VIDRL Mycobacterium Reference Laboratory

Quarterly Surveillance Report - Fourth Quarter 2001


*Due to the slow growing nature of Mycobacteria spp. this report will always be presented with a one period delay to maintain accuracy

Specimen Analysis

Most specimens (both primary & referred) and isolates are from Victorian patients. The majority of non-Victorian patients originate in the Northern Territory & the Solomon Islands

Primary Specimens
M. tb isolates
New Victorian M tb isolates
Non M. tb isolates
Negatives
Total
October
20
6
15
470
505
November
5
4
11
394
410
December
22
6
15
380
417
Referred Specimens
October
37
14
46
83
November
32
22
51
83
December
23
7
35
25
 
Total
139
59
173
1244
1556

 

 

 

Site details of M. tuberculosis isolates and resistant isolates by month

October
November
December
Site
Pulmonary
10
15
7
Extrapulmonary
10
11
6
 
Extrapulmonary Site Details

Lymph node (x5) ,
Urine (x1),
Pleural fluid (x1),
Blood (x1),
Chest wall tissue (x1)

Lymph Node (x3), Urine (x2),
Bronch. wash (x1),
Neck bx. (x2),
Bone (x1),
Foot (x1)
Lymph Node (x4),
Neck mass (x1),
Parietal pleura (x1)
Resistance 3x resistance to
Isoniazid,
1x resistance to
Isoniazid & Streptomycin
3x resistance to
Isoniazid,
1x resistance to
Isoniazid & Streptomycin
 

 

Direct Amplification (MTD)

 
October
November
December
Positive
2
-
1
Negative
50
50
23
Positive - culture negative
1
1
-
Inhibition - culture positive
1
1
1
Total
54
52
24

 

Comments


M. bovis BCG
Isolated from two patients. One isolate was pus from a vaccination site and the other was from an axillary abscess.

M. kansasii
Isolated from sputum of an elderly male and from tissue specimens, (right hand & right index finger) from two other men.

M. ulcerans
M. ulcerans PCR was requested from 15 specimens. There were three positive results, two from the same patient (arm biopsy & eyelid tissue). One patient had the organism isolated from culture and culture results from the other patient are pending. M. ulcerans was also identified from a referred isolate where no PCR was performed

Molecular identifying techniques were used to identify or confirm identification of 31 isolates, including one of M. intracellulare and one of M. interjectum. The last organism was detected in a mixed culture where M. tuberculosis was also isolated. M. interjectum was isolated from this patient on three different occasions, each one a month or more apart.

Mycobacterium generic PCR was performed on 25 specimens, 14 of which were paraffin embedded. M. tuberculosis complex DNA was detected in one paraffin embedded lung tissue where culture was never requested.

M. avium complex DNA was detected in three specimens. Two of these were from the same patient and M. abscessus DNA was also detected. These results were subsequently confirmed by culture.

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