Identification of Mycobacterium avium complex (MAC) was made using three DNAprobe tests for MAC: Gen-Probe
(R) Rapid Diagnostic System for the MAC (Gen-Probe Inc., San Diego, U.S.A.), AccuProbe
TM MAC Culture Identification or Confirmation Test (Gen- Probe Inc.); and SNAP
(R) Culture Identification Diagnostic Kit (MAC) (Syngene Inc., San Diego, U.S.A.). Various strains of MAC belonging to serovars 21 to 28 were identified bythe DNA probe tests and showed the following. First, Serovar 21 and 25 belonged to M.avium and M. intracellulare, respectively. Each of them reacted with species-specific probesused in the three DNA probe tests [ie., either M. avium-probe (in SNAP test; Probe A) or M. intracellulare-probe (in SNAP test; Probe I)]. Second, serovars 22-24 and 26-28consisted of M. intracellulare, MAC strains that reacted with Probe X of SNAP test butlacked the reactivity with M. avium and M. intracellulare-probes of all the DNA probetests, M. scrofulaceum that showed no reactivity with M. avium or M. intracellulareprobe or Probe X, and M. scrofulaceum that had only the reactivity with Prnhp
When the disease-associated MAC strains (35 strains), isolated in the Kanto to Kyushuareas in Japan, were identified using AccuProbe test, both the M. avium and M.intracellulare strains identified by the Gen-Probe test reacted with the MAC-probe but notwith the M. tuberculosis complex (MTC)-probe. Three MAC strains (strains N-417, N-420and N-428) failed to react with M. avium-probe and only had borderline reactivity with M. intracellulare-probe in the Gen-Probe test: These strains also failed to react with either the MAC- or MTC-probe in the AccuProbe test. They were, however, reacted withProbe X of SNAP test. Therefore, these peculiar strains could be identified as beeing Probe-X reactive MAC.
When the distribution of M. avium and M. intracellulare among the disease-associated MAC strains (123 strains) newly isolated in the western districts of Japan (Kinki toKyushu) was studied, the ratio of M. avium was larger than that of M. intracellulare inKinki district for those MAC strains identified using the SNAP test. On the other hand, areverse distribution was observed for the MAC strains isolated in the Chugoku, Shikoku and Kyushu districts. This was consistent with our previous findings in the identification ofdisease-associated MAC strains isolated in the various districts of Japan using Gen-Probetesting.
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