Visual endpoint detection of Escherichia coli O157:H7 using isothermal Genome Exponential Amplification Reaction (GEAR) assay and malachite green
Rapid and specific detection methods for bacterial agents in drinking water are important for disease prevention and responding to suspected contamination events. In this study, an isothermal Genome Exponential Amplification Reaction (GEAR) assay for Escherichia coli O157:H7 was designed specificall...
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Veröffentlicht in: | Journal of microbiological methods 2014-03, Vol.98, p.122-127 |
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description | Rapid and specific detection methods for bacterial agents in drinking water are important for disease prevention and responding to suspected contamination events. In this study, an isothermal Genome Exponential Amplification Reaction (GEAR) assay for Escherichia coli O157:H7 was designed specifically to recognize a 199-bp fragment of the lipopolysaccharide gene (rfbE) for rapid testing of water samples. The GEAR assay was found to be specific for E. coli O157:H7 using 10 isolates of E. coli O157:H7 and a panel of 86 bacterial controls. The GEAR assay was performed at a constant temperature of 65°C using SYTO 9 intercalating dye. Detection limits were determined to be 20CFU for the GEAR assay. When SYTO 9 fluorescence was measured using a real-time PCR instrument, the assay had the same detection limit as when malachite green was added to the reaction mix and a characteristic blue color was visually observed in positive reactions. The study also found that 50 and 20CFU of E. coli O157:H7 seeded into 100-liter of tap water could be detected by the GEAR assays after the sample was concentrated by hollow-fiber ultrafiltration (HFUF) and approximately 10% of HFUF concentrate was cultured using trypticase soy broth–novobiocin. When applied to 19 surface water samples collected from Tennessee and Kentucky, the GEAR assay and a published real-time PCR assay both detected E. coli O157:H7 in two of the samples. The results of this study indicate that the GEAR assay can be sensitive for rapid detection of E. coli O157:H7 in water samples using fluorometric instruments and visual endpoint determination.
•Genome Exponential Amplification Reaction (GEAR) method requires six primers.•Malachite green in the isothermal amplification reaction enables visual inspection.•Malachite green enables identification of positive reactions without opening tubes.•The GEAR assay for detection of E. coli O157:H7 was determined to be 100% specific.•GEAR is amenable to field use in resource-limited settings. |
doi_str_mv | 10.1016/j.mimet.2014.01.002 |
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•Genome Exponential Amplification Reaction (GEAR) method requires six primers.•Malachite green in the isothermal amplification reaction enables visual inspection.•Malachite green enables identification of positive reactions without opening tubes.•The GEAR assay for detection of E. coli O157:H7 was determined to be 100% specific.•GEAR is amenable to field use in resource-limited settings.</description><identifier>ISSN: 0167-7012</identifier><identifier>EISSN: 1872-8359</identifier><identifier>DOI: 10.1016/j.mimet.2014.01.002</identifier><identifier>PMID: 24424127</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>DNA, Bacterial - genetics ; E. coli O157:H7 ; Escherichia coli ; Escherichia coli O157 - genetics ; Escherichia coli O157 - isolation & purification ; Isothermal amplification ; Malachite green ; Molecular assay ; Real-Time Polymerase Chain Reaction - methods ; Rosaniline Dyes - chemistry ; Water Microbiology</subject><ispartof>Journal of microbiological methods, 2014-03, Vol.98, p.122-127</ispartof><rights>2014</rights><rights>Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-ac8cbfe7ea1be10796941ac539c1bf2b49db6e325c97f64e6db82d1a35a3d8643</citedby><cites>FETCH-LOGICAL-c392t-ac8cbfe7ea1be10796941ac539c1bf2b49db6e325c97f64e6db82d1a35a3d8643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mimet.2014.01.