Identification of differences in gene expression implicated in the Adherent-Invasive Escherichia coli phenotype during in vitro infection of intestinal epithelial cells
dc.contributor.author
dc.date.accessioned
2024-07-11T07:25:24Z
dc.date.available
2024-07-11T07:25:24Z
dc.date.issued
2023-09-11
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dc.description.abstract
Introduction: Adherent-invasive Escherichia coli (AIEC) is strongly associated with the pathogenesis of Crohn’s disease (CD). However, no molecular markers currently exist for AIEC identification. This study aimed to identify differentially expressed genes (DEGs) between AIEC and non-AIEC strains that may contribute to AIEC pathogenicity and to evaluate their utility as molecular markers.
Methods: Comparative transcriptomics was performed on two closely related AIEC/non-AIEC strain pairs during Intestine-407 cell infection. DEGs were quantified by RT-qPCR in the same RNA extracts, as well as in 14 AIEC and 23 non-AIEC strains to validate the results across a diverse strain collection. Binary logistical regression was performed to identify DEGs whose quantification could be used as AIEC biomarkers.
Results: Comparative transcriptomics revealed 67 differences in expression between the two phenotypes in the strain pairs, 50 of which (81.97%) were corroborated by RT-qPCR. When explored in the whole strain collection, 29 DEGs were differentially expressed between AIEC and non-AIEC phenotypes (p-value < 0.042), and 42 genes between the supernatant fraction of infected cell cultures and the cellular fraction containing adhered and intracellular bacteria (p-value < 0.049). Notably, six DEGs detected in the strain collection were implicated in arginine biosynthesis and five in colanic acid synthesis. Furthermore, two biomarkers based on wzb and cueR gene expression were proposed with an accuracy of ≥ 85% in our strain collection.
Discussion: This is the first transcriptomic study conducted using AIEC-infected cell cultures. We have identified several genes that may be involved in AIEC pathogenicity, two of which are putative biomarkers for identification
dc.description.sponsorship
This work was supported by the Universitat de Girona under Grants MPCUdG2016-009 and GdRCompetUdG2017; Spanish Ministry of Economy and Competitiveness (MINECO) under Grants PID2021-126699NB-I00/MCIN/AEI/10.13039/501100011033/FEDER, UE, SAF2017-82261-P and SAF2013-43284-P, being the last co-funded by the European Regional Development Fund. CC-F and QB-R were recipients of predoctoral fellowships (IF-UdG 2015 and IF-UdG 2019). ML-S was a Serra Húnter fellow
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application/pdf
dc.language.iso
eng
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Frontiers Media
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PID2021-126699NB-I00
SAF2017-82261-P
SAF2013-43284-P
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Reproducció digital del document publicat a: https://doi.org/10.3389/fcimb.2023.1228159
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Frontiers in Cellular and Infection Microbiology, 2023, vol. 13, art. núm. 1228159
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Articles publicats (D-B)
dc.rights
Attribution 4.0 International
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dc.subject
dc.title
Identification of differences in gene expression implicated in the Adherent-Invasive Escherichia coli phenotype during in vitro infection of intestinal epithelial cells
dc.type
info:eu-repo/semantics/article
dc.rights.accessRights
info:eu-repo/semantics/openAccess
dc.relation.projectID
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-126699NB-I00/ES/MONOCAPAS DERIVADAS DE ORGANOIDES INTESTINALES HUMANOS PARA ESTUDIAR LA PATOGENICIDAD DE AIEC Y ROL DE LA ALARMONA PPGPP EN LA VIRULENCIA DE AIEC/
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/SAF2017-82261-P/ES/BUSQUEDA DE NUEVOS FACTORES IMPLICADOS EN LA VIRULENCIA DEL PATOTIPO AIEC ASOCIADO A LA ENFERMEDAD DE CROHN: ESTUDIO TRANSCRIPTOMICO Y ROL DE LAS VESICULAS DE MEMBRANA EXTERNA/
info:eu-repo/grantAgreement/MINECO//SAF2013-43284-P/ES/DETERMINANTES GENETICOS IMPLICADOS EN EL PATOTIPO ESCHERICHIA COLI ADHERENTE INVASIVA (AIEC) PARA SU IDENTIFICACION EN LA ENFERMEDAD DE CROHN/
dc.type.version
info:eu-repo/semantics/publishedVersion
dc.identifier.doi
dc.identifier.idgrec
037382
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dc.type.peerreviewed
peer-reviewed
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dc.identifier.eissn
2235-2988