help button home button
AJRCCM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Online Data Supplement
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fukunaga, H.
Right arrow Articles by Ishihara, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fukunaga, H.
Right arrow Articles by Ishihara, T.
American Journal of Respiratory and Critical Care Medicine Vol 166. pp. 994-997, (2002)
© 2002 American Thoracic Society


Original Articles

Sensitivity of Acid-Fast Staining for Mycobacterium tuberculosis in Formalin-fixed Tissue

Hajime Fukunaga, Tomoyuki Murakami, Toshikazu Gondo, Kazuo Sugi and Tokuhiro Ishihara

First Department of Pathology, Yamaguchi University School of Medicine; and Department of Clinical Research, National Sanyo Hospital, Ube, Yamaguchi, Japan

Correspondence and requests for reprints should be addressed to Hajime Fukunaga, 1-1-1 Minamikogushi, Ube, Yamaguchi 755-8505, Japan. E-mail: fukunaga{at}sanyou.hosp.go.jp

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.

Key Words: formalin • xylene • real-time polymerase chain reaction




This article has been cited by other articles:


Home page
J. Clin. Microbiol.Home page
S. Chakravorty, M. K. Sen, and J. S. Tyagi
Diagnosis of Extrapulmonary Tuberculosis by Smear, Culture, and PCR Using Universal Sample Processing Technology
J. Clin. Microbiol., September 1, 2005; 43(9): 4357 - 4362.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
C. L. Fuller, J. L. Flynn, and T. A. Reinhart
In Situ Study of Abundant Expression of Proinflammatory Chemokines and Cytokines in Pulmonary Granulomas That Develop in Cynomolgus Macaques Experimentally Infected with Mycobacterium tuberculosis
Infect. Immun., December 1, 2003; 71(12): 7023 - 7034.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
M. J. Tobin
Tuberculosis, Lung Infections, Interstitial Lung Disease, and Journalology in AJRCCM 2002
Am. J. Respir. Crit. Care Med., February 1, 2003; 167(3): 345 - 355.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Cell Mol. Biol.
Copyright © 2002 American Thoracic Society