Eriksson Helena, Jansson Désirée S, Johansson Karl-Erik, Båverud Viveca, Chirico Jan, Aspán Anna
Department of Animal Health, National Veterinary Institute, SE-751 89 Uppsala, Sweden.
Vet Microbiol. 2009 May 28;137(1-2):98-104. doi: 10.1016/j.vetmic.2008.12.016. Epub 2008 Dec 25.
Erysipelothrix rhusiopathiae is the causative agent of erysipelas in mammals and birds, especially pigs and poultry. In order to investigate the suitability of different subtyping methods for genetic and phenotypic similarities among Swedish isolates of the organism, 45 isolates from poultry (n=23), pigs (n=17), emus (n=2) and the poultry red mite Dermanyssus gallinae (n=3) were investigated by serotyping, pulsed-field gel electrophoresis (PFGE) and antimicrobial susceptibility testing. Sequence analysis of the 16S rRNA gene was performed on eleven isolates from nine animal species. The results indicated a random scattering of serotypes throughout the dendrogram based on PFGE banding patterns following SmaI digestion. In three cases, isolates with an identical PFGE pattern were of differing serotypes. No differentiation into subgroups by antimicrobial susceptibility testing by broth microdilution was possible as results were similar for all isolates. The Minimum Inhibitory Concentrations for most antimicrobials, including penicillin and oxytetracycline, were low. The 16S rRNA gene sequences (1443 nts) from eight of eleven selected isolates of Erysipelothrix spp. were identical to that of the type strain E. rhusiopathiae ATCC 19414(T). The other three isolates differed from the type strain by two or three nucleotides. While this method may be useful for identification of Erysipelothrix spp., it is unsuitable for epidemiological investigations. Similarities in PFGE banding patterns between isolates from chickens and mites supported the hypothesis that D. gallinae may act as a reservoir and vector for E. rhusiopathiae. Further PFGE studies on E. rhusiopathiae isolates are appropriate to investigate the epidemiology of poultry erysipelas.
猪红斑丹毒丝菌是哺乳动物和鸟类尤其是猪和家禽丹毒的病原体。为了研究不同分型方法对于该生物体瑞典分离株之间遗传和表型相似性的适用性,通过血清分型、脉冲场凝胶电泳(PFGE)和药敏试验对来自家禽(n = 23)、猪(n = 17)、鸸鹋(n = 2)和家禽红螨(鸡皮刺螨,n = 3)的45株分离株进行了研究。对来自9个动物物种的11株分离株进行了16S rRNA基因序列分析。结果表明,基于SmaI消化后的PFGE条带模式,血清型在整个系统发育树中随机分布。在3个案例中,具有相同PFGE模式的分离株血清型不同。通过肉汤微量稀释法进行药敏试验无法将分离株分为亚组,因为所有分离株的结果相似。包括青霉素和土霉素在内的大多数抗菌药物的最低抑菌浓度都很低。11株红斑丹毒丝菌属选定分离株中的8株的16S rRNA基因序列(1443个核苷酸)与猪红斑丹毒丝菌模式菌株ATCC 19414(T)相同。其他3株分离株与模式菌株有2个或3个核苷酸的差异。虽然该方法可能有助于红斑丹毒丝菌属的鉴定,但不适用于流行病学调查。鸡和螨分离株之间PFGE条带模式的相似性支持了鸡皮刺螨可能作为猪红斑丹毒丝菌的储存宿主和传播媒介的假说。对猪红斑丹毒丝菌分离株进一步进行PFGE研究,对于调查家禽丹毒的流行病学是合适的。