Loading…
Optimized methods for detecting Salmonella Typhi in the environment using validated field sampling, culture and confirmatory molecular approaches
Aims This study evaluated detection methods for Salmonella Typhi (S. Typhi) in the environment, to establish a novel pathway from field sampling to isolation of viable organisms and molecular confirmation from complex environmental samples, thus enabling environmental surveillance of typhoid. Method...
Saved in:
Published in: | Journal of applied microbiology 2022-02, Vol.132 (2), p.1503-1517 |
---|---|
Main Authors: | , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3887-b486030f0e0897d469b5a3d8bcb3e3a98f78a55e89bf8f9a771a5904d5f80e603 |
---|---|
cites | cdi_FETCH-LOGICAL-c3887-b486030f0e0897d469b5a3d8bcb3e3a98f78a55e89bf8f9a771a5904d5f80e603 |
container_end_page | 1517 |
container_issue | 2 |
container_start_page | 1503 |
container_title | Journal of applied microbiology |
container_volume | 132 |
creator | Rigby, Jonathan Elmerhebi, Ezzeddine Diness, Yohane Mkwanda, Charity Tonthola, Katalina Galloway, Heather Miles, Rory Henrion, Marc Y. R. Edwards, Thomas Gauld, Jillian Msefula, Chisomo Johnston, Rob Nair, Satheesh Feasey, Nicholas Elviss, Nicola C. |
description | Aims
This study evaluated detection methods for Salmonella Typhi (S. Typhi) in the environment, to establish a novel pathway from field sampling to isolation of viable organisms and molecular confirmation from complex environmental samples, thus enabling environmental surveillance of typhoid.
Methods and Results
Multiple media were assessed using clinical isolates from the Public Health England's (PHE) Culture collection. The culture pathway selected consisted of a primary 2% bile broth and secondary Selenite F broth, followed by modified Chromogenic Agar for Salmonella Esterase (mCASE). A qPCR assay was adapted from a validated S. Typhi PCR panel for confirmation of isolates, with comparison to biochemical and serological tests showing good specificity. Sampling locations in Blantyre, Malawi were used to compare sampling methods. Viable S. Typhi were isolated from a mixture of trap and grab river water samples on six occasions.
Conclusions
Culture of viable S. Typhi from environmental samples was possible using effective capture and culture techniques.
Significance and impact of study
Whilst several studies have attempted to detect S. Typhi from the environment, this is the first successful attempt to isolate the organism from river water since the 1980s. Supplementing clinical data with environmental screening offers the potential for enhanced surveillance, which might inform interventions and assess vaccination programmes. |
doi_str_mv | 10.1111/jam.15237 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2621162312</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2621162312</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3887-b486030f0e0897d469b5a3d8bcb3e3a98f78a55e89bf8f9a771a5904d5f80e603</originalsourceid><addsrcrecordid>eNp1kMtu1TAQhiMEohdY8ALIEisk0voSx86yqoCCWnXRso6ceMzxkS_BdooOb8Eb1-0p3TGbGWm--Ub6m-YdwSek1ulW-RPCKRMvmkPCet7SXtCXj3PXcizoQXOU8xZjwjDvXzcHrGO0Ez0_bP5eL8V6-wc08lA2UWdkYkIaCszFhp_oRjkfAzin0O1u2VhkAyobQBDubIrBQyhozQ_knXJWq1JNxoLTKCu_uLr4hObVlTUBUkGjOQZjk1clph3y0UFdqoTUsqSo5g3kN80ro1yGt0_9uPnx5fPt-UV7ef312_nZZTszKUU7dbLHDBsMWA5Cd_0wccW0nOaJAVODNEIqzkEOk5FmUEIQxQfcaW4khnp63HzYe-vjXyvkMm7jmkJ9OdKeEtJTRmilPu6pOcWcE5hxSdartBsJHh_CH2v442P4lX3_ZFwnD_qZ_Jd2BU73wG_rYPd_0_j97GqvvAeihpEl</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2621162312</pqid></control><display><type>article</type><title>Optimized methods for detecting Salmonella Typhi in the environment using validated field sampling, culture and confirmatory molecular approaches</title><source>Alma/SFX Local Collection</source><creator>Rigby, Jonathan ; Elmerhebi, Ezzeddine ; Diness, Yohane ; Mkwanda, Charity ; Tonthola, Katalina ; Galloway, Heather ; Miles, Rory ; Henrion, Marc Y. R. ; Edwards, Thomas ; Gauld, Jillian ; Msefula, Chisomo ; Johnston, Rob ; Nair, Satheesh ; Feasey, Nicholas ; Elviss, Nicola C.</creator><creatorcontrib>Rigby, Jonathan ; Elmerhebi, Ezzeddine ; Diness, Yohane ; Mkwanda, Charity ; Tonthola, Katalina ; Galloway, Heather ; Miles, Rory ; Henrion, Marc Y. R. ; Edwards, Thomas ; Gauld, Jillian ; Msefula, Chisomo ; Johnston, Rob ; Nair, Satheesh ; Feasey, Nicholas ; Elviss, Nicola C.</creatorcontrib><description>Aims
This study evaluated detection methods for Salmonella Typhi (S. Typhi) in the environment, to establish a novel pathway from field sampling to isolation of viable organisms and molecular confirmation from complex environmental samples, thus enabling environmental surveillance of typhoid.
