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1 pxB abundance in Streptococcus sanguinis and Streptococcus gordonii.
2 n the binding of Streptococcus anginosus and Streptococcus gordonii.
3 al transformation of Streptococcus mitis and Streptococcus gordonii.
4 the surface of the human commensal bacterium Streptococcus gordonii.
5 re supernatants of Staphylococcus aureus and Streptococcus gordonii.
6 the presence of antecedent organisms such as Streptococcus gordonii.
7 s on rates of hydrogen peroxide synthesis by Streptococcus gordonii.
8 by adhering to early plaque bacteria such as Streptococcus gordonii.
9 commensal species Streptococcus sanguinis or Streptococcus gordonii.
10 with the antecedent oral biofilm constituent Streptococcus gordonii.
11  attaches and forms biofilms on substrata of Streptococcus gordonii.
12 ggregation receptor polysaccharides (RPS) of Streptococcus gordonii 38 and Streptococcus oralis J22 w
13                              Type 2Gn RPS of Streptococcus gordonii 38 and type 2G RPS of Streptococc
14              The cell wall polysaccharide of Streptococcus gordonii 38 functions as a coaggregation r
15 tion of this polysaccharide in transformable Streptococcus gordonii 38.
16 dominant salivary enzyme in humans, binds to Streptococcus gordonii, a primary colonizer of the tooth
17 oped in this study assessed a multi-species (Streptococcus gordonii, Actinobacillus actinomycetemcomi
18 ultispecies bacteria (Enterococcus faecalis, Streptococcus gordonii, Actinomyces naeslundii, and Lact
19                   In contrast, nonpathogenic Streptococcus gordonii adhered poorly to keratinocytes r
20 ed as Streptococcus oralis (RPS bearing) and Streptococcus gordonii (adhesin bearing).
21 equired for SRR glycoprotein export, Asp2 of Streptococcus gordonii also functions as an O-acetyltran
22  an important determinant of colonization by Streptococcus gordonii, an oral commensal and opportunis
23 nvestigated its role in biofilm formation by Streptococcus gordonii, an organism that colonizes human
24 erence of early colonizing organisms such as Streptococcus gordonii and Actinomyces naeslundii to the
25 en paired with two other initial colonizers, Streptococcus gordonii and Actinomyces oris, as well as
26 Structural studies of the type-C PPases from Streptococcus gordonii and Bacillus subtilis reveal a ho
27                                              Streptococcus gordonii and other viridans streptococci (
28 nge between two bacterial species, commensal Streptococcus gordonii and pathogenic Streptococcus muta
29 NAc-sensitive coaggregations with strains of Streptococcus gordonii and S. sanguis.
30 cause a similar activity is also secreted by Streptococcus gordonii and Staphylococcus aureus.
31                                              Streptococcus gordonii and Streptococcus mutans avidly c
32                                              Streptococcus gordonii and Streptococcus sanguinis are p
33  the human oral flora (Streptococcus mutans, Streptococcus gordonii and Streptococcus sanguinis) to d
34        Studies revealed that S. oralis, like Streptococcus gordonii and Streptococcus sanguinis, bind
35 igher, respectively, in the S-ECC group, and Streptococcus gordonii and Streptococcus sanguinis, whic
36 acid requirements for two oral streptococci: Streptococcus gordonii and Streptococcus sanguinis.
37 dulated by coculture with the oral commensal Streptococcus gordonii and the opportunistic commensal F
38 ction in vivo, mice were first infected with Streptococcus gordonii and then challenged with P. gingi
39  C, showed an increased ability to adhere to Streptococcus gordonii and to invade primary cultures of
40                                              Streptococcus gordonii and Veillonella atypica, two earl
41                                              Streptococcus gordonii and Veillonella atypica, two earl
42 two key initial colonizers of dental plaque, Streptococcus gordonii and Veillonella parvula, on gene
43 l was synthesized, and Streptococcus mutans, Streptococcus gordonii, and Streptococcus sanguinis were
44                    Oral streptococci such as Streptococcus gordonii are facultative anaerobes that in
45 enes (asp4 and asp5) essential for export in Streptococcus gordonii are missing in S. aureus.