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24424127$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jothikumar, Prithiviraj</creatorcontrib><creatorcontrib>Narayanan, Jothikumar</creatorcontrib><creatorcontrib>Hill, Vincent R.</creatorcontrib><title>Visual endpoint detection of Escherichia coli O157:H7 using isothermal Genome Exponential Amplification Reaction (GEAR) assay and malachite green</title><title>Journal of microbiological methods</title><addtitle>J Microbiol Methods</addtitle><description>Rapid and specific detection methods for bacterial agents in drinking water are important for disease prevention and responding to suspected contamination events. In this study, an isothermal Genome Exponential Amplification Reaction (GEAR) assay for Escherichia coli O157:H7 was designed specifically to recognize a 199-bp fragment of the lipopolysaccharide gene (rfbE) for rapid testing of water samples. The GEAR assay was found to be specific for E. coli O157:H7 using 10 isolates of E. coli O157:H7 and a panel of 86 bacterial controls. The GEAR assay was performed at a constant temperature of 65°C using SYTO 9 intercalating dye. Detection limits were determined to be 20CFU for the GEAR assay. When SYTO 9 fluorescence was measured using a real-time PCR instrument, the assay had the same detection limit as when malachite green was added to the reaction mix and a characteristic blue color was visually observed in positive reactions. The study also found that 50 and 20CFU of E. coli O157:H7 seeded into 100-liter of tap water could be detected by the GEAR assays after the sample was concentrated by hollow-fiber ultrafiltration (HFUF) and approximately 10% of HFUF concentrate was cultured using trypticase soy broth–novobiocin. When applied to 19 surface water samples collected from Tennessee and Kentucky, the GEAR assay and a published real-time PCR assay both detected E. coli O157:H7 in two of the samples. The results of this study indicate that the GEAR assay can be sensitive for rapid detection of E. coli O157:H7 in water samples using fluorometric instruments and visual endpoint determination.
•Genome Exponential Amplification Reaction (GEAR) method requires six primers.•Malachite green in the isothermal amplification reaction enables visual inspection.•Malachite green enables identification of positive reactions without opening tubes.•The GEAR assay for detection of E. coli O157:H7 was determined to be 100% specific.•GEAR is amenable to field use in resource-limited settings.</description><subject>DNA, Bacterial - genetics</subject><subject>E. coli O157:H7</subject><subject>Escherichia coli</subject><subject>Escherichia coli O157 - genetics</subject><subject>Escherichia coli O157 - isolation & purification</subject><subject>Isothermal amplification</subject><subject>Malachite green</subject><subject>Molecular assay</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>Rosaniline Dyes - chemistry</subject><subject>Water Microbiology</subject><issn>0167-7012</issn><issn>1872-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhi0EokvhCZCQj-WQ4LGdOEHisKqWLVKlShVwtRx70nqV2CFOKvoYvDFut3CEk6Xx9_8jzUfIW2AlMKg_HMrRj7iUnIEsGZSM8WdkA43iRSOq9jnZZEoVigE_Ia9SOjAGlZDNS3LCpeQSuNqQX999Ws1AMbgp-rBQhwvaxcdAY093yd7i7O2tN9TGwdMrqNTHC0XX5MMN9Sku-X_M-T2GOCLd_ZxiwLD4PNqO0-B7b81j2zWaY-3Zfre9fk9NSuaemuBojpu8YUF6MyOG1-RFb4aEb57eU_Lt8-7r-UVxebX_cr69LKxo-VIY29iuR4UGOgSm2rqVYGwlWgtdzzvZuq5GwSvbqr6WWLuu4Q6MqIxwTS3FKTk79k5z_LFiWvTok8VhMAHjmnS-XS0yx-v_oxWTUAGv24yKI2rnmNKMvZ5mP5r5XgPTD9r0QT9q0w_aNAOdteXUu6cFazei-5v54ykDn44A5ovceZx1sh6DRefnrEu76P-54Dd_KKsC</recordid><startdate>201403</startdate><enddate>201403</enddate><creator>Jothikumar, Prithiviraj</creator><creator>Narayanan, Jothikumar</creator><creator>Hill, Vincent R.