Sammra Osama, Balbutskaya Anna, Nagib Samy, Alber Jörg, Lämmler Christoph, Abdulmawjood Amir, Timke Markus, Kostrzewa Markus, Prenger-Berninghoff Ellen
Institut für Pharmakologie und Toxikologie, Justus-Liebig-Universität Giessen, Germany.
Institut für Lebensmittelqualität und -sicherheit, Stiftung Tierärztliche Hochschule Hannover, Germany.
Berl Munch Tierarztl Wochenschr. 2014 Jan-Feb;127(1-2):56-60.
The present study was designed to characterize phenotypically and genotypically an Arcanobacterium haemolyticum strain (A. haemolyticum P646) isolated from a purulent nasal discharge of a donkey. A. haemolyticum P646 showed, compared to sheep blood, an enhanced hemolytic reaction on rabbit blood agar, a synergistic CAMP-like reaction with Streptococcus agalactiae and Rhodococcus equi as indicator strains, a reverse CAMP reaction in the zone of Staphylococcus aureus beta-hemolysin and the typical biochemical properties of this species. The species identity could be confirmed by MALDI-TOF MS analysis, by sequencing the 16S rDNA and glyceraldehyde-3-phosphate dehydrogenase encoding gene gap and by amplification of A. haemolyticum specific parts of 16S-23S rDNA intergenic spacer region and 23S rDNA. A. haemolyticum P646 and the reference strain A. haemolyticum DSM 20595 were further characterized by amplification of the putative virulence genes encoding arcanolysin, phospholipase D, hemolysin A, CAMP factor family protein, a collagen binding protein and two neuraminidases which were present for A. haemolyticum DSM 20595. A. haemolyticum P646 showed a comparable gene spectrum but was negative for the genes encoding collagen binding protein and neuraminidase H. To our knowledge, the present study is the first phenotypic and genotypic characterization of an A. haemolyticum strain isolated from a donkey.
本研究旨在对从一头驴的脓性鼻分泌物中分离出的溶血隐秘杆菌菌株(溶血隐秘杆菌P646)进行表型和基因型特征分析。与绵羊血相比,溶血隐秘杆菌P646在兔血琼脂上表现出增强的溶血反应,与无乳链球菌和马红球菌作为指示菌株呈现协同CAMP样反应,在金黄色葡萄球菌β-溶血素区域呈现反向CAMP反应以及该菌种的典型生化特性。通过基质辅助激光解吸电离飞行时间质谱分析、对16S rDNA和编码甘油醛-3-磷酸脱氢酶的基因gap进行测序以及对16S-23S rDNA基因间隔区和23S rDNA的溶血隐秘杆菌特异性部分进行扩增,可确认该菌种的身份。通过扩增编码溶血素、磷脂酶D、溶血素A、CAMP因子家族蛋白、一种胶原结合蛋白和两种神经氨酸酶的假定毒力基因,对溶血隐秘杆菌P646和参考菌株溶血隐秘杆菌DSM 20595进行了进一步特征分析,这些基因在溶血隐秘杆菌DSM 20595中存在。溶血隐秘杆菌P646显示出类似的基因谱,但编码胶原结合蛋白和神经氨酸酶H的基因呈阴性。据我们所知,本研究是对从驴分离出的溶血隐秘杆菌菌株进行的首次表型和基因型特征分析。