Author/Authors :
Khosravi, Azar D School of Medicine - Ahwaz University of Medical Sciences , Stanford, John L UCL Medical School - London - UK
Abstract :
Isolation and differentiation of various species of mycobacteria are predominantly based on
conventional, cultural and biochemical tests. Among the non-tuberculous mycobacteria, these tests
are unable to differentiate M. scrofulaceum from M. avium-intracellulare (MAI) because of their
identical biochemical characteristics. For this reason, one hundred mycobacterial strains suspected to
be M. scrofulaceum, which had identical preliminary cultural and biochemical tests, were investigated
by immunodiffusion technique. The standard sonicated antigens of M. scrofulaceum (22, 159, 1281)
were used to sensitize rabbits and to produce specific antisera. The method was performed in plastic
petri dishes containing agar and sodium azide. Antiserum was placed in the central well of the agar
plate and the homologous ultrasonicates were in the peripheral wells. The results were observed one
week later and the mycobacterial strains were divided according to the number of produced
precipitation lines. Four different groups were identified on the basis of identical reaction with three
antisera (three groups were M. scrofulaceum). Group 1 produced identical precipitation lines with
antisera 22 and 1281, group 2 with antisera 22, 159 and 1281 and group 3 with antiserum 1281. The
present study showed that the technique was able to differentiate M. scrofulaceum from MAI and was
also able to identify the bacterium as distinct species. Moreover, by using different specific antisera, it
is possible to determine different serotypes of M. scrofulaceum.
Keywords :
Double diffusion , lymphadenitis , M. scrofulaceum , M. avium complex