Mycobacterium tuberculosis invasion of macrophages:: Linking bacterial gene expression to environmental cues

被引:289
作者
Rohde, Kyle H. [1 ]
Abramovitch, Robert B. [1 ]
Russell, David G. [1 ]
机构
[1] Cornell Univ, Coll Vet Med, Dept Microbiol & Immunol, Ithaca, NY 14853 USA
关键词
D O I
10.1016/j.chom.2007.09.006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A central feature of Mycobacterium tuberculosis (Mtb) pathogenesis is the ability of Mtb to survive within macrophages (M empty set). Despite its critical importance, our appreciation of the interplay between these two cells remains superficial. We employed microarrays to conduct a stepwise dissection of Mtb-M empty set interaction during the invasion of resting bone marrow M empty set. Contrary to many bacterial pathogens, engagement by M empty set receptors without internalization did not alter Mtb gene expression. Subsequently, a high-resolution profile of Mtb invasion-linked gene expression was generated by assaying the Mtb transcriptome at 20 min intervals up to 2 hr postinfection. Transcriptional responses were detected within minutes of phagocytosis, including gene subsets with distinct temporal profiles. Pharmacological manipulation of phagosomal pH and in vitro acid stress studies revealed that vacuole acidification is an important trigger for differential gene expression. Finally, there are marked species-specific differences in the response of Mtb and M. bovis BCG to intraphagosomal cues.
引用
收藏
页码:352 / 364
页数:13
相关论文
共 62 条
[1]   Comparison of the roles of reactive oxygen and nitrogen intermediates in the host response to Mycobacterium tuberculosis using transgenic mice [J].
Adams, LB ;
Dinauer, MC ;
Morgenstern, DE ;
Krahenbuhl, JL .
TUBERCLE AND LUNG DISEASE, 1997, 78 (5-6) :237-246
[2]   Effector molecules in expression of the antimicrobial activity of macrophages against Mycobacterium avium complex: roles of reactive nitrogen intermediates, reactive oxygen intermediates, and free fatty acids [J].
Akaki, T ;
Sato, K ;
Shimizu, T ;
Sano, C ;
Kajitani, H ;
Dekio, S ;
Tomioka, H .
JOURNAL OF LEUKOCYTE BIOLOGY, 1997, 62 (06) :795-804
[3]   PHAGOSOME-LYSOSOME INTERACTIONS IN CULTURED MACROPHAGES INFECTED WITH VIRULENT TUBERCLE-BACILLI - REVERSAL OF USUAL NONFUSION PATTERN AND OBSERVATIONS ON BACTERIAL SURVIVAL [J].
ARMSTRONG, JA ;
HART, PD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1975, 142 (01) :1-16
[4]   The virulence-associated twocomponent PhoP-PhoR system controls the biosynthesis of polyketide-derived lipids in Mycobacterium tuberculosis [J].
Asensio, JG ;
Maia, C ;
Ferrer, NL ;
Barilone, N ;
Laval, F ;
Soto, CY ;
Winter, N ;
Daffé, M ;
Gicquel, B ;
Martín, C ;
Jackson, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (03) :1313-1316
[5]   Regulation of Mycobacterium tuberculosis whiB3 in the mouse lung and macrophages [J].
Banaiee, N. ;
Jacobs, W. R., Jr. ;
Ernst, J. D. .
INFECTION AND IMMUNITY, 2006, 74 (11) :6449-6457
[6]   Comparative genomics of BCG vaccines by whole-genome DNA microarray [J].
Behr, MA ;
Wilson, MA ;
Gill, WP ;
Salamon, H ;
Schoolnik, GK ;
Rane, S ;
Small, PM .
SCIENCE, 1999, 284 (5419) :1520-1523
[7]   Mycobacterium bovis BCG response regulator essential for hypoxic dormancy [J].
Boon, C ;
Dick, T .
JOURNAL OF BACTERIOLOGY, 2002, 184 (24) :6760-6767
[8]   ESAT-6 proteins: protective antigens and virulence factors? [J].
Brodin, P ;
Rosenkrands, I ;
Andersen, P ;
Cole, ST ;
Brosch, R .
TRENDS IN MICROBIOLOGY, 2004, 12 (11) :500-508
[9]  
Butcher PD, 1998, METH MOL B, V101, P285, DOI 10.1385/0-89603-471-2:285
[10]   Identification of a virulence gene cluster of Mycobacterium tuberculosis by signature-tagged transposon mutagenesis [J].
Camacho, LR ;
Ensergueix, D ;
Perez, E ;
Gicquel, B ;
Guilhot, C .
MOLECULAR MICROBIOLOGY, 1999, 34 (02) :257-267