Agent-based model of fecal microbial transplant effect on bile acid metabolism on suppressing Clostridium difficile infection: an example of agent-based modeling of intestinal bacterial infection

Agent-based modeling is a computational modeling method that represents system-level behavior as arising from multiple interactions between the multiple components that make up a system. Biological systems are thus readily described using agent-based models (ABMs), as multi-cellular organisms can be...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of pharmacokinetics and pharmacodynamics 2014-10, Vol.41 (5), p.493-507
Hauptverfasser: Peer, Xavier, An, Gary
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 507
container_issue 5
container_start_page 493
container_title Journal of pharmacokinetics and pharmacodynamics
container_volume 41
creator Peer, Xavier
An, Gary
description Agent-based modeling is a computational modeling method that represents system-level behavior as arising from multiple interactions between the multiple components that make up a system. Biological systems are thus readily described using agent-based models (ABMs), as multi-cellular organisms can be viewed as populations of interacting cells, and microbial systems manifest as colonies of individual microbes. Intersections between these two domains underlie an increasing number of pathophysiological processes, and the intestinal tract represents one of the most significant locations for these inter-domain interactions, so much so that it can be considered an internal ecology of varying robustness and function. Intestinal infections represent significant disturbances of this internal ecology, and one of the most clinically relevant intestinal infections is Clostridium difficile infection (CDI). CDI is precipitated by the use of broad-spectrum antibiotics, involves the depletion of commensal microbiota, and alterations in bile acid composition in the intestinal lumen. We present an example ABM of CDI (the C. difficile Infection ABM, or CDIABM) to examine fundamental dynamics of the pathogenesis of CDI and its response to treatment with anti-CDI antibiotics and a newer treatment therapy, fecal microbial transplant. The CDIABM focuses on one specific mechanism of potential CDI suppression: commensal modulation of bile acid composition. Even given its abstraction, the CDIABM reproduces essential dynamics of CDI and its response to therapy, and identifies a paradoxical zone of behavior that provides insight into the role of intestinal nutritional status and the efficacy of anti-CDI therapies. It is hoped that this use case example of the CDIABM can demonstrate the usefulness of both agent-based modeling and the application of abstract functional representation as the biomedical community seeks to address the challenges of increasingly complex diseases with the goal of personalized medicine.
doi_str_mv 10.1007/s10928-014-9381-1
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4210368</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1639992584</sourcerecordid><originalsourceid>FETCH-LOGICAL-c573t-8ff5523dc340b2cac4871f4c13c801cd9e61079956ba91b2adfa8e93acd7e7783</originalsourceid><addsrcrecordid>eNp1Ul1rFTEQXUSxtfoDfJGAL75Ek_1MfBDKxS8o9KWCbyGbnVxTdpM1yYr-Pv9YJ9x6qYU-hISZM2fOTE5VveTsLWdseJc4k7WgjLdUNoJT_qg65d3QUDG07ePy7geK5_tJ9Syla8Z439XsaXVSd7wXrZCn1d_zPfhMR51gIkuYYCbBEgtGz2RxJobR4StH7dM6a58JWExmEjwZ3QxEG4d1kPUYZpeWEk_bukZIyfk92c0h5egmty1kctY6U4qcLxwu-PdEewK_9bJiFPvq-2IKB8adz5Cy8yhl1CZDLKKOLM-rJ1bPCV7c3mfVt08fr3Zf6MXl56-78wtqcCeZCmu7rm4m07RsrI02rRi4bQ1vjGDcTBJ6zgYpu37Uko-1nqwWIBttpgGGQTRn1YcD77qNC0wGtUY9qzW6Rcc_Kmin_s9490Ptwy_V1pw1fSF4c0sQw88NJ1KLSwZmXCyELSneN1LKuhMtQl_fg16HLeICCgpxSMgKIT-g8KNSimCPYjhTxSLqYBGFFlHFIopjzau7Uxwr_nkCAfUBkDDl9xDvtH6Q9Qb_gMz8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1616310308</pqid></control><display><type>article</type><title>Agent-based model of fecal microbial transplant effect on bile acid metabolism on suppressing Clostridium difficile infection: an example of agent-based modeling of intestinal bacterial infection</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Peer, Xavier ; An, Gary</creator><creatorcontrib>Peer, Xavier ; An, Gary</creatorcontrib><description>Agent-based modeling is a computational modeling method that represents system-level behavior as arising from multiple interactions between the multiple components that make up a