Evidence map›Paper›PMID 40369709›Full record

ReviewAnnals of the New York Academy of Sciences2025

Mechanisms governing bacterial capsular polysaccharide attachment and chain length.

Saroj Khadka, Emily L Kinney, Brooke E Ryan, Laura A Mike

Abstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Connections betweenInfection and immunity · 2026
    Article
  10. Article
  11. Article
  12. Review
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

4 authors.

Saroj KhadkaDepartment of Medicine/Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Emily L KinneyDepartment of Medicine/Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Brooke E RyanDepartment of Medical Microbiology and Immunology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio, USA.
Laura A MikeDepartment of Medicine/Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-3368-4184

Funding

UC San Diego RAPID Faculty Development Program in Infectious DiseasesR25AI147376 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ADRIANA H TREMOULET, Joann Trejo · 2020 to 2026
$2.5M
Control of Klebsiella capsule biosynthesis and attachmentR35GM150588 · NIGMS · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI Laura Anzaldi Mike · 2023 to 2026
$1.6M
American Heart Association 23CDA1056712American Heart Association 24PRE1197026American Heart Association-American Stroke Association 23CDA1056712American Heart Association-American Stroke Association 24PRE1197026NIAID NIH HHS R25 AI147376NIGMS NIH HHS R35 GM150588NIH HHS R35 GM150588
6 · The paper itself

Abstract

Capsular polysaccharides (CPSs) are high-molecular weight glycopolymers that form a capsule layer on the surface of many bacterial species. This layer serves as a crucial barrier between bacteria and their environment, protecting them from host immune responses and environmental stressors while facilitating adaptation to host niches. The capsule also affects other critical virulence factors of plant and human pathogens such as biofilm production and exchange of antimicrobial-resistance genes. Bacterial pathogens modulate several CPS properties including abundance, chain length, and cell surface retainment to optimize niche-specific fitness. CPS composition varies greatly among bacterial species due to differences in sugar units comprising the polymer. Despite the diversity in composition, three conserved CPS biosynthetic systems are common across bacterial species. Although less explored than CPS polymerization and export, the processes of chain length control and attachment are also broadly conserved among bacterial species. Here, we discuss the common strategies that bacteria use to retain CPS to their cell surface and the mechanisms by which bacteria define and control CPS chain length. Additionally, we highlight the outstanding questions related to these processes, identifying areas where future research is needed to gain better insights into these crucial CPS systems.

Indexed as

BacteriaBacterial CapsulesPolysaccharides, BacterialBiofilmsHumansPolysaccharides, Bacterialbacterial glycansbacterial virulencecapsular polysaccharidecapsuleCPSEPSextracellular polysaccharide

Identifiers

PMID40369709
PMCPMC12220298

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Registered trials

None linked

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.