REISOLATION OF MICROCOCCUS MUCILAGINOSUS MIGULA 1900
Identifieur interne : 001A23 ( Istex/Corpus ); précédent : 001A22; suivant : 001A24REISOLATION OF MICROCOCCUS MUCILAGINOSUS MIGULA 1900
Auteurs : Tom Bergan ; Kjell B Vre ; Berit HovigSource :
- Acta Pathologica Microbiologica Scandinavica Section B Microbiology and Immunology [ 0365-5563 ] ; 1970-03.
Abstract
In cultures from the pharynx, one frequently observed Gram‐positive, catalase positive cocci with characteristic transparent to grayish white colonies with a coherent consistency. These often adhered firmly to the agar surface. Eighteen such strains, including one from bronchial secretion and three from blood cultures, were subjected to detailed biochemical, serological and pathogenicity studies. They were also examined for lysostaphin sensitivity and the DNA base composition was determined. All the strains appeared as members of the same species. On the basis of a careful review of the literature, we found that this species had been named Staphylococcus salivarius Andrewes & Gordon 1907 and was reisolated by Gordon (19). However, the per cent (G + C) of these strains, their lysostaphin resistance and lack of anaerobic glycolysis are compatible only with the genus Micrococcus. The strains are not identical to Gaffkya tetragena, Diplococcus crassus, Micrococcus hyicus, or M. freudenreichii. On the other hand, they possess all the properties of M. mucilaginosus Migula 1900 which is therefore the earliest available epithet for this species and must be adopted. Micrococci have been reported to be typically novobiocin resistant. Neither the strains of M. mucilaginosus, nor those of M. freudenreichii examined by us adhered to this concept. M. mucilaginosus is important for its frequency of occurrence in cultures from the human pharynx, mostly without clear relation to disease. The possibility of potential pathogenicity in man cannot be decided.
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DOI: 10.1111/j.1699-0463.1970.tb04272.x
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These often adhered firmly to the agar surface. Eighteen such strains, including one from bronchial secretion and three from blood cultures, were subjected to detailed biochemical, serological and pathogenicity studies. They were also examined for lysostaphin sensitivity and the DNA base composition was determined. All the strains appeared as members of the same species. On the basis of a careful review of the literature, we found that this species had been named Staphylococcus salivarius Andrewes & Gordon 1907 and was reisolated by Gordon (19). However, the per cent (G + C) of these strains, their lysostaphin resistance and lack of anaerobic glycolysis are compatible only with the genus Micrococcus. The strains are not identical to Gaffkya tetragena, Diplococcus crassus, Micrococcus hyicus, or M. freudenreichii. On the other hand, they possess all the properties of M. mucilaginosus Migula 1900 which is therefore the earliest available epithet for this species and must be adopted. Micrococci have been reported to be typically novobiocin resistant. Neither the strains of M. mucilaginosus, nor those of M. freudenreichii examined by us adhered to this concept. M. mucilaginosus is important for its frequency of occurrence in cultures from the human pharynx, mostly without clear relation to disease. The possibility of potential pathogenicity in man cannot be decided.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Tom Bergan</name><affiliations><json:string>Kaptein W. Wilhelmsen og Frues Bakteriologiske Institutt, Rikshospitalet, University of Oslo, Oslo, Norway. (Head: Professor, dr. med. S. D. Henriksen)</json:string></affiliations></json:item><json:item><name>Kjell Bøvre</name><affiliations><json:string>Kaptein W. Wilhelmsen og Frues Bakteriologiske Institutt, Rikshospitalet, University of Oslo, Oslo, Norway. (Head: Professor, dr. med. S. D. Henriksen)</json:string></affiliations></json:item><json:item><name>Berit Hovig</name><affiliations><json:string>Kaptein W. Wilhelmsen og Frues Bakteriologiske Institutt, Rikshospitalet, University of Oslo, Oslo, Norway. (Head: Professor, dr. med. S. D. Henriksen)</json:string></affiliations></json:item></author><articleId><json:string>APM85</json:string></articleId><language><json:string>eng</json:string></language><abstract>In cultures from the pharynx, one frequently observed Gram‐positive, catalase positive cocci with characteristic transparent to grayish white colonies with a coherent consistency. These often adhered firmly to the agar surface. Eighteen such strains, including one from bronchial secretion and three from blood cultures, were subjected to detailed biochemical, serological and pathogenicity studies. They were also examined for lysostaphin sensitivity and the DNA base composition was determined. All the strains appeared as members of the same species. On the basis of a careful review of the literature, we found that this species had been named Staphylococcus salivarius Andrewes & Gordon 1907 and was reisolated by Gordon (19). However, the per cent (G + C) of these strains, their lysostaphin resistance and lack of anaerobic glycolysis are compatible only with the genus Micrococcus. The strains are not identical to Gaffkya tetragena, Diplococcus crassus, Micrococcus hyicus, or M. freudenreichii. On the other hand, they possess all the properties of M. mucilaginosus Migula 1900 which is therefore the earliest available epithet for this species and must be adopted. Micrococci have been reported to be typically novobiocin resistant. Neither the strains of M. mucilaginosus, nor those of M. freudenreichii examined by us adhered to this concept. M. mucilaginosus is important for its frequency of occurrence in cultures from the human pharynx, mostly without clear relation to disease. 