46         Viridans streptococci, which include Streptococcus gordonii, are pioneer oral bacteria that i
47                   Oral streptococci, such as Streptococcus gordonii, are the predominant early coloni
48                                     By using Streptococcus gordonii as a model organism for streptoco
49                                        Using Streptococcus gordonii as a model, we now show the mecha
50                                           In Streptococcus gordonii, Asp2 is required for the transpo
51 omyces naeslundii, Tannerella forsythia, and Streptococcus gordonii) associated with dysbiosis of the
52       In contrast, heterotypic P. gingivalis-Streptococcus gordonii biofilm formation was enhanced in
53 lpXP also enhanced heterotypic P. gingivalis-Streptococcus gordonii biofilm formation.
54                                    Layers of Streptococcus gordonii Blackburn or Streptococcus oralis
55                           Strains used were: Streptococcus gordonii Blackburn, 10558, Streptococcus m
56 velops biofilm microcolonies on substrata of Streptococcus gordonii but not on Streptococcus mutans.
57 of PMNs or HL-60 cells abolished adhesion of Streptococcus gordonii but was required for adhesion of
58 pathogen Porphyromonas gingivalis adheres to Streptococcus gordonii by interacting with a specific re
59                                              Streptococcus gordonii can mediate its platelet attachme
60                                          The Streptococcus gordonii cell surface glycoprotein GspB me
61                       The alpha-hemolysin of Streptococcus gordonii CH1 caused characteristic shifts
62                                   Planktonic Streptococcus gordonii CH1 killed HUVEC over a 5-h perio
63 agenesis identified a new competence gene in Streptococcus gordonii Challis designated comYA.
64  a 585-bp gene was cloned and sequenced from Streptococcus gordonii Challis encoding a 20.5-kDa amyla
65                                          The Streptococcus gordonii (Challis) glucosyltransferase-enc
66                                              Streptococcus gordonii colonizes multiple sites within t
67 tococcus pyogenes) exposed on the surface of Streptococcus gordonii commensal bacterial vectors: (i)
68 produced by the glucosyltransferase (GTF) of Streptococcus gordonii confer a hard, cohesive phenotype
69 nsortium members Fusobacterium nucleatum and Streptococcus gordonii confirmed the presence of all thr
70 tion with P. gingivalis, whereas noninvasive Streptococcus gordonii did not have a significant effect
71 acid-containing receptors is associated with Streptococcus gordonii DL1 (Challis) but not with a spon
72 dentified by transposon Tn916 mutagenesis of Streptococcus gordonii DL1 (Challis).
73 inactivate a coaggregation-relevant locus of Streptococcus gordonii DL1 (Challis).
74                  The accessory Sec system in Streptococcus gordonii DL1 is a specialized export syste
75 ageneric coaggregation, streptococci such as Streptococcus gordonii DL1 recognize receptor polysaccha
76 ne cluster and used to transform E. coli and Streptococcus gordonii DL1, a nonureolytic, dental plaqu
77                                           In Streptococcus gordonii DL1, inactivation of the ccpA gen
78 ating early colonizers of the tooth surface (Streptococcus gordonii DL1, Streptococcus oralis 34, and
79 he scaCBA operon in the human oral bacterium Streptococcus gordonii encodes the components of an ABC-
80                                              Streptococcus gordonii expresses two related adhesins, S
81 pV, a dipeptidase found in culture fluids of Streptococcus gordonii FSS2, was purified and characteri
82  polypeptide (259 kDa) in the oral bacterium Streptococcus gordonii, generates mutants that are marke
83                                              Streptococcus gordonii genes involved in beta-glucoside
84                  A DNA microarray identified Streptococcus gordonii genes regulated in response to co
85                                          The Streptococcus gordonii glucosyltransferase gene, gtfG, i
86 biofilm formation by Streptococcus mutans or Streptococcus gordonii grown in human plasma.
87 Previous studies of GspB (the SRR adhesin of Streptococcus gordonii) have shown that a glycine-rich m
88 mbriae by reducing P. gingivalis adhesion to Streptococcus gordonii in a dual-species biofilm model.
