Abstract

Background: The incidence of mycobacterial infection, in particular M. tuberculosis complex (MTC), is increasing in some Western countries, while nontuberculous mycobacteria (NTM) may be recognized more frequently in clinical specimens worldwide. The clinical scenario and available histopathology alone are often insufficient to separate these two categories of mycobacterial disease, whose behavior and treatment differ. In particular, NTM may be clinically unsuspected in pathological specimens and the opportunity for culturing missed. Methods: We developed two multiplex PCR assays, which distinguish MTC from NTM by detecting the IS6110 insert in the first tube and discriminating up to 14 NTM reference strains in the second by targeting the 16S-23S rRNA internal transcribed spacer. Test material included 594 routine clinical specimens with diverse pathology; many were granulomas unrelated to mycobacterial infection. About 75% were formalin-fixed paraffin blocks, the remainder mainly cytologic imprints or aspirates on FTA cards submitted on suspicion of mycobacterial infection either to avoid frozen sectioning (with the attendant risk of aerosolisation) or at the time of fine needle aspiration. Results: The paraffinized material yielded 53 MTC positives and the cytological 21 positives. A subset consisting of 337 specimens was also analyzed for NTM and yielded 51 positives. The frequency of simultaneous NTM infection in tuberculous patients was about 17%. Mycobacterium avium complex represented the dominant NTM species overall, showed a predilection for lung and lymph node, and together with M. haemophilum were the second most frequent NTM just behind M. ulcerans/M. marinum in skin and soft tissue, the category displaying the largest NTM diversity. Conclusions: Cytological and deparaffinized tissue analyzed in a new two-tube multiplex PCR allows for specific discrimination of causative agents in mycobacterial infection. MTC is readily distinguished from NTM for appropriate therapy, and NTM presumptively diagnosed at the species level allows appropriate choices of antimicrobials.

Highlights

  • Mycobacterial infection in western countries is increasingly common as a result of greater immigration from areas with a high incidence of tuberculosis, modern medicine’s growing reliance on therapies with immunosuppressive effects and the use of aggressive treatments in aging populations

  • We developed two multiplex PCR assays, which distinguish M. tuberculosis complex (MTC) from nontuberculous mycobacterial (NTM) by detecting the IS6110 insert in the first tube and discriminating up to 14 NTM reference strains in the second by targeting the 16S-23S rRNA internal transcribed spacer

  • To expedite the diagnosis of species commonly reported in human infection worldwide, in Europe or associated with immunodeficiency, as stated by the American Thoracic Society and Infectious Disease Societies of America [2], we developed a two-tube multiplex PCR (MPCR) with product detection by four-color capillary gel electrophoresis

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Summary

Introduction

Mycobacterial infection in western countries is increasingly common as a result of greater immigration from areas with a high incidence of tuberculosis, modern medicine’s growing reliance on therapies with immunosuppressive effects and the use of aggressive treatments in aging populations. Mycobacterial infection may be often overlooked and first suggested in a biopsy report at which time the only material available for culture may have been removed, fixed in formalin and embedded in paraffin. Clinical findings, including skin tests with PPD (purified protein derivative), in localized or disseminated infection do not always allow for the critical distinction of nontuberculous mycobacterial (NTM) disease from tuberculosis (MTC, M. tuberculosis complex). The incidence of mycobacterial infection, in particular M. tuberculosis complex (MTC), is increasing in some Western countries, while nontuberculous mycobacteria (NTM) may be recognized more frequently in clinical specimens worldwide. Test material included 594 routine clinical specimens with diverse pathology; many were granulomas unrelated to mycobacterial infection. Conclusions: Cytological and deparaffinized tissue analyzed in a new two-tube multiplex PCR allows for specific discrimination of causative agents in mycobacterial infection

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