Urban-Chmiel Renata, Wernicki Andrzej, Wawrzykowski Jacek, Puchalski Andrzej, Nowaczek Anna, Dec Marta, Stęgierska Diana, Alomari Mohammed Mijbas Mohammed
Sub-department of Veterinary Prevention and Avian Diseases, Institute of Biological Bases of Animal Diseases, Faculty of Veterinary Medicine, University of Life Sciences, 20-033, Lublin, Poland.
Department of Biochemistry, Faculty Veterinary Medicine, University of Life Sciences, 20-033, Lublin, Poland.
AMB Express. 2018 Jun 19;8(1):102. doi: 10.1186/s13568-018-0630-3.
The aim of study was to isolate, characterize and analyse the protein profiles of Myoviridae-like bacteriophages obtained from M. haemolytica using MALDI TOF mass spectrometry. The material consisted of the M. haemolytica reference strain ATCC BAA410, reference serotypes A1, A2, A5, A6, A7, A9, and A11, and wild-type isolates of serotype A1. Bacteriophage morphology was examined with a transmission electron microscope. The proteins were separated in SDS-PAGE and two-dimensional electrophoresis and characterized by MALDI-TOF. Among the phages obtained, seven were specific for strains A1, A2, A5, A6, A7 and 25, and PHL-1 was specific for the BAA410 strain. The protein profiles for the phages were very similar to one another, but differed from the reference phage in that they lacked protein fractions with molecular weights of 22.9, 56.3 and 73.1 kDa. 2D electrophoresis revealed significant differences in the size of proteins and their localization in the pH gradient. The most similar profiles were observed in phages specific for strains BAA-410 and A6. In all profiles two main spots were observed in the molecular weight range from 44 to 70 kDa at pH < 4. The results indicate that 2D electrophoresis is a very useful tool for characterization of phage protein profiles. An important objective was to determine the molecular differences between morphologically similar phages belonging to one family and to find similarities to phages specific for other pathogens. The study also assessed the suitability of the methods used to characterize phages.
本研究的目的是利用基质辅助激光解吸电离飞行时间质谱(MALDI TOF)对从溶血曼氏杆菌中获得的类肌尾噬菌体进行分离、表征和分析其蛋白质谱。材料包括溶血曼氏杆菌参考菌株ATCC BAA410、参考血清型A1、A2、A5、A6、A7、A9和A11,以及血清型A1的野生型分离株。用透射电子显微镜检查噬菌体形态。蛋白质在十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)和二维电泳中进行分离,并用MALDI-TOF进行表征。在所获得的噬菌体中,有七个对菌株A1、A2、A5、A6、A7和25具有特异性,而PHL-1对BAA410菌株具有特异性。噬菌体的蛋白质谱彼此非常相似,但与参考噬菌体不同的是,它们缺乏分子量为22.9、56.3和73.1 kDa的蛋白质组分。二维电泳显示蛋白质大小及其在pH梯度中的定位存在显著差异。在对BAA-410和A6菌株具有特异性的噬菌体中观察到最相似的谱。在所有谱中,在pH < 4时,在分子量范围为44至70 kDa处观察到两个主要斑点。结果表明,二维电泳是表征噬菌体蛋白质谱的非常有用的工具。一个重要目标是确定属于一个家族的形态相似的噬菌体之间的分子差异,并找到与其他病原体特异性噬菌体的相似性。该研究还评估了用于表征噬菌体的方法的适用性。