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...
Gespeichert in:
Veröffentlicht in: | Letters in applied microbiology 2014-12, Vol.59 (6), p.648-657 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 657 |
---|---|
container_issue | 6 |
container_start_page | 648 |
container_title | Letters in applied microbiology |
container_volume | 59 |
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1641425575</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3494361691</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4077-80be038d9939ca99214e2eb156949121923d753e7003ac14b78fdecc6e5045323</originalsourceid><addsrcrecordid>eNp1ks-KFDEQxoMo7jh68AU0sAh6mNkknXR3jsviPxjxoAvemup09Zgl3WmTtDo3fQOf0Scxa88qCOaSgvzq-4r6QshDzrY8nzMHw5aLQlS3yIrLSmyqUn24TVZMlOWmFkqekHsxXjHGai70XXIilGC8LPiKfA8w2Y7C2NHPNs7gqPN--vntx4CdhYQdtdGnjxiG_ATD5GxvDSTrRwoxwoEmTztMaBLdoe2jHy3QrwdnaZzbOG2XOkHYY7LjngJNAcY4-QgR6R5HvE_u9OAiPjjea3L54vn7i1eb3duXry_OdxsjWVVtatYiK-pO60Ib0FpwiQJbrkotNRdci6KrVIEVYwUYLtuq7js0pkTFpCpEsSZPF90p-E8zxtQMNhp0Dkb0c2x4KbkUSmWRNTn9B73ycxjzdJkSstRClXWmni2UCT7GgH0zBTtAODScNde5NDmX5ncumX10VJzbvNk_5E0QGXhyBCAacH1ekrHxL1drrqW8FjpbuC_W4eH_js3u_M2N9eOlowffwD5k1ct32VUxxuv8OVjxC2ChrmM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1624692568</pqid></control><display><type>article</type><title>rapid and visual loop‐mediated isothermal amplification assay to detect Leifsonia xyli subsp. xyli targeting a transposase gene</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><source>Alma/SFX Local Collection</source><source>EZB Electronic Journals Library</source><source>Oxford Journals</source><creator>Ghai, M ; Singh, V ; Martin, L.A ; McFarlane, S.A ; Antwerpen, T ; Rutherford, R.S</creator><creatorcontrib>Ghai, M ; Singh, V ; Martin, L.A ; McFarlane, S.A ; Antwerpen, T ; Rutherford, R.S</creatorcontrib><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.</description><identifier>ISSN: 0266-8254</identifier><identifier>EISSN: 1472-765X</identifier><identifier>DOI: 10.1111/lam.12327</identifier><identifier>PMID: 25201631</identifier><identifier>CODEN: LAMIE7</identifier><language>eng</language><publisher>Oxford: Published for the Society for Applied Bacteriology by Blackwell Scientific Publications [c1985-]</publisher><subject>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</subject><ispartof>Letters in applied microbiology, 2014-12, Vol.59 (6), p.648-657</ispartof><rights>2014 The Society for Applied Microbiology</rights><rights>2015 INIST-CNRS</rights><rights>2014 The Society for Applied Microbiology.</rights><rights>Copyright © 2014 The Society for Applied Microbiology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4077-80be038d9939ca99214e2eb156949121923d753e7003ac14b78fdecc6e5045323</citedby><cites>FETCH-LOGICAL-c4077-80be038d9939ca99214e2eb156949121923d753e7003ac14b78fdecc6e5045323</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Flam.12327$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Flam.12327$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28919447$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25201631$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>rapid and visual loop‐mediated isothermal amplification assay to detect Leifsonia xyli subsp. xyli targeting a transposase gene</title><title>Letters in applied microbiology</title><addtitle>Lett Appl Microbiol</addtitle><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.