{"title":"<i>Aggregatibacter actinomycetemcomitans</i> NadN contributes to neutrophil extracellular trap degradation.","authors":"Yaowapa Puanglai, Anongnard Kasorn, Oranart Matangkasombut, Dujduan Waraho-Zhmayev, Soraya Chaturongakul, Fabien Loison","doi":"10.1080/20002297.2026.2694756","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Neutrophils Extracellular Traps (NET) immobilize and kill extracellular pathogens. <i>Aggregatibacter actinomycetemcomitans (Aa)</i>, associated with aggressive forms of periodontitis, has been shown to induce NET release. However, it remains unknown whether <i>Aa</i> evades extracellular traps.</p><p><strong>Materials and methods: </strong>NETs were incubated with wild-type <i>Aa</i> (<i>Aa</i>-WT, strain Y4) or <i>Aa</i>-ΔCdtB, lacking a toxin inducing DNA breaks. NET degradation was measured by imaging and fluorometry. <i>Aa</i> survival and growth was measured by biofilm formation. <i>Aa</i>-WT membrane was fractionated on a sucrose gradient, and fractions positive for NET degradation were subjected to LC-MS/MS. The top protein candidate was expressed as a recombinant protein in <i>Lactococcus lactis</i> to confirm its NET-degrading activity.</p><p><strong>Results: </strong><i>Aa</i>-WT and <i>Aa</i>-ΔCdtB strains were captured by NETs but degraded the extracellular traps after three hours. <i>Aa</i> survival in the presence of NETs was independent of CdtB expression. NET degrading activity was not release but associated with cells. NAD nucleotidase (NadN) was identified via mass spectrometry from membrane fraction. <i>In vitro</i>, recombinant NadN degraded NETs, and heterologous expression of NadN in <i>L. lactis</i> was sufficient to confer a NET-degrading phenotype.</p><p><strong>Conclusions: </strong><i>Aa</i> degrades NETs to evade host immunity. NadN is a primary mediator of the NET-degrading activity of <i>Aggregatibacter actinomycetemcomitans.</i></p>","PeriodicalId":16598,"journal":{"name":"Journal of Oral Microbiology","volume":"18 1","pages":"2694756"},"PeriodicalIF":6.7000,"publicationDate":"2026-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13347837/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Oral Microbiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/20002297.2026.2694756","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Neutrophils Extracellular Traps (NET) immobilize and kill extracellular pathogens. Aggregatibacter actinomycetemcomitans (Aa), associated with aggressive forms of periodontitis, has been shown to induce NET release. However, it remains unknown whether Aa evades extracellular traps.
Materials and methods: NETs were incubated with wild-type Aa (Aa-WT, strain Y4) or Aa-ΔCdtB, lacking a toxin inducing DNA breaks. NET degradation was measured by imaging and fluorometry. Aa survival and growth was measured by biofilm formation. Aa-WT membrane was fractionated on a sucrose gradient, and fractions positive for NET degradation were subjected to LC-MS/MS. The top protein candidate was expressed as a recombinant protein in Lactococcus lactis to confirm its NET-degrading activity.
Results: Aa-WT and Aa-ΔCdtB strains were captured by NETs but degraded the extracellular traps after three hours. Aa survival in the presence of NETs was independent of CdtB expression. NET degrading activity was not release but associated with cells. NAD nucleotidase (NadN) was identified via mass spectrometry from membrane fraction. In vitro, recombinant NadN degraded NETs, and heterologous expression of NadN in L. lactis was sufficient to confer a NET-degrading phenotype.
Conclusions: Aa degrades NETs to evade host immunity. NadN is a primary mediator of the NET-degrading activity of Aggregatibacter actinomycetemcomitans.
期刊介绍:
As the first Open Access journal in its field, the Journal of Oral Microbiology aims to be an influential source of knowledge on the aetiological agents behind oral infectious diseases. The journal is an international forum for original research on all aspects of ''oral health''. Articles which seek to understand ''oral health'' through exploration of the pathogenesis, virulence, host-parasite interactions, and immunology of oral infections are of particular interest. However, the journal also welcomes work that addresses the global agenda of oral infectious diseases and articles that present new strategies for treatment and prevention or improvements to existing strategies.
Topics: ''oral health'', microbiome, genomics, host-pathogen interactions, oral infections, aetiologic agents, pathogenesis, molecular microbiology systemic diseases, ecology/environmental microbiology, treatment, diagnostics, epidemiology, basic oral microbiology, and taxonomy/systematics.
Article types: original articles, notes, review articles, mini-reviews and commentaries