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Cost-effectiveness of blood agar for isolation of mycobacteria.

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TLDR
Blood agar should be regarded as a first-line medium for culturing Mycobacterium species, it saves time, is cost-effective, is more sensitive than, and at least as rapid as the automated method, and for resource-limited countries in which the prevalence of tuberculosis is high.
Abstract
BackgroundMycobacterium species are grown using specific media that increase laboratory cost, thus hampering their diffusion in resource-limited countries. Preliminary data suggested that versatile blood agar may be also used for mycobacterial culture.MethodologyWe examined the growth of 41 different Mycobacterium species on 5% blood agar. Over a 24-month period we analysed isolation of mycobacteria after parallel inoculation of clinical specimens into both a reference automated system (BACTEC 9000 MB broth) and 5% blood agar slant tubes, after NaOH decontamination, and compared the cost of performing 1,000 analyses using these two techniques.ConclusionsMycobacterium reference species cultured on blood agar, with the exception of Mycobacterium ulcerans. Inoculation of 1,634 specimens yielded 95 Mycobacterium isolates. Blood agar performed significantly more efficiently than BACTEC 9000 MB broth (94 vs 88 isolates, P = 0.03). Decontamination of Candida albicans in 5 specimens by addition of amphotericin B in blood agar yielded one more M. tuberculosis isolate that could not be isolated in BACTEC broth. Uneven distribution of time to culture positivity for M. tuberculosis had a median (range) of 19±5 days using blood agar and 26±6 days using BACTEC 9000 MB broth. Cost for 1,000 analyses in France was estimated to be of 1,913 euros using the blood agar method and 8,990 euros using the BACTEC 9000 MB method. Blood agar should be regarded as a first-line medium for culturing Mycobacterium species. It saves time, is cost-effective, is more sensitive than, and at least as rapid as the automated method. This is of particular importance for resource-limited countries in which the prevalence of tuberculosis is high.

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Current and Past Strategies for Bacterial Culture in Clinical Microbiology

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Modern clinical microbiology: new challenges and solutions

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Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry identification of mycobacteria in routine clinical practice.

TL;DR: The data indicate that MALDI-TOF MS can be used as a first-line method for the routine identification of heat-inactivated mycobacteria and is an attractive method for implementation in clinical microbiology laboratories in both developed and developing countries.
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Steps towards the discovery of Mycobacterium tuberculosis by Robert Koch, 1882

TL;DR: It is thanks to R. Koch that one of the most lethal diseases in human history could be diagnosed, could be treated and cured after the discovery of streptomycin 65 years later, and could be efficiently prevented by isolation of cases.
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Repertoire of intensive care unit pneumonia microbiota

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References
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rpoB-Based Identification of Nonpigmented and Late-Pigmenting Rapidly Growing Mycobacteria

TL;DR: It is concluded that molecular identification by analysis of the 723-bp rpoB sequence is a rapid and accurate tool for identification of RGM.
Journal ArticleDOI

Buruli ulcer: emerging from obscurity

TL;DR: Considerable progress has been made in understanding the immune response to M ulcerans and there have been major advances in management of the disease with the introduction of rational antibiotic therapy.
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