Saccharibacteria (TM7) in the Human Oral Microbiome

被引:123
作者
Bor, B. [1 ,2 ]
Bedree, J. K. [1 ,3 ]
Shi, W. [1 ]
McLean, J. S. [4 ]
He, X. [1 ]
机构
[1] Forsyth Inst, 245 First St, Cambridge, MA 02142 USA
[2] Harvard Sch Dent Med, Dept Oral Med Infect & Immun, Boston, MA USA
[3] Univ Calif Los Angeles, Sch Dent, Sect Oral Biol, Div Oral Biol & Med, Los Angeles, CA 90024 USA
[4] Univ Washington, Dept Periodont, 1959 NE Pacific St, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
candidate phyla radiation; ultra-small bacteria; interspecies interaction; epiparasite; symbiont; periodontitis; AGGRESSIVE PERIODONTITIS; DIVISION TM7; DIVERSITY; BACTERIA; GENOME; CULTURE; CULTIVATION; BIOFILMS; HEALTH; TREE;
D O I
10.1177/0022034519831671
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Bacteria from the Saccharibacteria phylum (formerly known as TM7) are ubiquitous members of the human oral microbiome and are part of the Candidate Phyla Radiation. Recent studies have revealed remarkable 16S rRNA diversity in environmental and mammalian host-associated members across this phylum, and their association with oral mucosal infectious diseases has been reported. However, due to their recalcitrance to conventional cultivation, TM7's physiology, lifestyle, and role in health and diseases remain elusive. The recent cultivation and characterization of Nanosynbacter lyticus type strain TM7x (HMT_952)-the first Saccharibacteria strain coisolated as an ultrasmall obligate parasite with its bacterial host from the human oral cavity-provide a rare glimpse into the novel symbiotic lifestyle of these enigmatic human-associated bacteria. TM7x is unique among all bacteria: it has an ultrasmall size and lives on the surface of its host bacterium. With a highly reduced genome, it lacks the ability to synthesize any of its own amino acids, vitamins, or cell wall precursors and must parasitize other oral bacteria. TM7x displays a highly dynamic interaction with its bacterial hosts, as reflected by the reciprocal morphologic and physiologic changes in both partners. Furthermore, depending on environmental conditions, TM7x can exhibit virulent killing of its host bacterium. Thus, Saccharibacteria potentially affect oral microbial ecology by modulating the oral microbiome structure hierarchy and functionality through affecting the bacterial host's physiology, inhibiting the host's growth dynamics, or affecting the relative abundance of the host via direct killing. At this time, several other uncharacterized members of this phylum have been detected in various human body sites at high prevalence. In the oral cavity alone, at least 6 distinct groups vary widely in relative abundance across anatomic sites. Here, we review the current knowledge on the diversity and unique biology of this recently uncovered group of ultrasmall bacteria.
引用
收藏
页码:500 / 509
页数:10
相关论文
共 85 条
  • [21] Unusual respiratory capacity and nitrogen metabolism in a Parcubacterium (OD1) of the Candidate Phyla Radiation
    Castelle, Cindy J.
    Brown, Christopher T.
    Thomas, Brian C.
    Williams, Kenneth H.
    Banfield, Jillian F.
    [J]. SCIENTIFIC REPORTS, 2017, 7
  • [22] The Human Oral Microbiome Database: a web accessible resource for investigating oral microbe taxonomic and genomic information
    Chen, Tsute
    Yu, Wen-Han
    Izard, Jacques
    Baranova, Oxana V.
    Lakshmanan, Abirami
    Dewhirst, Floyd E.
    [J]. DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION, 2010, : baq013
  • [23] The oral microbiome and the immunobiology of periodontal disease and caries
    Costalonga, Massimo
    Herzberg, Mark C.
    [J]. IMMUNOLOGY LETTERS, 2014, 162 (02) : 22 - 38
  • [24] Members of the Candidate Phyla Radiation are functionally differentiated by carbon- and nitrogen-cycling capabilities
    Danczak, R. E.
    Johnston, M. D.
    Kenah, C.
    Slattery, M.
    Wrighton, K. C.
    Wilkins, M. J.
    [J]. MICROBIOME, 2017, 5 : 112
  • [25] The Canine Oral Microbiome
    Dewhirst, Floyd E.
    Klein, Erin A.
    Thompson, Emily C.
    Blanton, Jessica M.
    Chen, Tsute
    Milella, Lisa
    Buckley, Catherine M. F.
    Davis, Ian J.
    Bennett, Marie-Lousie
    Marshall-Jones, Zoe V.
    [J]. PLOS ONE, 2012, 7 (04):
  • [26] The Human Oral Microbiome
    Dewhirst, Floyd E.
    Chen, Tuste
    Izard, Jacques
    Paster, Bruce J.
    Tanner, Anne C. R.
    Yu, Wen-Han
    Lakshmanan, Abirami
    Wade, William G.
    [J]. JOURNAL OF BACTERIOLOGY, 2010, 192 (19) : 5002 - 5017
  • [27] In Search of an Uncultured Human-Associated TM7 Bacterium in the Environment
    Dinis, Jorge M.
    Barton, David E.
    Ghadiri, Jamsheed
    Surendar, Deepa
    Reddy, Kavitha
    Velasquez, Fernando
    Chaffee, Carol L.
    Lee, Mei-Chong Wendy
    Gavrilova, Helen
    Ozuna, Hazel
    Smits, Samuel A.
    Ouverney, Cleber C.
    [J]. PLOS ONE, 2011, 6 (06):
  • [28] Biofilm Formation Avoids Complement Immunity and Phagocytosis of Streptococcus pneumoniae
    Domenech, Mirian
    Ramos-Sevillano, Elisa
    Garica, Ernesto
    Moscoso, Miriam
    Yuste, Jose
    [J]. INFECTION AND IMMUNITY, 2013, 81 (07) : 2606 - 2615
  • [29] Biofilms: Survival mechanisms of clinically relevant microorganisms
    Donlan, RM
    Costerton, JW
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (02) : 167 - +
  • [30] Novel Microbial Diversity and Functional Potential in the Marine Mammal Oral Microbiome
    Dudek, Natasha K.
    Sun, Christine L.
    Burstein, David
    Kantor, Rose S.
    Goltsman, Daniela S. Aliaga
    Bik, Elisabeth M.
    Thomas, Brian C.
    Banfield, Jillian F.
    Relman, David A.
    [J]. CURRENT BIOLOGY, 2017, 27 (24) : 3752 - +