The aim of this study was to evaluate the in situ detection of living
mycobacterium TB rRNA by the mycobacterium TB direct assay (MTD) and its
clinical significance in the early diagnosis of extrapulmonary TB. Eighty-six
patients were recruited from the Shanghai Public Health Clinical Center from
June to November in 2010, having been diagnosed with extrapulmonary TB,
including tuberculous peritonitis (n=22), lymphatic TB (n=21), tuberculous
meningitis (n=15), HIV-associated TB (n=13), nephroTB (n=9), spinal TB (n=2),
cutaneous TB (n=13), parotid TB (n=1), chest wall TB (n=1), intestinal TB
(n=1). One hundred and five extrapulmonary specimens, including CSF, puncture
fluid, drainage, pleural fluid, urine, secretion, ascites, lymphatic tissue
and marrow were collected from the patients. The samples were examined using
acid-fast stain, solid culture, liquid culture and MTD in parallel. In MTD,
the target segments of MTB rRNA in either cultures or clinical specimens were
amplified prior to being qualitatively detected with the hybridization
protection assay (HPA). The sensitivities of MTD and acid-fast staining in
liquid and solid cultures were 48.6%, 41.9%, 20.0% and 14.3%, respectively.
MTD sensitivity was higher than that of the others and its specificity was
100%. We concluded that MTD rRNA detection is an effective, rapid,
convenient, sensitive and reliable method for the early diagnosis of
extrapulmonary TB.