ライフサイエンスコーパス: adhesin

1 icating that OspA may serve as a tick midgut adhesin.

2 teolytic cleavage to act as an intercellular adhesin.

3 s (LPG) coated with T4 bacteriophage (phage) adhesin.

4 ctivity of its type IV pili, a major surface adhesin.

5 rdetella pertussis filamentous hemagglutinin adhesin.

6 outer membrane protein intimin, a major EHEC adhesin.

7 nt to the gut by blocking the FimH bacterial adhesin.

8 ein F to be an important and ubiquitous NTHi adhesin.

9 growth of CRC cells through its unique FadA adhesin.

10 dence for a CBM40 as a novel bacterial mucus adhesin.

11 ting a domain from a Gram-positive bacterial adhesin.

12 ordonii modifies the Ser/Thr-rich repeats of adhesin.

13 s GtfB provides the primary binding site for adhesin.

14 capacitor coated with T4 bacteriophage gp37 adhesin.

15 factor CS23 but is negative for other known adhesins.

16 d stress and elevated expression of fimbrial adhesins.

17 stis in its hosts, in conjunction with other adhesins.

18 que and define a new class of polysaccharide adhesins.

19 iarrhea, colonizes the intestine by means of adhesins.

20 that involve microbial surface proteins, or adhesins.

21 and antigenic variation of the MgpB and MgpC adhesins.

22 ks are widespread in Gram-positive bacterial adhesins.

23 a family of serine-rich repeat streptococcal adhesins.

24 mably because of the absence of cell surface adhesins.

25 serine-rich repeat protein (SRRP) family of adhesins.

26 glycan binding of human pathogen lectins and adhesins.

27 icobacter pylori blood group antigen binding adhesin A (BabA) is more common in strains isolated from

28 Neisserial adhesin A (NadA), a trimeric autotransporter adhesin (TA

29 Yersinia adhesin A (YadA) belongs to a class of bacterial adhesin

30 ence strain (5/99, which included neisserial adhesin A), both of which were used in vaccine developme

31 entify the fusobacterial galactose-sensitive adhesin, a system for transposon mutagenesis in fusobact

32 nique gene locus encoding an amylase-binding adhesin AbpA and a sortase B in oral streptococci.

33 The collagen adhesin Acm was the first virulence determinant reported

34 forms a channel for translocation of the Hsa adhesin across the cytoplasmic membrane.

35 that the exoprotein possesses an additional adhesin activity.

36 It comprises stacked beta-sandwich adhesin (AD) and pilin (PD) domains, with the putative r

37 Here, we report that these adhesins also can bind C1q and act as inhibitors of the

38 e components: the pathogenic agent, a lectin/adhesin and a glycan ligand.

39 AmOmpA is both an adhesin and an invasin, as coating inert beads with it c

40 us assembly and traffic the pilus-associated adhesin and anti-retraction protein, PilY1, to the cell

41 colonization factors comprising a minor tip adhesin and major stalk-forming subunit.

42 lacking expression of pertactin, a bacterial adhesin and vaccine target, are emerging.

43 ofuranose-containing polysaccharides conceal adhesins and are important for membrane integrity.

44 e adaptations include expression of specific adhesins and cell wall re-modeling to attach to the root

45 l cells, the bacterium produces a variety of adhesins and delivers virulence factors.

46 ne exposure, these cells overproduce the Prg adhesins and display impaired envelope integrity, as evi

47 anisms to colonize host cells, as nearly all adhesins and effectors involved in host cell entry are d

48 tosA and affect the reciprocal expression of adhesins and flagella.

49 is governed by interactions between parasite adhesins and red blood cell receptors.

50 and fitness factors but do have a variety of adhesins and regulatory pathways.

51 overproduction, block production of the Prg adhesins and render cells insensitive to pheromone.

52 ad amino acid sequence homology to bacterial adhesins and structural homology to bacterial lysozyme i

53 tween the cytoplasmic tails of transmembrane adhesins and the actin-myosin motor.

54 gulation of principal virulence factors (eg, adhesins and toxins) and biofilm formation.

55 vB and PspC are pneumococcal surface-exposed adhesins and virulence factors exhibiting repetitive seq

56 contained allele 41 of fimH (type 1 fimbrial adhesin) and a narrow range of alleles of gyrA and parC

57 s the cwp cluster peaked within slpA, cwp66 (adhesin), and secA2 (secretory translocase).