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>201403</creationdate><title>Visual endpoint detection of Escherichia coli O157:H7 using isothermal Genome Exponential Amplification Reaction (GEAR) assay and malachite green</title><author>Jothikumar, Prithiviraj ; Narayanan, Jothikumar ; Hill, Vincent R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-ac8cbfe7ea1be10796941ac539c1bf2b49db6e325c97f64e6db82d1a35a3d8643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>DNA, Bacterial - genetics</topic><topic>E. coli O157:H7</topic><topic>Escherichia coli</topic><topic>Escherichia coli O157 - genetics</topic><topic>Escherichia coli O157 - isolation & purification</topic><topic>Isothermal amplification</topic><topic>Malachite green</topic><topic>Molecular assay</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>Rosaniline Dyes - chemistry</topic><topic>Water Microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jothikumar, Prithiviraj</creatorcontrib><creatorcontrib>Narayanan, Jothikumar</creatorcontrib><creatorcontrib>Hill, Vincent R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</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><jtitle>Journal of microbiological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jothikumar, Prithiviraj</au><au>Narayanan, Jothikumar</au><au>Hill, Vincent R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Visual endpoint detection of Escherichia coli O157:H7 using isothermal Genome Exponential Amplification Reaction (GEAR) assay and malachite green</atitle><jtitle>Journal of microbiological methods</jtitle><addtitle>J Microbiol Methods</addtitle><date>2014-03</date><risdate>2014</risdate><volume>98</volume><spage>122</spage><epage>127</epage><pages>122-127</pages><issn>0167-7012</issn><eissn>1872-8359</eissn><abstract>Rapid and specific detection methods for bacterial agents in drinking water are important for disease prevention and responding to suspected contamination events. In this study, an isothermal Genome Exponential Amplification Reaction (GEAR) assay for Escherichia coli O157:H7 was designed specifically to recognize a 199-bp fragment of the lipopolysaccharide gene (rfbE) for rapid testing of water samples. The GEAR assay was found to be specific for E. coli O157:H7 using 10 isolates of E. coli O157:H7 and a panel of 86 bacterial controls. The GEAR assay was performed at a constant temperature of 65°C using SYTO 9 intercalating dye. Detection limits were determined to be 20CFU for the GEAR assay. When SYTO 9 fluorescence was measured using a real-time PCR instrument, the assay had the same detection limit as when malachite green was added to the reaction mix and a characteristic blue color was visually observed in positive reactions. The study also found that 50 and 20CFU of E. coli O157:H7 seeded into 100-liter of tap water could be detected by the GEAR assays after the sample was concentrated by hollow-fiber ultrafiltration (HFUF) and approximately 10% of HFUF concentrate was cultured using trypticase soy broth–novobiocin. When applied to 19 surface water samples collected from Tennessee and Kentucky, the GEAR assay and a published real-time PCR assay both detected E. coli O157:H7 in two of the samples. The results of this study indicate that the GEAR assay can be sensitive for rapid detection of E. coli O157:H7 in water samples using fluorometric instruments and visual endpoint determination.
•Genome Exponential Amplification Reaction (GEAR) method requires six primers.•Malachite green in the isothermal amplification reaction enables visual inspection.•Malachite green enables identification of positive reactions without opening tubes.•The GEAR assay for detection of E. coli O157:H7 was determined to be 100% specific.•GEAR is amenable to field use in resource-limited settings.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>24424127</pmid><doi>10.1016/j.mimet.2014.01.002</doi><tpages>6</tpages></addata></record> |
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subjects | DNA, Bacterial - genetics E. coli O157:H7 Escherichia coli Escherichia coli O157 - genetics Escherichia coli O157 - isolation & purification Isothermal amplification Malachite green Molecular assay Real-Time Polymerase Chain Reaction - methods Rosaniline Dyes - chemistry Water Microbiology |
title | Visual endpoint detection of Escherichia coli O157:H7 using isothermal Genome Exponential Amplification Reaction (GEAR) assay and malachite green |
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