-
Články
Top novinky
Reklama- Vzdělávání
- Časopisy
Top články
Nové číslo
- Témata
Top novinky
Reklama- Videa
- Podcasty
Nové podcasty
Reklama- Kariéra
Doporučené pozice
Reklama- Praxe
Top novinky
ReklamaThe power of saliva: Antimicrobial and beyond
Autoři: Taissa Vila aff001; Alexandra M. Rizk aff001; Ahmed S. Sultan aff001; Mary Ann Jabra-Rizk aff001
Působiště autorů: Department of Oncology and Diagnostic Sciences, Dental School, University of Maryland, Baltimore, United States of America aff001; Department of Microbiology and Immunology, School of Medicine, University of Maryland, Baltimore, United States of America aff002
Vyšlo v časopise: The power of saliva: Antimicrobial and beyond. PLoS Pathog 15(11): e32767. doi:10.1371/journal.ppat.1008058
Kategorie: Pearls
doi: https://doi.org/10.1371/journal.ppat.1008058
Zdroje
1. Sultan AS, Kong EF, Jabra-Rizk MA. The oral microbiome: A lesson in co-existence. PLoS Pathog. 2018;14(1):e1006719. doi: 10.1371/journal.ppat.1006719 29370304
2. Amerongen A, Veerman E. Saliva: the defender of the oral cavity. Oral Dis. 2002;8(1):12–22. 11936451
3. Zhang CZ, Cheng XQ, Li JY, Zhang P, Yi P, Xu X, et al. Saliva in the diagnosis of diseases. Int J Oral Sci. 2016 8(3):133–7. doi: 10.1038/ijos.2016.38 27585820
4. Dawes C, Pedersen AM, Villa A, Ekström J, Proctor GB, Vissink A, et al. The functions of human saliva: A review sponsored by the World Workshop on Oral Medicine VI. Arch Oral Biol 2015;60(6):863–74. doi: 10.1016/j.archoralbio.2015.03.004 25841068
5. Salvatori O, Puri S, Tati S, Edgerton M. Innate immunity and saliva in Candida albicans-mediated oral diseases. J Dent Res. 2016;95(4):365–71. doi: 10.1177/0022034515625222 26747422
6. Sroussi HY, Epstein JB, Bensadoun RJ, Saunders DP, Lalla RV, Migliorati CA, et al. Common oral complications of head and neck cancer radiation therapy: mucositis, infections, saliva change, fibrosis, sensory dysfunctions, dental caries, periodontal disease, and osteoradionecrosis. Cancer Med. 2017;6(12):2918–31. doi: 10.1002/cam4.1221 29071801
7. van 't Hof W, Veerman EC, Nieuw Amerongen AV, Ligtenberg AJ. Antimicrobial defense systems in saliva. Monogr Oral Sci 2014; 24 : 52–60. 2014;24 : 40–51. doi: 10.1159/000358784
8. Gorr S. Antimicrobial peptides of the oral cavity. Periodontol 2000. 2009;51 : 152–80. doi: 10.1111/j.1600-0757.2009.00310.x 19878474
9. Mochon AB, Liu H. The antimicrobial peptide histatin-5 causes a spatially restricted disruption on the Candida albicans surface allowing rapid entry of the peptide into the cytoplasm. PLoS Pathog. 2008;4(10):e1000190. doi: 10.1371/journal.ppat.1000190 18974864
10. Edgerton M, Koshlukova SE, Araujo MWB, Patel RC, Dong J, Bruenn J. Salivary histatin 5 and human neutrophil defensin 1 kill Candida albicans via shared pathways. Animicrobial Agents and Chemotherapy. 2000;44(12):3310–6.
11. Khurshid Z, Naseem M, Yahya F, Mali M, Sannam KR, Sahibzada HA, et al. Significance and diagnostic role of antimicrobial cathelicidins (LL-37) peptides in oral health. Biomolecules. 2017;7(4): doi: 10.3390/biom7040080 29206168
12. Abiko Y, Nishimura M, Kaku T. Defensins in saliva and the salivary glands. Med Electron Microscopy. 2003;36 : 247–52.
