Literature DB >> 12704111

LipL21 is a novel surface-exposed lipoprotein of pathogenic Leptospira species.

Paul A Cullen1, David A Haake, Dieter M Bulach, Richard L Zuerner, Ben Adler.   

Abstract

Leptospira is the etiologic agent of leptospirosis, a bacterial zoonosis distributed worldwide. Leptospiral lipopolysaccharide is a protective immunogen, but the extensive serological diversity of leptospires has inspired a search for conserved outer membrane proteins (OMPs) that may stimulate heterologous immunity. Previously, a global analysis of leptospiral OMPs (P. A. Cullen, S. J. Cordwell, D. M. Bulach, D. A. Haake, and B. Adler, Infect. Immun. 70:2311-2318, 2002) identified pL21, a novel 21-kDa protein that is the second most abundant constituent of the Leptospira interrogans serovar Lai outer membrane proteome. In this study, we identified the gene encoding pL21 and found it to encode a putative lipoprotein; accordingly, the protein was renamed LipL21. Southern hybridization analysis revealed the presence of lipL21 in all of the pathogenic species but in none of the saprophytic species examined. Alignment of the LipL21 sequence from six strains of Leptospira revealed 96 to 100% identity. When specific polyclonal antisera to recombinant LipL21 were used, LipL21 was isolated together with other known leptospiral OMPs by both Triton X-114 extraction and sucrose density gradient membrane fractionation. All nine strains of pathogenic leptospires investigated by Western blotting, whether culture attenuated or virulent, were found to express LipL21. In contrast, the expression of LipL21 or an antigenically related protein could not be detected in nonpathogenic L. biflexa. Infected hamster sera and two of eight human leptospirosis sera tested were found to react with recombinant LipL21. Native LipL21 was found to incorporate tritiated palmitic acid, consistent with the prediction of a lipoprotein signal peptidase cleavage site. Biotinylation of the leptospiral surface resulted in selective labeling of LipL21 and the previously known OMPs LipL32 and LipL41. These findings show that LipL21 is a surface-exposed, abundant outer membrane lipoprotein that is expressed during infection and conserved among pathogenic Leptospira species.

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Year:  2003        PMID: 12704111      PMCID: PMC153295          DOI: 10.1128/IAI.71.5.2414-2421.2003

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  38 in total

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Journal:  Infect Immun       Date:  1991-03       Impact factor: 3.441

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Journal:  Infect Immun       Date:  1992-08       Impact factor: 3.441

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  44 in total

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Authors:  Paul A Cullen; Xiaoyi Xu; James Matsunaga; Yolanda Sanchez; Albert I Ko; David A Haake; Ben Adler
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Journal:  Vet Res Commun       Date:  2007-01-13       Impact factor: 2.459

Review 3.  Leptospira: a spirochaete with a hybrid outer membrane.

Authors:  David A Haake; James Matsunaga
Journal:  Mol Microbiol       Date:  2010-06-28       Impact factor: 3.501

Review 4.  Human leptospirosis vaccines in China.

Authors:  Yinghua Xu; Qiang Ye
Journal:  Hum Vaccin Immunother       Date:  2017-12-19       Impact factor: 3.452

5.  Response of Leptospira interrogans to physiologic osmolarity: relevance in signaling the environment-to-host transition.

Authors:  James Matsunaga; Miranda Lo; Dieter M Bulach; Richard L Zuerner; Ben Adler; David A Haake
Journal:  Infect Immun       Date:  2007-03-19       Impact factor: 3.441

Review 6.  Outer membrane proteins of pathogenic spirochetes.

Authors:  Paul A Cullen; David A Haake; Ben Adler
Journal:  FEMS Microbiol Rev       Date:  2004-06       Impact factor: 16.408

7.  Proteome analysis of Leptospira interrogans virulent strain.

Authors:  Monica L Vieira; Daniel C Pimenta; Zenaide M de Morais; Silvio A Vasconcellos; Ana L T O Nascimento
Journal:  Open Microbiol J       Date:  2009-05-07

8.  Global transcriptomic response of Leptospira interrogans serovar Copenhageni upon exposure to serum.

Authors:  Kanitha Patarakul; Miranda Lo; Ben Adler
Journal:  BMC Microbiol       Date:  2010-01-29       Impact factor: 3.605

9.  High-temperature protein G is an essential virulence factor of Leptospira interrogans.

Authors:  Amy M King; Gabriela Pretre; Thanatchaporn Bartpho; Rasana W Sermswan; Claudia Toma; Toshihiko Suzuki; Azad Eshghi; Mathieu Picardeau; Ben Adler; Gerald L Murray
Journal:  Infect Immun       Date:  2013-12-23       Impact factor: 3.441

10.  Immunoprotection of recombinant leptospiral immunoglobulin-like protein A against Leptospira interrogans serovar Pomona infection.

Authors:  Raghavan U M Palaniappan; Sean P McDonough; Thomas J Divers; Chia-Sui Chen; Ming-Jeng Pan; Mitsuharu Matsumoto; Yung-Fu Chang
Journal:  Infect Immun       Date:  2006-03       Impact factor: 3.441

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