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1 infected with antibiotic-resistant Neisseria gonorrhoeae).
2 namics of RMS and methylation patterns in N. gonorrhoeae.
3 t the radiant exposure used to inactivate N. gonorrhoeae.
4 that is conserved and surfaced exposed in N. gonorrhoeae.
5 gH1 to target the same enzyme from Neisseria gonorrhoeae.
6 ting studies against organisms other than N. gonorrhoeae.
7 xygen was involved in aBL inactivation of N. gonorrhoeae.
8 ynamics of microcolonies formed by Neisseria gonorrhoeae.
9 the generation of antibodies recognizing N. gonorrhoeae.
10 logical approach, for the inactivation of N. gonorrhoeae.
11 is of the closely related species, Neisseria gonorrhoeae.
12 meningitidis, no vaccine is available for N. gonorrhoeae.
13 bited rapid bactericidal activity against N. gonorrhoeae.
14 s in PBP2 underpins the ESC resistance of N. gonorrhoeae.
15 able expression amongst strains of Neisseria gonorrhoeae.
16 /mL for C. trachomatis and 1500CFU/mL for N. gonorrhoeae.
17 the global threat of multidrug-resistant N. gonorrhoeae.
18 exposure and decreased susceptibility of N. gonorrhoeae.
19 exposure and decreased susceptibility of N. gonorrhoeae.
20 mmon sexually transmitted pathogen Neisseria gonorrhoeae.
21 ections: Chlamydia trachomatis and Neisseria gonorrhoeae.
22 o modulate biofilm accumulation by Neisseria gonorrhoeae.
23 bal spread of antibiotic-resistant Neisseria gonorrhoeae.
24 uishable from infections caused by Neisseria gonorrhoeae.
25 ce for bacterial pathogens such as Neisseria gonorrhoeae.
26 IL-8 by endocervical cells infected with N. gonorrhoeae.
27 rce of antimicrobial resistance in Neisseria gonorrhoeae.
28 DA-approved gold-containing drugs against N. gonorrhoeae.
29 against an important eye pathogen, Neisseria gonorrhoeae.
30 both Streptococcus pneumoniae and Neisseria gonorrhoeae.
32 sting was 8.5% for C trachomatis, 7.1% for N gonorrhoeae, 16.1% for T vaginalis, 18.1% for bacterial
33 ed for C. trachomatis (887 specimens) and N. gonorrhoeae (890 specimens) at the Children's Hospital o
34 and diagnostic escape variants in Neisseria gonorrhoeae, a pathogen associated with a high burden of
36 spatus, Gardnerella vaginalis, and Neisseria gonorrhoeae All vaginal microbiota and N. gonorrhoeae ef
37 stasis affecting antibiotic resistance in N. gonorrhoeae and a generalizable approach for epistatic g
38 technology to examine the epidemiology of N. gonorrhoeae and associated AMR in the Australian populat
39 gative percent agreement for detection of N. gonorrhoeae and C. trachomatis for 3 investigational ass
40 gative percent agreement for detection of N. gonorrhoeae and C. trachomatis for three investigational
43 lection of urethral discharge to diagnose N. gonorrhoeae and Chlamydia trachomatis infection in certa
45 sserial heparin-binding antigen (NHBA) of N. gonorrhoeae and confirm its role in binding to several g
46 -based tool for genomic contact tracing of N gonorrhoeae and demonstrate local, national, and interna
47 pects of the colonization and survival of N. gonorrhoeae and may be a target for new antimicrobial or
49 However, only infection with pathogenic N. gonorrhoeae and not infection with the other bacteria te
50 he monoglyceride monocaprin rapidly kills N. gonorrhoeae and other bacterial species and is non-irrit
53 (ii) swabs seeded with C. trachomatis and N. gonorrhoeae and then placed in transport medium were tes
54 me (OR, 0.24; 95% 0.09, 0.66), and Neisseria gonorrhoeae and/or Chlamydia trachomatis had 92% lower o
57 eographical and temporal spread of AMR in N. gonorrhoeae, and improved understanding of the pharmacok
60 olone-resistant Campylobacter spp, Neisseria gonorrhoeae, and Salmonella typhi were included in the h
61 entified similar numbers of C trachomatis, N gonorrhoeae, and T vaginalis infections, but much higher
62 y rates for Chlamydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis DNA, detected usi
63 ecimens for Chlamydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis via commercial tr
64 ee well-defined species (N. meningitidis; N. gonorrhoeae; and Neisseria polysaccharea) and genomes of
65 ting several resistance threats including N. gonorrhoeae AR-Ng testing, a subactivity of the CDC's AR
66 e rising, and antibiotic-resistant Neisseria gonorrhoeae (AR-Ng) is an urgent public health threat.
