1 Lamont, R. J., Koo, H. & Hajishengallis, G. The oral microbiota: dynamic communities and host interactions. Nat Rev Microbiol 16, 745-759, doi:10.1038/s41579-018-0089-x (2018).
2 Fan, X. et al. Human oral microbiome and prospective risk for pancreatic cancer: a population-based nested case-control study. Gut 67, 120-127, doi:10.1136/gutjnl-2016-312580 (2018).
3 Flemer, B. et al. The oral microbiota in colorectal cancer is distinctive and predictive. Gut 67, 1454-1463, doi:10.1136/gutjnl-2017-314814 (2018).
4 Long, J. et al. Association of oral microbiome with type 2 diabetes risk. J Periodontal Res 52, 636-643, doi:10.1111/jre.12432 (2017).
5 Peters, B. A. et al. Oral Microbiome Composition Reflects Prospective Risk for Esophageal Cancers. Cancer research 77, 6777-6787, doi:10.1158/0008-5472.Can-17-1296 (2017).
6 Zhang, J. et al. Identification of abnormal fucosylated-glycans recognized by LTL in saliva of HBV-induced chronic hepatitis, cirrhosis, and hepatocellular carcinoma. Glycobiology 29, 242-259, doi:10.1093/glycob/cwy108 (2019).
7 Escapa, I. F. et al. New Insights into Human Nostril Microbiome from the Expanded Human Oral Microbiome Database (eHOMD): a Resource for the Microbiome of the Human Aerodigestive Tract. mSystems 3, doi:10.1128/mSystems.00187-18 (2018).
8 Belda-Ferre, P. et al. The oral metagenome in health and disease. The ISME journal 6, 46-56, doi:10.1038/ismej.2011.85 (2012).
9 Qin, Y. et al. Age- and sex-associated differences in the glycopatterns of human salivary glycoproteins and their roles against influenza A virus. Journal of proteome research 12, 2742-2754, doi:10.1021/pr400096w (2013).
10 Zhong, Y. et al. Avian Influenza Virus Infection Risk in Humans with Chronic Diseases. Scientific reports 5, 8971 (2015).
11 Shu, J., Yu, H., Li, X., Zhang, D. & Liu, X. Salivary glycopatterns as potential biomarkers for diagnosis of gastric cancer. Oncotarget 8, 35718-35727 (2017).
12 Liu, X. et al. Salivary Glycopatterns as Potential Biomarkers for Screening of Early-Stage Breast Cancer. EBioMedicine, 70-79 (2018).
13 Shu, J. et al. Identification of N- and O-linked glycans recognized by AAL in saliva of patients with atrophic gastritis and gastric cancer. Cancer Biomarkers 22, 669-681 (2018).
14 Kilian, M. A taxonomic study of the genus Haemophilus, with the proposal of a new species. J Gen Microbiol 93, 9-62, doi:10.1099/00221287-93-1-9 (1976).
15 Nørskov-Lauritsen, N. & Kilian, M. Reclassification of Actinobacillus actinomycetemcomitans, Haemophilus aphrophilus, Haemophilus paraphrophilus and Haemophilus segnis as Aggregatibacter actinomycetemcomitans gen. nov., comb. nov., Aggregatibacter aphrophilus comb. nov. and Aggregatibacter segnis comb. nov., and emended description of Aggregatibacter aphrophilus to include V factor-dependent and V factor-independent isolates. Int J Syst Evol Microbiol 56, 2135-2146, doi:10.1099/ijs.0.64207-0 (2006).
16 Revest, M., Egmann, G., Cattoir, V. & Tattevin, P. HACEK endocarditis: state-of-the-art. Expert Rev Anti Infect Ther 14, 523-530, doi:10.1586/14787210.2016.1164032 (2016).
17 Welch, W. D., Southern, P. M., Jr. & Schneider, N. R. Five cases of Haemophilus segnis appendicitis. J Clin Microbiol 24, 851-852, doi:10.1128/jcm.24.5.851-852.1986 (1986).
