Co-Occurrence of Symptoms and Gut Microbiota Composition Before Neoadjuvant Chemotherapy and Radiation Therapy for Rectal Cancer: A Proof of Concept

Purpose: To examine a) whether there are significant differences in gut microbial diversity and in the abundance of gut microbial taxa; and b) differences in predicted functional pathways of the gut microbiome between those participants with high co-occurring symptoms and those with low co-occurring...

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Veröffentlicht in:Biological research for nursing 2021-07, Vol.23 (3), p.513-523, Article 1099800421991656
Hauptverfasser: González-Mercado, Velda J., Lim, Jean, Yu, Gary, Penedo, Frank, Pedro, Elsa, Bernabe, Raul, Tirado-Gómez, Maribel, Aouizerat, Bradley
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container_issue 3
container_start_page 513
container_title Biological research for nursing
container_volume 23
creator González-Mercado, Velda J.
Lim, Jean
Yu, Gary
Penedo, Frank
Pedro, Elsa
Bernabe, Raul
Tirado-Gómez, Maribel
Aouizerat, Bradley
description Purpose: To examine a) whether there are significant differences in gut microbial diversity and in the abundance of gut microbial taxa; and b) differences in predicted functional pathways of the gut microbiome between those participants with high co-occurring symptoms and those with low co-occurring symptoms, prior to neoadjuvant chemotherapy and radiation therapy (CRT) for rectal cancer. Methods: Rectal cancer patients (n = 41) provided stool samples for 16 S rRNA gene sequencing and symptom ratings for fatigue, sleep disturbance, and depressive symptoms prior to CRT. Descriptive statistics were computed for symptoms. Gut microbiome data were analyzed using QIIME2, LEfSe, and the R statistical package. Results: Participants with high co-occurring symptoms (n = 19) had significantly higher bacterial abundances of Ezakiella, Clostridium sensu stricto, Porphyromonas, Barnesiella, Coriobacteriales Incertae Sedis, Synergistiaceae, Echerichia-Shigella, and Turicibacter compared to those with low co-occurring symptoms before CRT (n = 22). Biosynthesis pathways for lipopolysaccharide, L-tryptophan, and colanic acid building blocks were enriched in participants with high co-occurring symptoms. Participants with low co-occurring symptoms showed enriched abundances of Enterococcus and Lachnospiraceae, as well as pathways for β-D-glucoronosides, hexuronide/hexuronate, and nicotinate degradation, methanogenesis, and L-lysine biosynthesis. Conclusion: A number of bacterial taxa and predicted functional pathways were differentially abundant in patients with high co-occurring symptoms compared to those with low co-occurring symptoms before CRT for rectal cancer. Detailed examination of bacterial taxa and pathways mediating co-occurring symptoms is warranted.
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Methods: Rectal cancer patients (n = 41) provided stool samples for 16 S rRNA gene sequencing and symptom ratings for fatigue, sleep disturbance, and depressive symptoms prior to CRT. Descriptive statistics were computed for symptoms. Gut microbiome data were analyzed using QIIME2, LEfSe, and the R statistical package. Results: Participants with high co-occurring symptoms (n = 19) had significantly higher bacterial abundances of Ezakiella, Clostridium sensu stricto, Porphyromonas, Barnesiella, Coriobacteriales Incertae Sedis, Synergistiaceae, Echerichia-Shigella, and Turicibacter compared to those with low co-occurring symptoms before CRT (n = 22). Biosynthesis pathways for lipopolysaccharide, L-tryptophan, and colanic acid building blocks were enriched in participants with high co-occurring symptoms. Participants with low co-occurring symptoms showed enriched abundances of Enterococcus and Lachnospiraceae, as well as pathways for β-D-glucoronosides, hexuronide/hexuronate, and nicotinate degradation, methanogenesis, and L-lysine biosynthesis. Conclusion: A number of bacterial taxa and predicted functional pathways were differentially abundant in patients with high co-occurring symptoms compared to those with low co-occurring symptoms before CRT for rectal cancer. Detailed examination of bacterial taxa and pathways mediating co-occurring symptoms is warranted.</description><identifier>ISSN: 1099-8004</identifier><identifier>EISSN: 1552-4175</identifier><identifier>DOI: 10.1177/1099800421991656</identifier><identifier>PMID: 33541122</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Bacteria ; Fatigue ; Gastrointestinal Microbiome ; Humans ; Life Sciences &amp; Biomedicine ; Neoadjuvant Therapy ; Nursing ; Rectal Neoplasms - therapy ; Science &amp; Technology</subject><ispartof>Biological research for nursing, 2021-07, Vol.23 (3), p.513-523, Article 1099800421991656</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021 2021 SAGE Publications</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>6</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000619947200001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c434t-d462226898aa7eb6861c278cc9e4b48945f7064979eaae727a5d1c79e2b902d83</citedby><cites>FETCH-LOGICAL-c434t-d462226898aa7eb6861c278cc9e4b48945f7064979eaae727a5d1c79e2b902d83</cites><orcidid>0000-0002-7236-0182 ; 0000-0003-4578-5318</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1099800421991656$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1099800421991656$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,315,781,785,886,21824,27929,27930,39262,39263,43626,43627</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33541122$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>González-Mercado, Velda J.