89  parasanguinis, Streptococcus sanguinis, and Streptococcus gordonii, inhibit the growth of P. aerugin
90             Pioneer oral bacteria, including Streptococcus gordonii, initiate the formation of oral b
91 omonas gingivalis and the accessory pathogen Streptococcus gordonii interact to form communities in v
92                 The oral commensal bacterium Streptococcus gordonii interacts with salivary amylase v
93 ed by early dental plaque colonizers such as Streptococcus gordonii interfere with the subsequent col
94                                              Streptococcus gordonii is a frequent cause of infective
95 eptococcal coaggregation regulator (ScaR) of Streptococcus gordonii is a manganese-dependent transcri
96                          ScaA lipoprotein in Streptococcus gordonii is a member of the LraI family of
97                                              Streptococcus gordonii is a pioneer colonizer of the tee
98                                              Streptococcus gordonii is a primary colonizer of the hum
99                                              Streptococcus gordonii is a primary colonizer of the mul
100                                              Streptococcus gordonii is a primary etiological agent in
101                                              Streptococcus gordonii is an oral commensal and an early
102                  The accessory Sec system of Streptococcus gordonii is comprised of SecY2, SecA2, and
103                  The accessory Sec system of Streptococcus gordonii is essential for transport of the
104                                              Streptococcus gordonii is generally considered a benign
105                          Platelet binding by Streptococcus gordonii is mediated in large part by GspB
106                                              Streptococcus gordonii is shown to express, on the cell
107 ort, we show that the A regions from the two Streptococcus gordonii M5 antigen I/II proteins (SspA an
108 large cell-surface glycoprotein expressed by Streptococcus gordonii M99 that mediates binding of this
109                                              Streptococcus gordonii (mitis group) has been shown to b
110 he cytosolic O-glycosyltransferase GtfA/B of Streptococcus gordonii modifies the Ser/Thr-rich repeats
111                           The oral commensal Streptococcus gordonii must adapt to constantly fluctuat
112 ) was started 2 days before inoculation with Streptococcus gordonii or Staphylococcus aureus.
113 ed with PAAP(+) S. sanguis than with PAAP(-) Streptococcus gordonii or type II collagen, suggesting a
114                   Actinomyces naeslundii and Streptococcus gordonii, oral bacteria that possess Gal/G
115  p38 and then stimulated with oral commensal Streptococcus gordonii, oral pathogens Porphyromonas gin
116 r example, more Streptococcus sanguinis than Streptococcus gordonii organisms are consistently isolat
117                The ADS of the oral bacterium Streptococcus gordonii plays major roles in physiologic
118  oral commensals Streptococcus sanguinis and Streptococcus gordonii release DNA in a process induced
119                   In addition, we found that Streptococcus gordonii (S. gordonii) and Enterococcus fa
120 ory region with high homology to that of the Streptococcus gordonii ScaR binding domain.
121 nalling between Porphyromonas gingivalis and Streptococcus gordonii serves to constrain development o
122 ion of hydrogen peroxide in solution above a Streptococcus gordonii (Sg) bacterial biofilm was studie
123  could detect 65 +/- 10 muM H2O2 produced by Streptococcus gordonii (Sg) in a simulated biofilm at 50
124 monstrated that a peptide (BAR) derived from Streptococcus gordonii (Sg) potently inhibited adherence
125  species, namely Streptococcus mutants (SM), Streptococcus gordonii (SG), Moraxella catarrhalis (MC),
126 es, including commensal streptococci such as Streptococcus gordonii (Sg).
