Blake E. Sanders, Ariana Umaña, Tam T.D. Nguyen, Kevin J. Williams, Christopher C. Yoo, Michael A. Casasanta, Bryce Wozniak, Daniel J. Slade
{"title":"IV型菌毛促进有核梭杆菌的自然能力。","authors":"Blake E. Sanders, Ariana Umaña, Tam T.D. Nguyen, Kevin J. Williams, Christopher C. Yoo, Michael A. Casasanta, Bryce Wozniak, Daniel J. Slade","doi":"10.1016/j.anaerobe.2023.102760","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><p>Many bacterial species naturally take up DNA from their surroundings and recombine it into their chromosome through homologous gene transfer (HGT) to aid in survival and gain advantageous functions. Herein we present the first characterization of Type IV pili facilitated natural competence in <em>Fusobacterium nucleatum</em>, which is a Gram-negative, anaerobic bacterium that participates in a range of infections and diseases including periodontitis, preterm birth, and cancer<em>.</em></p></div><div><h3>Methods</h3><p>Here we used bioinformatics on multiple <em>Fusobacterium</em> species, as well as molecular genetics to characterize natural competence in strain <em>F. nucleatum</em> subsp. <em>nucleatum ATCC 23726.</em></p></div><div><h3>Results</h3><p>We bioinformatically identified components of the Type IV conjugal pilus machinery and show this is a conserved system within the <em>Fusobacterium</em> genus. We next validate Type IV pili in natural competence in <em>F. nucleatum</em> ATCC 23726 and show that gene deletions in key components of pilus deployment (<em>pilQ)</em> and cytoplasmic DNA import (<em>comEC)</em> abolish DNA uptake and chromosomal incorporation. We next show that natural competence may require native <em>F. nucleatum</em> DNA methylation to bypass restriction modification systems and allow subsequent genomic homologous recombination.</p></div><div><h3>Conclusions</h3><p>In summary, this proof of principle study provides the first characterization of natural competence in <em>Fusobacterium nucleatum</em> and highlights the potential to exploit this DNA import mechanism as a genetic tool to characterize virulence mechanisms of an opportunistic oral pathogen.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Type IV pili facilitated natural competence in Fusobacterium nucleatum\",\"authors\":\"Blake E. Sanders, Ariana Umaña, Tam T.D. Nguyen, Kevin J. Williams, Christopher C. Yoo, Michael A. Casasanta, Bryce Wozniak, Daniel J. Slade\",\"doi\":\"10.1016/j.anaerobe.2023.102760\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objectives</h3><p>Many bacterial species naturally take up DNA from their surroundings and recombine it into their chromosome through homologous gene transfer (HGT) to aid in survival and gain advantageous functions. Herein we present the first characterization of Type IV pili facilitated natural competence in <em>Fusobacterium nucleatum</em>, which is a Gram-negative, anaerobic bacterium that participates in a range of infections and diseases including periodontitis, preterm birth, and cancer<em>.</em></p></div><div><h3>Methods</h3><p>Here we used bioinformatics on multiple <em>Fusobacterium</em> species, as well as molecular genetics to characterize natural competence in strain <em>F. nucleatum</em> subsp. <em>nucleatum ATCC 23726.</em></p></div><div><h3>Results</h3><p>We bioinformatically identified components of the Type IV conjugal pilus machinery and show this is a conserved system within the <em>Fusobacterium</em> genus. We next validate Type IV pili in natural competence in <em>F. nucleatum</em> ATCC 23726 and show that gene deletions in key components of pilus deployment (<em>pilQ)</em> and cytoplasmic DNA import (<em>comEC)</em> abolish DNA uptake and chromosomal incorporation. We next show that natural competence may require native <em>F. nucleatum</em> DNA methylation to bypass restriction modification systems and allow subsequent genomic homologous recombination.</p></div><div><h3>Conclusions</h3><p>In summary, this proof of principle study provides the first characterization of natural competence in <em>Fusobacterium nucleatum</em> and highlights the potential to exploit this DNA import mechanism as a genetic tool to characterize virulence mechanisms of an opportunistic oral pathogen.</p></div>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2023-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1075996423000690\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1075996423000690","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Type IV pili facilitated natural competence in Fusobacterium nucleatum
Objectives
Many bacterial species naturally take up DNA from their surroundings and recombine it into their chromosome through homologous gene transfer (HGT) to aid in survival and gain advantageous functions. Herein we present the first characterization of Type IV pili facilitated natural competence in Fusobacterium nucleatum, which is a Gram-negative, anaerobic bacterium that participates in a range of infections and diseases including periodontitis, preterm birth, and cancer.
Methods
Here we used bioinformatics on multiple Fusobacterium species, as well as molecular genetics to characterize natural competence in strain F. nucleatum subsp. nucleatum ATCC 23726.
Results
We bioinformatically identified components of the Type IV conjugal pilus machinery and show this is a conserved system within the Fusobacterium genus. We next validate Type IV pili in natural competence in F. nucleatum ATCC 23726 and show that gene deletions in key components of pilus deployment (pilQ) and cytoplasmic DNA import (comEC) abolish DNA uptake and chromosomal incorporation. We next show that natural competence may require native F. nucleatum DNA methylation to bypass restriction modification systems and allow subsequent genomic homologous recombination.
Conclusions
In summary, this proof of principle study provides the first characterization of natural competence in Fusobacterium nucleatum and highlights the potential to exploit this DNA import mechanism as a genetic tool to characterize virulence mechanisms of an opportunistic oral pathogen.