Comparative Genomics of Two Leptospira interrogans Serovars Reveals Novel Insights into Physiology and Pathogenesis

Author:

Nascimento A. L. T. O.1,Ko A. I.23,Martins E. A. L.1,Monteiro-Vitorello C. B.4,Ho P. L.1,Haake D. A.56,Verjovski-Almeida S.7,Hartskeerl R. A.8,Marques M. V.9,Oliveira M. C.10,Menck C. F. M.9,Leite L. C. C.1,Carrer H.4,Coutinho L. L.4,Degrave W. M.11,Dellagostin O. A.12,El-Dorry H.7,Ferro E. S.9,Ferro M. I. T.13,Furlan L. R.13,Gamberini M.1,Giglioti E. A.14,Góes-Neto A.15,Goldman G. H.16,Goldman M. H. S.17,Harakava R.18,Jerônimo S. M. B19,Junqueira-de-Azevedo I. L. M.1,Kimura E. T.9,Kuramae E. E.20,Lemos E. G. M.13,Lemos M. V. F.13,Marino C. L.21,Nunes L. R.22,de Oliveira R. C.22,Pereira G. G.23,Reis M. S.24,Schriefer A.25,Siqueira W. J.25,Sommer P.19,Tsai S. M.26,Simpson A. J. G.27,Ferro J. A.13,Camargo L. E. A.4,Kitajima J. P.28,Setubal J. C.24,Van Sluys M. A.10

Affiliation:

1. Centro de Biotecnologia, Instituto Butantan

2. Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz/Ministério da Saúde

3. Division of International Medicine and Infectious Disease, Weill Medical College of Cornell University

4. Escola Superior de Agricultura Luiz de Queiroz

5. University of California—Los Angeles School of Medicine

6. Division of Infectious Diseases, Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California

7. Instituto de Química

8. KIT (Koninklijk Instituut voor de Tropen/Royal Tropical Institute), KIT Biomedical Research, Amsterdam, The Netherlands

9. Instituto de Ciências Biomédicas

10. Instituto de Biociências

11. Departamento de Bioquímica e Biologia Molecular, Instituto Oswaldo Cruz, Rio de Janeiro, Rio de Janeiro

12. Centro de Biotecnologia, Universidade Federal de Pelotas, Pelotas, Rio Grande do Sul

13. Faculdade de Ciências Agrárias e Veterinárias, Universidade Estadual Paulista, Jaboticabal

14. Centro de Ciências Agrárias, Universidade Federal de São Carlos, Araras

15. Laboratório de Pesquisa em Microbiologia (LAPEM), Departamento de Ciências Biológicas, Universidade Estadual de Feira de Santana (UEFS), Feira de Santana, Bahia

16. Faculdade de Ciencias Farmaceuticas de Ribeirão Preto

17. Faculdade de Filosofia, Ciências e Letras, Universidade de São Paulo, Ribeirão Preto

18. Instituto Biológico, Universidade de São Paulo, São Paulo

19. Centro de Biociências, Universidade Federal do Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil

20. Faculdade de Ciências Agronômicas

21. Instituto de Biociências, Universidade Estadual Paulista, Botucatu

22. Núcleo Integrado de Biotecnologia, Universidade de Mogi das Cruzes, Mogi das Cruzes

23. Departamento de Genética e Evolução

24. Instituto de Computação

25. Hospital Universitário Professor Edgard Santos, Serviço de Imunologia, Universidade Federal da Bahia, Salvador

26. Centro de Energia Nuclear na Agricultura, Universidade de São Paulo, Piracicaba

27. Ludwig Institute for Cancer Research, New York, New York

28. Centro de Biologia Molecular e Engenharia Genética, Universidade Estadual de Campinas, Campinas, São Paulo

Abstract

ABSTRACT Leptospira species colonize a significant proportion of rodent populations worldwide and produce life-threatening infections in accidental hosts, including humans. Complete genome sequencing of Leptospira interrogans serovar Copenhageni and comparative analysis with the available Leptospira interrogans serovar Lai genome reveal that despite overall genetic similarity there are significant structural differences, including a large chromosomal inversion and extensive variation in the number and distribution of insertion sequence elements. Genome sequence analysis elucidates many of the novel aspects of leptospiral physiology relating to energy metabolism, oxygen tolerance, two-component signal transduction systems, and mechanisms of pathogenesis. A broad array of transcriptional regulation proteins and two new families of afimbrial adhesins which contribute to host tissue colonization in the early steps of infection were identified. Differences in genes involved in the biosynthesis of lipopolysaccharide O side chains between the Copenhageni and Lai serovars were identified, offering an important starting point for the elucidation of the organism's complex polysaccharide surface antigens. Differences in adhesins and in lipopolysaccharide might be associated with the adaptation of serovars Copenhageni and Lai to different animal hosts. Hundreds of genes encoding surface-exposed lipoproteins and transmembrane outer membrane proteins were identified as candidates for development of vaccines for the prevention of leptospirosis.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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