58 stile interactions (i.e. hemolysins, pilins, adhesins), and exoenzymes with a potential mixotrophic g

59 lymerized backbone, RrgA, the tip-associated adhesin, and RrgC, which presumably associates the pilus

60 us haemagglutinin (FHA), a surface-displayed adhesin, and until now, the consequences of this interac

61 r of a diverse family of predicted bacterial adhesins, and although lacking a high degree of sequence

62 dorferi s. l. bacteria, recombinant borrelia adhesins, and an array of adhesion assays carried out bo

63 ted loci that include genes encoding toxins, adhesins, and other cell surface proteins, and over 200

64 site effector proteins, including perforins, adhesins, and proteases, are extensively proteolytically

65 repeats in toxin (RTX) toxins, RHS proteins, adhesins, and type IV pili] that likely mediate cell-cel

66 Here, we followed the adhesin Apa-specific T-cell responses in BCG-primed mice

67 These adhesins are delivered to the cell surface by a Bacteroi

68 To date, adhesins are only known to bind to host receptors non-co

69 We identified autotransporter adhesins as the preferred protein substrate of NGT in vi

70 d outer membrane localization included known adhesins, as well as Cag proteins required for activity

71 rpA, similar in sequence to platelet-binding adhesins associated with increased virulence in this dis

72 ens produces a unipolar polysaccharide (UPP) adhesin at single cell poles that contact surfaces.

73 Cpa, the adhesin at the pilus tip, was recently shown to have a t

74 cells is mediated by FimH, a mannose-binding adhesin at the tip of bacterial type 1 pili.

75 This attachment is facilitated by bacterial adhesins at the cell surface.

76 The Helicobacter pylori adhesin BabA binds mucosal ABO/Le(b) blood group (bg) ca

77 ructural analyses of the Helicobacter pylori adhesin BabA to determine how the bacteria discriminatel

78 oieties recognized by the well-characterized adhesins BabA and SabA.

79 also revealed unexpected roles for Borrelia adhesins BBK32 and OspC in bacterial burdens in the bloo

80 mental data of the filamentous hemagglutinin adhesin beta-barrel protein transporter solubilized by n

81 and an ALD mutant that specifically disrupts adhesin binding in vitro also supported normal invasion

82 We show that T4 phage adhesin binds E. coli B LPS in its native or denatured f

83 The adhesin binds Escherichia coli B (E. coli B) by precise

84 FimH, the type 1 adhesin, binds mannosylated glycoproteins on the surface

85 ch domain seen in the parental streptococcal adhesin, but flanking sequences at both N- and C-termini

86 ation of highly conserved serine-rich repeat adhesins by a series of glycosyltransferases.

87 utant led to the discovery that the putative adhesin CD0386 is anchored to the peptidoglycan of C. di

88 two sortase-anchored proteins, the putative adhesins CD2831 and CD3246, and determine the cell wall

89 olism rather than interacting with microneme adhesins, challenging the current model for apicomplexan

90 f heart tissue is dependent on the bacterial adhesin choline-binding protein A that binds to laminin

91 e major pilus backbone subunit (RrgB) or the adhesin component (RrgA) impaired pneumococcal associati

92 lycoproteins (SRRPs) are important bacterial adhesins conserved in streptococci and staphylococci.

93 The C-terminal part of the adhesin consists of the receptor-binding amino acid resi

94 The surface-localized S. mutans P1 adhesin contributes to tooth colonization and caries for

95 The multifunctional fibrillar adhesin CshA, which mediates binding to both host molecu

96 n experiments with other pneumococcal hTSP-1 adhesins demonstrated that PspC and PspC-like Hic recogn

97 ith c-di-GMP activation of surface-dependent adhesin deployment.

98 tridium perfringens comprising an N-terminal adhesin domain followed by 11 repeat domains.

99 Taken together, these data suggest that the adhesin domain of SabA is sufficient in isolation for sp

100 aphy, we show that the soluble extracellular adhesin domain of SabA shares distant similarity to the

101 , we were able to detect binding of the SabA adhesin domain to sialyl-Lewis(X) and Lewis(X) but not t

102 ing pocket abrogates the binding of the SabA adhesin domain to sialyl-Lewis(X) and Lewis(X).

103 Escherichia coli-bearing Dr-adhesins (Dr+ E. coli) cause chronic pyelonephritis in p

104 sequentially deploying a number of putative adhesins during its interactions with the host.

105 with the host and the importance of multiple adhesins during mammalian infection.

