Cloning, Expression, and Homology Modeling of GroEL Protein from Leptospira interrogans Serovar Autumnalis Strain N2

Leptospirosis is an infectious bacterial disease caused by Leptospira species. In this study, we cloned and sequenced the gene encoding the immunodominant protein GroEL from L. interrogans serovar Autumnalis strain N2, which was isolated from the urine of a patient during an outbreak of leptospirosis in Chennai, India. This groEL gene encodes a protein of 60 kDa with a high degree of homology (99% similarity) to those of other leptospiral serovars. Recombinant GroEL was overexpressed in Escherichia coli. Immunoblot analysis indicated that the sera from confirmed leptospirosis patients showed strong reactivity with the recombinant GroEL while no reactivity was observed with the sera from seronegative control patient. In addition, the 3D structure of GroEL was constructed using chaperonin complex cpn60 from Thermus thermophilus as template and validated. The results indicated a Z-score of −8.35, which is in good agreement with the expected value for a protein. The superposition of the Cα traces of cpn60 structure and predicted structure of leptospiral GroEL indicates good agreement of secondary structure elements with an RMSD value of 1.5 Å. Further study is necessary to evaluate GroEL for serological diagnosis of leptospirosis and for its potential as a vaccine component.

[1]  D. Haake,et al.  Molecular cloning and sequence analysis of the gene encoding OmpL1, a transmembrane outer membrane protein of pathogenic Leptospira spp , 1993, Journal of bacteriology.

[2]  Matthew A. Kayala,et al.  A Burkholderia pseudomallei protein microarray reveals serodiagnostic and cross-reactive antigens , 2009, Proceedings of the National Academy of Sciences.

[3]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[4]  R. Zuerner,et al.  The Leptospiral Major Outer Membrane Protein LipL32 Is a Lipoprotein Expressed during Mammalian Infection , 2000, Infection and Immunity.

[5]  R. Young,et al.  In Vivo Cytotoxic T Lymphocyte Elicitation by Mycobacterial Heat Shock Protein 70 Fusion Proteins Maps to a Discrete Domain and Is Cd4+ T Cell Independent , 2000, The Journal of experimental medicine.

[6]  B. Adler,et al.  Molecular analysis of the dnaK locus of Leptospira interrogans serovar Copenhageni. , 1998, Gene.

[7]  Radhey S. Gupta Evolution of the chaperonin families (HSP60, HSP 10 and TCP‐1) of proteins and the origin of eukaryotic cells , 1995, Molecular microbiology.

[8]  S. Sharma,et al.  Evolutionary Implication of Outer Membrane Lipoprotein-Encoding Genes ompL1, lipL32 and lipL41 of Pathogenic Leptospira Species , 2009, Genom. Proteom. Bioinform..

[9]  J. Timoney,et al.  Surface-associated Hsp60 chaperonin of Leptospira interrogans serovar Autumnalis N2 strain as an immunoreactive protein , 2011, European Journal of Clinical Microbiology & Infectious Diseases.

[10]  F. Gherardini,et al.  Heat shock response of spirochetes , 1991, Infection and immunity.

[11]  J. Thornton,et al.  PROCHECK: a program to check the stereochemical quality of protein structures , 1993 .

[12]  R. Ellis,et al.  Molecular Chaperones , 1993, Springer Netherlands.

[13]  K. Willison,et al.  Cystosolic chaperonin subunits have a conserved ATPase domain but diverged polypeptide-binding domains. , 1994, Trends in biochemical sciences.

[14]  B. Adler,et al.  Molecular analysis of the hsp (groE) operon of Leptospira interrogans serovar copenhageni , 1993, Molecular microbiology.

[15]  R. Hancock,et al.  The rare outer membrane protein, OmpL1, of pathogenic Leptospira species is a heat-modifiable porin , 1995, Infection and immunity.

[16]  M. Karplus,et al.  Evaluation of comparative protein modeling by MODELLER , 1995, Proteins.

[17]  C. Georgopoulos,et al.  The universally conserved GroE (Hsp60) chaperonins. , 1991, Annual review of microbiology.

[18]  M. Loos,et al.  A 66-kilodalton heat shock protein of Salmonella typhimurium is responsible for binding of the bacterium to intestinal mucus , 1992, Infection and immunity.

[19]  M. Salimans,et al.  Rapid and simple method for purification of nucleic acids , 1990, Journal of clinical microbiology.

[20]  S. Faine,et al.  Leptospira and leptospirosis. , 1994 .

[21]  P E Bourne,et al.  Protein structure alignment by incremental combinatorial extension (CE) of the optimal path. , 1998, Protein engineering.

[22]  T. Blundell,et al.  Comparative protein modelling by satisfaction of spatial restraints. , 1993, Journal of molecular biology.

[23]  S. Kaufmann,et al.  Role of Heat Shock Proteins in Protection from and Pathogenesis of Infectious Diseases , 1999, Clinical Microbiology Reviews.

[24]  S. Sharma,et al.  Leptospiral proteins expressed during acute & convalescent phases of human leptospirosis. , 2004, The Indian journal of medical research.

[25]  John P. Overington,et al.  Derivation of rules for comparative protein modeling from a database of protein structure alignments , 1994, Protein science : a publication of the Protein Society.

[26]  A. Seguro,et al.  Acute lung injury in leptospirosis: clinical and laboratory features, outcome, and factors associated with mortality. , 1999, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[27]  B. Ahn,et al.  Expression and immunologic characterization of recombinant heat shock protein 58 of Leptospira species: a major target antigen of the humoral immune response. , 1999, DNA and cell biology.

[28]  A Sali,et al.  Modeling mutations and homologous proteins. , 1995, Current opinion in biotechnology.

[29]  M. Reis,et al.  Leptospiral Proteins Recognized during the Humoral Immune Response to Leptospirosis in Humans , 2001, Infection and Immunity.

[30]  D. Haake,et al.  Molecular cloning and sequence analysis of the gene encoding LipL41, a surface-exposed lipoprotein of pathogenic Leptospira species , 1996, Infection and immunity.