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1 ting infection with the riboflavin auxotroph Streptococcus pyogenes.
2 can enter human cells and kill intracellular Streptococcus pyogenes.
3 yte activation in response to infection with Streptococcus pyogenes.
4 s II-bound peptide from the mucosal pathogen Streptococcus pyogenes.
5 ions of adhesion proteins from the bacterium Streptococcus pyogenes.
6 urface of invasive M3-type strain MGAS315 of Streptococcus pyogenes.
7 treptolysin O (SLO), a virulence factor from Streptococcus pyogenes.
8 e 8 charged residues in YtgP, a homolog from Streptococcus pyogenes.
9 lycoside-hydrolase secreted by the bacterium Streptococcus pyogenes.
10 plays an important role in the virulence of Streptococcus pyogenes.
11 cribes such a situation after infection with Streptococcus pyogenes.
12 occus pneumoniae, Staphylococcus aureus, and Streptococcus pyogenes.
13 using two rapid antigen detection assays for Streptococcus pyogenes.
14 ins are critical for the in vivo survival of Streptococcus pyogenes.
15 , including the clinically relevant pathogen Streptococcus pyogenes.
16 d to effectively identify DNA signatures for Streptococcus pyogenes.
17 phil peptide (HNP-1) with the human pathogen Streptococcus pyogenes.
18 AgI/II-family proteins are also expressed by Streptococcus pyogenes.
19 gous to the myosin cross-reactive antigen of Streptococcus pyogenes.
20 share homology with the mitogenic toxins of Streptococcus pyogenes.
21 Cas9 enzymes from Staphylococcus aureus and Streptococcus pyogenes.
22 toxins secreted by Staphylococcus aureus and Streptococcus pyogenes.
23 with PJI, namely, Staphylococcus aureus and Streptococcus pyogenes.
24 s aureus (10 [43.5%] vs 4 [12.9%]; P = .02), Streptococcus pyogenes (2 [8.7%] vs 19 [61.3%]; P < .001
26 mutagenesis approach, we have identified in Streptococcus pyogenes a gene that exhibits a receptor-l
27 r, pharyngitis resulting from infection with Streptococcus pyogenes (a group A Streptococcus [GAS]) c
35 ing a positive result for samples containing Streptococcus pyogenes and a negative result for those w
36 ride (RhaPS) that is essential for growth of Streptococcus pyogenes and contributes to its ability to
38 tudy, we created an RNase III null mutant of Streptococcus pyogenes and its RNA sequencing (RNA-Seq)
40 ce against lethal soft tissue infection with Streptococcus pyogenes and prevented bacterial dissemina
41 al effects against Staphylococcus aureus and Streptococcus pyogenes and protected against staphylococ
42 ive clinical diagnose include Staphylococci, Streptococcus pyogenes and Pseudomonas aeruginosa in ble
43 has never, or rarely, been reported for the Streptococcus pyogenes and S. bovis groups of species, e
45 mber of TCSs compared to the closely related Streptococcus pyogenes and Streptococcus pneumoniae, and
46 which includes common human pathogens, e.g., Streptococcus pyogenes and Streptococcus pneumoniae.
49 ular elements of patients with GP respond to Streptococcus pyogenes and whether this initial immune r
51 utagenesis of EndoS (an endoglycosidase from Streptococcus pyogenes ) and were found to be capable of
52 oth gram-positive (Staphylococcus aureus and Streptococcus pyogenes) and gram-negative bacteria (Pseu
55 ease onset in children and associations with Streptococcus Pyogenes, and influenza A H1N1-infection a
56 map between the significant human pathogen, Streptococcus pyogenes, and proteins from human saliva a
57 tein 9 (Cas9) from Staphylococcus aureus and Streptococcus pyogenes, and recombinant Cas9 and develop
58 in 8 patients, and Streptococcus agalactiae, Streptococcus pyogenes, and Streptococcus salivarius in
60 eus, methicillin-resistant S. aureus (MRSA), Streptococcus pyogenes, and vancomycin-resistant Enteroc
61 Herein, we report the development of the Streptococcus pyogenes anti-CRISPR/Cas9 protein, AcrIIA4
63 li of the nasty gram-positive human pathogen Streptococcus pyogenes are assembled as single, micromet
