TY - JOUR
T1 - Detection of animals carrying the hog cholera virus in a well-managed pig farm of Lima valley
AU - Iván Camargo, C.
AU - Hermelinda Rivera, G.
AU - Afredo Benito, Z.
PY - 2002/1/1
Y1 - 2002/1/1
N2 - © 2002 Universidad Nacional Mayor de San Marcos. All rights reserved. The objective of this study was to identify animal carriers of the Hog Cholera virus (HCV) post vaccination in a well-managed pig farm ofLima valley. A total of 166 serum samples were collected from 166piglets between 6 and 7 weeks of age, vaccinated against Hog Cholera 15 days befare sampling. Specific HCV antibodies were detected using a blocking ELISA test. Eighty eight (146/166) of animals reacted positively against HCV; 3% (5/166) and 9% (15/166) of animals were considered suspects and negatives to antibodies, respectively. A second sample was collected 30 days after the first collection from suspect (n=5) and negative (n=15) animals. HCV was detected by direct inmunofluorescence test using cultivated lymphocytes. At the time of the second sampling, 14 out of20 animals stayed at farm. Antibodies were detected in 6 animals and 8 were negative, however 4 ofthe latter were positive to HCV The results showed that the frequency ofHCV carrier animals was 2.4% (4/166). The lack of antibodies and the presence ofHCV in lymphocytes after vaccination, suggested that those animals were persistently infected and HCV carriers.
AB - © 2002 Universidad Nacional Mayor de San Marcos. All rights reserved. The objective of this study was to identify animal carriers of the Hog Cholera virus (HCV) post vaccination in a well-managed pig farm ofLima valley. A total of 166 serum samples were collected from 166piglets between 6 and 7 weeks of age, vaccinated against Hog Cholera 15 days befare sampling. Specific HCV antibodies were detected using a blocking ELISA test. Eighty eight (146/166) of animals reacted positively against HCV; 3% (5/166) and 9% (15/166) of animals were considered suspects and negatives to antibodies, respectively. A second sample was collected 30 days after the first collection from suspect (n=5) and negative (n=15) animals. HCV was detected by direct inmunofluorescence test using cultivated lymphocytes. At the time of the second sampling, 14 out of20 animals stayed at farm. Antibodies were detected in 6 animals and 8 were negative, however 4 ofthe latter were positive to HCV The results showed that the frequency ofHCV carrier animals was 2.4% (4/166). The lack of antibodies and the presence ofHCV in lymphocytes after vaccination, suggested that those animals were persistently infected and HCV carriers.
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M3 - Article
SN - 1682-3419
SP - 56
EP - 60
JO - Revista de Investigaciones Veterinarias del Peru
JF - Revista de Investigaciones Veterinarias del Peru
ER -