Methods and Results
Multiple media were assessed using clinical isolates from the Public Health England's (PHE) Culture collection. The culture pathway selected consisted of a primary 2% bile broth and secondary Selenite F broth, followed by modified Chromogenic Agar for Salmonella Esterase (mCASE). A qPCR assay was adapted from a validated S. Typhi PCR panel for confirmation of isolates, with comparison to biochemical and serological tests showing good specificity. Sampling locations in Blantyre, Malawi were used to compare sampling methods. Viable S. Typhi were isolated from a mixture of trap and grab river water samples on six occasions.
Conclusions
Culture of viable S. Typhi from environmental samples was possible using effective capture and culture techniques.
Significance and impact of study
Whilst several studies have attempted to detect S. Typhi from the environment, this is the first successful attempt to isolate the organism from river water since the 1980s. Supplementing clinical data with environmental screening offers the potential for enhanced surveillance, which might inform interventions and assess vaccination programmes.</description><identifier>ISSN: 1364-5072</identifier><identifier>EISSN: 1365-2672</identifier><identifier>DOI: 10.1111/jam.15237</identifier><identifier>PMID: 34324765</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>bile broth ; biofilm ; biofilms ; Clinical isolates ; Culture techniques ; Esterase ; Health surveillance ; Humans ; Identification ; Malawi ; mCASE ; Moore swabs ; PCR (polymerase chain reaction) ; Public health ; Real-Time Polymerase Chain Reaction ; river water ; Rivers ; Salmonella ; Salmonella Typhi ; Salmonella typhi - genetics ; Sampling ; Sampling methods ; Selenite ; selenite broth ; Serological tests ; Specimen Handling ; Typhoid ; Typhoid Fever - diagnosis ; Vaccination ; water ; Water analysis ; Water sampling</subject><ispartof>Journal of applied microbiology, 2022-02, Vol.132 (2), p.1503-1517</ispartof><rights>2021 The Authors. published by John Wiley & Sons Ltd on behalf of Society for Applied Microbiology</rights><rights>2021 The Authors. Journal of Applied Microbiology published by John Wiley & Sons Ltd on behalf of Society for Applied Microbiology.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3887-b486030f0e0897d469b5a3d8bcb3e3a98f78a55e89bf8f9a771a5904d5f80e603</citedby><cites>FETCH-LOGICAL-c3887-b486030f0e0897d469b5a3d8bcb3e3a98f78a55e89bf8f9a771a5904d5f80e603</cites><orcidid>0000-0003-4041-1405 ; 0000-0002-7297-1485 ; 0000-0001-9693-7700 ; 0000-0003-2304-886X ; 0000-0003-4058-4461 ; 0000-0003-1242-839X ; 0000-0001-5143-0981</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34324765$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rigby, Jonathan</creatorcontrib><creatorcontrib>Elmerhebi, Ezzeddine</creatorcontrib><creatorcontrib>Diness, Yohane</creatorcontrib><creatorcontrib>Mkwanda, Charity</creatorcontrib><creatorcontrib>Tonthola, Katalina</creatorcontrib><creatorcontrib>Galloway, Heather</creatorcontrib><creatorcontrib>Miles, Rory</creatorcontrib><creatorcontrib>Henrion, Marc Y. R.</creatorcontrib><creatorcontrib>Edwards, Thomas</creatorcontrib><creatorcontrib>Gauld, Jillian</creatorcontrib><creatorcontrib>Msefula, Chisomo</creatorcontrib><creatorcontrib>Johnston, Rob</creatorcontrib><creatorcontrib>Nair, Satheesh</creatorcontrib><creatorcontrib>Feasey, Nicholas</creatorcontrib><creatorcontrib>Elviss, Nicola C.</creatorcontrib><title>Optimized methods for detecting Salmonella Typhi in the environment using validated field sampling, culture and confirmatory molecular approaches</title><title>Journal of applied microbiology</title><addtitle>J Appl Microbiol</addtitle><description>Aims
This study evaluated detection methods for Salmonella Typhi (S. Typhi) in the environment, to establish a novel pathway from field sampling to isolation of viable organisms and molecular confirmation from complex environmental samples, thus enabling environmental surveillance of typhoid.
