Tetrazolium reduction methods for assessment of substrate oxidation and strain differentiation among mycoplasmas, with particular reference to Mycoplasma bovigenitalium and some members of the Mycoplasma mycoides cluster

Aims:  To apply a rapid nitroblue tetrazolium (NBT) reduction assay of substrate metabolism by mycoplasmas that would help to differentiate Mycoplasmas. Methods and Results:  Growth, substrate preferences and tetrazolium reduction were assessed for 18 strains of Mycoplasma bovigenitalium and Mycopla...

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Veröffentlicht in:Journal of applied microbiology 2008-08, Vol.105 (2), p.492-501
Hauptverfasser: Lin, Y.‐C., Agbanyim, C.N.M., Miles, R.J., Nicholas, R.A.J., Kelly, D.P., Wood, A.P.
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container_issue 2
container_start_page 492
container_title Journal of applied microbiology
container_volume 105
creator Lin, Y.‐C.
Agbanyim, C.N.M.
Miles, R.J.
Nicholas, R.A.J.
Kelly, D.P.
Wood, A.P.
description Aims:  To apply a rapid nitroblue tetrazolium (NBT) reduction assay of substrate metabolism by mycoplasmas that would help to differentiate Mycoplasmas. Methods and Results:  Growth, substrate preferences and tetrazolium reduction were assessed for 18 strains of Mycoplasma bovigenitalium and Mycoplasma ovine serogroup 11. NBT reduction was detectable in 1 h with 108 CFU ml−1. Use of α‐ketobutyrate, lactate and pyruvate to support growth and NBT reduction were correlated: pyruvate was preferred and lactate was used by only four of the 18 strains. Selected members of the Mycoplasma mycoides cluster were also assessed and monotetrazoles tested as alternatives to NBT. The NBT method was applied to a further 19 species. Conclusions:  This simple and reproducible method requires only small amounts of cells, enabling routine assessment of substrate use within 1 h, and the rapid assignment of numerous mycoplasmas to one of six physiological groups. The four physiological groups of M. bovigenitalium and Mycoplasma serogroup 11 strains were indistinguishable from each other, which supports the view that these belong to the same species. Significance and Impact of the Study:  Strain‐specific substrate‐utilization patterns by mycoplasmas can be obtained rapidly and reliably. The method has potential as a large‐scale semi‐automated procedure to monitor numerous strains and substrates simultaneously.
doi_str_mv 10.1111/j.1365-2672.2008.03772.x
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Methods and Results:  Growth, substrate preferences and tetrazolium reduction were assessed for 18 strains of Mycoplasma bovigenitalium and Mycoplasma ovine serogroup 11. NBT reduction was detectable in 1 h with 108 CFU ml−1. Use of α‐ketobutyrate, lactate and pyruvate to support growth and NBT reduction were correlated: pyruvate was preferred and lactate was used by only four of the 18 strains. Selected members of the Mycoplasma mycoides cluster were also assessed and monotetrazoles tested as alternatives to NBT. The NBT method was applied to a further 19 species. Conclusions:  This simple and reproducible method requires only small amounts of cells, enabling routine assessment of substrate use within 1 h, and the rapid assignment of numerous mycoplasmas to one of six physiological groups. The four physiological groups of M. bovigenitalium and Mycoplasma serogroup 11 strains were indistinguishable from each other, which supports the view that these belong to the same species. Significance and Impact of the Study:  Strain‐specific substrate‐utilization patterns by mycoplasmas can be obtained rapidly and reliably. The method has potential as a large‐scale semi‐automated procedure to monitor numerous strains and substrates simultaneously.</description><identifier>ISSN: 1364-5072</identifier><identifier>EISSN: 1365-2672</identifier><identifier>DOI: 10.1111/j.1365-2672.2008.03772.x</identifier><identifier>PMID: 18312568</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Bacteriological Techniques ; Base Sequence ; Biological and medical sciences ; Fundamental and applied biological sciences. 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Methods and Results:  Growth, substrate preferences and tetrazolium reduction were assessed for 18 strains of Mycoplasma bovigenitalium and Mycoplasma ovine serogroup 11. NBT reduction was detectable in 1 h with 108 CFU ml−1. Use of α‐ketobutyrate, lactate and pyruvate to support growth and NBT reduction were correlated: pyruvate was preferred and lactate was used by only four of the 18 strains. Selected members of the Mycoplasma mycoides cluster were also assessed and monotetrazoles tested as alternatives to NBT. The NBT method was applied to a further 19 species. Conclusions:  This simple and reproducible method requires only small amounts of cells, enabling routine assessment of substrate use within 1 h, and the rapid assignment of numerous mycoplasmas to one of six physiological groups. The four physiological groups of M. bovigenitalium and Mycoplasma serogroup 11 strains were indistinguishable from each other, which supports the view that these belong to the same species. 