rapid and visual loop‐mediated isothermal amplification assay to detect Leifsonia xyli subsp. xyli targeting a transposase gene

Leifsonia xyli subsp. xyli (Lxx), causal organism of ratoon stunt (RSD), does not produce any reliable internal or external symptoms on sugarcane. Its detection on a large scale is solely based on microscopic and serological methods. These methods require well‐equipped laboratories, are time consumi...

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Veröffentlicht in:Letters in applied microbiology 2014-12, Vol.59 (6), p.648-657
Hauptverfasser: Ghai, M, Singh, V, Martin, L.A, McFarlane, S.A, Antwerpen, T, Rutherford, R.S
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container_issue 6
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creator Ghai, M
Singh, V
Martin, L.A
McFarlane, S.A
Antwerpen, T
Rutherford, R.S
description Leifsonia xyli subsp. xyli (Lxx), causal organism of ratoon stunt (RSD), does not produce any reliable internal or external symptoms on sugarcane. Its detection on a large scale is solely based on microscopic and serological methods. These methods require well‐equipped laboratories, are time consuming and are not feasible for near‐field detection of Lxx. In this study, we developed a loop‐mediated isothermal amplification (LAMP) assay for rapid and sensitive detection of Lxx without the use of sophisticated equipment. To the best of our knowledge, this is the first report on the detection of Lxx in 30 min via an isothermal amplification method at 65°C. A transposase gene, ISLxx5, was used to design a set of six primers specifically targeting eight genomic sequences. The xylem sap was used as template, thus circumventing the need to isolate pure genomic DNA. The positive reactions were visually detected through a colour change of hydroxynaphthol blue (HNB) from violet to light blue, thus, eliminating the need for gel electrophoresis. The LAMP method was 10 times more sensitive than serological detection and as sensitive as immunofluorescence microscopy (IFM). The simplicity and sensitivity of the ISLxx5 LAMP assay makes it suitable for near‐field diagnosis of RSD. SIGNIFICANCE AND IMPACT OF THE STUDY: Detection of Leifsonia xyli subsp. xyli (Lxx) on a large scale is based on serological assays such as evaporative‐binding enzyme‐linked immunoassay (EB‐EIA). These methods are time consuming and require well‐equipped laboratories. This study presents the development of a loop‐mediated isothermal amplification (LAMP) assay which allows detection of Lxx in 30 min at 65°C, using xylem sap as the template. The assay requires minimal laboratory equipment and could be used at near farm conditions, thus saving time and money required to transfer samples from remote areas to diagnostic laboratories. The LAMP method shows potential as an alternative detection method for RSD.
doi_str_mv 10.1111/lam.12327
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Its detection on a large scale is solely based on microscopic and serological methods. These methods require well‐equipped laboratories, are time consuming and are not feasible for near‐field detection of Lxx. In this study, we developed a loop‐mediated isothermal amplification (LAMP) assay for rapid and sensitive detection of Lxx without the use of sophisticated equipment. To the best of our knowledge, this is the first report on the detection of Lxx in 30 min via an isothermal amplification method at 65°C. A transposase gene, ISLxx5, was used to design a set of six primers specifically targeting eight genomic sequences. The xylem sap was used as template, thus circumventing the need to isolate pure genomic DNA. The positive reactions were visually detected through a colour change of hydroxynaphthol blue (HNB) from violet to light blue, thus, eliminating the need for gel electrophoresis. The LAMP method was 10 times more sensitive than serological detection and as sensitive as immunofluorescence microscopy (IFM). The simplicity and sensitivity of the ISLxx5 LAMP assay makes it suitable for near‐field diagnosis of RSD. SIGNIFICANCE AND IMPACT OF THE STUDY: Detection of Leifsonia xyli subsp. xyli (Lxx) on a large scale is based on serological assays such as evaporative‐binding enzyme‐linked immunoassay (EB‐EIA). These methods are time consuming and require well‐equipped laboratories. This study presents the development of a loop‐mediated isothermal amplification (LAMP) assay which allows detection of Lxx in 30 min at 65°C, using xylem sap as the template. The assay requires minimal laboratory equipment and could be used at near farm conditions, thus saving time and money required to transfer samples from remote areas to diagnostic laboratories. 