Author | Barocchi, Michele A | |
Author | Ko, Albert Icksang | |
Author | Reis, Mitermayer Galvão dos | |
Author | McDonald, Kent L | |
Author | Riley, Lee Woodland | |
Access date | 2014-05-02T13:17:56Z | |
Available date | 2014-05-02T13:17:56Z | |
Document date | 2002 | |
Citation | BAROCCHI, M. A. et al. Rapid translocation of polarized MDCK cell monolayers by Leptospira interrogans, an invasive but nonintracellular pathogen. Infection and Immunity, v. 70, n. 12, p. 6926-6932, 2002. | pt_BR |
ISSN | 0019-9567 | |
URI | https://www.arca.fiocruz.br/handle/icict/7566 | |
Language | eng | pt_BR |
Publisher | American Society for Microbiology | pt_BR |
Rights | open access | pt_BR |
Title | Rapid translocation of polarized MDCK cell monolayers by Leptospira interrogans, an invasive but nonintracellular pathogen | pt_BR |
Type | Article | pt_BR |
DOI | 10.1128/IAI.70.12.6926–6932.2002 | |
Abstract | Pathogenic spirochetes of the genus Leptospira are a major cause of human zoonotic infectious disease
worldwide. After gaining entry through the skin, the organism causes disease by hematogenously disseminating
to multiple organs. The mechanism by which it penetrates the mammalian cell barriers to disseminate is not
well understood. In this study, we used a low-passage-number isolate of Leptospira interrogans to elucidate the
invasive potential of this spirochete. Quantification of bacteria by dark-field microscopy revealed that pathogenic
spirochetes were able to translocate through polarized MDCK cell monolayers at a rate significantly
greater than that of nonpathogenic Leptospira or a recognized invasive bacterial pathogen, Salmonella. In
contrast to Salmonella, L. interrogans did not alter transepithelial electrical resistance during cell translocation.
Both transmission and scanning electron microscopy revealed tight association of the extracellular spirochetes
with the host cell plasma membrane, without membrane perturbations suggestive of cytoskeletal rearrangement.
Spirochetes were not observed within intercellular junctions or membrane-bound compartments inside
cells. They were found within the cytoplasm of only 8% of the counted cells. These results indicate that
Leptospira is an invasive but not a facultative intracellular organism. We propose that the rapid translocation
of mammalian cells by pathogenic Leptospira is a mechanism designed to evade killing by host cells that
permits the organism to quickly reach the bloodstream and disseminate to multiple organs. | pt_BR |
Affilliation | Division of Infectious Diseases and Immunity. School of Public Health. Berkeley, California | pt_BR |
Affilliation | Fundação Oswaldo Cruz. Centro de Pesquisa Gonçalo Moniz. Salvador, BA, Brasil | pt_BR |
Affilliation | Fundação Oswaldo Cruz. Centro de Pesquisa Gonçalo Moniz. Salvador, BA, Brasil / Division of International Medicine and Infectious Diseases. Weil Medical College of Cornell University. New York, NY | pt_BR |
Affilliation | UC Berkeley Electron Microscopy Laboratory. University of California. Berkeley, Berkeley, California | pt_BR |
Affilliation | Division of Infectious Diseases and Immunity. School of Public Health. Berkeley, California | pt_BR |
DeCS | Polaridade Celular | pt_BR |
DeCS | Células Epiteliais/microbiologia | pt_BR |
DeCS | Leptospira interrogans/patogenicidade | pt_BR |
DeCS | Animais | pt_BR |
DeCS | Linhagem Celular | pt_BR |
DeCS | Cães | pt_BR |
DeCS | Condutividade Elétrica | pt_BR |
DeCS | Células Epiteliais/ultraestrutura | pt_BR |
DeCS | Interações Hospedeiro-Parasita | pt_BR |
DeCS | Junções Intercelulares/ultraestrutura | pt_BR |
DeCS | Rim/citologia | pt_BR |
DeCS | Rim/microbiologia | pt_BR |
DeCS | Microscopia Eletrônica de Varredura | pt_BR |
DeCS | Microvilosidades/ultraestrutura | pt_BR |
DeCS | Fatores de Tempo | pt_BR |
DeCS | Virulência | pt_BR |