Change in colony morphology influences the virulence as well as the biochemical properties of the Mycobacterium avium complex

被引:49
作者
Kansal, RG [1 ]
Gomez-Flores, R [1 ]
Mehta, RT [1 ]
机构
[1] Univ Texas, Md Anderson Canc Ctr, Dept Bioimmunotherapy, Houston, TX 77030 USA
关键词
Mycobacterium avium complex; colony morphology; virulence; growth rate; biochemical properties; MTT reduction;
D O I
10.1006/mpat.1998.0227
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Factors that influence colony morphology are of crucial importance for drug development as well as for understanding the virulence of Mycobacterium avium complex (MAC) strains. The MAC 101 strain used in the present study grows as smooth transparent (SmT) colonies that tend to become opaque and pigmented when incubated for long periods of time. However, when MAC was passaged in animals, two types of colonies were recovered. The new rough transparent (RgT) colony morphology appeared more flat and transparent, having a central spot, irregular edges at times, and a dry, granular appearance like that of the rough mutants. In animal studies, the RgT bacilli multiplied at a much faster rate than that of the SmT bacilli, causing 60-80% mortality compared with the 10% mortality observed in mice infected with SmT. in vitro studies indicated that the SmT MAC did not grow and multiply as well in reside;nt peritoneal macrophages as the RgT MAC did. The two morphotypes did not differ in their growth rates in vitro but the RgT MAC failed to reduce dimethylthiazol-diphenyltetrazolium bromide (MTT), alamar blue and neutral red, suggesting that there might be significant changes in the cell wall or elsewhere causing changes in cellular permeability. These two morphotypes could serve as models for studying the biochemical markers or the identification of factors responsible for the virulence of the MAC. (C) 1998 Academic Press.
引用
收藏
页码:203 / 214
页数:12
相关论文
共 27 条
[1]  
ANZ W, 1972, ZENTRALBL BAKT P INF, V221, P334
[2]  
BENSON CA, 1994, CLIN INFECT DIS S3, V18, P237
[3]   COMPARISON OF 15 LABORATORY AND PATIENT-DERIVED STRAINS OF MYCOBACTERIUM-AVIUM FOR ABILITY TO INFECT AND MULTIPLY IN CULTURED HUMAN MACROPHAGES [J].
CROWLE, AJ ;
TSANG, AY ;
VATTER, AE ;
MAY, MH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1986, 24 (05) :812-821
[4]   BEIGE MOUSE MODEL FOR MYCOBACTERIUM-AVIUM COMPLEX DISEASE [J].
GANGADHARAM, PRJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (08) :1647-1654
[5]   VIRULENCE OF MYCOBACTERIUM-AVIUM COMPLEX STRAINS FROM ACQUIRED IMMUNE-DEFICIENCY SYNDROME PATIENTS - RELATIONSHIP WITH CHARACTERISTICS OF THE PARASITE AND HOST [J].
GANGADHARAM, PRJ ;
PERUMAL, VK ;
JAIRAM, BT ;
PODAPATI, NR ;
TAYLOR, RB ;
LABRECQUE, JF .
MICROBIAL PATHOGENESIS, 1989, 7 (04) :263-278
[6]   Enhancement of antibacterial activity of clofazimine against Mycobacterium avium Mycobacterium intracellulare complex infection induced by IFN-gamma is mediated by TNF-alpha [J].
GomezFlores, R ;
Tucker, SD ;
Kansal, R ;
TamezGuerra, R ;
Mehta, RT .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 39 (02) :189-197
[7]   DETERMINATION OF MICS FOR MYCOBACTERIUM-AVIUM MYCOBACTERIUM-INTRACELLULARE COMPLEX IN LIQUID-MEDIUM BY A COLORIMETRIC METHOD [J].
GOMEZFLORES, R ;
GUPTA, S ;
TAMEZGUERRA, R ;
MEHTA, RT .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (07) :1842-1846
[8]   THE EPIDEMIOLOGY OF DISSEMINATED NONTUBERCULOUS MYCOBACTERIAL INFECTION IN THE ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS) [J].
HORSBURGH, CR ;
SELIK, RM .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 139 (01) :4-7
[9]   THE MYCOBACTERIUM-AVIUM COMPLEX [J].
INDERLIED, CB ;
KEMPER, CA ;
BERMUDEZ, LEM .
CLINICAL MICROBIOLOGY REVIEWS, 1993, 6 (03) :266-310
[10]   Therapeutic efficacy of liposomal clofazimine against Mycobacterium avium complex in mice depends on size of initial inoculum and duration of infection [J].
Kansal, RG ;
GomezFlores, R ;
Sinha, I ;
Mehta, RT .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (01) :17-23