106 tive highly conserved, chromosomally encoded adhesin, EaeH, engages the surfaces of intestinal epithe

107 onal adherence in planta was mediated by the adhesin EcpD in combination with the structural subunit,

108 . albicans and radD, an arginine-inhibitable adhesin-encoding gene in F. nucleatum that is involved i

109 Uropathogenic E coli containing prsG-adhesin-encoding plasmids agglutinated A(pae) but not gr

110 ted the fungal ligands to be the C. glabrata adhesins Epa1, Epa6, and Epa7 and demonstrated that clea

111 e serine-threonine-rich region of epithelial adhesin (Epa1) of Candida glabrata, and the carboxyl reg

112 ll wall proteins, the lectin-like epithelial adhesins (Epas).

113 llular receptors or bacterial outer membrane adhesins essential for this process are unknown.

114 we identify the HopQ protein as a genuine Hp adhesin, exploiting defined members of the carcinoembryo

115 udies advance our knowledge of regulation of adhesin expression associated with uropathogen colonizat

116 In staphylococci, the adhesins extracellular adherence protein (Eap) and autol

117 cleatum clinical isolates with FadA and Fap2 adhesins failed to induce inflammation and tumorigenesis

118 The adhesin family of polymorphic membrane proteins (Pmp) in

119 d to the serine-rich repeat of the bacterial adhesin, Fap1 of Streptococcus parasanguinis.

120 For example, the type 1 pilus adhesin FimH binds mannose on the bladder surface, and m

121 Here we study the bacterial adhesin FimH to address the role of the inactive conform

122 One example is the bacterial adhesin FimH, where the C-terminal pilin domain exerts n

123 nd FimH antagonists that block the bacterial adhesin FimH, which would otherwise mediate binding of u

124 antivirulence inhibitors of the type 1 pilus adhesin, FimH, demonstrated oral activity in animal mode

125 the carbohydrate-binding domain of the FimH adhesin (FimHL).

126 olved in bacterial virulence such as toxins, adhesins, flagella, and pili, among others.

127 The Fml adhesin FmlH binds galactose beta1-3 N-acetylgalactosami

128 YapV acted as an adhesin for alveolar epithelial cells and specific extra

129 el polysaccharide serves as an intercellular adhesin for the formation and maintenance of biofilms in

130 g protein (MUB), a multi-repeat cell-surface adhesin found in Lactobacillus inhabitants of the GI tra

131 We have investigated a putative cell-surface adhesin from Clostridium perfringens comprising an N-ter

132 ic cysteine protease LapG and release of the adhesin from the cell surface under conditions unfavorab

133 nd Random Forest analyses of known/suspected adhesins from 580 independent Typhimurium isolates ident

134 he first clinical evidence that fimbrial tip adhesins function as protective antigens.

135 as resolved based on fimH sequence (fimbrial adhesin gene: H subclone assignments), multilocus sequen

136 The adhesin (gp37) binds Escherichia coli B (E. coli B) by r

137 pear to be hypervirulent, no ligand for this adhesin has been described.

138 The specificity of LPS binding by adhesin has been tested with LPG-based device and confir

139 lactose and the first time that one of these adhesins has been shown to be required for binding of mu

140 onal classification and explain how Epa-like adhesins have evolved in C. glabrata and related fungal

141 tudies on a class of Gram-positive bacterial adhesins have revealed an intramolecular Cys-Gln thioest

142 ociated nsSNPs for FimH, the type 1 fimbrial adhesin, highlights the role of key allelic residues in

143 ed protein domain, based on the cell-surface adhesin HMW1A, is preferentially recognized by antibodie

144 lly infectious strains uniformly express Opa adhesins; however, their specificities were unknown at t

145 lysin/cytolysin (beta-h/c), surface-anchored adhesin HvgA, and capsule to study the role of CovR in U

146 coli, FimH, we demonstrate that locking the adhesin in a low-binding conformation induces the produc

147 ollagenous structures and may function as an adhesin in a process that is required to prevent bacteri

148 The major surface adhesin in HCG is called Cha, which mediates bacterial a

149 ity accompanying overproduction of PrgB-like adhesins in E. faecalis and other clinically-important G

150 A range of fimbrial adhesins in ETEC strains determines host and tissue trop

151 efine the biological roles of B. burgdorferi adhesins in tissue-specific vascular interactions.

152 mophilus influenzae, expressing cell-surface adhesins including N-Glc, to establish a connection betw

153 reus expresses a panel of cell wall-anchored adhesins, including proteins belonging to the microbial

154 NTHi express several adhesins, including the high molecular weight (HMW) adhe

155 The MAM(HS) adhesin interacted with a range of host receptors, throu

156 The arsenal of pneumococcal adhesins interacts with a multitude of extracellular mat

157 tivate the conformational change of the FimH adhesin into its stronger state but also lower than the

158 ecognition receptors detecting the bacterial adhesin invasin (Inv).