system. Biological systems are thus readily described using agent-based models (ABMs), as multi-cellular organisms can be viewed as populations of interacting cells, and microbial systems manifest as colonies of individual microbes. Intersections between these two domains underlie an increasing number of pathophysiological processes, and the intestinal tract represents one of the most significant locations for these inter-domain interactions, so much so that it can be considered an internal ecology of varying robustness and function. Intestinal infections represent significant disturbances of this internal ecology, and one of the most clinically relevant intestinal infections is Clostridium difficile infection (CDI). CDI is precipitated by the use of broad-spectrum antibiotics, involves the depletion of commensal microbiota, and alterations in bile acid composition in the intestinal lumen. We present an example ABM of CDI (the C. difficile Infection ABM, or CDIABM) to examine fundamental dynamics of the pathogenesis of CDI and its response to treatment with anti-CDI antibiotics and a newer treatment therapy, fecal microbial transplant. The CDIABM focuses on one specific mechanism of potential CDI suppression: commensal modulation of bile acid composition. Even given its abstraction, the CDIABM reproduces essential dynamics of CDI and its response to therapy, and identifies a paradoxical zone of behavior that provides insight into the role of intestinal nutritional status and the efficacy of anti-CDI therapies. It is hoped that this use case example of the CDIABM can demonstrate the usefulness of both agent-based modeling and the application of abstract functional representation as the biomedical community seeks to address the challenges of increasingly complex diseases with the goal of personalized medicine.</description><identifier>ISSN: 1567-567X</identifier><identifier>EISSN: 1573-8744</identifier><identifier>DOI: 10.1007/s10928-014-9381-1</identifier><identifier>PMID: 25168489</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Anti-Bacterial Agents - therapeutic use ; Bacteria ; Bile Acids and Salts - metabolism ; Biochemistry ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Clostridium difficile ; Enterocolitis, Pseudomembranous - drug therapy ; Enterocolitis, Pseudomembranous - metabolism ; Enterocolitis, Pseudomembranous - microbiology ; Enterocolitis, Pseudomembranous - therapy ; Feces - microbiology ; Humans ; Models, Biological ; Original Paper ; Pharmacology/Toxicology ; Pharmacy ; Transplantation ; Veterinary Medicine/Veterinary Science</subject><ispartof>Journal of pharmacokinetics and pharmacodynamics, 2014-10, Vol.41 (5), p.493-507</ispartof><rights>Springer Science+Business Media New York 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c573t-8ff5523dc340b2cac4871f4c13c801cd9e61079956ba91b2adfa8e93acd7e7783</citedby><cites>FETCH-LOGICAL-c573t-8ff5523dc340b2cac4871f4c13c801cd9e61079956ba91b2adfa8e93acd7e7783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10928-014-9381-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10928-014-9381-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27922,27923,41486,42555,51317</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25168489$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peer, Xavier</creatorcontrib><creatorcontrib>An, Gary</creatorcontrib><title>Agent-based model of fecal microbial transplant effect on bile acid metabolism on suppressing Clostridium difficile infection: an example of agent-based modeling of intestinal bacterial infection</title><title>Journal of pharmacokinetics and pharmacodynamics</title><addtitle>J Pharmacokinet Pharmacodyn</addtitle><addtitle>J Pharmacokinet Pharmacodyn</addtitle><description>Agent-based modeling is a computational modeling method that represents system-level behavior as arising from multiple interactions between the multiple components that make up a system. Biological systems are thus readily described using agent-based models (ABMs), as multi-cellular organisms can be viewed as populations of interacting cells, and microbial systems manifest as colonies of individual microbes. Intersections between these two domains underlie an increasing number of pathophysiological processes, and the intestinal tract represents one of the most significant locations for these inter-domain interactions, so much so that it can be considered an