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Psychology</topic><topic>gel electrophoresis</topic><topic>genes</topic><topic>Genes, Bacterial</topic><topic>hydroxynaphthol blue</topic><topic>ISLxx5</topic><topic>laboratory equipment</topic><topic>Leifsonia xyli subsp</topic><topic>Leifsonia xyli subsp. xyli</topic><topic>loop-mediated isothermal amplification</topic><topic>Microbiology</topic><topic>Nucleic Acid Amplification Techniques - methods</topic><topic>nucleotide sequences</topic><topic>Plant Diseases - microbiology</topic><topic>ratoon stunt</topic><topic>Saccharum - microbiology</topic><topic>sap</topic><topic>Sensitivity and Specificity</topic><topic>sugarcane</topic><topic>Transposases - genetics</topic><topic>xylem</topic><topic>Xylem - microbiology</topic><topic>Xyli</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ghai, M</creatorcontrib><creatorcontrib>Singh, V</creatorcontrib><creatorcontrib>Martin, L.A</creatorcontrib><creatorcontrib>McFarlane, S.A</creatorcontrib><creatorcontrib>Antwerpen, T</creatorcontrib><creatorcontrib>Rutherford, R.S</creatorcontrib><collection>AGRIS</collection><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>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Letters in applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ghai, M</au><au>Singh, V</au><au>Martin, L.A</au><au>McFarlane, S.A</au><au>Antwerpen, T</au><au>Rutherford, R.S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>rapid and visual loop‐mediated isothermal amplification assay to detect Leifsonia xyli subsp. xyli targeting a transposase gene</atitle><jtitle>Letters in applied microbiology</jtitle><addtitle>Lett Appl Microbiol</addtitle><date>2014-12</date><risdate>2014</risdate><volume>59</volume><issue>6</issue><spage>648</spage><epage>657</epage><pages>648-657</pages><issn>0266-8254</issn><eissn>1472-765X</eissn><coden>LAMIE7</coden><abstract>Leifsonia xyli subsp. xyli (Lxx), causal organism of ratoon stunt (RSD), does not produce any reliable internal or external symptoms on sugarcane. Its detection on a large scale is solely based on microscopic and serological methods. These methods require well‐equipped laboratories, are time consuming and are not feasible for near‐field detection of Lxx. In this study, we developed a loop‐mediated isothermal amplification (LAMP) assay for rapid and sensitive detection of Lxx without the use of sophisticated equipment. To the best of our knowledge, this is the first report on the detection of Lxx in 30 min via an isothermal amplification method at 65°C. A transposase gene, ISLxx5, was used to design a set of six primers specifically targeting eight genomic sequences. The xylem sap was used as template, thus circumventing the need to isolate pure genomic DNA. The positive reactions were visually detected through a colour change of hydroxynaphthol blue (HNB) from violet to light blue, thus, eliminating the need for gel electrophoresis. The LAMP method was 10 times more sensitive than serological detection and as sensitive as immunofluorescence microscopy (IFM). The simplicity and sensitivity of the ISLxx5 LAMP assay makes it suitable for near‐field diagnosis of RSD. SIGNIFICANCE AND IMPACT OF THE STUDY: Detection of Leifsonia xyli subsp. xyli (Lxx) on a large scale is based on serological assays such as evaporative‐binding enzyme‐linked immunoassay (EB‐EIA). These methods are time consuming and require well‐equipped laboratories. This study presents the development of a loop‐mediated isothermal amplification (LAMP) assay which allows detection of Lxx in 30 min at 65°C, using xylem sap as the template. The assay requires minimal laboratory equipment and could be used at near farm conditions, thus saving time and money required to transfer samples from remote areas to diagnostic laboratories. The LAMP method shows potential as an alternative detection method for RSD.</abstract><cop>Oxford</cop><pub>Published for the Society for Applied Bacteriology by Blackwell Scientific Publications [c1985-]</pub><pmid>25201631</pmid><doi>10.1111/lam.12327</doi><tpages>10</tpages></addata></record>
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source MEDLINE; Wiley Online Library All Journals; Alma/SFX Local Collection; EZB Electronic Journals Library; Oxford Journals
subjects Actinomycetales - enzymology
Actinomycetales - genetics
Actinomycetales - isolation & purification
Base Sequence
Biological and medical sciences
color
diagnosis
DNA
DNA Primers
enzyme-linked immunosorbent assay
farms
fluorescence microscopy
Fundamental and applied biological sciences. Psychology
gel electrophoresis
genes
Genes, Bacterial
hydroxynaphthol blue
ISLxx5
laboratory equipment
Leifsonia xyli subsp
Leifsonia xyli subsp. xyli
loop-mediated isothermal amplification
Microbiology
Nucleic Acid Amplification Techniques - methods
nucleotide sequences
Plant Diseases - microbiology
ratoon stunt
Saccharum - microbiology
sap
Sensitivity and Specificity
sugarcane
Transposases - genetics
xylem
Xylem - microbiology
Xyli
title rapid and visual loop‐mediated isothermal amplification assay to detect Leifsonia xyli subsp. xyli targeting a transposase gene
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