Evidence map›Paper›PMID 25404032›Full record

ArticleInfection and immunity2015

Pleiotropic effects of cell wall amidase LytA on Streptococcus pneumoniae sensitivity to the host immune response.

Elisa Ramos-Sevillano, Ana Urzainqui, Susana Campuzano, Miriam Moscoso, Fernando González-Camacho, Mirian Domenech, Santiago Rodríguez de Córdoba, Francisco Sánchez-Madrid, Jeremy S Brown, Ernesto García and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 70 citations in OpenAlex.

  1. Trial
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  3. Identification ofJournal of proteome research · 2025
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  7. Novel processes to obtain pneumococcal surface proteins for vaccines.Applied microbiology and biotechnology · 2025
    Review
  8. Review
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  10. Diverse Functions of C4b-Binding Protein in Health and Disease.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Frontiers in cellular and infection microbiology · 2022
    Review
  15. Article
  16. Review
  17. Altered Signal Transduction in the Immune Response to Influenza Virus andInternational journal of molecular sciences · 2021
    Review
  18. Article
  19. A molecular link between cell wall biosynthesis, translation fidelity, and stringent response inProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  20. 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 at 7 institutions in 2 countries.

Elisa Ramos-SevillanoCentro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain CIBER de Enfermedades Respiratorias (CIBERES), Madrid, Spain Spanish Pneumococcal Reference Laboratory, Centro Nacional de Microbiología, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Ana UrzainquiDepartment of Immunology, Hospital Universitario de la Princesa, Instituto Investigación Sanitaria Princesa (IIS-IP), Madrid, Spain.
Susana CampuzanoDepartment of Analytical Chemistry, School of Chemistry, Universidad Complutense de Madrid, Madrid, Spain.
Miriam MoscosoCentro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain CIBER de Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Fernando González-CamachoConfocal Microscopy Facility, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Madrid, Spain.
Mirian DomenechCentro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain CIBER de Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Santiago Rodríguez de CórdobaCentro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain CIBER de Enfermedades Raras (CIBERER), Madrid, Spain.
Francisco Sánchez-MadridDepartment of Immunology, Hospital Universitario de la Princesa, Instituto Investigación Sanitaria Princesa (IIS-IP), Madrid, Spain.
Jeremy S BrownCentre for Inflammation and Tissue Repair, University College London, London, United Kingdom.
Ernesto GarcíaCentro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain CIBER de Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Jose YusteCIBER de Enfermedades Respiratorias (CIBERES), Madrid, Spain Spanish Pneumococcal Reference Laboratory, Centro Nacional de Microbiología, Instituto de Salud Carlos III (ISCIII), Madrid, Spain jyuste@isciii.es.
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESHospital Universitario de La Princesa · ESCentro de Investigaciones Biológicas Margarita Salas · ESInstituto de Investigación de Enfermedades Raras · ESInstituto de Salud Carlos III · ESUniversidad Complutense de Madrid · ESUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complement system is a key component of the host immune response for the recognition and clearance of Streptococcus pneumoniae. In this study, we demonstrate that the amidase LytA, the main pneumococcal autolysin, inhibits complement-mediated immunity independently of effects on pneumolysin by a complex process of impaired complement activation, increased binding of complement regulators, and direct degradation of complement C3. The use of human sera depleted of either C1q or factor B confirmed that LytA prevented activation of both the classical and alternative pathways, whereas pneumolysin inhibited only the classical pathway. LytA prevented binding of C1q and the acute-phase protein C-reactive protein to S. pneumoniae, thereby reducing activation of the classical pathway on the bacterial surface. In addition, LytA increased recruitment of the complement downregulators C4BP and factor H to the pneumococcal cell wall and directly cleaved C3b and iC3b to generate degradation products. As a consequence, C3b deposition and phagocytosis increased in the absence of LytA and were markedly enhanced for the lytA ply double mutant, confirming that a combination of LytA and Ply is essential for the establishment of pneumococcal pneumonia and sepsis in a murine model of infection. These data demonstrate that LytA has pleiotropic effects on complement activation, a finding which, in combination with the effects of pneumolysin on complement to assist with pneumococcal complement evasion, confirms a major role of both proteins for the full virulence of the microorganism during septicemia.

Indexed as

AnimalsBacterial CapsulesBacterial ProteinsCell WallComplement ActivationComplement C3Complement Factor HHistocompatibility AntigensHost-Pathogen InteractionsMiceMice, Inbred C57BLN-Acetylmuramoyl-L-alanine AmidasePhagocytosisPhosphorylcholinePneumococcal InfectionsPolysaccharides, BacterialBacterial ProteinsC4bp protein, mouseComplement C3Complement Factor HHistocompatibility AntigensN-Acetylmuramoyl-L-alanine AmidasePhosphorylcholineplY protein, Streptococcus pneumoniaePolysaccharides, BacterialSpsA protein, Streptococcus pneumoniaeStreptolysins

Identifiers

PMID25404032
PMCPMC4294232
OpenAlexW1994924549

What OpenQuestion holds

Textmetadata
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.