The major Alternaria alternata allergen, Alt a 1: A reliable and specific marker of fungal contamination in citrus fruits

The ubiquitously present spores of Alternaria alternata can spoil a wide variety of foodstuffs, including a variety of fruits belonging to the Citrus genus. The major allergenic protein of A. alternata, Alt a 1, is a species-specific molecular marker that has been strongly associated with allergenic...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of food microbiology 2017-09, Vol.257, p.26-30
Hauptverfasser: Gabriel, M.F., Uriel, N., Teifoori, F., Postigo, I., Suñén, E., Martínez, J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 30
container_issue
container_start_page 26
container_title International journal of food microbiology
container_volume 257
creator Gabriel, M.F.
Uriel, N.
Teifoori, F.
Postigo, I.
Suñén, E.
Martínez, J.
description The ubiquitously present spores of Alternaria alternata can spoil a wide variety of foodstuffs, including a variety of fruits belonging to the Citrus genus. The major allergenic protein of A. alternata, Alt a 1, is a species-specific molecular marker that has been strongly associated with allergenicity and phytopathogenicity of this fungal species. This study aimed to evaluate the potential of the detection of Alt a 1 as a reliable indicator of A. alternata contamination in citrus fruits. To accomplish this aim, sixty oranges were artificially infected with a spore suspension of A. alternata. Internal fruit material was collected at different incubation times (one, two and three weeks after the fungal inoculation) and used for both total RNA extraction and protein extraction. Alt a 1 detection was then performed by polymerase chain reaction (PCR) amplification using Alt a 1 specific primers and by enzyme-linked immunosorbent assay (ELISA). The experimental model presented in this work was effective to simulate the typical Alternaria black rot phenotype and its progression. Although both PCR and ELISA techniques have been successfully carried out for detecting Alt a 1 allergen in A. alternata infected oranges, the PCR method was found to be more sensitive than ELISA. Nevertheless, ELISA results were highly valuable to demonstrate that considerable amounts of Alt a 1 are produced during A. alternata fruit infection process, corroborating the recently proposed hypothesis that this protein plays a role in the pathogenicity and virulence of Alternaria species. Such evidence suggests that the detection of Alt a 1 by PCR-based assay may be used as a specific indicator of the presence of pathogenic and allergenic fungal species, A. alternata, in fruits. This knowledge can be employed to control the fungal infection and mitigate agricultural losses as well as human exposure to A. alternata allergens and toxins. •Alternaria black rot was experimentally induced in citrus fruits by A. alternata inoculation.•During the A. alternata fruit infection high amounts of Alt a 1 are produced.•ELISA and PCR are valuable tools for detecting Alt a 1 in moldy fruits.•Alt a 1 may be used as a specific biosecurity indicator of contamination by A. alternata.
doi_str_mv 10.1016/j.ijfoodmicro.2017.06.006
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1912195009</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S016816051730274X</els_id><sourcerecordid>1957223478</sourcerecordid><originalsourceid>FETCH-LOGICAL-c405t-f14c3cfd004d636acabfd0cf8fbf00108486faf173f3b7939d61da06a652ba673</originalsourceid><addsrcrecordid>eNqNkc1u1DAUhS1E1U5LXwEZsWHRhOs4cRJ2oxE_lSqxKWvLsa-LgxMPdlKpb4-jKQixYuVj-bvnyucQ8oZByYCJ92PpRhuCmZyOoayAtSWIEkC8IDvWtX3BawEvyS6zXcEENBfkMqURABrO4ZxcVJ3IouE78nT_HemkxhDp3i8YZxWdouokl015jA8432zPVFH2ge5pRO_U4JGq2dB0RO2s09kl_sBIg6V2nR-UpzrMi5pc9nFhpm6m2i1xTdTG1S3pFTmzyie8fj6vyLdPH-8PX4q7r59vD_u7QtfQLIVltebaGoDaCC6UVkO-aNvZwQIw6OpOWGVZyy0f2p73RjCjQCjRVIMSLb8i706-xxh-rpgWObmk0Xs1Y1iTZD2rWN8A9Bl9-w86hjXn4DeqaauK122Xqf5E5fBTimjlMbr8-SfJQG79yFH-1Y_c-pEgZO4nz75-3rAOE5o_k78LycDhBGCO5NFhlEk7nDUaF1Ev0gT3H2t-Aar9p_U</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1957223478</pqid></control><display><type>article</type><title>The major Alternaria alternata allergen, Alt a 1: A reliable and specific marker of fungal contamination in citrus fruits</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Gabriel, M.F. ; Uriel, N. ; Teifoori, F. ; Postigo, I. ; Suñén, E. ; Martínez, J.