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Journal of Clinical Microbiology, December 1999, p. 3901-3905, Vol. 37, No. 12
Department of Mycobacteriology,
Received 6 April 1999/Returned for modification 22 June
1999/Accepted 8 September 1999
In the present study we compared the clinical presentations of
patients with a clinical diagnosis of AIDS and disseminated Mycobacterium genavense infection (n = 12)
with those of patients with AIDS and disseminated M. avium
complex (MAC) infection (n = 24). Abdominal pain was
seen more frequently in the group of patients infected with M. genavense than in patients infected with MAC (P = 0.003). Analysis of microbiological data revealed that stool
specimens from patients infected with M. genavense were
more often smear positive than stool specimens from patients infected
with MAC (P = 0.00002). However, M. genavense could be cultured on solid media from only 15.4% of
the stool specimens, whereas MAC could be cultured from 71.4% of the
specimens. Bone marrow and liver biopsy specimens yielded growth of
M. genavense within a reasonably short time, allowing
species identification by DNA technology. Microbiological data clearly
demonstrated the importance of acidic liquid medium for primary
culture, the avoidance of pretreatment and the use of additives in
culture, and the necessity for prolonged incubation if M. genavense is suspected. Susceptibility testing showed that
M. genavense is sensitive to rifamycins, fluoroquinolones, and macrolides, whereas it is resistant to isoniazid. Susceptibility to
ethambutol and clofazimine could not be evaluated. The mean survival
times of patients in the two groups were similar.
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Disseminated Infection with Mycobacterium
genavense: a Challenge to Physicians and
Mycobacteriologists
and
*
Corresponding author. Mailing address: Department of
Mycobacteriology, Statens Serum Institut, Artillerivej 5, 2300 Copenhagen S, Denmark. Phone: 45 32 68 37 04. Fax: 45 32 68 38 71. E-mail: vot{at}ssi.dk.
Present address: Department of Clinical Microbiology, Århus
University Hospital, Århus, Denmark.
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