Evidence map›Paper›PMID 22069491›Full record

ArticlePloS one2011

Pseudomonas aeruginosa elastase provides an escape from phagocytosis by degrading the pulmonary surfactant protein-A.

Zhizhou Kuang, Yonghua Hao, Brent E Walling, Jayme L Jeffries, Dennis E Ohman, Gee W Lau

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 142 citations in OpenAlex.

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  13. Chemical Optimization of SelectiveACS infectious diseases · 2023
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  17. Frontiers in microbiology · 2022
    Review
  18. Article
  19. Adsorption of extracellular proteases and pyocyanin produced byCurrent research in microbial sciences · 2022
    Article
  20. Article

13 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Zhizhou KuangDepartment of Pathobiology, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.
Yonghua Hao
Brent E Walling
Jayme L Jeffries
Dennis E Ohman
Gee W Lau
University of Illinois Urbana-Champaign · USVirginia Commonwealth University · US

Funding

Mechanisms of Pseudomonas Resistance to Membrane Permeabilization by SP-AR01HL090699 · NHLBI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI LAU, GEE W · 2009 to 2012
$1.6M
UIUC COLLEGE VET MED COMPLETION SHELL SPACEC06RR016515 · NCRR · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI WHITELEY, HERBERT E · 2001 to 2001
$1.5M
NCRR NIH HHS C06 RR016515NCRR NIH HHS C06 RR 16515-01NHLBI NIH HHS HL090699NHLBI NIH HHS R01 HL090699
6 · The paper itself

Abstract

Pseudomonas aeruginosa is an opportunistic pathogen that causes both acute pneumonitis in immunocompromised patients and chronic lung infections in individuals with cystic fibrosis and other bronchiectasis. Over 75% of clinical isolates of P. aeruginosa secrete elastase B (LasB), an elastolytic metalloproteinase that is encoded by the lasB gene. Previously, in vitro studies have demonstrated that LasB degrades a number of components in both the innate and adaptive immune systems. These include surfactant proteins, antibacterial peptides, cytokines, chemokines and immunoglobulins. However, the contribution of LasB to lung infection by P. aeruginosa and to inactivation of pulmonary innate immunity in vivo needs more clarification. In this study, we examined the mechanisms underlying enhanced clearance of the ΔlasB mutant in mouse lungs. The ΔlasB mutant was attenuated in virulence when compared to the wild-type strain PAO1 during lung infection in SP-A+/+ mice. However, the ΔlasB mutant was as virulent as PAO1 in the lungs of SP-A⁻/⁻ mice. Detailed analysis showed that the ΔlasB mutant was more susceptible to SP-A-mediated opsonization but not membrane permeabilization. In vitro and in vivo phagocytosis experiments revealed that SP-A augmented the phagocytosis of ΔlasB mutant bacteria more efficiently than the isogenic wild-type PAO1. The ΔlasB mutant was found to have a severely reduced ability to degrade SP-A, consequently making it unable to evade opsonization by the collectin during phagocytosis. These results suggest that P. aeruginosa LasB protects against SP-A-mediated opsonization by degrading the collectin.

Indexed as

AnimalsBacterial ProteinsBlotting, WesternCell Membrane PermeabilityEnzyme-Linked Immunosorbent AssayFlow CytometryHumansLungMacrophagesMetalloendopeptidasesMiceMice, Inbred C3HMice, KnockoutMutationOpsonin ProteinsPhagocytosisBacterial ProteinsMetalloendopeptidasesOpsonin Proteinspseudolysin, Pseudomonas aeruginosaPulmonary Surfactant-Associated Protein A

Identifiers

PMID22069491
PMCPMC3206073
OpenAlexW2094417413

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.