</creator><creatorcontrib>Gabriel, M.F. ; Uriel, N. ; Teifoori, F. ; Postigo, I. ; Suñén, E. ; Martínez, J.</creatorcontrib><description>The ubiquitously present spores of Alternaria alternata can spoil a wide variety of foodstuffs, including a variety of fruits belonging to the Citrus genus. The major allergenic protein of A. alternata, Alt a 1, is a species-specific molecular marker that has been strongly associated with allergenicity and phytopathogenicity of this fungal species. This study aimed to evaluate the potential of the detection of Alt a 1 as a reliable indicator of A. alternata contamination in citrus fruits. To accomplish this aim, sixty oranges were artificially infected with a spore suspension of A. alternata. Internal fruit material was collected at different incubation times (one, two and three weeks after the fungal inoculation) and used for both total RNA extraction and protein extraction. Alt a 1 detection was then performed by polymerase chain reaction (PCR) amplification using Alt a 1 specific primers and by enzyme-linked immunosorbent assay (ELISA). The experimental model presented in this work was effective to simulate the typical Alternaria black rot phenotype and its progression. Although both PCR and ELISA techniques have been successfully carried out for detecting Alt a 1 allergen in A. alternata infected oranges, the PCR method was found to be more sensitive than ELISA. Nevertheless, ELISA results were highly valuable to demonstrate that considerable amounts of Alt a 1 are produced during A. alternata fruit infection process, corroborating the recently proposed hypothesis that this protein plays a role in the pathogenicity and virulence of Alternaria species. Such evidence suggests that the detection of Alt a 1 by PCR-based assay may be used as a specific indicator of the presence of pathogenic and allergenic fungal species, A. alternata, in fruits. This knowledge can be employed to control the fungal infection and mitigate agricultural losses as well as human exposure to A. alternata allergens and toxins. •Alternaria black rot was experimentally induced in citrus fruits by A. alternata inoculation.•During the A. alternata fruit infection high amounts of Alt a 1 are produced.•ELISA and PCR are valuable tools for detecting Alt a 1 in moldy fruits.•Alt a 1 may be used as a specific biosecurity indicator of contamination by A. alternata.</description><identifier>ISSN: 0168-1605</identifier><identifier>EISSN: 1879-3460</identifier><identifier>DOI: 10.1016/j.ijfoodmicro.2017.06.006</identifier><identifier>PMID: 28633053</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Allergenicity ; Allergens ; Alt a 1 detection ; Alternaria ; Alternaria - immunology ; Alternaria - isolation &amp; purification ; Alternaria alternata ; Alternaria black rot ; Antigens, Fungal - analysis ; Antigens, Fungal - immunology ; Black rot ; Citrus - microbiology ; Citrus fruits ; Computer simulation ; Contamination ; ELISA ; Enzyme-linked immunosorbent assay ; Enzyme-Linked Immunosorbent Assay - methods ; Food biosecurity ; Food contamination &amp; poisoning ; Food Contamination - analysis ; Fruit - microbiology ; Fruits ; Fungal Proteins - analysis ; Fungi ; Humans ; Infections ; Inoculation ; Pathogenicity ; Pathogens ; Phenotypes ; Polymerase chain reaction ; Primers ; Proteins ; Ribonucleic acid ; RNA ; Species ; Spores ; Spores, Fungal - immunology ; Spores, Fungal - isolation &amp; purification ; Toxins ; Virulence</subject><ispartof>International journal of food microbiology, 2017-09, Vol.257, p.26-30</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Sep 18, 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-f14c3cfd004d636acabfd0cf8fbf00108486faf173f3b7939d61da06a652ba673</citedby><cites>FETCH-LOGICAL-c405t-f14c3cfd004d636acabfd0cf8fbf00108486faf173f3b7939d61da06a652ba673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijfoodmicro.2017.06.