159 ernalization is interaction of the bacterial adhesins invasin and YadA with host cell beta1 integrin,

160 Many genes encoding known adhesins involved in epithelial adherence were upregulat

161 In conclusion the hyperglucosylated adhesin is the first example of an N-glucosylated native

162 One such UPEC adhesin is the nonfimbrial adhesin TosA, which mediates

163 a stabilized form of the CFA/I fimbrial tip adhesin, is a protective antigen, using a lethal neonata

164 rominent function in the regulation of other adhesins, is also hypothesized to contribute to tos oper

165 ce to host epithelium, mediated by bacterial adhesins, is one of the first steps in NTHi colonization

166 ered on a subset of plasmid-encoded fimbrial adhesins known as colonization factors and heat-labile t

167 ification of a yet uncharacterized bacterial adhesin, LabA, which specifically recognizes lacdiNAc.

168 in LapD, and resulting in proteolysis of the adhesin LapA and the subsequent release of biofilm cells

169 cteria use their envelope proteins and their adhesin lectins to recognize the glycan residues present

170 we identified FLO9, which encodes a putative adhesin-like cell wall mannoprotein of C. albicans and r

171 olled by modifications of the stage-specific adhesin lipophosphoglycan (LPG).

172 Of these the 21 kDa Leptospira surface adhesin, Lsa21 had strong TLR2 and TLR4 activity leading

173 of clinical isolates are negative for known adhesins, making it difficult to identify antigens for b

174 er, our results demonstrate that the E. coli adhesin MAM(HS) facilitates retention of a gut commensal

175 polymeric microbeads functionalized with the adhesin MAM7 to a burn infected with multidrug-resistant

176 Cells expressing large amounts of HMW adhesins may be critical for the establishment and maint

177 The BabA adhesin mediates high-affinity binding of Helicobacter p

178 suggesting that a single galactose-sensitive adhesin might mediate the interaction of fusobacteria wi

179 antigens, including a novel highly conserved adhesin molecule, EaeH.

180 und to the high-affinity conformation of the adhesin more avidly than to the low-affinity form.

181 ve cycle of T. gondii including secretion of adhesins, motility, invasion, and egress.

182 its in vivo include trimeric autotransporter adhesins, O antigens, and type IV pili (T4P).

183 EfbA is a PavA-like fibronectin adhesin of Enterococcus faecalis previously shown to be

184 CfaE, the tip adhesin of enterotoxigenic Escherichia coli colonization

185 by using a common mannose-specific fimbrial adhesin of Escherichia coli, FimH, we demonstrate that l

186 tion of the protein, named bacterial surface adhesin of GBS (BsaB), depended both on a central BID1 d

187 Hia is a major adhesin of nontypeable Haemophilus influenzae (NTHi) and

188 P1 (antigen I/II) is a sucrose-independent adhesin of Streptococcus mutans whose functional archite

189 We show that the major adhesin of the pneumococcal pilus-1, RrgA, binds both re

190 o the increased surface exposure of the Als3 adhesin on slr1Delta/Delta cells.

191 P1 is an adhesin on the surface of Streptococcus mutans.

192 egarding pilus stiffness and the location of adhesins on pili.

193 tly because of the absence of RemA and other adhesins on the cell surface.

194 against CFA/I minor pilin subunit (CfaE) tip adhesin or colonization factor I (CFA/I) fimbraie (posit

195 The polysaccharide intercellular adhesin or the cell wall-anchored accumulation-associate

196 ocused predominantly on the role of parasite adhesins or signaling pathways and the identity of bindi

197 ease with O7 serogroup (P = .034) and PapGII adhesin (OR, 2.3 [95% CI, 1.2-4.5], P = .015).

198 de known as the polysaccharide intercellular adhesin, or poly N-acetylglucosamine (PIA/PNAG).

199 operon, which encodes another important UPEC adhesin, P fimbria.

200 ignificantly altered, including reduction of adhesin P1 and glucan-binding proteins B and C.

201 The adhesin P1 is localized on the surface of the oral patho

202 riogenic bacterium Streptococcus mutans uses adhesin P1 to adhere to tooth surfaces, extracellular ma

203 dently from the polysaccharide intercellular adhesin PIA.