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Micrococci have been reported to be typically novobiocin resistant. Neither the strains of M. mucilaginosus, nor those of M. freudenreichii examined by us adhered to this concept. M. mucilaginosus is important for its frequency of occurrence in cultures from the human pharynx, mostly without clear relation to disease. 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Wilhelmsen og Frues Bakteriologiske Institutt, Rikshospitalet, University of Oslo, Oslo, Norway. (Head: Professor, dr. med. S. D. Henriksen)</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><p>In cultures from the pharynx, one frequently observed Gram‐positive, catalase positive cocci with characteristic transparent to grayish white colonies with a coherent consistency. These often adhered firmly to the agar surface. Eighteen such strains, including one from bronchial secretion and three from blood cultures, were subjected to detailed biochemical, serological and pathogenicity studies. They were also examined for lysostaphin sensitivity and the DNA base composition was determined. All the strains appeared as members of the same species. On the basis of a careful review of the literature, we found that this species had been named <i>Staphylococcus salivarius</i> Andrewes & Gordon 1907 and was reisolated by <i>Gordon</i> (19). However, the per cent (G + C) of these strains, their lysostaphin resistance and lack of anaerobic glycolysis are compatible only with the genus <i>Micrococcus.</i> The strains are not identical to <i>Gaffkya tetragena, Diplococcus crassus, Micrococcus hyicus</i>, or <i>M. freudenreichii.</i> On the other hand, they possess all the properties of <i>M. mucilaginosus</i> Migula 1900 which is therefore the earliest available epithet for this species and must be adopted. Micrococci have been reported to be typically novobiocin resistant. Neither the strains of <i>M. mucilaginosus</i>, nor those of <i>M. freudenreichii</i> examined by us adhered to this concept. <i>M. mucilaginosus</i> is important for its frequency of occurrence in cultures from the human pharynx, mostly without clear relation to disease. The possibility of potential pathogenicity in man cannot be decided.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>REISOLATION OF MICROCOCCUS MUCILAGINOSUS MIGULA 1900</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>REISOLATION OF</title></titleInfo><name type="personal"><namePart type="given">Tom</namePart><namePart type="family">Bergan</namePart><affiliation>Kaptein W. Wilhelmsen og Frues Bakteriologiske Institutt, Rikshospitalet, University of Oslo, Oslo, Norway. (Head: Professor, dr. med. S. D. Henriksen)</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Kjell</namePart><namePart type="family">Bøvre</namePart><affiliation>Kaptein W. Wilhelmsen og Frues Bakteriologiske Institutt, Rikshospitalet, University of Oslo, Oslo, Norway. (Head: Professor, dr. med. S. D. Henriksen)</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Berit</namePart><namePart type="family">Hovig</namePart><affiliation>Kaptein W. Wilhelmsen og Frues Bakteriologiske Institutt, Rikshospitalet, University of Oslo, Oslo, Norway. (Head: Professor, dr. med. S. D. Henriksen)</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">1970-03</dateIssued><edition>Received 10.vii.69</edition><copyrightDate encoding="w3cdtf">1970</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="references">42</extent></physicalDescription><abstract lang="en">In cultures from the pharynx, one frequently observed Gram‐positive, catalase positive cocci with characteristic transparent to grayish white colonies with a coherent consistency. These often adhered firmly to the agar surface. Eighteen such strains, including one from bronchial secretion and three from blood cultures, were subjected to detailed biochemical, serological and pathogenicity studies. They were also examined for lysostaphin sensitivity and the DNA base composition was determined. All the strains appeared as members of the same species. On the basis of a careful review of the literature, we found that this species had been named Staphylococcus salivarius Andrewes & Gordon 1907 and was reisolated by Gordon (19). However, the per cent (G + C) of these strains, their lysostaphin resistance and lack of anaerobic glycolysis are compatible only with the genus Micrococcus. The strains are not identical to Gaffkya tetragena, Diplococcus crassus, Micrococcus hyicus, or M. freudenreichii. On the other hand, they possess all the properties of M. mucilaginosus Migula 1900 which is therefore the earliest available epithet for this species and must be adopted. Micrococci have been reported to be typically novobiocin resistant. Neither the strains of M. mucilaginosus, nor those of M. freudenreichii examined by us adhered to this concept. M. mucilaginosus is important for its frequency of occurrence in cultures from the human pharynx, mostly without clear relation to disease. The possibility of potential pathogenicity in man cannot be decided.</abstract><relatedItem type="host"><titleInfo><title>Acta Pathologica Microbiologica Scandinavica Section B Microbiology and Immunology</title></titleInfo><genre type="Journal">journal</genre><identifier type="ISSN">0365-5563</identifier><identifier type="eISSN">1600-0463</identifier><identifier type="DOI">10.1111/(ISSN)1600-0463g</identifier><identifier type="PublisherID">APM</identifier><part><date>1970</date><detail type="volume"><caption>vol.</caption><number>78B</number></detail><detail type="issue"><caption>no.</caption><number>1</number></detail><extent unit="pages"><start>85</start><end>97</end><total>13</total></extent></part></relatedItem><identifier type="istex">C50C882DE2B9DEEA3F07B0688443F72D08E30F78</identifier><identifier type="DOI">10.1111/j.1699-0463.1970.tb04272.x</identifier><identifier type="ArticleID">APM85</identifier><accessCondition type="use and reproduction" contentType="copyright">© 1970 Acta Pathologica, Microbiologica et Immunologica Scandinavica</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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