Methods and Results
Multiple media were assessed using clinical isolates from the Public Health England's (PHE) Culture collection. The culture pathway selected consisted of a primary 2% bile broth and secondary Selenite F broth, followed by modified Chromogenic Agar for Salmonella Esterase (mCASE). A qPCR assay was adapted from a validated S. Typhi PCR panel for confirmation of isolates, with comparison to biochemical and serological tests showing good specificity. Sampling locations in Blantyre, Malawi were used to compare sampling methods. Viable S. Typhi were isolated from a mixture of trap and grab river water samples on six occasions.
Conclusions
Culture of viable S. Typhi from environmental samples was possible using effective capture and culture techniques.
Significance and impact of study
Whilst several studies have attempted to detect S. Typhi from the environment, this is the first successful attempt to isolate the organism from river water since the 1980s. Supplementing clinical data with environmental screening offers the potential for enhanced surveillance, which might inform interventions and assess vaccination programmes.</description><subject>bile broth</subject><subject>biofilm</subject><subject>biofilms</subject><subject>Clinical isolates</subject><subject>Culture techniques</subject><subject>Esterase</subject><subject>Health surveillance</subject><subject>Humans</subject><subject>Identification</subject><subject>Malawi</subject><subject>mCASE</subject><subject>Moore swabs</subject><subject>PCR (polymerase chain reaction)</subject><subject>Public health</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>river water</subject><subject>Rivers</subject><subject>Salmonella</subject><subject>Salmonella Typhi</subject><subject>Salmonella typhi - genetics</subject><subject>Sampling</subject><subject>Sampling methods</subject><subject>Selenite</subject><subject>selenite broth</subject><subject>Serological tests</subject><subject>Specimen Handling</subject><subject>Typhoid</subject><subject>Typhoid Fever - diagnosis</subject><subject>Vaccination</subject><subject>water</subject><subject>Water analysis</subject><subject>Water sampling</subject><issn>1364-5072</issn><issn>1365-2672</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp1kMtu1TAQhiMEohdY8ALIEisk0voSx86yqoCCWnXRso6ceMzxkS_BdooOb8Eb1-0p3TGbGWm--Ub6m-YdwSek1ulW-RPCKRMvmkPCet7SXtCXj3PXcizoQXOU8xZjwjDvXzcHrGO0Ez0_bP5eL8V6-wc08lA2UWdkYkIaCszFhp_oRjkfAzin0O1u2VhkAyobQBDubIrBQyhozQ_knXJWq1JNxoLTKCu_uLr4hObVlTUBUkGjOQZjk1clph3y0UFdqoTUsqSo5g3kN80ro1yGt0_9uPnx5fPt-UV7ef312_nZZTszKUU7dbLHDBsMWA5Cd_0wccW0nOaJAVODNEIqzkEOk5FmUEIQxQfcaW4khnp63HzYe-vjXyvkMm7jmkJ9OdKeEtJTRmilPu6pOcWcE5hxSdartBsJHh_CH2v442P4lX3_ZFwnD_qZ_Jd2BU73wG_rYPd_0_j97GqvvAeihpEl</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Rigby, Jonathan</creator><creator>Elmerhebi, Ezzeddine</creator><creator>Diness, Yohane</creator><creator>Mkwanda, Charity</creator><creator>Tonthola, Katalina</creator><creator>Galloway, Heather</creator><creator>Miles, Rory</creator><creator>Henrion, Marc Y. R.</creator><creator>Edwards, Thomas</creator><creator>Gauld, Jillian</creator><creator>Msefula, Chisomo</creator><creator>Johnston, Rob</creator><creator>Nair, Satheesh</creator><creator>Feasey, Nicholas</creator><creator>Elviss, Nicola C.