64 The heme-binding proteins Shp and HtsA of Streptococcus pyogenes are part of the heme acquisition
66 organisms, such as Staphylococcus aureus and Streptococcus pyogenes, are the dominant organisms isola
67 HIV-1 Gag-p24 on the tip of the T3 pilus of Streptococcus pyogenes as a fusion to the Cpa protein (L
68 inhibits growth of the pathogenic bacterium Streptococcus pyogenes as effectively as melittin create
70 (FUD), a polypeptide based on F1 adhesin of Streptococcus pyogenes, binds by anti-parallel beta-stra
71 ustom DNA-binding modules, the nuclease-dead Streptococcus pyogenes Cas9 (dCas9) protein, which recog
74 e-wide off-target effects of the widely used Streptococcus pyogenes Cas9 (SpCas9) are imperfect, poss
79 ontains a mutation in TCAP, treated with the Streptococcus pyogenes Cas9 (SpCas9) nuclease revealed t
80 first synthetic small-molecule inhibitors of Streptococcus pyogenes Cas9 (SpCas9) that weigh <500 Da
81 e this constraint, we engineered variants of Streptococcus pyogenes Cas9 (SpCas9) to eliminate the NG
82 udy by Walton et al. structurally engineered Streptococcus pyogenes Cas9 (SpCas9) to near-PAMless SpR
84 because commonly used endonucleases, such as Streptococcus pyogenes Cas9 (SpCas9), can tolerate up to
85 SaCas9), which is significantly smaller than Streptococcus pyogenes Cas9 (SpCas9), to facilitate effi
90 NA cleavage beyond the 44 degrees C limit of Streptococcus pyogenes Cas9 (SpyCas9) and the 70 degrees
91 uman oral and fecal metagenomes that inhibit Streptococcus pyogenes Cas9 (SpyCas9) in Escherichia col
92 he most commonly used genome editing protein Streptococcus pyogenes Cas9 (SpyCas9), we used both self
93 o 70 degrees C, compared to 45 degrees C for Streptococcus pyogenes Cas9 (SpyCas9), which expands the
95 icity, selectivity, and reaction kinetics of Streptococcus pyogenes Cas9 activity, we challenged libr
97 ng activity that are also among the smallest Streptococcus pyogenes Cas9 base editors described to da
100 fications to the sugar-phosphate backbone of Streptococcus pyogenes Cas9 CRISPR RNA (crRNA) to probe
102 DNA vectors expressing maize codon-optimized Streptococcus pyogenes Cas9 endonuclease and single guid
103 Here, we report the crystal structure of Streptococcus pyogenes Cas9 in complex with sgRNA and it
104 g guide RNA (stgRNA) that repeatedly directs Streptococcus pyogenes Cas9 nuclease activity toward the
105 also compared the cleavage efficiency of the Streptococcus pyogenes Cas9 protein based on expression
106 cular structures of the catalytically active Streptococcus pyogenes Cas9 R-loop that show the displac
107 hese inhibitors also blocked the widely used Streptococcus pyogenes Cas9 when assayed in Escherichia
108 protein containing a catalytically defective Streptococcus pyogenes Cas9, a cytidine deaminase, and a
110 egulatory sequences to conditionally express Streptococcus pyogenes Cas9, and V. carteri U6 RNA gene
111 ing method using only the well-characterized Streptococcus pyogenes Cas9, by incorporating MS2 or PP7
112 However, in M. tuberculosis, the existing Streptococcus pyogenes Cas9-based CRISPRi system is of l
119 d expression and activity of SLO, DNase, and Streptococcus pyogenes cell envelope protease in vitro.
121 etween sequence, stability, and folding, the Streptococcus pyogenes collagenous domain CL (Gly-Xaa-Ya
125 Type-II CRISPR-Cas systems, such as the Streptococcus pyogenes CRISPR-Cas9 system, can be adapte
129 reveal that a bacterial endoglycosidase from Streptococcus pyogenes , EndoS, is complementary to othe
130 ant bacterial pathogens in humans, including Streptococcus pyogenes, express surface proteins that bi
131 -residue functional upstream domain (FUD) of Streptococcus pyogenes F1 adhesin interacts with fibrone
133 to the surface of the human pathogen group A Streptococcus pyogenes (GAS) and subsequent hPg activati
141 -mediated opsonophagocytosis enables group A Streptococcus pyogenes (GAS) to establish infection.
