Literature DB >> 17593671

Rapid differentiation of Mycobacterium tuberculosis and Mycobacterium leprae from sputum by polymerase chain reaction.

Bishwa Raj Sapkota1, Chaman Ranjit, Murdo Macdonald.   

Abstract

Differentiation of M tuberculosis and M leprae by polymerase chain reaction (PCR), when acid-fast bacilli (AFB) were present in sputum from patients at Anandaban hospital, was carried out. Thirty sputum samples microscopy positive for AFB were collected and were subjected to culture. Bacterial DNA was extracted and PCR was performed using primers specific for Mycobacterium tuberculosis and Mycobacterium leprae DNA. Twenty samples were from patients with clinical TB and 10 from patients with clinical leprosy. Fifteen of the TB samples were positive in both TB PCR and culture, among the reminders four were TB PCR negative and one was positive for TB PCR. All TB samples were negative for leprosy PCR. Of the leprosy samples, five were TB PCR and culture positive, and negative for leprosy PCR. The remaining five samples were negative for both TB PCR and culture but positive in leprosy PCR. Five often clinical leprosy samples were positive for tuberculosis. This indicates that AFB in the sputum of leprosy patients might be M. tuberculosis or M. leprae. Thus PCR can be used for rapid differentiation of M. tuberculosis and M. leprae present in sputum where AFB microscopy is inconclusive.

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Year:  2007        PMID: 17593671

Source DB:  PubMed          Journal:  Nepal Med Coll J


  2 in total

1.  Coinfection of leprosy and tuberculosis.

Authors:  Seema Shetty; Shashikiran Umakanth; Bhawani Manandhar; Pankaj Bahadur Nepali
Journal:  BMJ Case Rep       Date:  2018-03-15

2.  Detection of Mycobacterium leprae by PCR testing of sputa from a patient with pulmonary cryptococcus coinfection in northern Australia.

Authors:  Laura J Edwards; Ric N Price; Vicki L Krause; Sarah E Huffam; Maria Globan; Janet Fyfe; Krispin M Hajkowicz
Journal:  J Clin Microbiol       Date:  2014-07-23       Impact factor: 5.948

  2 in total

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