Watson Eleanor, Alberdi M Pilar, Inglis Neil F, Lainson Alex, Porter Megan E, Manson Erin, Imrie Lisa, Mclean Kevin, Smith David G E
Moredun Research Institute, Bush Loan, Penicuik, United Kingdom.
Moredun Research Institute, Bush Loan, Penicuik, United Kingdom; Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Vet Microbiol. 2014 Dec 5;174(3-4):448-455. doi: 10.1016/j.vetmic.2014.10.002. Epub 2014 Nov 8.
Lawsonia intracellularis is the aetiological agent of the commercially significant porcine disease, proliferative enteropathy. Current understanding of host-pathogen interaction is limited due to the fastidious microaerophilic obligate intracellular nature of the bacterium. In the present study, expression of bacterial proteins during infection was investigated using a mass spectrometry approach. LC-ESI-MS/MS analysis of two isolates of L. intracellularis from heavily-infected epithelial cell cultures and database mining using fully annotated L. intracellularis genome sequences identified 19 proteins. According to the Clusters of Orthologous Groups (COG) functional classification, proteins were identified with roles in cell metabolism, protein synthesis and oxidative stress protection; seven proteins with putative or unknown function were also identified. Detailed bioinformatic analyses of five uncharacterised proteins, which were expressed by both isolates, identified domains and motifs common to other outer membrane-associated proteins with important roles in pathogenesis including adherence and invasion. Analysis of recombinant proteins on Western blots using immune sera from L. intracellularis-infected pigs identified two proteins, LI0841 and LI0902 as antigenic. The detection of five outer membrane proteins expressed during infection, including two antigenic proteins, demonstrates the potential of this approach to interrogate L. intracellularis host-pathogen interactions and identify novel targets which may be exploited in disease control.
胞内劳森菌是具有重要商业意义的猪病——增生性肠炎的病原体。由于该细菌苛求微需氧、专性胞内寄生的特性,目前对宿主-病原体相互作用的了解有限。在本研究中,采用质谱方法研究了感染过程中细菌蛋白的表达情况。对来自严重感染上皮细胞培养物的两株胞内劳森菌进行液相色谱-电喷雾串联质谱(LC-ESI-MS/MS)分析,并利用完全注释的胞内劳森菌基因组序列进行数据库挖掘,鉴定出了19种蛋白。根据直系同源簇(COG)功能分类,鉴定出了在细胞代谢、蛋白质合成和氧化应激保护中发挥作用的蛋白;还鉴定出了7种功能推定或未知的蛋白。对两株菌均表达的5种未表征蛋白进行详细的生物信息学分析,确定了与其他外膜相关蛋白共有的结构域和基序,这些蛋白在包括黏附和侵袭在内的发病机制中具有重要作用。使用来自胞内劳森菌感染猪的免疫血清对重组蛋白进行蛋白质印迹分析,确定了两种蛋白LI0841和LI0902具有抗原性。检测到感染过程中表达的5种外膜蛋白,包括两种抗原性蛋白,证明了这种方法在研究胞内劳森菌宿主-病原体相互作用以及鉴定可用于疾病控制的新靶点方面的潜力。