TY - JOUR
T1 - Detección de una proteína asociada a la enfermedad de la necrosis hepatopancreática aguda (AHPND) en Litopenaeus vannamei bajo cultivo semi-intensivo en Ecuador
AU - Saavedra-Olivos, Katherine Yuliana
AU - Peralta-Ortiz, Tessy
AU - Ordinola-Zapata, Alberto
AU - Sandoval-Ramayoni, John Estuardo
AU - Vieyra-Peña, Enedia Graciela
AU - Zapata-Cruz, Marco Antonio
AU - Hidalgo-Mogollón, Auberto
AU - Morán-Ávila, Braulio
AU - Mendoza-Neyra, Oscar Augusto
AU - Mendoza-Dioses, Magno Ego
AU - Campoverde-Peña, Sigrid Yamile
N1 - Publisher Copyright:
© 2018 Universidad Nacional Mayor de San Marcos. All Rights Reserved.
PY - 2018
Y1 - 2018
N2 - The present study aimed to detect a protein associated with acute hepatopancreatic necrosis (AHPND) by mass spectrometry, reared under semi-intensive farming in Ecuador. Sick shrimps from three farms were collected in the Bellavista area in the El Oro province. The hepatopancreas were macerated and cultured in TCBS medium and subcultured in TSA and LB broth. In the bacterial strains obtained, the proteins were extracted using a commercial kit and separated by SDS-PAGE gel migration. These were analyzed with a MALDI TOF/TOF mass spectrometer. The confirmation of the strains was performed by PCR using TUMSAT-Vp3 primers, which are specific for detecting AHPND. One of the strains had peptide sequences similar to that of the PirvpB protein causing AHPND, and was identified as belonging to Vibrio parahaemolyticus and carrying the gene coding for PirvpB. The results showed that it is possible to use MALDI TOF/TOF mass spectrometry in the detection of AHPND-associated proteins in shrimp culture.
AB - The present study aimed to detect a protein associated with acute hepatopancreatic necrosis (AHPND) by mass spectrometry, reared under semi-intensive farming in Ecuador. Sick shrimps from three farms were collected in the Bellavista area in the El Oro province. The hepatopancreas were macerated and cultured in TCBS medium and subcultured in TSA and LB broth. In the bacterial strains obtained, the proteins were extracted using a commercial kit and separated by SDS-PAGE gel migration. These were analyzed with a MALDI TOF/TOF mass spectrometer. The confirmation of the strains was performed by PCR using TUMSAT-Vp3 primers, which are specific for detecting AHPND. One of the strains had peptide sequences similar to that of the PirvpB protein causing AHPND, and was identified as belonging to Vibrio parahaemolyticus and carrying the gene coding for PirvpB. The results showed that it is possible to use MALDI TOF/TOF mass spectrometry in the detection of AHPND-associated proteins in shrimp culture.
KW - AHPND
KW - Early mortality syndrome
KW - Litopenaus vannamei
KW - PirvpB
KW - Shrimp
KW - Vibrio parahaemolitycus
UR - http://www.scopus.com/inward/record.url?scp=85045951841&partnerID=8YFLogxK
U2 - 10.15381/rivep.v29i1.14194
DO - 10.15381/rivep.v29i1.14194
M3 - Artículo
AN - SCOPUS:85045951841
SN - 1682-3419
VL - 29
SP - 328
EP - 338
JO - Revista de Investigaciones Veterinarias del Peru
JF - Revista de Investigaciones Veterinarias del Peru
IS - 1
ER -