Literature DB >> 2394846

Studies of experimental Jembrana disease in Bali cattle. I. Transmission and persistence of the infectious agent in ruminants and pigs, and resistance of recovered cattle to re-infection.

S Soeharsono1, N Hartaningsih, M Soetrisno, G Kertayadnya, G E Wilcox.   

Abstract

The agent causing Jembrana disease, an enzootic disease of Bos javanicus (Bali cattle) occurring in Bali, Indonesia, was shown to occur at high titres in the blood of animals during the febrile period of the disease and to persist in cattle for 25 months after clinical recovery. During the febrile period of the disease, most of the infectious agent appeared to be associated with the plasma fraction of whole blood. There was a linear relationship between the number of organisms inoculated into susceptible Bali cattle and the incubation period, which varied from 4.5 to 12 days. Seventeen of 18 animals in which Jembrana disease had been experimentally induced up to 22 months previously did not develop clinical signs when re-challenged with the infectious agent. Ongole cattle (Bos indicus), Friesian cattle (Bos taurus), buffaloes (Bubalus bubalis) and pigs, but not sheep or goats, developed a mild febrile response, but no other overt clinical signs of the disease after inoculation with the Jembrana disease agent. Ongole and Friesian cattle, buffaloes, and sheep developed a persistent infection after inoculation; the infectious agent persisted in blood or spleen for at least 9 months in buffaloes and for shorter periods in the other species.

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Year:  1990        PMID: 2394846     DOI: 10.1016/s0021-9975(08)80134-x

Source DB:  PubMed          Journal:  J Comp Pathol        ISSN: 0021-9975            Impact factor:   1.311


  5 in total

1.  Use of reverse transcription loop-mediated isothermal amplification combined with lateral flow dipstick for an easy and rapid detection of Jembrana disease virus.

Authors:  Asmarani Kusumawati; Issabellina Dwades Tampubolon; Narendra Yoga Hendarta; Siti Isrina Oktavia Salasia; Tenri Ashari Wanahari; Basofi Ashari Mappakaya; Sri Hartati
Journal:  Virusdisease       Date:  2015-08-26

2.  TaqMan real-time reverse transcription-PCR and JDVp26 antigen capture enzyme-linked immunosorbent assay to quantify Jembrana disease virus load during the acute phase of in vivo infection.

Authors:  Meredith Stewart; Moira Desport; Nining Hartaningsih; Graham Wilcox
Journal:  J Clin Microbiol       Date:  2005-11       Impact factor: 5.948

3.  Characterization of the Jembrana disease virus tat gene and the cis- and trans-regulatory elements in its long terminal repeats.

Authors:  H Chen; G Wilcox; G Kertayadnya; C Wood
Journal:  J Virol       Date:  1999-01       Impact factor: 5.103

4.  The transmission of Jembrana disease, a lentivirus disease of Bos javanicus cattle.

Authors:  S Soeharsono; G E Wilcox; A A Putra; N Hartaningsih; K Sulistyana; M Tenaya
Journal:  Epidemiol Infect       Date:  1995-10       Impact factor: 2.451

5.  Comparative functional analysis of Jembrana disease virus Tat protein on lentivirus long terminal repeat promoters: evidence for flexibility at its N-terminus.

Authors:  Yang Su; Gang Deng; Yuanming Gai; Yue Li; Yang Gao; Jiansen Du; Yunqi Geng; Qimin Chen; Wentao Qiao
Journal:  Virol J       Date:  2009-10-28       Impact factor: 4.099

  5 in total

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