</description><subject>Actinomycetales - enzymology</subject><subject>Actinomycetales - genetics</subject><subject>Actinomycetales - isolation & purification</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>color</subject><subject>diagnosis</subject><subject>DNA</subject><subject>DNA Primers</subject><subject>enzyme-linked immunosorbent assay</subject><subject>farms</subject><subject>fluorescence microscopy</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gel electrophoresis</subject><subject>genes</subject><subject>Genes, Bacterial</subject><subject>hydroxynaphthol blue</subject><subject>ISLxx5</subject><subject>laboratory equipment</subject><subject>Leifsonia xyli subsp</subject><subject>Leifsonia xyli subsp. xyli</subject><subject>loop-mediated isothermal amplification</subject><subject>Microbiology</subject><subject>Nucleic Acid Amplification Techniques - methods</subject><subject>nucleotide sequences</subject><subject>Plant Diseases - microbiology</subject><subject>ratoon stunt</subject><subject>Saccharum - microbiology</subject><subject>sap</subject><subject>Sensitivity and Specificity</subject><subject>sugarcane</subject><subject>Transposases - genetics</subject><subject>xylem</subject><subject>Xylem - microbiology</subject><subject>Xyli</subject><issn>0266-8254</issn><issn>1472-765X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1ks-KFDEQxoMo7jh68AU0sAh6mNkknXR3jsviPxjxoAvemup09Zgl3WmTtDo3fQOf0Scxa88qCOaSgvzq-4r6QshDzrY8nzMHw5aLQlS3yIrLSmyqUn24TVZMlOWmFkqekHsxXjHGai70XXIilGC8LPiKfA8w2Y7C2NHPNs7gqPN--vntx4CdhYQdtdGnjxiG_ATD5GxvDSTrRwoxwoEmTztMaBLdoe2jHy3QrwdnaZzbOG2XOkHYY7LjngJNAcY4-QgR6R5HvE_u9OAiPjjea3L54vn7i1eb3duXry_OdxsjWVVtatYiK-pO60Ib0FpwiQJbrkotNRdci6KrVIEVYwUYLtuq7js0pkTFpCpEsSZPF90p-E8zxtQMNhp0Dkb0c2x4KbkUSmWRNTn9B73ycxjzdJkSstRClXWmni2UCT7GgH0zBTtAODScNde5NDmX5ncumX10VJzbvNk_5E0QGXhyBCAacH1ekrHxL1drrqW8FjpbuC_W4eH_js3u_M2N9eOlowffwD5k1ct32VUxxuv8OVjxC2ChrmM</recordid><startdate>201412</startdate><enddate>201412</enddate><creator>Ghai, M</creator><creator>Singh, V</creator><creator>Martin, L.A</creator><creator>McFarlane, S.A</creator><creator>Antwerpen, T</creator><creator>Rutherford, R.S</creator><general>Published for the Society for Applied Bacteriology by Blackwell Scientific Publications [c1985-]</general><general>Blackwell</general><general>Oxford University Press</general><scope>FBQ</scope><scope>IQODW</scope><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>7QL</scope><scope>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>201412</creationdate><title>rapid and visual loop‐mediated isothermal amplification assay to detect Leifsonia xyli subsp. xyli targeting a transposase gene</title><author>Ghai, M ; Singh, V ; Martin, L.A ; McFarlane, S.A ; Antwerpen, T ; Rutherford, R.S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4077-80be038d9939ca99214e2eb156949121923d753e7003ac14b78fdecc6e5045323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Actinomycetales - enzymology</topic><topic>Actinomycetales - genetics</topic><topic>Actinomycetales - isolation & purification</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>color</topic><topic>diagnosis</topic><topic>DNA</topic><topic>DNA Primers</topic><topic>enzyme-linked immunosorbent assay</topic><topic>farms</topic><topic>fluorescence microscopy</topic><topic>Fundamental and applied biological sciences. 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> |
fulltext | fulltext |
identifier | ISSN: 0266-8254 |
ispartof | Letters in applied microbiology, 2014-12, Vol.59 (6), p.648-657 |
issn | 0266-8254 1472-765X |
language | eng |
recordid | cdi_proquest_miscellaneous_1641425575 |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T09%3A44%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=rapid%20and%20visual%20loop%E2%80%90mediated%20isothermal%20amplification%20assay%20to%20detect%20Leifsonia%20xyli%20subsp.%20xyli%20targeting%20a%20transposase%20gene&rft.jtitle=Letters%20in%20applied%20microbiology&rft.au=Ghai,%20M&rft.date=2014-12&rft.volume=59&rft.issue=6&rft.spage=648&rft.epage=657&rft.pages=648-657&rft.issn=0266-8254&rft.eissn=1472-765X&rft.coden=LAMIE7&rft_id=info:doi/10.1111/lam.12327&rft_dat=%3Cproquest_cross%3E3494361691%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1624692568&rft_id=info:pmid/25201631&rfr_iscdi=true |