127                                              Streptococcus gordonii (Sg)/S. oralis (So)/S. sanguinis
128                                              Streptococcus gordonii shows promise as a live mucosal v
129 uence motif within the C-terminal portion of Streptococcus gordonii SspB (AgI/II) is bound by Porphyr
130 tion between Streptococcus mutans AgI/II and Streptococcus gordonii SspB in their interaction with th
131 icroorganisms, e.g., Veillonella parvula and Streptococcus gordonii, stimulated higher levels of ROS
132 ns (SLBRs) from two strains of streptococci, Streptococcus gordonii strain Challis (SLBR(Hsa)) and St
133                                     However, Streptococcus gordonii strain M99 encodes SecA and SecY
134                    The gspB-secY2A2 locus of Streptococcus gordonii strain M99 encodes the platelet-b
135                          Platelet binding by Streptococcus gordonii strain M99 is dependent on expres
136                          Platelet binding by Streptococcus gordonii strain M99 is mediated predominan
137                          Platelet binding by Streptococcus gordonii strain M99 is predominantly media
138                          Platelet binding by Streptococcus gordonii strain M99 is strongly correlated
139 ologous serine-rich surface glycoproteins of Streptococcus gordonii strains M99 and Challis, respecti
140 nces in virulence among seven representative Streptococcus gordonii strains were observed by using th
141 infantis group, Corynebacterium matruchotii, Streptococcus gordonii, Streptococcus cristatus, Capnocy
142  (Streptococcus mitis, Streptococcus oralis, Streptococcus gordonii, Streptococcus cristatus, Strepto
143 t AgI/II family polypeptides from strains of Streptococcus gordonii, Streptococcus intermedius and St
144 omologous enzymes in Streptococcus pyogenes, Streptococcus gordonii, Streptococcus mutans, Staphyloco
145 phylococcus aureus, Streptococcus sanguinis, Streptococcus gordonii, Streptococcus oralis, and Strept
146 nt understanding of accessory Sec systems in Streptococcus gordonii, Streptococcus parasanguinis, Myc
147 racterized and closely related oral species, Streptococcus gordonii, Streptococcus sanguinis, and car
148 -seq) on cocultures of S. mutans with either Streptococcus gordonii, Streptococcus sanguinis, or Stre
149 lizes lactate produced by the oral bacterium Streptococcus gordonii, suggesting the potential for cro
150  Hsa are homologous surface glycoproteins of Streptococcus gordonii that bind sialic acid moieties on
151  (30-day) colonization of smooth surfaces by Streptococcus gordonii that incorporates the nutrient fl
152 spB is a serine-rich glycoprotein adhesin of Streptococcus gordonii that is exported to the bacterial
153                         In the gram-positive Streptococcus gordonii, the ability to form disulfide bo
154                                           In Streptococcus gordonii, the SRR glycoprotein GspB has a
155 ococcus mutans, Streptococcus sanguinis, and Streptococcus gordonii, they exhibited antibacterial eff
156 ies have shown that P. gingivalis adheres to Streptococcus gordonii through interaction of the minor
157 SspB (antigen I/II family proteins) can bind Streptococcus gordonii to other oral bacteria and also t
158                                Attachment of Streptococcus gordonii to the acquired pellicle of the t
159 the attachment of pioneer organisms, such as Streptococcus gordonii, to tooth surfaces.
160                                           In Streptococcus gordonii, transport of the serine-rich gly
161 erobes, including aerotolerant ones, such as Streptococcus gordonii, use pyruvate dehydrogenase to de
162 heterologous bacteria Lactococcus lactis and Streptococcus gordonii was demonstrated.
163      The amylase-binding protein A (AbpA) of Streptococcus gordonii was found to be undetectable in s
164 tA gene in the human oral commensal organism Streptococcus gordonii was insertionally inactivated.
165 tococcus oralis, Streptococcus sanguinis, or Streptococcus gordonii was investigated using flow cell
166 gnated atlS, encoding a major autolysin from Streptococcus gordonii, was identified and characterized
167   To investigate disulfide bond formation in Streptococcus gordonii, we identified five putative TDOR
168 enes encoding adhesins of the oral bacterium Streptococcus gordonii were differentially expressed dep
169                                              Streptococcus gordonii were spotted onto the membranes a
170 n homologous to the platelet adhesin GspB in Streptococcus gordonii, were identified.
171 yces gereneseriae, Actinomyces israelli, and Streptococcus gordonii when compared with Group EP.
172                                              Streptococcus gordonii Wicky becomes competent only afte

 
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