pubmed-article:9705393 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9705393 | lifeskim:mentions | umls-concept:C0445913 | lld:lifeskim |
pubmed-article:9705393 | lifeskim:mentions | umls-concept:C0033414 | lld:lifeskim |
pubmed-article:9705393 | lifeskim:mentions | umls-concept:C0018270 | lld:lifeskim |
pubmed-article:9705393 | lifeskim:mentions | umls-concept:C0348080 | lld:lifeskim |
pubmed-article:9705393 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:9705393 | pubmed:dateCreated | 1998-9-16 | lld:pubmed |
pubmed-article:9705393 | pubmed:abstractText | Our studies show that microaerophilic conditions promote the growth of Mycobacterium genavense in semisolid medium. The growth of M. genavense at 2.5 or 5% oxygen was superior to that obtained at 21% oxygen in BACTEC primary cultures (Middlebrook 7H12, pH 6.0, without additives). By using nondecontaminated specimens, it was possible to detect growth with very small inocula (25 bacilli/ml) of 12 different M. genavense strains (from nude mice) within 6 weeks of incubation under low oxygen tension; conversely, with 21% oxygen, no growth of 8 of 12 (66.7%) M. genavense strains was detected (growth index, <10). The same beneficial effect of 2.5 or 5% oxygen was observed in primary cultures of a decontaminated clinical specimen. Low oxygen tension (2.5 or 5%) is recommended for the primary isolation of M. genavense. Microaerophilic cultivation of other atypical mycobacteria, especially slow-growing (e.g., Mycobacterium avium) and difficult-to-grow (e.g., Mycobacterium ulcerans) species, is discussed. | lld:pubmed |
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pubmed-article:9705393 | pubmed:language | eng | lld:pubmed |
pubmed-article:9705393 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9705393 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:9705393 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9705393 | pubmed:month | Sep | lld:pubmed |
pubmed-article:9705393 | pubmed:issn | 0095-1137 | lld:pubmed |
pubmed-article:9705393 | pubmed:author | pubmed-author:PortaelsFF | lld:pubmed |
pubmed-article:9705393 | pubmed:author | pubmed-author:HirschelBB | lld:pubmed |
pubmed-article:9705393 | pubmed:author | pubmed-author:PalominoJJ | lld:pubmed |
pubmed-article:9705393 | pubmed:author | pubmed-author:De RidderKK | lld:pubmed |
pubmed-article:9705393 | pubmed:author | pubmed-author:RealiniLL | lld:pubmed |
pubmed-article:9705393 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9705393 | pubmed:volume | 36 | lld:pubmed |
pubmed-article:9705393 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9705393 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9705393 | pubmed:pagination | 2565-70 | lld:pubmed |
pubmed-article:9705393 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:9705393 | pubmed:year | 1998 | lld:pubmed |
pubmed-article:9705393 | pubmed:articleTitle | Microaerophilic conditions promote growth of Mycobacterium genavense. | lld:pubmed |
pubmed-article:9705393 | pubmed:affiliation | Mycobacteriology Unit, Department of Microbiology, Institute of Tropical Medicine, Antwerp, Belgium. realini@microbiol.itg.be | lld:pubmed |
pubmed-article:9705393 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:9705393 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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