PCR DETECTION OF OVINE HERPESVIRUS-2 DNA IN INDONESIAN RUMINANTS - NORMAL SHEEP AND CLINICAL CASES OF MALIGNANT CATARRHAL FEVER

Citation
A. Wiyono et al., PCR DETECTION OF OVINE HERPESVIRUS-2 DNA IN INDONESIAN RUMINANTS - NORMAL SHEEP AND CLINICAL CASES OF MALIGNANT CATARRHAL FEVER, Veterinary microbiology, 42(1), 1994, pp. 45-52
Citations number
29
Categorie Soggetti
Microbiology,"Veterinary Sciences
Journal title
ISSN journal
03781135
Volume
42
Issue
1
Year of publication
1994
Pages
45 - 52
Database
ISI
SICI code
0378-1135(1994)42:1<45:PDOOHD>2.0.ZU;2-G
Abstract
Malignant catarrhal fever (MCF), a fatal viral disease of cattle and o ther large ruminants, has a worldwide distribution. There are two form s of the disease, one of which, is caused by Alcelaphine herpesvirus-1 (AHV-1) and is derived from wildebeest. The other form is associated with domestic sheep and is caused by ovine herpesvirus-2 (OHV-2). The disease in Indonesia is sheep-associated with the preferred livestock of this area, Balinese cattle (Bos javanicus) and water buffalo (Bubal us bubalis), both highly susceptible to SA-MCF. The incidence in these species is thought to be high but the prevalence and economic losses attributable to SA-MCF have been difficult to assess. A polymerase cha in reaction (PCR) test, based on a cloned OHV-2 gene sequence, was suc cessfully applied to the detection of OHV-2 DNA in normal sheep and an imals affected with SA-MCF. OHV-2 DNA was detected in eleven confirmed cases of SA-MCF and in the peripheral blood leucocyte (PBL) fraction of six latently infected sheep. These findings have confirmed that the PCR can be of value in establishing a diagnosis of MCF and that the a etiological agent of MCF in Indonesia is OHV-2. The amplification of D NA from the PBL of goats suggests that they are infected with a simila r or identical herpesvirus.