204 In addition to polysaccharide intercellular adhesin (PIA) and extracellular DNA, surface proteins ap

205 oduction of the polysaccharide intracellular adhesin (PIA) in either strain because the amount of PIA

206 opolysaccharide polysaccharide intercellular adhesin (PIA) were central to the regulatory impact of R

207 e production of polysaccharide intercellular adhesin (PIA), a well-characterized, robust matrix molec

208 es, such as the polysaccharide intercellular adhesin (PIA), with the bacterial cell surface.

209 , we have established that the HMW1 and HMW2 adhesins play a major role in facilitating colonization

210 s cells carrying pCF10 produce three surface adhesins (PrgA, PrgB or Aggregation Substance, PrgC) and

211 uch that as the number of repeats increases, adhesin production decreases.

212 mber affects both hmwA transcription and HMW-adhesin production such that as the number of repeats in

213 -molecule force spectroscopy to show that an adhesin protein can regenerate its thioester in the abse

214 orrelated with reduced expression of the Flp adhesin proteins in the (p)ppGpp mutant but not in the d

215 n is required for the export and function of adhesin proteins that mediate the attachment of pathogen

216 of the domains of the LapA family of biofilm adhesin proteins.

217 produce a unique set of defined glucosylated adhesin proteins.

218 el) the interaction between the pneumococcal adhesin PspC and the human glycoprotein vitronectin.

219 glycosylate the serine-rich repeat (SRR) of adhesin PsrP (pneumococcal serine-rich repeat protein),

220 luding those encoding secreted proteins (the adhesins RapA2, RapB and RapC, two cadherins and the gly

221 n that the type 1 fimbria shaft and the FimH adhesin-receptor interaction are optimized to each other

222 imbriae can reduce fluid shear stress on the adhesin-receptor interaction by which the bacterium adhe

223 a model that describes how the force on the adhesin-receptor interaction of a type 1 fimbria varies

224 in bacterial colonization, and the nature of adhesin-receptor interactions determines bacterial local

225 also deficient in secretion of the motility adhesin RemA but retained the ability to secrete SprB.

226 ted from Denmark, suggesting that this novel adhesin represents an important variant.

227 ow that they promote expression of the curli adhesin, repress the expression of tryptophan metabolism

228 nding protein homolog 5 (PfRH5), a merozoite adhesin required for erythrocyte invasion, is highly sus

229 face exposition of various proteins, such as adhesins, required for gliding motility in Flavobacteriu

230 eumococcal pilus-1, which includes the pilus adhesin RrgA, promotes bacterial penetration through the

231 proteinaceous nature of potential bacterial adhesin(s) for hTSP-1.

232 However, the bacterial adhesin(s) remain elusive.

233 environment of the digestive system are the adhesins SabA and BabA; these molecules belong to the sa

234 dings indicate that the dscCfaE fimbrial tip adhesin serves as a protective passive vaccine antigen i

235 population of adherent cells in spite of HMW adhesin specific antibody-mediated immunity.

236 cur greater fitness costs when faced with an adhesin-specific antibody-mediated immune response.

237 In tissue, Scl1 adhesin specifically recognizes the wound microenvironme

238 These include the surface adhesin SprB that forms filaments about 160 nm long by 6

239 The T9SS secretes the cell surface motility adhesins SprB and RemA and the chitinase ChiA.

240 The propulsion of a cell-surface adhesin, SprB, is known to enable gliding.

241 Studying the pilus tip adhesin Spy0125 of Streptococcus pyogenes, we developed

242 s.S. sanguinisexpresses a serine-rich repeat adhesin, SrpA, similar in sequence to platelet-binding a

243 Here, we describe a novel S. sonnei adhesin, SSO1327 which is a multivalent adhesion molecul

244 ly, these findings establish a new bacterial adhesin structure that has in effect been hijacked by a

245 astric epithelium via outer membrane protein adhesins such as SabA.

246 Gliding results from the movement of adhesins such as SprB and RemA along the cell surface.

247 Members of the Trimeric Autotransporter Adhesin (TAA) family play a crucial role in the adhesion

248 adhesin A (NadA), a trimeric autotransporter adhesin (TAA) that acts in adhesion to and invasion of h

249 ogenesis of UpaG, a trimeric autotransporter adhesin (TAA).

250 Trimeric autotransporter adhesins (TAAs) are important virulence factors of many

251 -related gene encoding a yet-uncharacterized adhesin, termed agg5A.