</creatorcontrib><creatorcontrib>Lim, Jean</creatorcontrib><creatorcontrib>Yu, Gary</creatorcontrib><creatorcontrib>Penedo, Frank</creatorcontrib><creatorcontrib>Pedro, Elsa</creatorcontrib><creatorcontrib>Bernabe, Raul</creatorcontrib><creatorcontrib>Tirado-Gómez, Maribel</creatorcontrib><creatorcontrib>Aouizerat, Bradley</creatorcontrib><title>Co-Occurrence of Symptoms and Gut Microbiota Composition Before Neoadjuvant Chemotherapy and Radiation Therapy for Rectal Cancer: A Proof of Concept</title><title>Biological research for nursing</title><addtitle>BIOL RES NURS</addtitle><addtitle>Biol Res Nurs</addtitle><description>Purpose: To examine a) whether there are significant differences in gut microbial diversity and in the abundance of gut microbial taxa; and b) differences in predicted functional pathways of the gut microbiome between those participants with high co-occurring symptoms and those with low co-occurring symptoms, prior to neoadjuvant chemotherapy and radiation therapy (CRT) for rectal cancer. Methods: Rectal cancer patients (n = 41) provided stool samples for 16 S rRNA gene sequencing and symptom ratings for fatigue, sleep disturbance, and depressive symptoms prior to CRT. Descriptive statistics were computed for symptoms. Gut microbiome data were analyzed using QIIME2, LEfSe, and the R statistical package. Results: Participants with high co-occurring symptoms (n = 19) had significantly higher bacterial abundances of Ezakiella, Clostridium sensu stricto, Porphyromonas, Barnesiella, Coriobacteriales Incertae Sedis, Synergistiaceae, Echerichia-Shigella, and Turicibacter compared to those with low co-occurring symptoms before CRT (n = 22). Biosynthesis pathways for lipopolysaccharide, L-tryptophan, and colanic acid building blocks were enriched in participants with high co-occurring symptoms. Participants with low co-occurring symptoms showed enriched abundances of Enterococcus and Lachnospiraceae, as well as pathways for β-D-glucoronosides, hexuronide/hexuronate, and nicotinate degradation, methanogenesis, and L-lysine biosynthesis. Conclusion: A number of bacterial taxa and predicted functional pathways were differentially abundant in patients with high co-occurring symptoms compared to those with low co-occurring symptoms before CRT for rectal cancer. 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AHCI)</collection><collection>Web of Science - Social Sciences Citation Index – 2021</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biological research for nursing</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>González-Mercado, Velda J.</au><au>Lim, Jean</au><au>Yu, Gary</au><au>Penedo, Frank</au><au>Pedro, Elsa</au><au>Bernabe, Raul</au><au>Tirado-Gómez, Maribel</au><au>Aouizerat, Bradley</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Co-Occurrence of Symptoms and Gut Microbiota Composition Before Neoadjuvant Chemotherapy and Radiation Therapy for Rectal Cancer: A Proof of Concept</atitle><jtitle>Biological research for nursing</jtitle><stitle>BIOL RES NURS</stitle><addtitle>Biol Res Nurs</addtitle><date>2021-07-01</date><risdate>2021</risdate><volume>23</volume><issue>3</issue><spage>513</spage><epage>523</epage><pages>513-523</pages><artnum>1099800421991656</artnum><issn>1099-8004</issn><eissn>1552-4175</eissn><abstract>Purpose: To examine a) whether there are significant differences in gut microbial diversity and in the abundance of gut microbial taxa; and b) differences in predicted functional pathways of the gut microbiome between those participants with high co-occurring symptoms and those with low co-occurring symptoms, prior to neoadjuvant chemotherapy and radiation therapy (CRT) for rectal cancer. Methods: Rectal cancer patients (n = 41) provided stool samples for 16 S rRNA gene sequencing and symptom ratings for fatigue, sleep disturbance, and depressive symptoms prior to CRT. Descriptive statistics were computed for symptoms. Gut microbiome data were analyzed using QIIME2, LEfSe, and the R statistical package. Results: Participants with high co-occurring symptoms (n = 19) had significantly higher bacterial abundances of Ezakiella, Clostridium sensu stricto, Porphyromonas, Barnesiella, Coriobacteriales Incertae Sedis, Synergistiaceae, Echerichia-Shigella, and Turicibacter compared to those with low co-occurring symptoms before CRT (n = 22). Biosynthesis pathways for lipopolysaccharide, L-tryptophan, and colanic acid building blocks were enriched in participants with high co-occurring symptoms. 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subjects Bacteria
Fatigue
Gastrointestinal Microbiome
Humans
Life Sciences & Biomedicine
Neoadjuvant Therapy
Nursing
Rectal Neoplasms - therapy
Science & Technology
title Co-Occurrence of Symptoms and Gut Microbiota Composition Before Neoadjuvant Chemotherapy and Radiation Therapy for Rectal Cancer: A Proof of Concept
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