Brucella intracellular life:: from invasion to intracellular replication

被引:230
作者
Gorvel, JP [1 ]
Moreno, E
机构
[1] CNRS, Ctr Immunol, INSERM, F-13288 Marseille 9, France
[2] Univ Nacl, Escuela Med Vet, Programa Invest Enfermedades Trop, Heredia 3000, Costa Rica
关键词
Brucella; BvrR/BvrS; virB; bacterial invasion; intracellular trafficking;
D O I
10.1016/S0378-1135(02)00214-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Brucella organisms are pathogens that ultimate goal is to propagate in their preferred niche, the cell. Upon cell contact the bacteria is internalized via receptor molecules by activating small GTPases of the Rho subfamily and by a moderate recruitment of actin filaments. Once inside cells, Brucella localizes in early phagosomes, where it avoids fusion with late endosomes and lysosomes. These early events require the control of Rab small GTPases, and cytokines such as the G-CSF. Then, the bacterium redirects its trafficking to autophagosomes and finally reaches the endoplasmic reticulum, where it extensively replicates. Some of the bacterial molecular determinants involved in the internalization and early events after ingestion are controlled by the BvrS/BvrR two component regulatory system, whereas the intracellular trafficking beyond this early compartments are controlled by the VirB type IV secretion system. Once inside the endoplasmic reticulum, Brucella extensively replicates without restricting basic cellular functions or inducing obvious damage to cells. The integrity of Brucella LPS on the bacterial surface is one of the required factors for Brucella intracellular survival, and therefore for virulence. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:281 / 297
页数:17
相关论文
共 65 条
[1]  
Abu Kwaik Y, 2001, ASM NEWS, V67, P240
[2]   BOVINE ILEAL DOME LYMPHOEPITHELIAL CELLS - ENDOCYTOSIS AND TRANSPORT OF BRUCELLA-ABORTUS STRAIN-19 [J].
ACKERMANN, MR ;
CHEVILLE, NF ;
DEYOE, BL .
VETERINARY PATHOLOGY, 1988, 25 (01) :28-35
[3]   Transposon-derived Brucella abortus rough mutants are attenuated and exhibit reduced intracellular survival [J].
Allen, CA ;
Adams, LG ;
Ficht, TA .
INFECTION AND IMMUNITY, 1998, 66 (03) :1008-1016
[4]  
AMANO K, 1987, J BIOL CHEM, V262, P4740
[5]   PATHOGENESIS OF PLACENTITIS IN THE GOAT INOCULATED WITH BRUCELLA-ABORTUS .1. GROSS AND HISTOLOGIC LESIONS [J].
ANDERSON, TD ;
MEADOR, VP ;
CHEVILLE, NF .
VETERINARY PATHOLOGY, 1986, 23 (03) :219-226
[6]  
ANDERSON TD, 1986, AM J PATHOL, V124, P226
[7]   PATHOGENESIS OF PLACENTITIS IN THE GOAT INOCULATED WITH BRUCELLA-ABORTUS .2. ULTRASTRUCTURAL STUDIES [J].
ANDERSON, TD ;
CHEVILLE, NF ;
MEADOR, VP .
VETERINARY PATHOLOGY, 1986, 23 (03) :227-239
[8]  
Brade H, 1999, ENDOTOXIN IN HEALTH AND DISEASE, P229
[9]   INDUCTION OF SALMONELLA STRESS PROTEINS UPON INFECTION OF MACROPHAGES [J].
BUCHMEIER, NA ;
HEFFRON, F .
SCIENCE, 1990, 248 (4956) :730-732
[10]   MECHANISMS OF BINDING OF BRUCELLA-ABORTUS TO MONONUCLEAR PHAGOCYTES FROM COWS NATURALLY RESISTANT OR SUSCEPTIBLE TO BRUCELLOSIS [J].
CAMPBELL, GA ;
ADAMS, LG ;
SOWA, BA .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1994, 41 (3-4) :295-306