Otsuka Taketo, Kirkham Charmaine, Brauer Aimee, Koszelak-Rosenblum Mary, Malkowski Michael G, Murphy Timothy F
Division of Infectious Diseases, Department of Medicine, University at Buffalo, State University of New York, Buffalo, New York, USA Clinical and Translational Research Center, University at Buffalo, State University of New York, Buffalo, New York, USA.
Department of Structural Biology, University at Buffalo, State University of New York, Buffalo, New York, USA Hauptman Woodward Medical Research Institute, Buffalo, New York, USA.
Infect Immun. 2015 Nov 23;84(2):432-8. doi: 10.1128/IAI.00799-15. Print 2016 Feb.
Moraxella catarrhalis is an exclusively human pathogen that is an important cause of otitis media in children and lower respiratory tract infections in adults with chronic obstructive pulmonary disease. A vaccine to prevent M. catarrhalis infections would have an enormous global impact in reducing morbidity resulting from these infections. Substrate binding protein 2 (SBP2) of an ABC transporter system has recently been identified as a promising vaccine candidate antigen on the bacterial surface of M. catarrhalis. In this study, we showed that SBP1, -2, and -3 individually bind different basic amino acids with exquisite specificity. We engineered mutants that each expressed a single SBP from this gene cluster and showed in growth experiments that SBP1, -2, and -3 serve a nutritional function through acquisition of amino acids for the bacterium. SBP2 mediates uptake of arginine, a strict growth requirement of M. catarrhalis. Adherence and invasion assays demonstrated that SBP1 and SBP3 play a role in invasion of human respiratory epithelial cells, consistent with a nutritional role in intracellular survival in the human respiratory tract. This work demonstrates that the SBPs of an ABC transporter system function in the uptake of basic amino acids to support growth of M. catarrhalis. The critical role of SBP2 in arginine uptake may contribute to its potential as a vaccine antigen.
卡他莫拉菌是一种仅感染人类的病原体,是儿童中耳炎以及慢性阻塞性肺疾病成人患者下呼吸道感染的重要病因。一种预防卡他莫拉菌感染的疫苗将对降低这些感染导致的发病率产生巨大的全球影响。ABC转运蛋白系统的底物结合蛋白2(SBP2)最近被确定为卡他莫拉菌细菌表面一种有前景的疫苗候选抗原。在本研究中,我们表明SBP1、-2和-3分别以极高的特异性结合不同的碱性氨基酸。我们构建了各自表达该基因簇中单个SBP的突变体,并在生长实验中表明SBP1、-2和-3通过为细菌获取氨基酸发挥营养功能。SBP2介导精氨酸的摄取,精氨酸是卡他莫拉菌严格的生长必需物质。黏附和侵袭试验表明SBP1和SBP3在人呼吸道上皮细胞的侵袭中起作用,这与它们在人类呼吸道细胞内存活中的营养作用一致。这项工作表明ABC转运蛋白系统的SBPs在摄取碱性氨基酸以支持卡他莫拉菌生长中发挥作用。SBP2在精氨酸摄取中的关键作用可能有助于其作为疫苗抗原的潜力。