Helicobacter pylori Growth Stage Determines the Size, Protein Composition, and Preferential Cargo Packaging of Outer Membrane Vesicles

被引:104
作者
Zavan, Lauren [1 ]
Bitto, Natalie J. [1 ]
Johnston, Ella L. [1 ]
Greening, David W. [2 ,3 ]
Kaparakis-Liaskos, Maria [1 ,3 ]
机构
[1] La Trobe Univ, Dept Physiol Anat & Microbiol, Bundoora, Vic 3086, Australia
[2] La Trobe Univ, La Trobe Inst Mol Sci, Dept Biochem & Genet, Bundoora, Vic 3086, Australia
[3] La Trobe Univ, Res Ctr Extracellular Vesicles, Bundoora, Vic 3086, Australia
基金
英国医学研究理事会;
关键词
growth stage; Helicobacter pylori; IL-8; outer membrane vesicles; proteomics; size; GRAM-NEGATIVE BACTERIA; PSEUDOMONAS-AERUGINOSA; FUNCTIONAL-CHARACTERIZATION; ACINETOBACTER-BAUMANNII; PERIPLASMIC PROTEINS; BIOGENESIS; RESISTANCE; SECRETION; INFECTION; MUTANTS;
D O I
10.1002/pmic.201800209
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gram-negative bacteria release outer membrane vesicles (OMVs) as part of their normal growth that contain a range of cargo from their parent bacterium, including DNA, RNA, and proteins. The protein content of OMVs is suggested to be similar in composition to various sub-cellular locations of their parent bacterium. However, very little is known regarding the effect of bacterial growth stage on the size, content, and selective packaging of proteins into OMVs. In this study, the global proteome of Helicobacter pylori and their OMVs throughout bacterial growth are examined to determine if bacterial growth stage affected OMV cargo composition. Analysis of OMVs produced by H. pylori reveals that bacterial growth stage affects the size, composition, and selection of protein cargo into OMVs. Proteomic analysis identifies that the proteome of H. pylori OMVs is vastly different throughout bacterial growth and that OMVs contain a range of proteins compared to their parent bacteria. In addition, bacterial growth stage affects the ability of OMVs to induce the production of IL-8 by human epithelial cells. Therefore, the findings identify that the size, proteome, and immunogenicity of OMVs produced during various stages of bacterial growth is not comparable. Collectively, these findings highlight the importance of considering the bacterial growth stage from which OMVs are isolated, as this will impact their size, protein composition, and ultimately their biological functions.
引用
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页数:14
相关论文
共 47 条
[1]   Purification of outer membrane vesicles from Pseudomonas aeruginosa and their activation of an IL-8 response [J].
Bauman, Susanne J. ;
Kuehn, Meta J. .
MICROBES AND INFECTION, 2006, 8 (9-10) :2400-2408
[2]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[3]   Escherichia coli tol-pal mutants form outer membrane vesicles [J].
Bernadac, A ;
Gavioli, M ;
Lazzaroni, JC ;
Raina, S ;
Lloubès, R .
JOURNAL OF BACTERIOLOGY, 1998, 180 (18) :4872-4878
[4]   NOD-Like Receptor Activation by Outer Membrane Vesicles from Vibrio cholerae Non-O1 Non-O139 Strains Is Modulated by the Quorum-Sensing Regulator HapR [J].
Bielig, H. ;
Rompikuntal, P. K. ;
Dongre, M. ;
Zurek, B. ;
Lindmark, B. ;
Ramstedt, M. ;
Wai, S. N. ;
Kufer, T. A. .
INFECTION AND IMMUNITY, 2011, 79 (04) :1418-1427
[5]   The Therapeutic Benefit of Bacterial Membrane Vesicles [J].
Bitto, Natalie J. ;
Kaparakis-Liaskos, Maria .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (06)
[6]  
BLASER MJ, 1995, CANCER RES, V55, P2111
[7]   cag, a pathogenicity island of Helicobacter pylori, encodes type I-specific and disease-associated virulence factors [J].
Censini, S ;
Lange, C ;
Xiang, ZY ;
Crabtree, JE ;
Ghiara, P ;
Borodovsky, M ;
Rappuoli, R ;
Covacci, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14648-14653
[8]   MOLECULAR CHARACTERIZATION OF THE 128-KDA IMMUNODOMINANT ANTIGEN OF HELICOBACTER-PYLORI-ASSOCIATED WITH CYTOTOXICITY AND DUODENAL-ULCER [J].
COVACCI, A ;
CENSINI, S ;
BUGNOLI, M ;
PETRACCA, R ;
BURRONI, D ;
MACCHIA, G ;
MASSONE, A ;
PAPINI, E ;
XIANG, ZY ;
FIGURA, N ;
RAPPUOLI, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (12) :5791-5795
[9]   Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ [J].
Cox, Juergen ;
Hein, Marco Y. ;
Luber, Christian A. ;
Paron, Igor ;
Nagaraj, Nagarjuna ;
Mann, Matthias .
MOLECULAR & CELLULAR PROTEOMICS, 2014, 13 (09) :2513-2526
[10]   MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification [J].
Cox, Juergen ;
Mann, Matthias .
NATURE BIOTECHNOLOGY, 2008, 26 (12) :1367-1372