13. Meade KG, O'Farrelly C. β-Defensins: Farming the microbiome for homeostasis and health. Front Immunol. 2019 25(9):3072.
14. Oppenheim FG, Xu T, McMillian FM, Levitz SM, Diamond RD, Offner GD, et al. Histatins, a novel family of histidine-rich proteins in human parotid secretion. The Journal of Biological Chemistry. 1988;263(16):7472–7. 3286634
15. Edgerton M, Koshlukova S, Lo T, Chrzan B, Straubinger R, Raj P. Candidacidal activity of salivary histatins. J Biol Chem. 1998;272(32):20438–47.
16. Li XS, Reddy MS, Baev D, Edgerton M. Candida albicans Ssa1/2p is the cell envelope binding protein for human salivary histatin 5. The Journal of Biological Chemistry. 2003;278(31):28553–61. doi: 10.1074/jbc.M300680200 12761219
17. Gyurko C, Lendenmann U, Helmerhorst EJ, Troxler RF, Oppenheim FG. Killing of Candida albicans by histatin 5: cellular uptake and energy requirement. Antonie van Leeuwenhoek. 2001;79 : 297–309. doi: 10.1023/a:1012070600340 11816973
18. Leito JT, Ligtenberg AJ, Nazmi K, Veerman EC. Identification of salivary components that induce transition of hyphae to yeast in Candida albicans. FEMS Yeast Res. 2009;9(7):1102–10. doi: 10.1111/j.1567-1364.2009.00575.x 19799638
19. Jabra-Rizk MA, Kong E, Tsui C, Nguyen M, Clancy C, Fidel P, et al. Candida albicans pathogenesis: Fitting within the host-microbe damage response framework. Infect Immun. 2016;84(10):2724–39. doi: 10.1128/IAI.00469-16 27430274
20. Moffa EB, Mussi MCM, Xiao Y, Garrido SS, Machado MAAM, Giampaolo ET, et al. Histatin 5 inhibits adhesion of C. albicans to reconstructed human oral epithelium. Front Microbiol. 2015;6(885): doi: 10.3389/fmicb.2015.00885 26379655
21. Vivino F, Bunya VY, Massaro-Giordano G, Johr CR, Giattino SL, Schorpion A, et al. Sjogren's syndrome: An update on disease pathogenesis, clinical manifestations and treatment. Clin Immunol. 2019 22: doi: 10.1016/j.clim.2019.04.009 31022578
22. Sweet SP, Denbury AN, Challacombe SJ. Salivary calprotectin levels are aised in patients with oral candidiasis or Sjögren’s syndrome but decreased by HIV infection. Oral Microbiol Immunol 2001;16(2):119–23. doi: 10.1034/j.1399-302x.2001.016002119.x 11240866
23. Lin AL, Johnson DA, Stephan KT, Yeh CK. Alteration in salivary function in early HIV infection. J Dent Res. 2003 8;2(9):719–24.
24. Khan SA, Fidel P Jr, Al Thunayyan A, Meiller T, Jabra-Rizk MA. Impaired histatin-5 level and salivary antimicrobial activity against C. albicans in HIV-infected individuals. J AIDS Clin Res. 2013;4(2):1–6.