142 rt a population genomic study of the group A Streptococcus pyogenes (GAS), a human pathogen with high
143 treptococcus pyogenes (gram-positive group A Streptococcus pyogenes [GAS]) recruit host single-chain
144 The normalized fluorescence intensity of the Streptococcus pyogenes gave a signal that is up to 16.4
147 tics is a global concern in the treatment of Streptococcus pyogenes (group A Streptococcus [GAS]) inf
148 Rgg2 and Rgg3 (Rgg2/3) regulatory circuit of Streptococcus pyogenes (group A streptococcus [GAS]) is
155 e role of zinc efflux in the pathogenesis of Streptococcus pyogenes (group A Streptococcus [GAS]), a
156 d an RNase Y ortholog has been identified in Streptococcus pyogenes (group A streptococcus [GAS]).
157 a, including one (stk) in the human pathogen Streptococcus pyogenes (group A streptococcus [GAS]).
158 t to which glucose alters gene expression in Streptococcus pyogenes (group A streptococcus) and the c
160 the Gram-positive human-restricted pathogen Streptococcus pyogenes (Group A Streptococcus, GAS) has
162 ity of North-East Asian serotype M12 (emm12) Streptococcus pyogenes (group A Streptococcus, GAS) to c
166 of many human pathogenic bacteria, including Streptococcus pyogenes (Group A Streptococcus; GAS), Str
168 rammed genome editing using CRISPR/Cas9 from Streptococcus pyogenes has enabled rapid and accessible
169 , formed autocatalytically, in the pili from Streptococcus pyogenes has highlighted the role that suc
170 mbinant immunoglobulin G-degrading enzyme of Streptococcus pyogenes (IdeS) followed by chemical reduc
172 bacterial protease, IgG-degrading enzyme of Streptococcus pyogenes (IdeS), cleaves the hinge region
173 A bacterial enzyme, IgG-degrading enzyme of Streptococcus pyogenes (IdeS), was shown to specifically
174 use of immunoglobulin G-degrading enzyme of Streptococcus pyogenes (IdeS), which is capable of diges
175 A reactivity against IgG-degrading enzyme of Streptococcus pyogenes (IdeS)- or pepsin-generated F(ab'
177 occus aureus, Staphylococcus epidermidis and Streptococcus pyogenes in a soft-tissue wound biofilm mo
179 pha2 exhibited considerable activity against Streptococcus pyogenes, indicating a role of PSMs in the
180 rate that type I interferons produced during Streptococcus pyogenes infection are required to prevent
181 ated as an adjunctive treatment for clinical Streptococcus pyogenes infection however, the protein ta
182 , and laboratory testing for confirmation of Streptococcus pyogenes infection is required to prevent
183 ontrast to infection of superficial tissues, Streptococcus pyogenes infection of deeper tissue can be
189 owed that the adhesive is capable of killing Streptococcus pyogenes introduced subcutaneously at the
195 The ExPortal protein secretion organelle in Streptococcus pyogenes is an anionic phospholipid-contai
200 epeats (CRISPR)-associated protein Cas9 from Streptococcus pyogenes is an RNA-guided DNA endonuclease
211 h year, millions of people are infected with Streptococcus pyogenes, leading to an estimated 500,000
212 ombined with focused experimental testing in Streptococcus pyogenes, led to a better understanding of
213 f a catalytically inactive Cas9 (dCas9) from Streptococcus pyogenes loaded with single guide RNAs (sg
214 r Staphylococcus aureus (</=0.12 microg/mL), Streptococcus pyogenes (</=0.12 microg/mL), Streptococcu
215 nella enterica, Clostridioides difficile, or Streptococcus pyogenes, multiple highly conserved DNA MT
217 ected mutagenesis of an endoglycosidase from Streptococcus pyogenes of serotype M49 (Endo-S2) and the
223 ginosus group, Streptococcus pneumoniae, and Streptococcus pyogenes), positive percent agreement (PPA
230 ar analysis conducted on streptolysin O from Streptococcus pyogenes revealed that this CDC also has g
233 en was used to identify mutations in rgg2 of Streptococcus pyogenes (rgg2Sp ) that conferred pheromon
235 The AF, but not the meconium SALSA, bound to Streptococcus pyogenes, S. agalactiae, S. gordonii, and
236 resent in pathogenic streptococci, including Streptococcus pyogenes, S. agalactiae, S. pneumoniae, an
240 human pathogens Streptococcus pneumoniae and Streptococcus pyogenes, SEER identifies relevant previou
241 cluding that in group A Streptococcus (GAS) (Streptococcus pyogenes Ser/Thr kinase (SP-STK)), regulat
242 the eukaryote-type serine/threonine kinase (Streptococcus pyogenes serine/threonine kinase; SP-STK)