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28633053$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gabriel, M.F.</creatorcontrib><creatorcontrib>Uriel, N.</creatorcontrib><creatorcontrib>Teifoori, F.</creatorcontrib><creatorcontrib>Postigo, I.</creatorcontrib><creatorcontrib>Suñén, E.</creatorcontrib><creatorcontrib>Martínez, J.</creatorcontrib><title>The major Alternaria alternata allergen, Alt a 1: A reliable and specific marker of fungal contamination in citrus fruits</title><title>International journal of food microbiology</title><addtitle>Int J Food Microbiol</addtitle><description>The ubiquitously present spores of Alternaria alternata can spoil a wide variety of foodstuffs, including a variety of fruits belonging to the Citrus genus. The major allergenic protein of A. alternata, Alt a 1, is a species-specific molecular marker that has been strongly associated with allergenicity and phytopathogenicity of this fungal species. This study aimed to evaluate the potential of the detection of Alt a 1 as a reliable indicator of A. alternata contamination in citrus fruits. To accomplish this aim, sixty oranges were artificially infected with a spore suspension of A. alternata. Internal fruit material was collected at different incubation times (one, two and three weeks after the fungal inoculation) and used for both total RNA extraction and protein extraction. Alt a 1 detection was then performed by polymerase chain reaction (PCR) amplification using Alt a 1 specific primers and by enzyme-linked immunosorbent assay (ELISA). The experimental model presented in this work was effective to simulate the typical Alternaria black rot phenotype and its progression. Although both PCR and ELISA techniques have been successfully carried out for detecting Alt a 1 allergen in A. alternata infected oranges, the PCR method was found to be more sensitive than ELISA. Nevertheless, ELISA results were highly valuable to demonstrate that considerable amounts of Alt a 1 are produced during A. alternata fruit infection process, corroborating the recently proposed hypothesis that this protein plays a role in the pathogenicity and virulence of Alternaria species. Such evidence suggests that the detection of Alt a 1 by PCR-based assay may be used as a specific indicator of the presence of pathogenic and allergenic fungal species, A. alternata, in fruits. This knowledge can be employed to control the fungal infection and mitigate agricultural losses as well as human exposure to A. alternata allergens and toxins. •Alternaria black rot was experimentally induced in citrus fruits by A. alternata inoculation.•During the A. alternata fruit infection high amounts of Alt a 1 are produced.•ELISA and PCR are valuable tools for detecting Alt a 1 in moldy fruits.•Alt a 1 may be used as a specific biosecurity indicator of contamination by A. alternata.</description><subject>Allergenicity</subject><subject>Allergens</subject><subject>Alt a 1 detection</subject><subject>Alternaria</subject><subject>Alternaria - immunology</subject><subject>Alternaria - isolation &amp; purification</subject><subject>Alternaria alternata</subject><subject>Alternaria black rot</subject><subject>Antigens, Fungal - analysis</subject><subject>Antigens, Fungal - immunology</subject><subject>Black rot</subject><subject>Citrus - microbiology</subject><subject>Citrus fruits</subject><subject>Computer simulation</subject><subject>Contamination</subject><subject>ELISA</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Food biosecurity</subject><subject>Food contamination &amp; poisoning</subject><subject>Food Contamination - analysis</subject><subject>Fruit - microbiology</subject><subject>Fruits</subject><subject>Fungal Proteins - analysis</subject><subject>Fungi</subject><subject>Humans</subject><subject>Infections</subject><subject>Inoculation</subject><subject>Pathogenicity</subject><subject>Pathogens</subject><subject>Phenotypes</subject><subject>Polymerase chain