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Psychology</topic><topic>Microbiology</topic><topic>Molecular Sequence Data</topic><topic>Mycoplasma</topic><topic>Mycoplasma - genetics</topic><topic>Mycoplasma - isolation &amp; purification</topic><topic>Mycoplasma - metabolism</topic><topic>Mycoplasma bovigenitalium</topic><topic>Mycoplasma bovigenitalium - genetics</topic><topic>Mycoplasma bovigenitalium - isolation &amp; purification</topic><topic>Mycoplasma bovigenitalium - metabolism</topic><topic>Mycoplasma mycoides</topic><topic>Mycoplasma mycoides - genetics</topic><topic>Mycoplasma mycoides - isolation &amp; purification</topic><topic>Mycoplasma mycoides - metabolism</topic><topic>Mycoplasma serogroup 11</topic><topic>Oxidation-Reduction</topic><topic>Ribotyping</topic><topic>Substrate Specificity</topic><topic>tetrazolium reduction</topic><topic>Tetrazolium Salts - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Y.‐C.</creatorcontrib><creatorcontrib>Agbanyim, C.N.M.</creatorcontrib><creatorcontrib>Miles, R.J.</creatorcontrib><creatorcontrib>Nicholas, R.A.J.</creatorcontrib><creatorcontrib>Kelly, D.P.</creatorcontrib><creatorcontrib>Wood, A.P.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Y.‐C.</au><au>Agbanyim, C.N.M.</au><au>Miles, R.J.</au><au>Nicholas, R.A.J.</au><au>Kelly, D.P.</au><au>Wood, A.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tetrazolium reduction methods for assessment of substrate oxidation and strain differentiation among mycoplasmas, with particular reference to Mycoplasma bovigenitalium and some members of the Mycoplasma mycoides cluster</atitle><jtitle>Journal of applied microbiology</jtitle><addtitle>J Appl Microbiol</addtitle><date>2008-08</date><risdate>2008</risdate><volume>105</volume><issue>2</issue><spage>492</spage><epage>501</epage><pages>492-501</pages><issn>1364-5072</issn><eissn>1365-2672</eissn><abstract>Aims:  To apply a rapid nitroblue tetrazolium (NBT) reduction assay of substrate metabolism by mycoplasmas that would help to differentiate Mycoplasmas. Methods and Results:  Growth, substrate preferences and tetrazolium reduction were assessed for 18 strains of Mycoplasma bovigenitalium and Mycoplasma ovine serogroup 11. NBT reduction was detectable in 1 h with 108 CFU ml−1. Use of α‐ketobutyrate, lactate and pyruvate to support growth and NBT reduction were correlated: pyruvate was preferred and lactate was used by only four of the 18 strains. Selected members of the Mycoplasma mycoides cluster were also assessed and monotetrazoles tested as alternatives to NBT. The NBT method was applied to a further 19 species. Conclusions:  This simple and reproducible method requires only small amounts of cells, enabling routine assessment of substrate use within 1 h, and the rapid assignment of numerous mycoplasmas to one of six physiological groups. The four physiological groups of M. bovigenitalium and Mycoplasma serogroup 11 strains were indistinguishable from each other, which supports the view that these belong to the same species. Significance and Impact of the Study:  Strain‐specific substrate‐utilization patterns by mycoplasmas can be obtained rapidly and reliably. The method has potential as a large‐scale semi‐automated procedure to monitor numerous strains and substrates simultaneously.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18312568</pmid><doi>10.1111/j.1365-2672.2008.03772.x</doi><tpages>10</tpages></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Bacteriological Techniques
Base Sequence
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Microbiology
Molecular Sequence Data
Mycoplasma
Mycoplasma - genetics
Mycoplasma - isolation & purification
Mycoplasma - metabolism
Mycoplasma bovigenitalium
Mycoplasma bovigenitalium - genetics
Mycoplasma bovigenitalium - isolation & purification
Mycoplasma bovigenitalium - metabolism
Mycoplasma mycoides
Mycoplasma mycoides - genetics
Mycoplasma mycoides - isolation & purification
Mycoplasma mycoides - metabolism
Mycoplasma serogroup 11
Oxidation-Reduction
Ribotyping
Substrate Specificity
tetrazolium reduction
Tetrazolium Salts - metabolism
title Tetrazolium reduction methods for assessment of substrate oxidation and strain differentiation among mycoplasmas, with particular reference to Mycoplasma bovigenitalium and some members of the Mycoplasma mycoides cluster
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