Molecular characterization of the spike gene of the porcine epidemic diarrhea virus in Mexico, 2013–2016

被引:0
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作者
Rocío Lara-Romero
Luis Gómez-Núñez
José Luis Cerriteño-Sánchez
Laura Márquez-Valdelamar
Susana Mendoza-Elvira
Humberto Ramírez-Mendoza
José Francisco Rivera-Benítez
机构
[1] Instituto Nacional de Investigaciones Forestales,Laboratorio de Virología, Centro Nacional de Investigación Disciplinaria en Microbiología Animal
[2] Agrícolas y Pecuarias,Facultad de Estudios Superiores Cuautitlán
[3] UNAM,Laboratorio de Secuenciación Genómica de la Biodiversidad y de la Salud, Instituto de Biología
[4] CONACYT-FMVZ,Laboratorio de Microbiología y Virología de las Enfermedades Respiratorias del Cerdo, Facultad de Estudios Superiores Cuautitlán
[5] UNAM,Departamento de Microbiología e Inmunología, Facultad de Medicina Veterinaria y Zootecnia
[6] UNAM,undefined
[7] UNAM,undefined
[8] UNAM,undefined
来源
Virus Genes | 2018年 / 54卷
关键词
Porcine epidemic diarrhea virus; Spike gene; Neutralizing epitopes; Phylogenetic analysis; Pigs;
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摘要
In Mexico, the first outbreaks suggestive of the circulation of the porcine epidemic diarrhea virus (PEDV) were identified at the beginning of July 2013. To identify the molecular characteristics of the PEDV Spike (S) gene in Mexico, 116 samples of the intestine and diarrhea of piglets with clinical signs of porcine epidemic diarrhea (PED) were obtained. Samples were collected from 14 farms located in six states of Mexico (Jalisco, Puebla, Sonora, Veracruz, Guanajuato, and Michoacán) from 2013 to 2016. To identify PEDV, we used real-time RT-PCR to discriminate between non-INDEL and INDEL strains. We chose samples according to state and year to characterize the S gene. After amplification of the S gene, the obtained products were sequenced and assembled. The complete amino acid sequences of the spike protein were used to perform an epitope analysis, which was used to determine null mutations in regions SS2, SS6, and 2C10 compared to the sequences of G2. A phylogenetic analysis determined the circulation of G2b and INDEL strains in Mexico. However, several mutations were recorded in the collagenase equivalent (COE) region that were related to the change in polarity and charge of the amino acid residues. The PEDV strain circulating in Jalisco in 2016 has an insertion of three amino acids (232LGL234) and one change in the antigenic site of the COE region, and strains from the years 2015 and 2016 changed the index of the surface probability, which could be related to the re-emergence of disease outbreaks.
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页码:215 / 224
页数:9
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