reaction</subject><subject>Primers</subject><subject>Proteins</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Species</subject><subject>Spores</subject><subject>Spores, Fungal - immunology</subject><subject>Spores, Fungal - isolation &amp; purification</subject><subject>Toxins</subject><subject>Virulence</subject><issn>0168-1605</issn><issn>1879-3460</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhS1E1U5LXwEZsWHRhOs4cRJ2oxE_lSqxKWvLsa-LgxMPdlKpb4-jKQixYuVj-bvnyucQ8oZByYCJ92PpRhuCmZyOoayAtSWIEkC8IDvWtX3BawEvyS6zXcEENBfkMqURABrO4ZxcVJ3IouE78nT_HemkxhDp3i8YZxWdouokl015jA8432zPVFH2ge5pRO_U4JGq2dB0RO2s09kl_sBIg6V2nR-UpzrMi5pc9nFhpm6m2i1xTdTG1S3pFTmzyie8fj6vyLdPH-8PX4q7r59vD_u7QtfQLIVltebaGoDaCC6UVkO-aNvZwQIw6OpOWGVZyy0f2p73RjCjQCjRVIMSLb8i706-xxh-rpgWObmk0Xs1Y1iTZD2rWN8A9Bl9-w86hjXn4DeqaauK122Xqf5E5fBTimjlMbr8-SfJQG79yFH-1Y_c-pEgZO4nz75-3rAOE5o_k78LycDhBGCO5NFhlEk7nDUaF1Ev0gT3H2t-Aar9p_U</recordid><startdate>20170918</startdate><enddate>20170918</enddate><creator>Gabriel, M.F.</creator><creator>Uriel, N.</creator><creator>Teifoori, F.</creator><creator>Postigo, I.</creator><creator>Suñén, E.</creator><creator>Martínez, J.</creator><general>Elsevier B.V</general><general>Elsevier BV</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>7QL</scope><scope>7QO</scope><scope>7QR</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20170918</creationdate><title>The major Alternaria alternata allergen, Alt a 1: A reliable and specific marker of fungal contamination in citrus fruits</title><author>Gabriel, M.F. ; Uriel, N. ; Teifoori, F. ; Postigo, I. ; Suñén, E. ; Martínez, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-f14c3cfd004d636acabfd0cf8fbf00108486faf173f3b7939d61da06a652ba673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Allergenicity</topic><topic>Allergens</topic><topic>Alt a 1 detection</topic><topic>Alternaria</topic><topic>Alternaria - immunology</topic><topic>Alternaria - isolation &amp; purification</topic><topic>Alternaria alternata</topic><topic>Alternaria black rot</topic><topic>Antigens, Fungal - analysis</topic><topic>Antigens, Fungal - immunology</topic><topic>Black rot</topic><topic>Citrus - microbiology</topic><topic>Citrus fruits</topic><topic>Computer simulation</topic><topic>Contamination</topic><topic>ELISA</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>Food biosecurity</topic><topic>Food contamination &amp; poisoning</topic><topic>Food Contamination - analysis</topic><topic>Fruit - microbiology</topic><topic>Fruits</topic><topic>Fungal Proteins - analysis</topic><topic>Fungi</topic><topic>Humans</topic><topic>Infections</topic><topic>Inoculation</topic><topic>Pathogenicity</topic><topic>Pathogens</topic><topic>Phenotypes</topic><topic>Polymerase chain reaction</topic><topic>Primers</topic><topic>Proteins</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Species</topic><topic>Spores</topic><topic>Spores, Fungal - immunology</topic><topic>Spores, Fungal - isolation &amp; purification</topic><topic>Toxins</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gabriel, M.F.</creatorcontrib><creatorcontrib>Uriel, N.</creatorcontrib><creatorcontrib>Teifoori, F.</creatorcontrib><creatorcontrib>Postigo, I.</creatorcontrib><creatorcontrib>Suñén, E.</creatorcontrib><creatorcontrib>Martínez, J.</creatorcontrib><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>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of food microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gabriel, M.F.</au><au>Uriel, N.</au><au>Teifoori, F.</au><au>Postigo, I.</au><au>Suñén, E.