internal ecology of varying robustness and function. Intestinal infections represent significant disturbances of this internal ecology, and one of the most clinically relevant intestinal infections is Clostridium difficile infection (CDI). CDI is precipitated by the use of broad-spectrum antibiotics, involves the depletion of commensal microbiota, and alterations in bile acid composition in the intestinal lumen. We present an example ABM of CDI (the C. difficile Infection ABM, or CDIABM) to examine fundamental dynamics of the pathogenesis of CDI and its response to treatment with anti-CDI antibiotics and a newer treatment therapy, fecal microbial transplant. The CDIABM focuses on one specific mechanism of potential CDI suppression: commensal modulation of bile acid composition. Even given its abstraction, the CDIABM reproduces essential dynamics of CDI and its response to therapy, and identifies a paradoxical zone of behavior that provides insight into the role of intestinal nutritional status and the efficacy of anti-CDI therapies. It is hoped that this use case example of the CDIABM can demonstrate the usefulness of both agent-based modeling and the application of abstract functional representation as the biomedical community seeks to address the challenges of increasingly complex diseases with the goal of personalized medicine.</description><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Bacteria</subject><subject>Bile Acids and Salts - metabolism</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Clostridium difficile</subject><subject>Enterocolitis, Pseudomembranous - drug therapy</subject><subject>Enterocolitis, Pseudomembranous - metabolism</subject><subject>Enterocolitis, Pseudomembranous - microbiology</subject><subject>Enterocolitis, Pseudomembranous - therapy</subject><subject>Feces - microbiology</subject><subject>Humans</subject><subject>Models, Biological</subject><subject>Original Paper</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Transplantation</subject><subject>Veterinary Medicine/Veterinary Science</subject><issn>1567-567X</issn><issn>1573-8744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1Ul1rFTEQXUSxtfoDfJGAL75Ek_1MfBDKxS8o9KWCbyGbnVxTdpM1yYr-Pv9YJ9x6qYU-hISZM2fOTE5VveTsLWdseJc4k7WgjLdUNoJT_qg65d3QUDG07ePy7geK5_tJ9Syla8Z439XsaXVSd7wXrZCn1d_zPfhMR51gIkuYYCbBEgtGz2RxJobR4StH7dM6a58JWExmEjwZ3QxEG4d1kPUYZpeWEk_bukZIyfk92c0h5egmty1kctY6U4qcLxwu-PdEewK_9bJiFPvq-2IKB8adz5Cy8yhl1CZDLKKOLM-rJ1bPCV7c3mfVt08fr3Zf6MXl56-78wtqcCeZCmu7rm4m07RsrI02rRi4bQ1vjGDcTBJ6zgYpu37Uko-1nqwWIBttpgGGQTRn1YcD77qNC0wGtUY9qzW6Rcc_Kmin_s9490Ptwy_V1pw1fSF4c0sQw88NJ1KLSwZmXCyELSneN1LKuhMtQl_fg16HLeICCgpxSMgKIT-g8KNSimCPYjhTxSLqYBGFFlHFIopjzau7Uxwr_nkCAfUBkDDl9xDvtH6Q9Qb_gMz8</recordid><startdate>20141001</startdate><enddate>20141001</enddate><creator>Peer, Xavier</creator><creator>An, Gary</creator><general>Springer US</general><general>Springer Nature B.V</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>3V.</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20141001</creationdate><title>Agent-based model of fecal microbial transplant effect on bile acid metabolism on suppressing Clostridium difficile infection: an example of agent-based modeling of intestinal bacterial infection</title><author>Peer, Xavier ; An, Gary</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c573t-8ff5523dc340b2cac4871f4c13c801cd9e61079956ba91b2adfa8e93acd7e7783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Bacteria</topic><topic>Bile Acids and Salts - metabolism</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Clostridium difficile</topic><topic>Enterocolitis, Pseudomembranous - drug therapy</topic><topic>Enterocolitis, Pseudomembranous - metabolism</topic><topic>Enterocolitis, Pseudomembranous - microbiology</topic><topic>Enterocolitis, Pseudomembranous - therapy</topic><topic>Feces - microbiology</topic><topic>Humans</topic><topic>Models, Biological</topic><topic>Original Paper</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Transplantation</topic><topic>Veterinary Medicine/Veterinary Science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peer, Xavier</creatorcontrib><creatorcontrib>An, Gary</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of pharmacokinetics and pharmacodynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peer, Xavier</au><au>An, Gary</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Agent-based model of