A comprehensive approach to identification of surface-exposed, outer membrane-spanning proteins of Leptospira interrogans.

Leptospirosis is a zoonosis with worldwide distribution caused by pathogenic spirochetes belonging to the genus Leptospira. The leptospiral life cycle involves transmission via fresh water and colonization of the renal tubules of their reservoir hosts or infection of accidental hosts, including huma...

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Main Authors: Marija Pinne, David A Haake
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-06-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2698987?pdf=render
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spelling doaj-882decede7b049858c5543b6a994f29c2020-11-24T21:54:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-06-0146e607110.1371/journal.pone.0006071A comprehensive approach to identification of surface-exposed, outer membrane-spanning proteins of Leptospira interrogans.Marija PinneDavid A HaakeLeptospirosis is a zoonosis with worldwide distribution caused by pathogenic spirochetes belonging to the genus Leptospira. The leptospiral life cycle involves transmission via fresh water and colonization of the renal tubules of their reservoir hosts or infection of accidental hosts, including humans. Bacterial outer membrane proteins (OMPs), particularly those with surface-exposed regions, play crucial roles in virulence mechanisms of pathogens and the adaptation to various environmental conditions, including those of the mammalian host. Little is known about the surface-exposed OMPs in Leptospira, particularly those with outer membrane-spanning domains. Herein, we describe a comprehensive strategy for identification and characterization of leptospiral transmembrane OMPs. The genomic sequence of L. interrogans serovar Copenhageni strain Fiocruz L1-130 allowed us to employ the beta-barrel prediction programs, PRED-TMBB and TMBETA-NET, to identify potential transmembrane OMPs. Several complementary methods were used to characterize four novel OMPs, designated OmpL36, OmpL37, OmpL47 and OmpL54. In addition to surface immunofluorescence and surface biotinylation, we describe surface proteolysis of intact leptospires as an improved method for determining the surface exposure of leptospiral proteins. Membrane integration was confirmed using techniques for removal of peripheral membrane proteins. We also demonstrate deficiencies in the Triton X-114 fractionation method for assessing the outer membrane localization of transmembrane OMPs. Our results establish a broadly applicable strategy for the elucidation of novel surface-exposed outer membrane-spanning proteins of Leptospira, an essential step in the discovery of potential virulence factors, diagnostic antigens and vaccine candidates.http://europepmc.org/articles/PMC2698987?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Marija Pinne
David A Haake
spellingShingle Marija Pinne
David A Haake
A comprehensive approach to identification of surface-exposed, outer membrane-spanning proteins of Leptospira interrogans.
PLoS ONE
author_facet Marija Pinne
David A Haake
author_sort Marija Pinne
title A comprehensive approach to identification of surface-exposed, outer membrane-spanning proteins of Leptospira interrogans.
title_short A comprehensive approach to identification of surface-exposed, outer membrane-spanning proteins of Leptospira interrogans.
title_full A comprehensive approach to identification of surface-exposed, outer membrane-spanning proteins of Leptospira interrogans.
title_fullStr A comprehensive approach to identification of surface-exposed, outer membrane-spanning proteins of Leptospira interrogans.
title_full_unstemmed A comprehensive approach to identification of surface-exposed, outer membrane-spanning proteins of Leptospira interrogans.
title_sort comprehensive approach to identification of surface-exposed, outer membrane-spanning proteins of leptospira interrogans.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-06-01
description Leptospirosis is a zoonosis with worldwide distribution caused by pathogenic spirochetes belonging to the genus Leptospira. The leptospiral life cycle involves transmission via fresh water and colonization of the renal tubules of their reservoir hosts or infection of accidental hosts, including humans. Bacterial outer membrane proteins (OMPs), particularly those with surface-exposed regions, play crucial roles in virulence mechanisms of pathogens and the adaptation to various environmental conditions, including those of the mammalian host. Little is known about the surface-exposed OMPs in Leptospira, particularly those with outer membrane-spanning domains. Herein, we describe a comprehensive strategy for identification and characterization of leptospiral transmembrane OMPs. The genomic sequence of L. interrogans serovar Copenhageni strain Fiocruz L1-130 allowed us to employ the beta-barrel prediction programs, PRED-TMBB and TMBETA-NET, to identify potential transmembrane OMPs. Several complementary methods were used to characterize four novel OMPs, designated OmpL36, OmpL37, OmpL47 and OmpL54. In addition to surface immunofluorescence and surface biotinylation, we describe surface proteolysis of intact leptospires as an improved method for determining the surface exposure of leptospiral proteins. Membrane integration was confirmed using techniques for removal of peripheral membrane proteins. We also demonstrate deficiencies in the Triton X-114 fractionation method for assessing the outer membrane localization of transmembrane OMPs. Our results establish a broadly applicable strategy for the elucidation of novel surface-exposed outer membrane-spanning proteins of Leptospira, an essential step in the discovery of potential virulence factors, diagnostic antigens and vaccine candidates.
url http://europepmc.org/articles/PMC2698987?pdf=render
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