Microculture in biphasic medium with silicone-coated slides for isolation of mycobacteria.

H Shibayama, F J Galván, C Contreras
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Abstract

The study reported here, seeking to develop a simple, practical, sensitive, and inexpensive technique for microbial diagnosis of tuberculosis, used a combination of biphasic media and microculture techniques to augment the sensitivity of traditional culture methods. A total of 540 sputum samples (5 mL each) were obtained from 180 patients with suspected tuberculosis in Mexico City. These samples were treated with Hanks reagent, neutralized with 25% HCl, and centrifuged. In each case the resulting residue was combined with liquid media (Sula medium or a phosphate-buffered control solution) and was inoculated into a bottle containing a solid medium (Löwenstein-Jensen-Holm or Middlebrook). A silicone-coated slide appropriate for culture of hydrophobic mycobacteria was inserted in each bottle, and the cultures (examined weekly) were incubated at 37 degrees C until the first macroscopic bacterial growth was detected or for up to eight weeks if none was detected. When such growth was detected, or at the end of eight weeks, each slide was withdrawn from the bottle, sterilized, stained by Kinyoun's method, and examined microscopically. Following 2-4 weeks of incubation, macroscopic bacterial growth was detected in 71 bottles and was confirmed by microscopic examination of the corresponding slides. No macroscopic bacterial growth was found in any of the remaining 469 bottles, but microscopic growth was observed on 77 of the slides examined after eight weeks. The authors conclude that this method represents a noteworthy improvement over standard culture methods in terms of bacterial isolation and suggest that its case, economy, and practicality make it suitable for application in developing countries.

硅胶包覆载玻片双相培养基微培养分离分枝杆菌。
本文报道的这项研究旨在开发一种简单、实用、敏感、廉价的结核病微生物诊断技术,采用双相培养基和微培养技术相结合的方法来提高传统培养方法的灵敏度。从墨西哥城的180例疑似结核病患者中共采集了540份痰样本(每份5 mL)。这些样品用Hanks试剂处理,用25%的盐酸中和,然后离心。在每种情况下,将所得残留物与液体培养基(Sula培养基或磷酸盐缓冲对照溶液)结合,并接种到含有固体培养基(Löwenstein-Jensen-Holm或Middlebrook)的瓶子中。在每个瓶子中插入适合培养疏水性分枝杆菌的硅胶涂布载玻片,培养物(每周检查一次)在37℃下孵育,直到第一次肉眼可见的细菌生长被检测到,如果没有检测到,则孵育长达8周。当检测到这种生长时,或在八周结束时,将每张载玻片从瓶中取出,消毒,用金扬法染色,并在显微镜下检查。孵育2-4周后,在71瓶中检测到肉眼可见的细菌生长,并通过显微镜检查相应的载玻片证实。在剩下的469个瓶子中没有发现肉眼可见的细菌生长,但在8周后检查的载玻片中,有77个发现了显微镜下的细菌生长。作者得出结论,这种方法在细菌分离方面比标准培养方法有了显著的改进,并建议它的案例、经济和实用性使其适合在发展中国家应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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