245 limitations, we have developed CRISPR-RGR, a Streptococcus pyogenes (Sp)Cas9-based gene editing syste
246 The CRISPR-associated endonuclease Cas9 from Streptococcus pyogenes (spCas9) along with a single guid
247 arget and off-target activities of Cas9 from Streptococcus pyogenes (SpCas9) and the SpCas9 variants
248 (CRISPR)-associated endonuclease (Cas)9 from Streptococcus pyogenes (SpCas9) can be used to edit sing
249 The RNA-guided CRISPR-Cas9 nuclease from Streptococcus pyogenes (SpCas9) has been widely repurpos
250 he exogenous protein Cas9 from the bacterium Streptococcus pyogenes (SpCas9) in plasma samples by mea
252 In vitro assays demonstrate that Cas9 from Streptococcus pyogenes (SpCas9) is more active in creati
253 (CRISPR)-associated endonuclease (Cas)9 from Streptococcus pyogenes (SpCas9) is used to deplete VEGFR
254 ver, the size of the commonly used Cas9 from Streptococcus pyogenes (SpCas9) limits its utility for b
255 c Cas9, the most widely used is derived from Streptococcus pyogenes (SpCas9), with a complementary sm
258 acCas9 to its well-established ortholog from Streptococcus pyogenes (SpyCas9), and further engineer a
259 e measured affinities of Cas9 nucleases from Streptococcus pyogenes, Staphylococcus aureus, and Franc
260 for entry of other virulent pathogens (e.g., Streptococcus pyogenes, Staphylococcus aureus, and poten
261 e first complete, closed genome sequences of Streptococcus pyogenes strains NCTC 8198(T) and CCUG 420
262 identifying variation, we pooled DNA of 100 Streptococcus pyogenes strains of different emm types in
264 Enterococcus faecalis, Enterococcus faecium, Streptococcus pyogenes, Streptococcus agalactiae, and St
265 eruginosa, S. aureus, Enterococcus faecalis, Streptococcus pyogenes, Streptococcus agalactiae, and vi
266 pathogens, including Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae, Helico
267 against local and/or systemic infections by Streptococcus pyogenes, Streptococcus pneumoniae, Lister
268 rsA homologues encoded by Bacillus subtilis, Streptococcus pyogenes, Streptococcus pneumoniae, Strept
269 reproduce the canonical PAM preferences for Streptococcus pyogenes, Streptococcus thermophilus CRISP
273 /SpyCatcher), based on a protein domain from Streptococcus pyogenes, that locks itself together via s
274 toxin production and increased virulence in Streptococcus pyogenes The nature of the polymorphism is
275 type M1 and M3 strains of the human pathogen Streptococcus pyogenes (the group A Streptococcus [GAS])
277 l streptococci, including the human pathogen Streptococcus pyogenes(the group A Streptococcus[GAS]),
278 r model organisms, Staphylococcus aureus and Streptococcus pyogenes, the activity is dependent on pri
279 Herein we report that in the human pathogen Streptococcus pyogenes, the adaptive response to Mn limi
280 toxins produced by Staphylococcus aureus and Streptococcus pyogenes, the superantigens (SAgs) are the
282 protein against the Gram-positive bacterium Streptococcus pyogenes This protein is composed of two d
284 ontaining Lancefield group A carbohydrate of Streptococcus pyogenes to study the effects of bacterial
285 ction of Staphylococcus aureus harboring the Streptococcus pyogenes type II-A CRISPR-Cas system.
286 To overcome these challenges, the pathogen Streptococcus pyogenes utilizes the protein Cpa, a pilus
287 n-mediated translocation (CMT), performed by Streptococcus pyogenes, utilizes the cholesterol-depende
289 ermore, utilization of supplied 5-CHO-THF by Streptococcus pyogenes was shown to require expression o
291 Studying the pilus tip adhesin Spy0125 of Streptococcus pyogenes, we developed a single molecule a
292 elical peptide epitope from the M protein of Streptococcus pyogenes, were designed by exchanging one
293 h a fluorescent antibody complex specific to Streptococcus pyogenes, were volumetrically normalized a
294 cterial enzyme IdeS (IgG-degrading enzyme of Streptococcus pyogenes), which selectively cleaves IgG a
295 betabetaalpha/metal-dependent nuclease from Streptococcus pyogenes, which is encoded by the SF370.1
297 e also analyzed promiscuity of epitopes from Streptococcus pyogenes, which is known to exhibit epitop
298 tting a pilin subunit from a human pathogen, Streptococcus pyogenes, which usually undergoes intramol
299 lence of many bacterial pathogens, including Streptococcus pyogenes, which utilizes the cholesterol-d