Extensive gross-contamination of specimens with Mycobacterium tuberculosisin a reference laboratory

Citation
Md. Ramos et al., Extensive gross-contamination of specimens with Mycobacterium tuberculosisin a reference laboratory, J CLIN MICR, 37(4), 1999, pp. 916-919
Citations number
15
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF CLINICAL MICROBIOLOGY
ISSN journal
00951137 → ACNP
Volume
37
Issue
4
Year of publication
1999
Pages
916 - 919
Database
ISI
SICI code
0095-1137(199904)37:4<916:EGOSWM>2.0.ZU;2-9
Abstract
A striking increase in the numbers of cultures positive for Mycobacterium t uberculosis was noticed in a mycobacterial reference laboratory in Campinas , Sao Paulo State, Brazil, in May 1995. A contaminated bronchoscope was the suspected cause of the increase. All 91 M. tuberculosis isolates grown fro m samples from patients between 8 May and 18 July 1995 were characterized b y spoligotyping and IS6110 fingerprinting. Sixty-one of the 91 isolates had identical spoligotype patterns, and the pattern was arbitrarily designated S36. The 61 specimens containing these isolates had been processed and cul tured in a 21-day period ending on 1 June 1995, but only 1 sample was smear positive for acid-fast bacilli. The patient from whom this sample was obta ined was considered to be the index case patient and had a 4+ smear-positiv e lymph node aspirate that had been sent to the laboratory on 10 May. Virtu ally all organisms with spoligotype S36 had the same IS6110 fingerprint pat tern. Extensive review of the patients' charts and investigation of laborat ory procedures revealed that cross-contamination of specimens had occurred. Because the same strain was grown from all types of specimens, the broncho scope was ruled out as the outbreak source. The most likely source of conta mination was a multiple-use reagent used for specimen processing. The organ ism was cultured from two of the solutions 3 weeks after mock contamination . This investigation strongly supports the idea that M. tuberculosis grown from smear-negative specimens should be analyzed by rapid and reliable stra in differentiation techniques, such as spoligotyping, to help rule out labo ratory contamination.