Evidence map›Paper›PMID 39133001›Full record

ArticleApplied and environmental microbiology2024

Exploring strain-level diversity in the gut microbiome through mucin particle adhesion.

Keita Nishiyama, Ryuta Murakami, Masaki Nakahata, Binghui Zhou, Nanami Hashikura, Hiroki Kaneko, Fu Namai, Wakako Ikeda-Ohtsubo, Jin-Zhong Xiao, Haruki Kitazawa and 1 more

Abstract read
In one paragraph

Article in Applied and environmental microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Frontiers in microbiology · 2024
    Article
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

11 authors.

Keita NishiyamaGraduate School of Agricultural Science, Tohoku University, Aoba-ku, Sendai, Japan.ORCID 0000-0001-6483-0669
Ryuta MurakamiNext Generation Science Institute, Morinaga Milk Industry Co., Ltd, Zama, Kanagawa, Japan.
Masaki NakahataDepartment of Macromolecular Science, Osaka University, Toyonaka, Osaka, Japan.
Binghui ZhouGraduate School of Agricultural Science, Tohoku University, Aoba-ku, Sendai, Japan.
Nanami HashikuraNext Generation Science Institute, Morinaga Milk Industry Co., Ltd, Zama, Kanagawa, Japan.
Hiroki KanekoNext Generation Science Institute, Morinaga Milk Industry Co., Ltd, Zama, Kanagawa, Japan.
Fu NamaiGraduate School of Agricultural Science, Tohoku University, Aoba-ku, Sendai, Japan.
Wakako Ikeda-OhtsuboGraduate School of Agricultural Science, Tohoku University, Aoba-ku, Sendai, Japan.
Jin-Zhong XiaoNext Generation Science Institute, Morinaga Milk Industry Co., Ltd, Zama, Kanagawa, Japan.
Haruki KitazawaGraduate School of Agricultural Science, Tohoku University, Aoba-ku, Sendai, Japan.
Toshitaka OdamakiNext Generation Science Institute, Morinaga Milk Industry Co., Ltd, Zama, Kanagawa, Japan.ORCID 0000-0001-6019-9240

Funding

IFO 2021MEXT | Japan Society for the Promotion of Science (JSPS) 23H02358MEXT | Japan Society for the Promotion of Science (JSPS) 23K18072MEXT | Japan Society for the Promotion of Science (JSPS) JP19H05719MEXT | Japan Society for the Promotion of Science (JSPS) JP23K04863
6 · The paper itself

Abstract

Mucin glycoproteins are a significant source of carbon for the gut bacteria. Various gut microbial species possess diverse hydrolytic enzymes and catabolic pathways for breaking down mucin glycans, resulting in competition for the limited nutrients within the gut environment. Adherence to mucin glycans represents a crucial strategy used by gut microbes to access nutrient reservoirs. Understanding these properties is pivotal for comprehending the survival mechanisms of bacteria in the gastrointestinal tract. However, characterization of individual strains within the vast array of coexisting bacteria in the microbiome is challenging. To investigate this, we developed mucin-immobilized particles by immobilizing porcine gastric mucin (PGM) onto glass beads chemically modified with boronic acid. These PGM-immobilized particles were then anaerobically cultured with human fecal microbiota, and the bacteria adhering to PGM were isolated. Interestingly, the microbiome composition remained largely unchanged irrespective of PGM immobilization. Nonetheless, bacteria isolated from PGM-immobilized glass particles exhibited notably higher IMPORTANCE: Metabolism of mucin glycans by gut bacteria represents a crucial strategy for accessing nutrient reservoirs. The efficacy of mucin glycan utilization among gut bacteria hinges on the metabolic capabilities of individual strains, necessitating meticulous strain-level characterization. In this investigation, we used glass beads chemically immobilized with mucins to selectively enrich bacteria from fecal fermentation cultures, based on their superior adhesion to and metabolism of mucin glycoproteins. These findings lend support to the hypothesis that the physical interactions between bacteria and mucin glycoprotein components directly correlate with their capacity to utilize mucins as nutrient sources. Furthermore, our study implies that physical proximity may significantly influence bacterial nutrient acquisition within the ecosystem, facilitating gut bacteria's access to carbohydrate components.

Indexed as

BacteriaBacterial AdhesionGastrointestinal MicrobiomeAnimalsFecesGastric MucinsHumansMucinsSwineGastric MucinsMucinsadhesionbacteroidesgut microbiomemetabolismmucinstrain diversity

Identifiers

PMID39133001
PMCPMC11409716

What OpenQuestion holds

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Registered trials

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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.