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Original ArticleOpen Access
Detection of Mycobacterium tuberculosis from Sputum CoUected on Filter Paper and Stored at Room Tempt!rature for 5 Days by PCR Assay and Culture
Tansuphasiri U 
The efficacy of PCR assay and culture for direct detection of
M. tuberculosis
(MTB) from
sputum specimens collected on filter paper and stored at room temperature for 5 days was eva-
luated in comparison with conventional culture of fresh sputum specimen. A total of 231 sputum
specimens were examined. MTB was recovered from 124 samples by culture from fresh sputum
samples before storage. The culture positivity rate was significantly decreased to 70 per cent after
5 day's storage on filter paper. For PCR assay, a fragment of 377-bp of the
IS61 10
sequence was
amplified and detected using nested PCR. Compared with culture results performed on fresh sputum
samples, the sensitivity, specificity, and efficiency for the nested PCR were 96.0, 97.2 and 96.5 per
cent, respectively. The nested PCR showed sensitivity and specificity with no significant difference
(p>0.05) from culture of fresh sputum specimens.
Conclusion
: The collection and storage of sputum on filter paper at room temperature
for 5 days had no apparent effect on the performance of nested PCR. Sputum samples collected by
this method could be sent by post in a minimum of space and inexpensive way and will enable a
large number of samples collected in the field or from peripheral health centers to be sent to central
laboratories for analysis by trained technicians and under a well-equipped and well-established
quality control system. The rapid and reliable detection by PCR-based assay will be helpful for
optimal patient management of therapy and effective control of tuberculosis.
Key word
:
Mycobacterium tuberculosis,
Sputum Storage, Filter Paper, PCR, Culture
M. tuberculosis
(MTB) from
sputum specimens collected on filter paper and stored at room temperature for 5 days was eva-
luated in comparison with conventional culture of fresh sputum specimen. A total of 231 sputum
specimens were examined. MTB was recovered from 124 samples by culture from fresh sputum
samples before storage. The culture positivity rate was significantly decreased to 70 per cent after
5 day's storage on filter paper. For PCR assay, a fragment of 377-bp of the
IS61 10
sequence was
amplified and detected using nested PCR. Compared with culture results performed on fresh sputum
samples, the sensitivity, specificity, and efficiency for the nested PCR were 96.0, 97.2 and 96.5 per
cent, respectively. The nested PCR showed sensitivity and specificity with no significant difference
(p>0.05) from culture of fresh sputum specimens.
Conclusion
: The collection and storage of sputum on filter paper at room temperature
for 5 days had no apparent effect on the performance of nested PCR. Sputum samples collected by
this method could be sent by post in a minimum of space and inexpensive way and will enable a
large number of samples collected in the field or from peripheral health centers to be sent to central
laboratories for analysis by trained technicians and under a well-equipped and well-established
quality control system. The rapid and reliable detection by PCR-based assay will be helpful for
optimal patient management of therapy and effective control of tuberculosis.
Key word
:
Mycobacterium tuberculosis,
Sputum Storage, Filter Paper, PCR, Culture
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