Evidence map›Paper›PMID 25892864›Full record

ArticleWorld journal of gastroenterology2015

Changes in the colon microbiota and intestinal cytokine gene expression following minimal intestinal surgery.

Susan Lapthorne, Julie E Bines, Fiona Fouhy, Nicole L Dellios, Guineva Wilson, Sarah L Thomas, Michelle Scurr, Catherine Stanton, Paul D Cotter, Prue M Pereira-Fantini

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 37 citations in OpenAlex.

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  19. The role of the microbiota in surgical recovery.Current opinion in clinical nutrition and metabolic care · 2016
    Article
  20. The intestinal microbiome and surgical disease.Current problems in surgery · 2016
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Susan LapthorneSusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Julie E BinesSusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Fiona FouhySusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Nicole L DelliosSusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Guineva WilsonSusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Sarah L ThomasSusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Michelle ScurrSusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Catherine StantonSusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Paul D CotterSusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Prue M Pereira-FantiniSusan Lapthorne, Nicole L Dellios, Sarah L Thomas, Michelle Scurr, Prue M Pereira-Fantini, Intestinal Failure and Clinical Nutrition group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Royal Children's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the impact of minor abdominal surgery on the caecal microbial population and on markers of gut inflammation.

methodsFour week old piglets were randomly allocated to a no-surgery "control" group (n = 6) or a "transection surgery" group (n = 5). During the transection surgery procedure, a conventional midline incision of the lower abdominal wall was made and the small intestine was transected at a site 225 cm proximal to the ileocaecal valve, a 2 cm segment was removed and the intestine was re-anastomosed. Piglets received a polymeric infant formula diet throughout the study period and were sacrificed at two weeks post-surgery. Clinical outcomes including weight, stool consistency and presence of stool fat globules were monitored. High throughput DNA sequencing of colonic content was used to detect surgery-related disturbances in microbial composition at phylum, family and genus level. Diversity and richness estimates were calculated for the control and minor surgery groups. As disturbances in the gut microbial community are linked to inflammation we compared the gene expression of key inflammatory cytokines (TNF, IL1B, IL18, IL12, IL8, IL6 and IL10) in ileum, terminal ileum and colon mucosal extracts obtained from control and abdominal surgery groups at two weeks post-surgery.

resultsChanges in the relative abundance of bacterial species at family and genus level were confined to bacterial members of the Proteobacteria and Bacteroidetes phyla. Family level compositional shifts included a reduction in the relative abundance of Enterobacteriaceae (22.95 ± 5.27 vs 2.07 ± 0.72, P < 0.01), Bacteroidaceae (2.54 ± 0.56 vs 0.86 ± 0.43, P < 0.05) and Rhodospirillaceae (0.40 ± 0.14 vs 0.00 ± 0.00, P < 0.05) following transection surgery. Similarly, at the genus level, changes associated with transection surgery were restricted to members of the Proteobacteria and Bacteroidetes phyla and included decreased relative abundance of Enterobacteriaceae (29.20 ± 6.74 vs 2.88 ± 1.08, P < 0.01), Alistipes (4.82 ± 1.73 vs 0.18 ± 0.13, P < 0.05) and Thalassospira (0.53 ± 0.19 vs 0.00 ± 0.00, P < 0.05). Surgery-associated microbial dysbiosis was accompanied by increased gene expression of markers of inflammation. Within the ileum IL6 expression was decreased (4.46 ± 1.60 vs 0.24 ± 0.06, P < 0.05) following transection surgery. In the terminal ileum, gene expression of TNF was decreased (1.51 ± 0.13 vs 0.80 ± 0.16, P < 0.01) and IL18 (1.21 ± 0.18 vs 2.13 ± 0.24, P < 0.01), IL12 (1.04 ± 0.16 vs 1.82 ± 0.32, P < 0.05) and IL10 (1.04 ± 0.06 vs 1.43 ± 0.09, P < 0.01) gene expression increased following transection surgery. Within the colon, IL12 (0.72 ± 0.13 vs 1.78 ± 0.28, P < 0.01) and IL10 (0.98 ± 0.02 vs 1.95 ± 0.14, P < 0.01) gene expression were increased following transection surgery.

conclusionThis study suggests that minor abdominal surgery in infants, results in long-term alteration of the colonic microbial composition and persistent gastrointestinal inflammation.

Indexed as

ColonInflammation MediatorsMicrobiotaAnimalsAnimals, NewbornBacteriaColitisCytokinesDigestive System Surgical ProceduresDysbiosisFemaleGene Expression RegulationHigh-Throughput Nucleotide SequencingIleitisIleumSwineCytokinesInflammation MediatorsBacteriaDysbiosisInfantInflammationIntestinalMicrobiotaPediatricSurgeryTransection

Identifiers

PMID25892864
PMCPMC4394075
OpenAlexW2332909709

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.