</creator><general>Oxford University Press</general><scope>24P</scope><scope>WIN</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>7T7</scope><scope>7TM</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0003-4041-1405</orcidid><orcidid>https://orcid.org/0000-0002-7297-1485</orcidid><orcidid>https://orcid.org/0000-0001-9693-7700</orcidid><orcidid>https://orcid.org/0000-0003-2304-886X</orcidid><orcidid>https://orcid.org/0000-0003-4058-4461</orcidid><orcidid>https://orcid.org/0000-0003-1242-839X</orcidid><orcidid>https://orcid.org/0000-0001-5143-0981</orcidid></search><sort><creationdate>202202</creationdate><title>Optimized methods for detecting Salmonella Typhi in the environment using validated field sampling, culture and confirmatory molecular approaches</title><author>Rigby, Jonathan ; Elmerhebi, Ezzeddine ; Diness, Yohane ; Mkwanda, Charity ; Tonthola, Katalina ; Galloway, Heather ; Miles, Rory ; Henrion, Marc Y. R. ; Edwards, Thomas ; Gauld, Jillian ; Msefula, Chisomo ; Johnston, Rob ; Nair, Satheesh ; Feasey, Nicholas ; Elviss, Nicola C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3887-b486030f0e0897d469b5a3d8bcb3e3a98f78a55e89bf8f9a771a5904d5f80e603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>bile broth</topic><topic>biofilm</topic><topic>biofilms</topic><topic>Clinical isolates</topic><topic>Culture techniques</topic><topic>Esterase</topic><topic>Health surveillance</topic><topic>Humans</topic><topic>Identification</topic><topic>Malawi</topic><topic>mCASE</topic><topic>Moore swabs</topic><topic>PCR (polymerase chain reaction)</topic><topic>Public health</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>river water</topic><topic>Rivers</topic><topic>Salmonella</topic><topic>Salmonella Typhi</topic><topic>Salmonella typhi - genetics</topic><topic>Sampling</topic><topic>Sampling methods</topic><topic>Selenite</topic><topic>selenite broth</topic><topic>Serological tests</topic><topic>Specimen Handling</topic><topic>Typhoid</topic><topic>Typhoid Fever - diagnosis</topic><topic>Vaccination</topic><topic>water</topic><topic>Water analysis</topic><topic>Water sampling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rigby, Jonathan</creatorcontrib><creatorcontrib>Elmerhebi, Ezzeddine</creatorcontrib><creatorcontrib>Diness, Yohane</creatorcontrib><creatorcontrib>Mkwanda, Charity</creatorcontrib><creatorcontrib>Tonthola, Katalina</creatorcontrib><creatorcontrib>Galloway, Heather</creatorcontrib><creatorcontrib>Miles, Rory</creatorcontrib><creatorcontrib>Henrion, Marc Y. R.</creatorcontrib><creatorcontrib>Edwards, Thomas</creatorcontrib><creatorcontrib>Gauld, Jillian</creatorcontrib><creatorcontrib>Msefula, Chisomo</creatorcontrib><creatorcontrib>Johnston, Rob</creatorcontrib><creatorcontrib>Nair, Satheesh</creatorcontrib><creatorcontrib>Feasey, Nicholas</creatorcontrib><creatorcontrib>Elviss, Nicola C.</creatorcontrib><collection>Open Access: Wiley-Blackwell Open Access Journals</collection><collection>Wiley Online Library Free Content</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>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology 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>Genetics Abstracts</collection><jtitle>Journal of applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rigby, Jonathan</au><au>Elmerhebi, Ezzeddine</au><au>Diness, Yohane</au><au>Mkwanda, Charity</au><au>Tonthola, Katalina</au><au>Galloway, Heather</au><au>Miles, Rory</au><au>Henrion, Marc Y. R.</au><au>Edwards, Thomas</au><au>Gauld, Jillian</au><au>Msefula, Chisomo</au><au>Johnston, Rob</au><au>Nair, Satheesh</au><au>Feasey, Nicholas</au><au>Elviss, Nicola C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimized methods for detecting Salmonella Typhi in the environment using validated field sampling, culture and confirmatory molecular approaches</atitle><jtitle>Journal of applied microbiology</jtitle><addtitle>J Appl Microbiol</addtitle><date>2022-02</date><risdate>2022</risdate><volume>132</volume><issue>2</issue><spage>1503</spage><epage>1517</epage><pages>1503-1517</pages><issn>1364-5072</issn><eissn>1365-2672</eissn><abstract>Aims
This study evaluated detection methods for Salmonella Typhi (S. Typhi) in the environment, to establish a novel pathway from field sampling to isolation of viable organisms and molecular confirmation from complex environmental samples, thus enabling environmental surveillance of typhoid.