252 y discovered a widespread group of bacterial adhesins, termed Multivalent Adhesion Molecules (MAMs) t

253 ecifically associates with the transmembrane adhesin TgMIC2.

254 nized functions in addition to serving as an adhesin that binds Le(b).

255 EtpA is a secreted two-partner adhesin that is conserved within the ETEC pathovar.

256 that PKG regulates the secretion of TRAP, an adhesin that is essential for motility.

257 2 is a galactose-sensitive hemagglutinin and adhesin that is likely to play a role in the virulence o

258 lude that BsaB represents a newly identified adhesin that participates in GBS attachment to epithelia

259 As an adhesin that promotes bacterial interaction with fibrone

260 ri and show that HopQ is the surface-exposed adhesin that specifically binds human CEACAM1, CEACAM3,

261 Micronemal protein 2 (MIC2) is the key adhesin that supports gliding motility and host cell inv

262 y to OmpA of A. phagocytophilum (ApOmpA), an adhesin that uses key lysine and glycine residues to int

263 picomplexan parasites depend on cell-surface adhesins that are translocated via an actin-myosin motor

264 , which are extracellular fibers tipped with adhesins that bind mucosal surfaces of the urinary tract

265 sin A (YadA) belongs to a class of bacterial adhesins that form trimeric structures.

266 ues requires the presence of surface-exposed adhesins that have been difficult to identify due to the

267 They also possess putative adhesins that have not been described in encapsulated pn

268 s, including the high molecular weight (HMW) adhesins that mediate attachment to the respiratory epit

269 t the NTHi HMW1 and HMW2 proteins are potent adhesins that mediate efficient in vitro adherence to cu

270 e is an obligate intracellular organism, its adhesins that mediate entry into host cells are essentia

271 tion in surface-exposed molecules, including adhesins that promote host colonization.

272 ETEC adhesion is mediated by lectins (adhesins) that bind to glycoconjugates on the surface of

273 w paradigm for target binding by a bacterial adhesin, the identification of which will inform future

274 enting it from cleaving a cell surface-bound adhesin, thereby promoting cell adhesion.

275 oprotein CD0873 was identified as a putative adhesin through a bioinformatics approach.

276 The pilus adhesin tip protein Cpa promoted Alab49 survival in whol

277 Expression of ace (adhesin to collagen of Enterococcus faecalis), encoding

278 tes of inflammation, and allow the bacterial adhesin to selectively associate with surface-bound liga

279 brium reactivity allows thioester-containing adhesins to sample potential substrates without irrevers

280 For example, the RTX nonfimbrial adhesin TosA mediates adherence to host cells derived fr

281 One such UPEC adhesin is the nonfimbrial adhesin TosA, which mediates adherence to the epithelium

282 wide variety of virulence factors, including adhesins, toxins and type III secretion systems, to caus

283 esentation of cell wall synthesis machinery, adhesins, transporter solute-binding proteins, and degra

284 As the only HSV-1 protein predicted to be an adhesin, UL26.5 is a promising vaccine target.

285 hmwA, which encodes the HMW adhesin, undergoes phase variation mediated by 7-base pa

286 ine triad protein D (PhtD), an S. pneumoniae adhesin vaccine candidate, for its ability to prevent in

287 slocation of apically secreted transmembrane adhesins via their interaction with the parasite actomyo

288 prominent Znf2-downstream adhesion protein (adhesin), was identified to be responsible for the parac

289 n of BsaB in GBS, like that of several other adhesins, was regulated by the CsrRS two-component syste

290 st host proteins recognized by S. pneumoniae adhesins, we showed that S. pneumoniae uptake by cardiom

291 the vicinity of binding pocket-Ser155 for Dr-adhesin were mutated to alanine and subjected to tempora

292 Helicobacter pylori strains express the BabA adhesin, which binds to ABO/Leb blood group antigens on

293 definitive identification of a C. difficile adhesin, which now allows work to devise improved measur

294 w velocities and that the maximum stress the adhesin will experience is limited to approximately 120

295 This is the first report of a borrelial adhesin with a metal ion-dependent adhesion site (MIDAS)

296 ts a fimbrial subunit that forms a polymeric adhesin with a unique arrangement of dual receptor bindi

297 evidence that the borrelial OMP P66, a known adhesin with pore-forming activity, forms a beta-barrel

298 y the interaction between numerous bacterial adhesins with components of the extracellular matrix (EC

299 niae is directly mediated by interactions of adhesins with eukaryotic cellular receptors or indirectl

300 ion, and egress by connecting the micronemal adhesins with the actomyosin system.