fecal microbial transplant effect on bile acid metabolism on suppressing Clostridium difficile infection: an example of agent-based modeling of intestinal bacterial infection</atitle><jtitle>Journal of pharmacokinetics and pharmacodynamics</jtitle><stitle>J Pharmacokinet Pharmacodyn</stitle><addtitle>J Pharmacokinet Pharmacodyn</addtitle><date>2014-10-01</date><risdate>2014</risdate><volume>41</volume><issue>5</issue><spage>493</spage><epage>507</epage><pages>493-507</pages><issn>1567-567X</issn><eissn>1573-8744</eissn><abstract>Agent-based modeling is a computational modeling method that represents system-level behavior as arising from multiple interactions between the multiple components that make up a system. Biological systems are thus readily described using agent-based models (ABMs), as multi-cellular organisms can be viewed as populations of interacting cells, and microbial systems manifest as colonies of individual microbes. Intersections between these two domains underlie an increasing number of pathophysiological processes, and the intestinal tract represents one of the most significant locations for these inter-domain interactions, so much so that it can be considered an internal ecology of varying robustness and function. Intestinal infections represent significant disturbances of this internal ecology, and one of the most clinically relevant intestinal infections is Clostridium difficile infection (CDI). CDI is precipitated by the use of broad-spectrum antibiotics, involves the depletion of commensal microbiota, and alterations in bile acid composition in the intestinal lumen. We present an example ABM of CDI (the C. difficile Infection ABM, or CDIABM) to examine fundamental dynamics of the pathogenesis of CDI and its response to treatment with anti-CDI antibiotics and a newer treatment therapy, fecal microbial transplant. The CDIABM focuses on one specific mechanism of potential CDI suppression: commensal modulation of bile acid composition. Even given its abstraction, the CDIABM reproduces essential dynamics of CDI and its response to therapy, and identifies a paradoxical zone of behavior that provides insight into the role of intestinal nutritional status and the efficacy of anti-CDI therapies. It is hoped that this use case example of the CDIABM can demonstrate the usefulness of both agent-based modeling and the application of abstract functional representation as the biomedical community seeks to address the challenges of increasingly complex diseases with the goal of personalized medicine.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>25168489</pmid><doi>10.1007/s10928-014-9381-1</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1567-567X
ispartof Journal of pharmacokinetics and pharmacodynamics, 2014-10, Vol.41 (5), p.493-507
issn 1567-567X
1573-8744
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4210368
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Anti-Bacterial Agents - therapeutic use
Bacteria
Bile Acids and Salts - metabolism
Biochemistry
Biomedical and Life Sciences
Biomedical Engineering and Bioengineering
Biomedicine
Clostridium difficile
Enterocolitis, Pseudomembranous - drug therapy
Enterocolitis, Pseudomembranous - metabolism
Enterocolitis, Pseudomembranous - microbiology
Enterocolitis, Pseudomembranous - therapy
Feces - microbiology
Humans
Models, Biological
Original Paper
Pharmacology/Toxicology
Pharmacy
Transplantation
Veterinary Medicine/Veterinary Science
title Agent-based model of fecal microbial transplant effect on bile acid metabolism on suppressing Clostridium difficile infection: an example of agent-based modeling of intestinal bacterial infection
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T07%3A57%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Agent-based%20model%20of%20fecal%20microbial%20transplant%20effect%20on%20bile%20acid%20metabolism%20on%20suppressing%20Clostridium%20difficile%20infection:%20an%20example%20of%20agent-based%20modeling%20of%20intestinal%20bacterial%20infection&rft.jtitle=Journal%20of%20pharmacokinetics%20and%20pharmacodynamics&rft.au=Peer,%20Xavier&rft.date=2014-10-01&rft.volume=41&rft.issue=5&rft.spage=493&rft.epage=507&rft.pages=493-507&rft.issn=1567-567X&rft.eissn=1573-8744&rft_id=info:doi/10.1007/s10928-014-9381-1&rft_dat=%3Cproquest_pubme%3E1639992584%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1616310308&rft_id=info:pmid/25168489&rfr_iscdi=true