genotype B SRLVs are widely distributed in Mexico; a highly conserved LTR region among the sequences evaluated in this study was also found.
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spelling pubmed-65358812019-06-18 Genotyping Based on the LTR Region of Small Ruminant Lentiviruses from Naturally Infected Sheep and Goats from Mexico Mendiola, Wolfang P. S. Tórtora, Jorge L. Martínez, Humberto A. García, María M. Cuevas-Romero, Sandra Cerriteño, José L. Ramírez, Hugo Biomed Res Int Research Article Small ruminant lentiviruses (SRLVs) belong to the genus Lentivirus in the Retroviridae family. There are five genotypes (A, B, C, D, and E), where genotypes A and B have a global distribution and genotypes C, D, and E are limited to Europe. The presence of SRLV has been confirmed in Mexico, with genotype B detected in the central region of the country. We examined the presence of SRLVs and genotype prevalence in 1014 sheep and 1383 goats from 12 Mexican states. Using a commercial competitive ELISA (cELISA) test, we detected SRLV antibodies in 107 sheep (10.55%) and 466 goats (33.69%). We used an endpoint PCR to amplify the LTR region on seropositive animals. A total of 50 sheep and 75 goats tested positive via PCR. Positive amplicons from 11 sheep and 17 goats from ten Mexican States were cloned and sequenced. With the LTR sequence data obtained in this study, a phylogenetic analysis was performed; we also constructed a phylogenetic tree using the obtained sequences and GenBank's available sequences. All studied sequences were associated with genotype B, specifically with the FESC-752 isolate previously identified in Mexico. Highly conserved transcription factor binding sites were observed in analyzed alignments, such as AML (vis), AP-4, and TATA box. However, we identified nucleotide differences at site AP-1 that suggest function loss. Our study found that ovine and caprine genotype B SRLVs are widely distributed in Mexico; a highly conserved LTR region among the sequences evaluated in this study was also found. Hindawi 2019-05-12 /pmc/articles/PMC6535881/ /pubmed/31214614 http://dx.doi.org/10.1155/2019/4279573 Text en Copyright © 2019 Wolfang P. S. Mendiola et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mendiola, Wolfang P. S.
Tórtora, Jorge L.
Martínez, Humberto A.
García, María M.
Cuevas-Romero, Sandra
Cerriteño, José L.
Ramírez, Hugo
Genotyping Based on the LTR Region of Small Ruminant Lentiviruses from Naturally Infected Sheep and Goats from Mexico
title Genotyping Based on the LTR Region of Small Ruminant Lentiviruses from Naturally Infected Sheep and Goats from Mexico
title_full Genotyping Based on the LTR Region of Small Ruminant Lentiviruses from Naturally Infected Sheep and Goats from Mexico
title_fullStr Genotyping Based on the LTR Region of Small Ruminant Lentiviruses from Naturally Infected Sheep and Goats from Mexico
title_full_unstemmed Genotyping Based on the LTR Region of Small Ruminant Lentiviruses from Naturally Infected Sheep and Goats from Mexico
title_short Genotyping Based on the LTR Region of Small Ruminant Lentiviruses from Naturally Infected Sheep and Goats from Mexico
title_sort genotyping based on the ltr region of small ruminant lentiviruses from naturally infected sheep and goats from mexico
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535881/
https://www.ncbi.nlm.nih.gov/pubmed/31214614
http://dx.doi.org/10.1155/2019/4279573
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