GROWTH OF FRANCISELLA-TULARENSIS LVS IN MACROPHAGES - THE ACIDIC INTRACELLULAR COMPARTMENT PROVIDES ESSENTIAL IRON REQUIRED FOR GROWTH

被引:130
作者
FORTIER, AH
LEIBY, DA
NARAYANAN, RB
ASAFOADJEI, E
CRAWFORD, RM
NACY, CA
MELTZER, MS
机构
[1] WALTER REED ARMY INST RES,DEPT CELLULAR IMMUNOL,WASHINGTON,DC 20307
[2] WALTER REED ARMY INST RES,DEPT PATHOL,WASHINGTON,DC 20307
关键词
D O I
10.1128/IAI.63.4.1478-1483.1995
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Murine macrophages supported exponential intracellular growth of Francisella tularensis LVS in vitro with a doubling time of 4 to 6 h, LVS was internalized and remained in a vacuolar compartment throughout its growth cycle, The importance of endosome acidification to intracellular growth of this bacterium was assessed by treatment of LVS-infected macrophages with several different lysosomotropic agents (chloroquine, NH4Cl, and ouabain), Regardless of the agent used or its mechanism of action, macrophages treated with agents that blocked endosome acidification no longer supported replication of LVS, Over several experiments for each lysosomotropic agent, the number of CFU of LVS recovered from treated macrophage cultures was equivalent to the input inoculum (approximately 10(4) CFU) at 72 h, In contrast, over 10(8) CFU was consistently recovered from untreated cultures, Pretreatment of macrophages with these endosome acidification inhibitors did not alter their ingestion of bacteria. Further, the effects of the inhibitors were completely reversible: inhibitor-pretreated LVS-infected macrophages washed free of the agent and cultured in medium fully supported LVS growth over 72 h, Endosome acidification is an important cellular event essential for release of iron from transferrin, The growth-inhibitory effects of both chloroquine and NH4Cl were completely reversed by addition of ferric PPi, a transferrin-independent iron source, at a neutral pH but not by addition of excess holotransferrin, Thus, intracellular localization in an acidic vesicle which facilitates the availability of iron essential for Francisella growth is a survival tactic of this bacterium, and iron depletion is one mechanism that macrophages use to inhibit its growth.
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页码:1478 / 1483
页数:6
相关论文
共 33 条
[1]   GROWTH OF FRANCISELLA-SPP IN RODENT MACROPHAGES [J].
ANTHONY, LSD ;
BURKE, RD ;
NANO, FE .
INFECTION AND IMMUNITY, 1991, 59 (09) :3291-3296
[2]   RESPONSE OF CULTURED MACROPHAGES TO MYCOBACTERIUM-TUBERCULOSIS, WITH OBSERVATIONS ON FUSION OF LYSOSOMES WITH PHAGOSOMES [J].
ARMSTRONG, JA ;
HART, PD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1971, 134 (03) :713-+
[3]   ANTIMICROBIAL SUSCEPTIBILITY TESTING OF FRANCISELLA-TULARENSIS WITH A MODIFIED MUELLER-HINTON BROTH [J].
BAKER, CN ;
HOLLIS, DG ;
THORNSBERRY, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1985, 22 (02) :212-215
[4]   THE ABILITY OF SALMONELLA-TYPHIMURIUM TO PRODUCE THE SIDEROPHORE ENTEROBACTIN IS NOT A VIRULENCE FACTOR IN MOUSE TYPHOID [J].
BENJAMIN, WH ;
TURNBOUGH, CL ;
POSEY, BS ;
BRILES, DE .
INFECTION AND IMMUNITY, 1985, 50 (02) :392-397
[5]  
BHATNAGAR NB, 1990, INFECT IMMUNOL, V58, P2875
[6]   THE INFLUENCE OF ENVIRONMENT ON ENVELOPE PROPERTIES AFFECTING SURVIVAL OF BACTERIA IN INFECTIONS [J].
BROWN, MRW ;
WILLIAMS, P .
ANNUAL REVIEW OF MICROBIOLOGY, 1985, 39 :527-556
[7]   CHLOROQUINE INHIBITS THE INTRACELLULAR MULTIPLICATION OF LEGIONELLA-PNEUMOPHILA BY LIMITING THE AVAILABILITY OF IRON - A POTENTIAL NEW MECHANISM FOR THE THERAPEUTIC EFFECT OF CHLOROQUINE AGAINST INTRACELLULAR PATHOGENS [J].
BYRD, TF ;
HORWITZ, MA .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (01) :351-357
[8]   THE ANEMIA OF INFECTION .2. THE EXPERIMENTAL PRODUCTION OF HYPOFERREMIA AND ANEMIA IN DOGS [J].
CARTWRIGHT, GE ;
LAURITSEN, MA ;
HUMPHREYS, S ;
JONES, PJ ;
MERRILL, IM ;
WINTROBE, MM .
JOURNAL OF CLINICAL INVESTIGATION, 1946, 25 (01) :81-86
[9]   MULTIPLICATION OF A HUMAN PARASITE (LEISHMANIA-DONOVANI) IN PHAGOLYSOSOMES OF HAMSTER MACROPHAGES INVITRO [J].
CHANG, KP ;
DWYER, DM .
SCIENCE, 1976, 193 (4254) :678-680
[10]   A STUDY OF THE SENSITIVITY OF LEISHMANIA-DONOVANI PROMASTIGOTES AND AMASTIGOTES TO HYDROGEN-PEROXIDE .2. POSSIBLE MECHANISMS INVOLVED IN PROTECTIVE H2O2 SCAVENGING [J].
CHANNON, JY ;
BLACKWELL, JM .
PARASITOLOGY, 1985, 91 (OCT) :207-217