Sensitivity of acid-fast staining for Mycobacterium tuberculosis in formalin-fixed tissue

被引:71
作者
Fukunaga, H
Murakami, T
Gondo, T
Sugi, K
Ishihara, T
机构
[1] Yamaguchi Univ, Sch Med, Dept Pathol 1, Ube, Yamaguchi 755, Japan
[2] Natl Sanyo Hosp, Dept Clin Res, Ube, Yamaguchi, Japan
关键词
formalin; xylene; real-time polymerase chain reaction;
D O I
10.1164/rccm.2111028
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Microscopic examination of tissue sections of mycobacterial lesions frequently results in few or no bacilli seen, even if the lesions appear active histologically. This might be due to the effects of the fixative fluid and/or organic solvent, both of which are conventionally used to make tissue sections for histopathology, on the acid-fast staining of bacteria. The present study was performed to examine how formalin and xylene lower the sensitivity of acid-fast staining for Mycobacterium tuberculosis and to clarify the meaning of the staining result in tissue sections. Microscopic observation of mycobacteria smeared on glass slides revealed that both of these agents greatly reduced the sensitivity of acid-fast staining. Moreover, the number of bacilli was calculated in 30 samples of paraffin-embedded granulomatous lesions using acid-fast microscopy and real-time polymerase chain reaction. The numbers of bacilli present that were estimated by real-time polymerase chain reaction were considerably higher than those counted with a microscope. These results suggest that the bacilli are frequently missed or underestimated with acid-fast microscopy on formalin-fixed, paraffin-embedded tissue.
引用
收藏
页码:994 / 997
页数:4
相关论文
共 34 条
[1]   A rapid real-time quantitative polymerase chain reaction for hepatitis B virus [J].
Brechtbuehl, K ;
Whalley, SA ;
Dusheiko, GM ;
Saunders, NA .
JOURNAL OF VIROLOGICAL METHODS, 2001, 93 (1-2) :105-113
[2]  
Cocito C, 1985, Eur J Epidemiol, V1, P202, DOI 10.1007/BF00234095
[3]  
CSERNI G, 1995, AM J CLIN PATHOL, V103, P114
[4]   Diagnosis of varicella-zoster virus infections in the clinical laboratory by LightClycler PCR [J].
Espy, MJ ;
Teo, R ;
Ross, TK ;
Svien, KA ;
Wold, AD ;
Uhl, JR ;
Smith, TF .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (09) :3187-3189
[5]  
Fite G L, 1965, Int J Lepr, V33, P324
[6]  
HARADA K, 1976, MICROSC ACTA, V78, P21
[7]  
Hardman WJ, 1996, AM J CLIN PATHOL, V106, P384
[8]   Direct detection of Legionella species from bronchoalveolar lavage and open lung biopsy specimens:: Comparison of LightCycler PCR, in situ hybridization, direct fluorescence antigen detection, and culture [J].
Hayden, RT ;
Uhl, JR ;
Qian, X ;
Hopkins, MK ;
Aubry, MC ;
Limper, AH ;
LLoyd, RV ;
Cockerill, FR .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (07) :2618-2626
[9]   Persistence of DNA from Mycobacterium tuberculosis in superficially normal lung tissue during latent infection [J].
Hernández-Pando, R ;
Jeyanathan, M ;
Mengistu, G ;
Aguilar, D ;
Orozco, H ;
Harboe, M ;
Rook, GAW ;
Bjune, G .
LANCET, 2000, 356 (9248) :2133-2138
[10]   Sensitive identification of mycobacterial species using PCR-RFLP on bronchial washings [J].
Hidaka, E ;
Honda, T ;
Ueno, I ;
Yamasaki, Y ;
Kubo, K ;
Katsuyama, T .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 161 (03) :930-934