2008
DOI: 10.1016/s0255-0857(21)01813-2
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The Utility of Is6110 Sequence Based Polymerase Chain Reaction in Comparison to Conventional Methods in the Diagnosis of Extra-Pulmonary Tuberculosis

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Cited by 7 publications
(3 citation statements)
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“…In our study, the real-time PCR positivity rate (38.7%) was lower than that reported in previous studies, which indicated a positivity rate that varies from 60 to 70%, but only in acid-fast bacilli (AFB) positive samples [10,12]. The low PCR-positivity of our results could be attributed to the small size of the sample [14]; absence or fewer copies of sequence IS6110 in some strains of Mycobacterium tuberculosis [10]; or DNA structural changes of paraffinembedded tissues due to prolonged formalin fixation [12]. These findings raise the possibility that some local mycobacteria might not harbor the sequence IS6110.…”
Section: Discussioncontrasting
confidence: 88%
See 1 more Smart Citation
“…In our study, the real-time PCR positivity rate (38.7%) was lower than that reported in previous studies, which indicated a positivity rate that varies from 60 to 70%, but only in acid-fast bacilli (AFB) positive samples [10,12]. The low PCR-positivity of our results could be attributed to the small size of the sample [14]; absence or fewer copies of sequence IS6110 in some strains of Mycobacterium tuberculosis [10]; or DNA structural changes of paraffinembedded tissues due to prolonged formalin fixation [12]. These findings raise the possibility that some local mycobacteria might not harbor the sequence IS6110.…”
Section: Discussioncontrasting
confidence: 88%
“…Real-time PCR could be used in tuberculosis diagnosis, and has a higher sensitivity and specificity than culture or stains [10]. IS6110 is a DNA target sequence present only in mycobacteria, that is commonly used for Mycobacterium tuberculosiscomplex detection by real-time PCR [11].…”
Section: Introductionmentioning
confidence: 99%
“…A fragment of the IS6110 insertion sequence of M. tuberculosis was amplified using polymerase chain reaction (PCR) for the cases that could not be diagnosed by ZN stain. DNA was obtained from the FF-PE tissues using the phenol-chloroform technique [18,19]. The genomic DNA concentration was calculated at 100 ng/μL for each reaction.…”
Section: Determination Of M Tuberculosis By Ziehl-neelsen Staining An...mentioning
confidence: 99%