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Molecular Epidemiology of Campylobacter jejuni in Broiler Flocks Using Randomly Amplified Polymorphic DNA-PCR and 23S rRNA-PCR and Role of Litter in Its Transmission

机译:肉鸡空肠弯曲菌空肠弯曲菌的分子流行病学研究-随机扩增多态性DNA-PCR和23S rRNA-PCR及其在传播中的作用

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摘要

Poultry has long been cited as a reservoir for Campylobacter spp., and litter has been implicated as a vehicle in their transmission. Chicks were raised on litter removed from a broiler house positive for Campylobacter jejuni. Litter was removed from the house on days 0, 3, and 9 after birds were removed for slaughter. Chicks were raised on these three litters under controlled conditions in flocks of 25. None of these birds yielded C. jejuni in their cecal droppings through 7 weeks. Two successive flocks from the same Campylobacter-positive broiler house were monitored for Campylobacter colonization. Campylobacter jejuni prevalence rates were determined for each flock. Randomly amplified polymorphic DNA (RAPD)-PCR and 23S rRNA-PCR typing methods were used to group isolates. A high prevalence (60%) of C. jejuni in flock 1 coincided with the presence of an RAPD profile not appearing in flock 2, which had a lower rate of prevalence (28%). A 23S rRNA-PCR typing method was used to determine if strains with different RAPD profiles and different prevalence rates contained different 23S sequences. RAPD profiles detected with higher prevalence rates contained a spacer in the 23S rRNA region 100% of the time, while RAPD profiles found with lower prevalence rates contained an intervening sequence less than 2% of the time. Data suggest varying colonizing potentials of different RAPD profiles and a source other than previously used litter as a means of transmission of C. jejuni. These molecular typing methods demonstrate their usefulness, when used together, in this epidemiologic investigation.
机译:长期以来,人们一直将家禽作为弯曲杆菌属的储存库,而垃圾也被认为是传播其的媒介。在从空肠弯曲杆菌阳性的肉鸡舍中取出的垫料上饲养小鸡。在将家禽移出进行屠宰后的第0、3和9天,将其从房屋中移出。在受控条件下,在这三个窝中以25只鸡群饲养小鸡。这些鸡在7周内没有盲肠粪便产生空肠弯曲杆菌。监测来自同一弯曲杆菌阳性肉鸡场的两个连续的鸡群弯曲杆菌的定殖情况。确定每个鸡群的空肠弯曲菌患病率。使用随机扩增多态性DNA(RAPD)-PCR和23S rRNA-PCR分型方法对分离株进行分组。鸡群1中空肠弯曲杆菌的高患病率(60%)与鸡群2中未出现的RAPD分布相符,其患病率较低(28%)。使用23S rRNA-PCR分型方法确定具有不同RAPD谱和不同患病率的菌株是否包含不同的23S序列。以较高的患病率检测到的RAPD谱图在100%的时间中在23S rRNA区域中包含一个间隔区,而以较低的患病率发现的RAPD谱图包含的介入序列少于2%的时间。数据表明,不同的RAPD分布图具有不同的定殖潜力,并且是以前使用的垫料作为空肠弯曲杆菌传播手段的来源。这些分子分型方法在流行病学研究中一起使用时证明了其有用性。

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