18 Carson, H. J., Rezmer, S. & Belli, J. Haemophilus segnis cholecystitis: a case report and literature review. The Journal of infection 35, 85-86, doi:10.1016/s0163-4453(97)91193-2 (1997).
19 Whitfield, C. & Trent, M. S. Biosynthesis and export of bacterial lipopolysaccharides. Annu Rev Biochem 83, 99-128, doi:10.1146/annurev-biochem-060713-035600 (2014).
20 Harriott, M. M. & Noverr, M. C. Importance of Candida-bacterial polymicrobial biofilms in disease. Trends in microbiology 19, 557-563, doi:10.1016/j.tim.2011.07.004 (2011).
21 Casarin, R. C. et al. Subgingival biodiversity in subjects with uncontrolled type-2 diabetes and chronic periodontitis. J Periodontal Res 48, 30-36, doi:10.1111/j.1600-0765.2012.01498.x (2013).
22 Wang, X. et al. Purification of sialoglycoproteins from bovine milk using serotonin-functionalized magnetic particles and their application against influenza A virus. Food & Function 11, 6911-6920, doi:10.1039/D0FO01447H (2020).
23 Bowen, W. H., Burne, R. A., Wu, H. & Koo, H. Oral Biofilms: Pathogens, Matrix, and Polymicrobial Interactions in Microenvironments. Trends in microbiology 26, 229-242, doi:10.1016/j.tim.2017.09.008 (2018).
24 Marsh, P. D. & Zaura, E. Dental biofilm: ecological interactions in health and disease. Journal of clinical periodontology 44 Suppl 18, S12-s22, doi:10.1111/jcpe.12679 (2017).
25 Takahashi, N. & Nyvad, B. The role of bacteria in the caries process: ecological perspectives. Journal of dental research 90, 294-303, doi:10.1177/0022034510379602 (2011).
26 Dabdoub, S. M., Ganesan, S. M. & Kumar, P. S. Comparative metagenomics reveals taxonomically idiosyncratic yet functionally congruent communities in periodontitis. Scientific reports 6, 38993, doi:10.1038/srep38993 (2016).
27 Lu, M., Xuan, S. & Wang, Z. Oral microbiota: A new view of body health. Food Science and Human Wellness 8, 8-15, doi:https://doi.org/10.1016/j.fshw.2018.12.001 (2019).
28 Tanner, A. C. R., Kressirer, C. A., Rothmiller, S., Johansson, I. & Chalmers, N. I. The Caries Microbiome: Implications for Reversing Dysbiosis. Advances in dental research 29, 78-85, doi:10.1177/0022034517736496 (2018).
29 Mark Welch, J. L., Rossetti, B. J., Rieken, C. W., Dewhirst, F. E. & Borisy, G. G. Biogeography of a human oral microbiome at the micron scale. Proc Natl Acad Sci U S A 113, E791-800, doi:10.1073/pnas.1522149113 (2016).
30 Suwannakul, S., Stafford, G. P., Whawell, S. A. & Douglas, C. W. I. Identification of bistable populations of Porphyromonas gingivalis that differ in epithelial cell invasion. Microbiology (Reading, England) 156, 3052-3064, doi:10.1099/mic.0.038075-0 (2010).
31 Valm, A. M. et al. Systems-level analysis of microbial community organization through combinatorial labeling and spectral imaging. Proc Natl Acad Sci U S A 108, 4152-4157, doi:10.1073/pnas.1101134108 (2011).
32 Yang, K. et al. Microbial diversity in combined UAF–UBAF system with novel sludge and coal cinder ceramic fillers for tetracycline wastewater treatment. Chemical Engineering Journal 285, 319-330, doi:https://doi.org/10.1016/j.cej.2015.10.019 (2016).
33 Kim, D. S. et al. Both α2,3- and α2,6-linked sialic acids on O-linked glycoproteins act as functional receptors for porcine Sapovirus. PLoS Pathog 10, e1004172, doi:10.1371/journal.ppat.1004172 (2014).