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      Streptococcus endopeptidases promote HPV infection in vitro

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          Abstract

          Both cervical and throat cancers are associated with human papillomavirus ( HPV). HPV infection requires cleavage of the minor capsid protein L2 by furin. While furin is present in the vaginal epithelium, it is absent in oral epithelial basal cells where HPV infection occurs. The objective of this study was to investigate whether common oral bacteria express furin‐like peptidases. By screening strains representing 12 oral Streptococcus and Enterococcus species, we identified that eight Streptococcus strains displayed high levels of furin‐like peptidase activity, with S. gordonii V2016 the highest. We constructed null mutations for 14 genes encoding putative endopeptidases in S. gordonii V2016. Results showed that three endopeptidases, PepO, PulO, and SepM, had furin‐like activities. All three mutants showed decreased natural transformation by chromosomal DNA, while the pepO mutant also showed reduced transformation by plasmid DNA, indicating involvement of these endopeptidases in competence development. The purified S. gordonii PepO protein promoted infection of epithelial 293 TT cells in vitro by HPV16 pseudovirus. In conclusion, oral bacteria might promote HPV infection and contribute to HPV tissue tropism and subsequent carcinogenesis in the oral cavity and throat by providing furin‐like endopeptidases.

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          Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectors

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            Changes in Abundance of Oral Microbiota Associated with Oral Cancer

            Individual bacteria and shifts in the composition of the microbiome have been associated with human diseases including cancer. To investigate changes in the microbiome associated with oral cancers, we profiled cancers and anatomically matched contralateral normal tissue from the same patient by sequencing 16S rDNA hypervariable region amplicons. In cancer samples from both a discovery and a subsequent confirmation cohort, abundance of Firmicutes (especially Streptococcus) and Actinobacteria (especially Rothia) was significantly decreased relative to contralateral normal samples from the same patient. Significant decreases in abundance of these phyla were observed for pre-cancers, but not when comparing samples from contralateral sites (tongue and floor of mouth) from healthy individuals. Weighted UniFrac principal coordinates analysis based on 12 taxa separated most cancers from other samples with greatest separation of node positive cases. These studies begin to develop a framework for exploiting the oral microbiome for monitoring oral cancer development, progression and recurrence.
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              Tongue and tonsil carcinoma: increasing trends in the U.S. population ages 20-44 years.

              An increasing incidence of oral carcinoma among young adults has been reported in the U.S. and Europe. Although the association between human papillomavirus infection and tonsillar carcinoma is now well established, to the authors' knowledge little is known about incidence trends in tonsillar carcinoma among younger adults. The objective of the current study was to explore the trends in both oral cavity and pharyngeal squamous cell carcinoma (SCC) in younger U.S. populations, in particular tongue and tonsillar SCC. Using the 1973-2001 Surveillance, Epidemiology and End Results (SEER) database, we computed age, race, and site-specific trends of oral and pharyngeal (excluding nasopharynx) carcinoma incidence rates. The percent change (PC) and annual percent change (APC) were computed to explore trends in incidence rates over time. There were 2262 SCC of the oral cavity and 1251 SCC of the pharynx reported to the SEER program from 1973 to 2001 in adults aged 20-44 years. There was a statistically significant increase in the incidence of oral tongue SCC (APC = +2.1; P < 0.001), base of tongue SCC (APC = +1.7; P = 0.04), and palatine tonsil SCC (APC = +3.9; P < 0.001) among younger white individuals, whereas the incidence of SCC in all other oral and pharyngeal sites decreased or remained constant. The increase in tonsil SCC incidence from 1973 to 2001 paralleled the increase in tongue SCC, whereas SCC in all other oral and pharyngeal sites remained constant or decreased. This may suggest similar etiologic factors for SCC affecting the palatine tonsils and tongue in younger populations. (c) 2005 American Cancer Society.
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                Author and article information

                Contributors
                ltao@uic.edu
                Journal
                Microbiologyopen
                Microbiologyopen
                10.1002/(ISSN)2045-8827
                MBO3
                MicrobiologyOpen
                John Wiley and Sons Inc. (Hoboken )
                2045-8827
                19 April 2018
                January 2019
                : 8
                : 1 ( doiID: 10.1002/mbo3.2019.8.issue-1 )
                : e00628
                Affiliations
                [ 1 ] Department of Oral Biology College of Dentistry University of Illinois at Chicago Chicago IL USA
                [ 2 ] Department of Microbiology and Immunology College of Medicine University of Illinois at Chicago Chicago IL USA
                [ 3 ] Department of Medicinal Chemistry and Pharmacognosy Center for Biomolecular Sciences College of Pharmacy University of Illinois at Chicago Chicago IL USA
                [ 4 ] Department of Oral Medicine and Diagnostic Sciences College of Dentistry University of Illinois at Chicago Chicago IL USA
                Author notes
                [*] [* ] Correspondence

                Lin Tao,

                Department of Oral Biology, College of Dentistry, University of Illinois at Chicago, Chicago, IL, USA.

                Email: ltao@ 123456uic.edu

                Author information
                http://orcid.org/0000-0001-7172-6974
                Article
                MBO3628
                10.1002/mbo3.628
                6341032
                29675996
                238d029c-f4f6-4035-8288-a3457b5f5a20
                © 2018 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 17 January 2018
                : 26 February 2018
                : 27 February 2018
                Page count
                Figures: 4, Tables: 2, Pages: 14, Words: 9522
                Funding
                Funded by: Burroughs Wellcome, American Heart Association
                Award ID: 15PRE22710027
                Funded by: National Institutes of Health
                Award ID: R01‐AI091779
                Categories
                Original Article
                Original Research
                Custom metadata
                2.0
                mbo3628
                January 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.5.6 mode:remove_FC converted:21.01.2019

                Microbiology & Virology
                cancer,furin,hpv,peptidase,streptococcus,transformation
                Microbiology & Virology
                cancer, furin, hpv, peptidase, streptococcus, transformation

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