{
  "abstract": "Streptococcus pneumoniae is a leading human respiratory pathogen, yet its success depends not on disease but on its ability to persist as an asymptomatic colonizer of the nasopharynx. The nasopharyngeal mucosa is lined with mucus, whose heavily O-glycosylated mucin proteins are the most abundant macromolecules in the pneumococcal natural niche. While mucus is canonically viewed as a host defense barrier, we found that mucin actively reprograms pneumococcal physiology to promote colonization through two distinct mechanisms. First, mucin suppresses pneumococcal autolysis by specifically inhibiting the enzymatic activity of the major autolysin LytA, prolonging bacterial survival and restricting release of the cholesterol-dependent cytotoxin pneumolysin, thereby reducing host cell damage. Second, mucin induces de novo biosynthesis and extracellular release of tryptophan, an essential amino acid that humans cannot synthesize and that serves as a substrate for host immunomodulatory pathways. Tryptophan biosynthesis was critical for pneumococcal survival against macrophage killing, and its disruption abolished both colonization and invasive disease. Transcriptomic analysis revealed that tryptophan biosynthesis enables the pneumococcus to survive a bactericidal macrophage state while preventing macrophage transition to proliferative tissue repair. Together, these findings reveal that mucin is not merely a barrier but an active signal that reprograms the pneumococcus toward a persistent, host-tolerant state, identifying a distinctive repertoire of colonization mechanisms that allow a virulent respiratory pathogen to sustain long-term asymptomatic carriage in its human reservoir.",
  "abstract_shown": true,
  "affiliations": [
    "St Jude Children's Research Hospital"
  ],
  "article_type": "New results",
  "arxiv": null,
  "author_total": 12,
  "authors": [
    {
      "name": "C. N. Johnson"
    },
    {
      "affs": [
        0
      ],
      "name": "J. Rosch"
    },
    {
      "name": "M. W. Frank"
    },
    {
      "name": "Y. Laguna-Terai"
    },
    {
      "name": "W. MacCain"
    },
    {
      "name": "T. S. Simmons"
    },
    {
      "name": "S. Zamakhaeva"
    },
    {
      "name": "N. Korotkova"
    },
    {
      "name": "C. Aherne"
    },
    {
      "name": "E. Tuomanen"
    },
    {
      "name": "C. Evans"
    },
    {
      "name": "K. Ribbeck"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/1jv2pxp3snt8x.bib",
  "cited_by": 0,
  "doi": "10.64898/2026.11.06.764952",
  "fulltext_url": "https://www.biorxiv.org/content/10.64898/2026.11.06.764952v1.full",
  "id": "1jv2pxp3snt8x",
  "issns": [],
  "landing_url": "https://www.biorxiv.org/content/10.64898/2026.11.06.764952v1",
  "language": null,
  "licence": "CC-BY-NC-ND",
  "licence_label": "CC BY-NC-ND",
  "licence_source": "article",
  "licence_url": "https://creativecommons.org/licenses/by-nc-nd/4.0/",
  "metadata_licence": null,
  "native_subjects": [
    [
      "biorxiv",
      "microbiology"
    ]
  ],
  "openalex": null,
  "pdf_url": "https://www.biorxiv.org/content/10.64898/2026.11.06.764952v1.full.pdf",
  "pmcid": null,
  "pmid": null,
  "published": "2026-11-06",
  "publisher": null,
  "ris": "https://research.draconitic.com/paper/1jv2pxp3snt8x.ris",
  "sources": [
    {
      "first_seen": "2026-11-10T00:30:16Z",
      "native_id": "10.64898/2026.11.06.764952",
      "source": "biorxiv",
      "url": "https://www.biorxiv.org/content/10.64898/2026.11.06.764952v1"
    }
  ],
  "subjects": [
    {
      "field": "biology",
      "origin": "biorxiv:microbiology",
      "subfield": "microbiology"
    }
  ],
  "title": "Mucin promotes pneumococcal colonization via autolysis suppression and tryptophan-mediated immune modulation",
  "title_text": "Mucin promotes pneumococcal colonization via autolysis suppression and tryptophan-mediated immune modulation",
  "type": "preprint",
  "updated_at": "2026-11-10T00:30:16Z",
  "url": "https://research.draconitic.com/paper/1jv2pxp3snt8x",
  "venue": "bioRxiv",
  "versions": []
}