Mzula Alexanda, Masola Selemani N, Kasanga Christopher J, Wambura Philemon N
Department of Veterinary Microbiology and Parasitology, Sokoine University of Agriculture, P.O. Box 3019, Morogoro, Tanzania,
Trop Anim Health Prod. 2014 Jun;46(5):711-6. doi: 10.1007/s11250-014-0552-2. Epub 2014 Feb 21.
Fowlpox virus (FPV) is one example of poultry viruses which undergoes recombination with Reticuloendotheliosis virus (REV). Trepidation had been raised, and it was well established on augmented pathogenicity of the FPV upon integration of the full intact REV. In this study, we therefore intended at assessing the integration of REV into FPV genome of the field isolates obtained in samples collected from different regions of Tanzania. DNA extraction of 85 samples (scabs) was performed, and FPV-specific PCR was done by the amplification of the highly conserved P4b gene. Evaluation of FPV-REV recombination was done to FPV-specific PCR positively identified samples by amplifying the env gene and REV long terminal repeats (5' LTR). A 578-bp PCR product was amplified from 43 samples. We are reporting for the first time in Tanzania the existence of variant stains of FPV integrated with REV in its genome as 65 % of FPV identified isolates were having full intact REV integration, 21 % had partial FPV-REV env gene integration and 5 % had partial 5' LTR integration. Despite of the fact that FPV-REV integrated stains prevailed, FPV-REV-free isolates (9 %) also existed. In view of the fact that full intact REV integration is connected with increased pathogenicity of FPV, its existence in the FPV genome of most field isolates could have played a role in increased endemic, sporadic and recurring outbreaks in selected areas in Tanzania.
禽痘病毒(FPV)是与网状内皮组织增生症病毒(REV)发生重组的禽类病毒之一。人们对此感到担忧,并且充分证实了完整的REV整合后FPV的致病性增强。因此,在本研究中,我们旨在评估REV整合到从坦桑尼亚不同地区采集的样本中获得的田间分离株的FPV基因组中的情况。对85个样本(痂皮)进行了DNA提取,并通过扩增高度保守的P4b基因进行了FPV特异性PCR。通过扩增env基因和REV长末端重复序列(5'LTR),对FPV特异性PCR阳性鉴定的样本进行了FPV-REV重组评估。从43个样本中扩增出了一个578 bp的PCR产物。我们首次在坦桑尼亚报告了在其基因组中与REV整合的FPV变异株的存在,因为鉴定出的FPV分离株中有65%具有完整的REV整合,21%具有部分FPV-REV env基因整合,5%具有部分5'LTR整合。尽管存在FPV-REV整合株,但也存在无FPV-REV的分离株(9%)。鉴于完整的REV整合与FPV致病性增加有关,其在大多数田间分离株的FPV基因组中的存在可能在坦桑尼亚某些地区的地方病、散发病例和反复暴发增加中起了作用。