Acid-Fast Positive and Acid-Fast Negative Mycobacterium tuberculosis: The Koch Paradox

被引:61
作者
Vilcheze, Catherine [1 ]
Kremer, Laurent [2 ]
机构
[1] Albert Einstein Coll Med, Howard Hughes Med Inst, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[2] Univ Montpellier, CNRS, IDRIM, IRIM ExCPBS UMR 9004, F-34293 Montpellier, France
来源
MICROBIOLOGY SPECTRUM | 2017年 / 5卷 / 02期
关键词
ZIEHL-NEELSEN STAIN; IN-VITRO; PULMONARY TUBERCULOSIS; FLUORESCENCE MICROSCOPY; SER/THR PHOSPHORYLATION; LABORATORY DIAGNOSIS; FOAMY MACROPHAGES; OUTER-MEMBRANE; TRIACYLGLYCEROL; SPUTUM;
D O I
10.1128/microbiolspec.TBTB2-0003-2015
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Acid-fast (AF) staining, also known as Ziehl-Neelsen stain microscopic detection, developed over a century ago, is even today the most widely used diagnostic method for tuberculosis. Herein we present a short historical review of the evolution of AF staining methods and discuss Koch's paradox, in which non-AF tubercle bacilli can be detected in tuberculosis patients or in experimentally infected animals. The conversion of Mycobacterium tuberculosis from an actively growing, AF-positive form to a nonreplicating, AF-negative form during the course of infection is now well documented. The mechanisms of loss of acid-fastness are not fully understood but involve important metabolic processes, such as the accumulation of triacylglycerol-containing intracellular inclusions and changes in the composition and spatial architecture of the cell wall. Although the precise component(s) responsible for the AF staining method remains largely unknown, analysis of a series of genetically defined M. tuberculosis mutants, which are attenuated in mice, pointed to the primary role of mycolic acids and other cell wall-associated (glyco) lipids as molecular markers responsible for the AF property of mycobacteria. Further studies are now required to better describe the cell wall reorganization that occurs during dormancy and to develop new staining procedures that are not affected by such cell wall alterations and that are capable of detecting AF-negative cells.
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页数:14
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共 99 条
  • [1] QUALITY-CONTROL IN TUBERCULOSIS BACTERIOLOGY .1. LABORATORY STUDIES ON ISOLATED POSITIVE CULTURES AND THE EFFICIENCY OF DIRECT SMEAR EXAMINATION
    ABER, VR
    ALLEN, BW
    MITCHISON, DA
    AYUMA, P
    EDWARDS, EA
    KEYES, AB
    [J]. TUBERCLE, 1980, 61 (03): : 123 - 133
  • [2] ALAUSA KO, 1977, AFR J MED MED SCI, V6, P103
  • [3] ALLEN JL, 1992, MED LAB SCI, V49, P99
  • [4] Use of specific rRNA oligonucleotide probes for microscopic detection of Mycobacterium tuberculosis in culture and tissue specimens
    Amand, ALS
    Frank, DN
    De Groote, MA
    Basaraba, RJ
    Orme, IM
    Pace, NR
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (10) : 5369 - 5371
  • [5] Angra P, 2007, INT J TUBERC LUNG D, V11, P1160
  • [6] The virulence-associated twocomponent PhoP-PhoR system controls the biosynthesis of polyketide-derived lipids in Mycobacterium tuberculosis
    Asensio, JG
    Maia, C
    Ferrer, NL
    Barilone, N
    Laval, F
    Soto, CY
    Winter, N
    Daffé, M
    Gicquel, B
    Martín, C
    Jackson, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (03) : 1313 - 1316
  • [7] Ba F, 1999, INT J TUBERC LUNG D, V3, P1101
  • [8] Mycobacterium tuberculosis Lacking All Mycolic Acid Cyclopropanation Is Viable but Highly Attenuated and Hyperinflammatory in Mice
    Barkan, Daniel
    Hedhli, Dorsaf
    Yan, Han-Guang
    Huygen, Kris
    Glickman, Michael S.
    [J]. INFECTION AND IMMUNITY, 2012, 80 (06) : 1958 - 1968
  • [9] Mycolic Acid Cyclopropanation is Essential for Viability, Drug Resistance, and Cell Wall Integrity of Mycobacterium tuberculosis
    Barkan, Daniel
    Liu, Zhen
    Sacchettini, James C.
    Glickman, Michael S.
    [J]. CHEMISTRY & BIOLOGY, 2009, 16 (05): : 499 - 509
  • [10] Performance of light-emitting diode fluorescence microscope for diagnosis of tuberculosis
    Bhalla, Manpreet
    Sidiq, Zeeshan
    Sharma, P. P.
    Singhal, Ritu
    Myneedu, V. P.
    Sarin, Rohit
    [J]. INTERNATIONAL JOURNAL OF MYCOBACTERIOLOGY, 2013, 2 (03) : 174 - 178