Methods and Results
Multiple media were assessed using clinical isolates from the Public Health England's (PHE) Culture collection. The culture pathway selected consisted of a primary 2% bile broth and secondary Selenite F broth, followed by modified Chromogenic Agar for Salmonella Esterase (mCASE). A qPCR assay was adapted from a validated S. Typhi PCR panel for confirmation of isolates, with comparison to biochemical and serological tests showing good specificity. Sampling locations in Blantyre, Malawi were used to compare sampling methods. Viable S. Typhi were isolated from a mixture of trap and grab river water samples on six occasions.
Conclusions
Culture of viable S. Typhi from environmental samples was possible using effective capture and culture techniques.
Significance and impact of study
Whilst several studies have attempted to detect S. Typhi from the environment, this is the first successful attempt to isolate the organism from river water since the 1980s. Supplementing clinical data with environmental screening offers the potential for enhanced surveillance, which might inform interventions and assess vaccination programmes.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>34324765</pmid><doi>10.1111/jam.15237</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-4041-1405</orcidid><orcidid>https://orcid.org/0000-0002-7297-1485</orcidid><orcidid>https://orcid.org/0000-0001-9693-7700</orcidid><orcidid>https://orcid.org/0000-0003-2304-886X</orcidid><orcidid>https://orcid.org/0000-0003-4058-4461</orcidid><orcidid>https://orcid.org/0000-0003-1242-839X</orcidid><orcidid>https://orcid.org/0000-0001-5143-0981</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1364-5072 |
ispartof | Journal of applied microbiology, 2022-02, Vol.132 (2), p.1503-1517 |
issn | 1364-5072 1365-2672 |
language | eng |
recordid | cdi_proquest_journals_2621162312 |
source | Alma/SFX Local Collection |
subjects | bile broth biofilm biofilms Clinical isolates Culture techniques Esterase Health surveillance Humans Identification Malawi mCASE Moore swabs PCR (polymerase chain reaction) Public health Real-Time Polymerase Chain Reaction river water Rivers Salmonella Salmonella Typhi Salmonella typhi - genetics Sampling Sampling methods Selenite selenite broth Serological tests Specimen Handling Typhoid Typhoid Fever - diagnosis Vaccination water Water analysis Water sampling |
title | Optimized methods for detecting Salmonella Typhi in the environment using validated field sampling, culture and confirmatory molecular approaches |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T10%3A04%3A55IST&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=Optimized%20methods%20for%20detecting%20Salmonella%20Typhi%20in%20the%20environment%20using%20validated%20field%20sampling,%20culture%20and%20confirmatory%20molecular%20approaches&rft.jtitle=Journal%20of%20applied%20microbiology&rft.au=Rigby,%20Jonathan&rft.date=2022-02&rft.volume=132&rft.issue=2&rft.spage=1503&rft.epage=1517&rft.pages=1503-1517&rft.issn=1364-5072&rft.eissn=1365-2672&rft_id=info:doi/10.1111/jam.15237&rft_dat=%3Cproquest_cross%3E2621162312%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3887-b486030f0e0897d469b5a3d8bcb3e3a98f78a55e89bf8f9a771a5904d5f80e603%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2621162312&rft_id=info:pmid/34324765&rfr_iscdi=true |