Enhanced capacity of a widespread strain of Mycobacterium tuberculosis to grow in human macrophages

被引:126
作者
Zhang, M
Gong, JH
Yang, ZH
Samten, B
Cave, MD
Barnes, PF
机构
[1] Univ Texas, Ctr Hlth, Ctr Pulm & Infect Dis Control, Dept Med, Tyler, TX 75708 USA
[2] Univ Texas, Dept Cell Biol, Tyler, TX 75708 USA
[3] Univ Arkansas Med Sci, Dept Pathol, Little Rock, AR 72205 USA
[4] Univ Arkansas Med Sci, Dept Anat, Little Rock, AR 72205 USA
[5] John L McClellan Mem Vet Adm Med Ctr, Med Res Serv, Little Rock, AR USA
关键词
D O I
10.1086/314738
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To determine whether the extent of spread of Mycobacterium tuberculosis strains in the community correlated with their capacity to replicate in human macrophages, intracellular growth rates of M. tuberculosis patient isolates were measured. Strain 210 caused disease in 43 patients in central Los Angeles, 3 "small-cluster" strains caused disease in 8-23 patients, and 5 "unique" strains each caused disease in only 1 patient who was positive by sputum acid-fast smear and spent substantial amounts of time at homeless shelters that were tuberculosis transmission sites. Strain 210 isolates grew significantly more rapidly than small-cluster and unique strains in macrophages. All strains elicited production of similar amounts of tumor necrosis factor-cu, interleukin (IL)-6, IL-10, and IL-12 and were equally susceptible to reactive nitrogen intermediates. It was concluded that the extensive spread of an M. tuberculosis strain correlated with its capacity to replicate rapidly in human macrophages, which may be a marker of virulence.
引用
收藏
页码:1213 / 1217
页数:5
相关论文
共 24 条
[1]   TRANSMISSION OF TUBERCULOSIS IN NEW-YORK-CITY - AN ANALYSIS BY DNA-FINGERPRINTING AND CONVENTIONAL EPIDEMIOLOGIC METHODS [J].
ALLAND, D ;
KALKUT, GE ;
MOSS, AR ;
MCADAM, RA ;
HAHN, JA ;
BOSWORTH, W ;
DRUCKER, E ;
BLOOM, BR .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (24) :1710-1716
[2]   Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency [J].
Altare, F ;
Durandy, A ;
Lammas, D ;
Emile, JF ;
Lamhamedi, S ;
Le Deist, F ;
Drysdale, P ;
Jouanguy, E ;
Döffinger, R ;
Bernaudin, F ;
Jeppsson, O ;
Gollob, JA ;
Meinl, E ;
Segal, AW ;
Fischer, A ;
Kumararatne, D ;
Casanova, JL .
SCIENCE, 1998, 280 (5368) :1432-1435
[3]   Tuberculosis transmission in central Los Angeles [J].
Barnes, PF ;
Yang, ZH ;
PrestonMartin, S ;
Pogoda, JM ;
Jones, BE ;
Otaya, M ;
Eisenach, KD ;
Knowles, L ;
Harvey, S ;
Cave, MD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 278 (14) :1159-1163
[4]   DNA fingerprinting with two probes decreases clustering of Mycobacterium tuberculosis [J].
Burman, WJ ;
Reves, RR ;
Hawkes, AP ;
Rietmeijer, CA ;
Yang, ZH ;
ElHajj, H ;
Bates, JH ;
Cave, MD .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 155 (03) :1140-1146
[5]   KILLING OF VIRULENT MYCOBACTERIUM-TUBERCULOSIS BY REACTIVE NITROGEN INTERMEDIATES PRODUCED BY ACTIVATED MURINE MACROPHAGES [J].
CHAN, J ;
XING, Y ;
MAGLIOZZO, RS ;
BLOOM, BR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (04) :1111-1122
[6]   Interleukin 12 (IL-12) is crucial to the development of protective immunity in mice intravenously infected with Mycobacterium tuberculosis [J].
Cooper, AM ;
Magram, J ;
Ferrante, J ;
Orme, IM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (01) :39-45
[7]  
de Jong R, 1998, SCIENCE, V280, P1435
[8]   TUMOR-NECROSIS-FACTOR-ALPHA IS REQUIRED IN THE PROTECTIVE IMMUNE-RESPONSE AGAINST MYCOBACTERIUM-TUBERCULOSIS IN MICE [J].
FLYNN, JL ;
GOLDSTEIN, MM ;
CHAN, J ;
TRIEBOLD, KJ ;
PFEFFER, K ;
LOWENSTEIN, CJ ;
SCHREIBER, R ;
MAK, TW ;
BLOOM, BR .
IMMUNITY, 1995, 2 (06) :561-572
[9]   Widespread dissemination of a drug-susceptible strain of Mycobacterium tuberculosis [J].
Friedman, CR ;
Quinn, GC ;
Kreiswirth, BN ;
Perlman, DC ;
Salomon, N ;
Schluger, N ;
Lutfey, M ;
Berger, J ;
Poltoratskaia, N ;
Riley, LW .
JOURNAL OF INFECTIOUS DISEASES, 1997, 176 (02) :478-484
[10]  
Frucht DM, 1996, J IMMUNOL, V157, P411