</au><au>Martínez, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The major Alternaria alternata allergen, Alt a 1: A reliable and specific marker of fungal contamination in citrus fruits</atitle><jtitle>International journal of food microbiology</jtitle><addtitle>Int J Food Microbiol</addtitle><date>2017-09-18</date><risdate>2017</risdate><volume>257</volume><spage>26</spage><epage>30</epage><pages>26-30</pages><issn>0168-1605</issn><eissn>1879-3460</eissn><abstract>The ubiquitously present spores of Alternaria alternata can spoil a wide variety of foodstuffs, including a variety of fruits belonging to the Citrus genus. The major allergenic protein of A. alternata, Alt a 1, is a species-specific molecular marker that has been strongly associated with allergenicity and phytopathogenicity of this fungal species. This study aimed to evaluate the potential of the detection of Alt a 1 as a reliable indicator of A. alternata contamination in citrus fruits. To accomplish this aim, sixty oranges were artificially infected with a spore suspension of A. alternata. Internal fruit material was collected at different incubation times (one, two and three weeks after the fungal inoculation) and used for both total RNA extraction and protein extraction. Alt a 1 detection was then performed by polymerase chain reaction (PCR) amplification using Alt a 1 specific primers and by enzyme-linked immunosorbent assay (ELISA). The experimental model presented in this work was effective to simulate the typical Alternaria black rot phenotype and its progression. Although both PCR and ELISA techniques have been successfully carried out for detecting Alt a 1 allergen in A. alternata infected oranges, the PCR method was found to be more sensitive than ELISA. Nevertheless, ELISA results were highly valuable to demonstrate that considerable amounts of Alt a 1 are produced during A. alternata fruit infection process, corroborating the recently proposed hypothesis that this protein plays a role in the pathogenicity and virulence of Alternaria species. Such evidence suggests that the detection of Alt a 1 by PCR-based assay may be used as a specific indicator of the presence of pathogenic and allergenic fungal species, A. alternata, in fruits. This knowledge can be employed to control the fungal infection and mitigate agricultural losses as well as human exposure to A. alternata allergens and toxins. •Alternaria black rot was experimentally induced in citrus fruits by A. alternata inoculation.•During the A. alternata fruit infection high amounts of Alt a 1 are produced.•ELISA and PCR are valuable tools for detecting Alt a 1 in moldy fruits.•Alt a 1 may be used as a specific biosecurity indicator of contamination by A. alternata.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28633053</pmid><doi>10.1016/j.ijfoodmicro.2017.06.006</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0168-1605
ispartof International journal of food microbiology, 2017-09, Vol.257, p.26-30
issn 0168-1605
1879-3460
language eng
recordid cdi_proquest_miscellaneous_1912195009
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Allergenicity
Allergens
Alt a 1 detection
Alternaria
Alternaria - immunology
Alternaria - isolation & purification
Alternaria alternata
Alternaria black rot
Antigens, Fungal - analysis
Antigens, Fungal - immunology
Black rot
Citrus - microbiology
Citrus fruits
Computer simulation
Contamination
ELISA
Enzyme-linked immunosorbent assay
Enzyme-Linked Immunosorbent Assay - methods
Food biosecurity
Food contamination & poisoning
Food Contamination - analysis
Fruit - microbiology
Fruits
Fungal Proteins - analysis
Fungi
Humans
Infections
Inoculation
Pathogenicity
Pathogens
Phenotypes
Polymerase chain reaction
Primers
Proteins
Ribonucleic acid
RNA
Species
Spores
Spores, Fungal - immunology
Spores, Fungal - isolation & purification
Toxins
Virulence
title The major Alternaria alternata allergen, Alt a 1: A reliable and specific marker of fungal contamination in citrus fruits
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T23%3A53%3A22IST&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=The%20major%20Alternaria%20alternata%20allergen,%20Alt%20a%201:%20A%20reliable%20and%20specific%20marker%20of%20fungal%20contamination%20in%20citrus%20fruits&rft.jtitle=International%20journal%20of%20food%20microbiology&rft.au=Gabriel,%20M.F.&rft.date=2017-09-18&rft.volume=257&rft.spage=26&rft.epage=30&rft.pages=26-30&rft.issn=0168-1605&rft.eissn=1879-3460&rft_id=info:doi/10.1016/j.ijfoodmicro.2017.06.006&rft_dat=%3Cproquest_cross%3E1957223478%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=1957223478&rft_id=info:pmid/28633053&rft_els_id=S016816051730274X&rfr_iscdi=true