Pejchalová M, Dostalíková E, Slámová M, Brozková I, Vytrasová J
Department of Biological and Biochemical Sciences, Faculty of Chemical Technology, University of Pardubice, Strossova 239, 53003 Pardubice, Czech Republic.
J Food Prot. 2008 Apr;71(4):719-27. doi: 10.4315/0362-028x-71.4.719.
The aim of this study was to examine 634 samples of chicken, lamb, pork, beef, fish, samples from the intensive animal industry and from poultry for slaughter, as well as from the domestic breeding of poultry, horses, pigs, and lambs, from surface water, and from clinical samples for the presence of Arcobacter. All the samples were examined with a cultivation method, followed by confirmation by multiplex PCR. The method of multiplex PCR applied directly to a liquid medium after enrichment was applied only to the samples with the highest probability of the presence of arcobacters. Arcobacter spp. were detected in 11.8% of the samples, of which A. butzleri, A. cryaerophilus, and A. skirrowii were found in 6.6, 5.1, and 0.2% of the samples, respectively. The sources of the arcobacters were chicken meat from the retail market, intensive animal production facilities, domestic chicken breeding facilities, lamb raising environments, surface water and wastewater, and beef swabs taken in a meat processing factory. No occurrence of arcobacters was identified in the swabs from slaughter turkeys, ducks, and wild poultry. No arcobacters were found in horse and pig breeding environments, on pork, or on the swabs of fish. Forty-two rectal swabs taken from humans were also free of Arcobacter. Seventeen isolates of Arcobacter were further identified by sequencing the 16S rRNA gene. Varied genotypes were observed among A. butzleri from chicken meat and chicken breeds, and A. cryaerophilus from wastewater and chicken breeds. They were similar to the genotypes present in wastewater, porcine feces, human stool, and human blood obtained from databases. Our results revealed that the chicken meat from the retail market is an important source of arcobacters. Cross-contamination during handling of chicken carcass practices could play a key role in the spread of Arcobacter.
本研究的目的是检测634份鸡肉、羊肉、猪肉、牛肉、鱼肉样本,这些样本来自集约化畜牧业、待屠宰家禽,以及家禽、马、猪和羊的家庭养殖,还包括地表水样本和临床样本,以检测其中是否存在弓形杆菌。所有样本均采用培养法进行检测,随后通过多重聚合酶链反应(multiplex PCR)进行确认。富集后直接应用于液体培养基的多重聚合酶链反应方法仅应用于最有可能存在弓形杆菌的样本。在11.8%的样本中检测到了弓形杆菌属,其中在6.6%、5.1%和0.2%的样本中分别发现了布氏弓形杆菌、嗜低温弓形杆菌和斯氏弓形杆菌。弓形杆菌的来源包括零售市场的鸡肉、集约化动物生产设施、家庭养鸡设施、养羊环境、地表水和废水,以及肉类加工厂采集的牛肉拭子。在屠宰火鸡、鸭子和野生家禽的拭子中未发现弓形杆菌。在马和猪的养殖环境、猪肉或鱼的拭子中也未发现弓形杆菌。从人类采集的42份直肠拭子中也未检测到弓形杆菌。通过对16S rRNA基因进行测序,进一步鉴定了17株弓形杆菌分离株。在来自鸡肉和鸡品种的布氏弓形杆菌以及来自废水和鸡品种的嗜低温弓形杆菌中观察到了不同的基因型。它们与数据库中废水、猪粪便、人类粪便和人类血液中存在的基因型相似。我们的结果表明,零售市场的鸡肉是弓形杆菌的重要来源。处理鸡胴体过程中的交叉污染可能在弓形杆菌的传播中起关键作用。