25. Gaffen S H-SN, Peterson A. IL-17 Signaling in host defense against Candida albicans. Immunol Res. 2011;50 : 181–7. doi: 10.1007/s12026-011-8226-x 21717069
26. Linden SK, Sutton P, Karlsson NG, Korolik V, McGuckin MA. Mucins in the mucosal barrier to infection. Mucosal Immunol. 2008;1(3):183–97. doi: 10.1038/mi.2008.5 19079178
27. Brand H, Ligtenberg A, Veerman E. Saliva and wound healing. Monogr Oral Sci. 2014;24 52–60. doi: 10.1159/000358784 24862594
28. Torres P, Castro M, Reyes M, Torres VA. Histatins, wound healing and cell migration. Oral Dis. 2018;24 : 1150–60. doi: 10.1111/odi.12816 29230909
29. Oudhoff MJ, Bolscher JGM, Nazmi K, Kalay H, van 't Hof W, Nieuw Amerongen AV, et al. Histatins are the major wound-closure stimulating factors in human saliva as identified in a cell culture assay. The FASEB Journal. 2008;22 : 3805–12. doi: 10.1096/fj.08-112003 18650243
30. Wisner A, Dufour E, Messaoudi M, Nejdi A, Marcel A, Ungeheuer MN, et al. Human opiorphin, a natural antinociceptive modulator of opioid-dependent pathways. Proc Natl Acad Sci U S A. 2006;103(47):17979–84. doi: 10.1073/pnas.0605865103 17101991
31. Shah S. Salivaomics: The current scenario. J Oral Maxillofac Pathol 2018 22(3):375–81. doi: 10.4103/jomfp.JOMFP_171_18 30651683
32. Wong D.T. Salivaomics. J Am Dent Assoc. 2012;143(10 Suppl):19S–24S.
33. Tasoulas J, Patsouris E, Giaginis C, Theocharis S. Salivaomics for oral diseases biomarkers detection. Expert Rev Molec Diag 2016 16(3):285–95
34. Ilea A, Andrei V, Feurdean CN, Băbțan AM, Petrescu NB, Câmpian RS, et al. Saliva, a magic biofluid available for multilevel assessment and a mirror of general health-A systematic review. Biosensors. 2019;9(1): doi: 10.3390/bios9010027 30769890
Štítky
Hygiena a epidemiologie Infekční lékařství Laboratoř
Článek Host signaling and EGR1 transcriptional control of human cytomegalovirus replication and latencyČlánek Chromatin dynamics and the transcriptional competence of HSV-1 genomes during lytic infectionsČlánek Candida albicans triggers NADPH oxidase-independent neutrophil extracellular traps through dectin-2Článek N-glycosylation of the protein disulfide isomerase Pdi1 ensures full Ustilago maydis virulence
Článek vyšel v časopisePLOS Pathogens
Nejčtenější tento týden
2019 Číslo 11- Jak souvisí postcovidový syndrom s poškozením mozku?
- Měli bychom postcovidový syndrom léčit antidepresivy?
- Farmakovigilanční studie perorálních antivirotik indikovaných v léčbě COVID-19
- 10 bodů k očkování proti COVID-19: stanovisko České společnosti alergologie a klinické imunologie ČLS JEP
-
Všechny články tohoto čísla
- The ETS transcription factor ELF1 regulates a broadly antiviral program distinct from the type I interferon response
- N-glycosylation of the protein disulfide isomerase Pdi1 ensures full Ustilago maydis virulence
- HCMV miR-US22 down-regulation of EGR-1 regulates CD34+ hematopoietic progenitor cell proliferation and viral reactivation
- Multi-strain Tn-Seq reveals common daptomycin resistance determinants in Staphylococcus aureus
- Electrostatic interactions at the five-fold axis alter heparin-binding phenotype and drive EV-A71 virulence in mice
- Trickle infection and immunity to Trichuris muris
- Activation of Shigella flexneri type 3 secretion requires a host-induced conformational change to the translocon pore
- Mitochondrial dynamics in parasitic protists
- Clostridium perfringens epsilon toxin induces blood brain barrier permeability via caveolae-dependent transcytosis and requires expression of MAL
- Host signaling and EGR1 transcriptional control of human cytomegalovirus replication and latency
- Subclinical in utero Zika virus infection is associated with interferon alpha sequelae and sex-specific molecular brain pathology in asymptomatic porcine offspring
- Chlamydia trachomatis and human herpesvirus 6 infections in ovarian cancer—Casual or causal?
