Diagnosis of Mycobacterium microti Infections among Humans by Using Novel Genetic Markers

Author:

van Soolingen Dick1,van der Zanden Adri G. M.2,de Haas Petra E. W.1,Noordhoek Gerda T.3,Kiers Albert4,Foudraine Norbert A.5,Portaels Francoise6,Kolk Arend H. J.7,Kremer Kristin1,van Embden Jan D. A.8

Affiliation:

1. Diagnostic Laboratory for Infectious Diseases and Perinatal Screening1 and

2. National Institute of Public Health and the Environment, 3720 BA Bilthoven, Regional Public Health Laboratory Deventer, 7400 GD Deventer,2

3. Regional Public Health Laboratory Friesland, 8900 JA Leeuwarden,3

4. Municipal Health Service Noord Friesland, 8901 BK Leeuwarden,4

5. National AIDS Therapy Evaluation Centre, Academical Medical Centre,5 and

6. Mycobacteriology Unit, Institute of Tropical Medicine Prince Leopold, 2000 Antwerp, Belgium6

7. Department of Biomedical Research, Royal Tropical Institute,7 1105 AZ Amsterdam, The Netherlands, and

8. Research Laboratory for Infectious Diseases,8

Abstract

ABSTRACT As a result of DNA typing of Mycobacterium microti isolates from animals in the United Kingdom and The Netherlands, we diagnosed four human M. microti infections. These are the first M. microti infections among humans to be reported. Three of the patients were immunocompromised and suffered from generalized forms of tuberculosis. The fourth patient was a 34-year-old immunocompetent male with a persistent cough and undefined X-ray abnormalities. Two of the M. microti infections were recognized by their IS 6110 restriction fragment length polymorphism (RFLP) patterns, which showed a high degree of similarity with those of M. microti strains isolated from a pig and a ferret in The Netherlands. The two other human M. microti infections were recognized by using the recently developed DNA fingerprinting method, “spoligotyping,” directly on clinical material. All M. microti isolates from the United Kingdom and The Netherlands were found to contain an exceptionally short genomic direct repeat region, resulting in identical two-spacer sequence reactions in spoligotyping. In contrast, the highly similar IS 6110 RFLP patterns of the vole strains from the United Kingdom differed considerably from the RFLPs of all M. microti strains isolated in The Netherlands, suggesting that geographic isolation led to divergent strains in the United Kingdom and on the continent.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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