Experimental Zooprophylactic Institute of Apulia and Basilicata, Via Manfredonia 20, 71121 Foggia, Italy.
Department of Biosciences, University of Milan, Via Celoria 26, 20133 Milano, Italy.
Syst Appl Microbiol. 2021 May;44(3):126204. doi: 10.1016/j.syapm.2021.126204. Epub 2021 Apr 2.
During a sampling of wild red foxes (Vulpes vulpes) for the detection of Epsilonproteobacteria, 14 strains were isolated from the caecal contents of 14 epidemiologically-unrelated animals. A genus-specific PCR indicated that the isolates belonged to the genus Campylobacter. Based on the results of a species-specific PCR, the isolates were initially identified as C. upsaliensis. However, multi-locus sequence typing (MLST) revealed that the isolates were significantly different from the C. upsaliensis present in the MLST database. A polyphasic study, including conventional biochemical and tolerance characteristics, morphology by transmission electron microscopy (TEM), MALDI-TOF analysis, and genetic comparisons based on partial 16S rDNA and atpA gene sequences, was undertaken. Finally, the complete genome sequence of the type strain 251/13 and the draft genome sequences of the other isolates were determined. Average nucleotide identity, average amino acid identity and in silico DNA-DNA hybridization analyses confirmed that the isolates represent a novel taxon for which the name Campylobacter vulpis sp. nov. is proposed, with isolate 251/13 (=CCUG 70587 = LMG 30110) as the type strain. In order to allow a rapid discrimination of C. vulpis from the closely-related C. upsaliensis, a specific PCR test was designed, based on atpA gene sequences.
在对野生红狐(Vulpes vulpes)进行埃希氏菌科(Epsilonproteobacteria)检测的抽样中,从 14 只流行病学上无关的动物的盲肠内容物中分离出 14 株菌。属特异性 PCR 表明这些分离株属于弯曲菌属(Campylobacter)。根据种特异性 PCR 的结果,这些分离株最初被鉴定为 C. upsaliensis。然而,多位点序列分型(MLST)显示,这些分离株与 MLST 数据库中存在的 C. upsaliensis 有很大的不同。进行了多相研究,包括常规生化和耐受特性、透射电子显微镜(TEM)形态学、MALDI-TOF 分析以及基于部分 16S rDNA 和 atpA 基因序列的遗传比较。最后,确定了模式株 251/13 的全基因组序列和其他分离株的草图基因组序列。平均核苷酸同一性、平均氨基酸同一性和计算机 DNA-DNA 杂交分析证实,这些分离株代表了一个新的分类群,建议将其命名为 Campylobacter vulpis sp. nov.,其中分离株 251/13(=CCUG 70587 = LMG 30110)作为模式株。为了能够快速区分 C. vulpis 和密切相关的 C. upsaliensis,根据 atpA 基因序列设计了一种特定的 PCR 检测方法。