- The power of saliva: Antimicrobial and beyond
- Ammonium transceptors: Novel regulators of fungal development
- Human monoclonal antibodies against chikungunya virus target multiple distinct epitopes in the E1 and E2 glycoproteins
- The male mosquito contribution towards malaria transmission: Mating influences the Anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites
- Mycobacterium abscessus virulence traits unraveled by transcriptomic profiling in amoeba and macrophages
- Chromatin dynamics and the transcriptional competence of HSV-1 genomes during lytic infections
- Alphaherpesvirus infection of mice primes PNS neurons to an inflammatory state regulated by TLR2 and type I IFN signaling
- Host nutritional status affects alphavirus virulence, transmission, and evolution
- Candida albicans triggers NADPH oxidase-independent neutrophil extracellular traps through dectin-2
- Influenza viruses that require 10 genomic segments as antiviral therapeutics
- NEDD4 family ubiquitin ligases associate with LCMV Z’s PPXY domain and are required for virus budding, but not via direct ubiquitination of Z
- CDR3α drives selection of the immunodominant Epstein Barr virus (EBV) BRLF1-specific CD8 T cell receptor repertoire in primary infection
- The Crohn’s disease-associated Escherichia coli strain LF82 relies on SOS and stringent responses to survive, multiply and tolerate antibiotics within macrophages
- Porphyromonas gingivalis induces penetration of lipopolysaccharide and peptidoglycan through the gingival epithelium via degradation of junctional adhesion molecule 1
- Amblyomma americanum ticks utilizes countervailing pro and anti-inflammatory proteins to evade host defense
- EV71 infection induces neurodegeneration via activating TLR7 signaling and IL-6 production
- Aging boosts antiviral CD8+T cell memory through improvedengagement of diversified recall response determinants
- Trypanosoma brucei infection protects mice against malaria
- 14-3-3 scaffold proteins mediate the inactivation of trim25 and inhibition of the type I interferon response by herpesvirus deconjugases
- Modulation of flagellar rotation in surface-attached bacteria: A pathway for rapid surface-sensing after flagellar attachment
- NCOA2 promotes lytic reactivation of Kaposi’s sarcoma-associated herpesvirus by enhancing the expression of the master switch protein RTA
- Regulation of macrophage activity by surface receptors contained within Borrelia burgdorferi-enriched phagosomal fractions
- Kinetics of HTLV-1 reactivation from latency quantified by single-molecule RNA FISH and stochastic modelling
- Reprogramming the unfolded protein response for replication by porcine reproductive and respiratory syndrome virus
- Correction: Eight RGS and RGS-like Proteins Orchestrate Growth, Differentiation, and Pathogenicity of Magnaporthe oryzae
- The mosquito melanization response requires hierarchical activation of non-catalytic clip domain serine protease homologs
- Correction: The bZIP Transcription Factor MoAP1 Mediates the Oxidative Stress Response and is Critical for Pathogenicity of the Rice Blast Fungus Magnaporthe oryzae
- PLOS Pathogens
- Archiv čísel
- Aktuální číslo
- Informace o časopisu
Nejčtenější v tomto čísle- Candida albicans triggers NADPH oxidase-independent neutrophil extracellular traps through dectin-2
- Mycobacterium abscessus virulence traits unraveled by transcriptomic profiling in amoeba and macrophages
- Porphyromonas gingivalis induces penetration of lipopolysaccharide and peptidoglycan through the gingival epithelium via degradation of junctional adhesion molecule 1
- Activation of Shigella flexneri type 3 secretion requires a host-induced conformational change to the translocon pore
Kurzy
Zvyšte si kvalifikaci online z pohodlí domova
Současné možnosti léčby obezity
nový kurzAutoři: MUDr. Martin Hrubý
Autoři: prof. MUDr. Hana Rosolová, DrSc.
Všechny kurzyPřihlášení#ADS_BOTTOM_SCRIPTS#Zapomenuté hesloZadejte e-mailovou adresu, se kterou jste vytvářel(a) účet, budou Vám na ni zaslány informace k nastavení nového hesla.
- Vzdělávání