Department of Bacteriology, National Institute for Research in Tuberculosis (Indian Council of Medical Research), Chennai, India.
BMC Infect Dis. 2013 Jan 28;13:44. doi: 10.1186/1471-2334-13-44.
Phage lysin, extracted from three bacteriophages was used in place of antibiotics to control the overgrowth of normal flora in processed sputum samples leading to the sensitive detection of Mycobacterium tuberculosis using diagnostic luciferase reporter phage assay (DLRPA).
A total of 129 sputum samples were processed by modified Petroff's method. Two Lowenstein Jensen slopes were inoculated from the processed sputum deposit thus obtained. The remaining deposits were transferred to 7 ml of Middlebrook 7H9 complete medium supplemented with phage lysin and incubated at 37°C. DLRPA was done using phAE129 at days 7, 9, 14 and 21. At the end of day 21, the samples were centrifuged and the pellets were inoculated on to 2 more LJ slopes to validate DLRPA results.
The sensitivity and specificity of DLRPA in detecting M. tuberculosis from sputum specimens was 90% and 81% respectively compared to conventional LJ culture. The agreement between the methods was 87%. The rate of contamination for DLRPA using phage lysin was 9.3%.
Phage lysin can be used to decontaminate sputum samples for the detection of M. tuberculosis by DLRPA directly from processed sputum specimens.
从三种噬菌体中提取的噬菌体裂解酶被用于替代抗生素,以控制处理后的痰样本中正常菌群的过度生长,从而利用诊断性荧光素酶报告噬菌体检测法(DLRPA)灵敏地检测结核分枝杆菌。
共处理了 129 份痰样本,采用改良的Petroff 法进行处理。从获得的处理痰沉积物中接种两个 Lowenstein Jensen 斜面。将剩余的沉积物转移到 7ml 的 Middlebrook 7H9 完全培养基中,补充噬菌体裂解酶,并在 37°C 下孵育。在第 7、9、14 和 21 天使用 phAE129 进行 DLRPA。在第 21 天结束时,将样品离心,将沉淀物接种到另外 2 个 LJ 斜面上,以验证 DLRPA 结果。
与传统的 LJ 培养相比,DLRPA 检测痰标本中结核分枝杆菌的灵敏度和特异性分别为 90%和 81%。两种方法的一致性为 87%。使用噬菌体裂解酶的 DLRPA 的污染率为 9.3%。
噬菌体裂解酶可用于处理痰样本,通过直接从处理后的痰标本中进行 DLRPA 检测结核分枝杆菌。