69 ork supported the laboratory capacity for N. gonorrhoeae AST and associated genetic marker detection,
70 e primary outcome was clearance of Neisseria gonorrhoeae at all initially infected sites, defined as
72 ipants were tested for C. trachomatis and N. gonorrhoeae at three sites (anorectum, pharynx, and uret
74 on of patients with eradication of genital N gonorrhoeae based on culture at test of cure, assessed i
77 her, the study identifies transmission of N. gonorrhoeae between HIV-positive and HIV-negative indivi
78 uenzner and Hauck (2020) find that Neisseria gonorrhoeae blocks exfoliation by producing nitric oxide
79 o detect Chlamydia trachomatis and Neisseria gonorrhoeae, but no commercial tests are cleared by the
80 sed to investigate transmission of Neisseria gonorrhoeae, but to date, most studies have not combined
81 nofin reduced the burden of intracellular N. gonorrhoeae by over 99% outperforming the drug of choice
82 cal urine and swab specimens positive for N. gonorrhoeae by the Cobas assay, 71% could be genotyped.
86 s two, Neisseria meningitidis, and Neisseria gonorrhoeae, cause invasive disease: the other eight are
89 A antibodies that bound to the surface of N. gonorrhoeae cells, as shown by indirect fluorescent anal
91 NGU was considered idiopathic when Neisseria gonorrhoeae, Chlamydia trachomatis, Mycoplasma genitaliu
93 administered intravaginally (10 mug/d) to N. gonorrhoeae-colonized mice were equally efficacious.
94 The objective of this work was to assess N. gonorrhoeae confirmation in over 13,000 N. gonorrhoeae s
97 post collection, 100% yielded concordant N. gonorrhoeae culture results compared to immediate proces
102 med a meta-analysis of seven large Neisseria gonorrhoeae datasets, as well as Klebsiella pneumoniae a
105 ction methods that maximize the amount of N. gonorrhoeae DNA sequenced while minimizing contaminating
106 e sequencing can detect sufficient Neisseria gonorrhoeae DNA to reconstruct whole genomes directly fr
107 ia gonorrhoeae All vaginal microbiota and N. gonorrhoeae efficiently colonized the 3-D surface, local
108 The human-restricted pathogen Neisseria gonorrhoeae encodes a single N-acetylmuramyl-l-alanine a
109 he ceftriaxone plus azithromycin group had N gonorrhoeae eradication at test of cure (difference -4.0
110 mice to study mechanisms by which Neisseria gonorrhoeae evades host-derived antimicrobial factors an
111 We demonstrate for the first time that N. gonorrhoeae exploits this host strategy in a novel defen
113 rolide use and azithromycin resistance in N. gonorrhoeae, finding that population-wide macrolide use
115 81% sensitivity and 100% specificity for N. gonorrhoeae from isolates with a representative database
123 nfluenzae, Neisseria meningitidis, Neisseria gonorrhoeae, Helicobacter pylori, Moraxella catarrhalis,
124 trachomatis and rectum and oropharynx for N. gonorrhoeae Hence, extragenital screening is critical fo
125 n of nucleic acid amplification tests for N. gonorrhoeae identification, the capacity for culturing N
128 sensitivity of Cobas for the detection of N. gonorrhoeae in female specimens was 94.8% (95% CI, 89.6%
129 ty and specificity of Cobas for detecting N. gonorrhoeae in male urine were 100.0% (95% CI, 95.8% to
130 and cefixime-resistant strains of Neisseria gonorrhoeae in MSM in England, which was applied to data
132 ssay (Xpert) to detect C. trachomatis and N. gonorrhoeae in rectal and pharyngeal samples from 224 me
134 dentification, the capacity for culturing N. gonorrhoeae in the United States has declined, along wit
136 tion and alters the infection dynamics of N. gonorrhoeae in vitro Furthermore, miR-718 regulates the
137 glucose inhibited 48 clinical isolates of N. gonorrhoeae including multidrug-resistant strains at a c
138 cated that aBL preferentially inactivated N. gonorrhoeae, including antibiotic-resistant strains, ove
139 ng of FH/FHL-1 through domains 6 and 7 to N. gonorrhoeae increased with truncation of the heptose I (
140 We previously reported FH binding to N. gonorrhoeae independently of lipooligosaccharide (LOS) s
142 n populations at high risk of contracting N. gonorrhoeae induces an increase in MIC and may result in
143 n populations at high risk of contracting N. gonorrhoeae induces an increase in MIC, and may result i
145 iated with bacterial burden during Neisseria gonorrhoeae infection and alters the infection dynamics
146 are Gram stain testing to diagnose Neisseria gonorrhoeae infection and nongonococcal urethritis (NGU)
147 nsequences of sexually transmitted Neisseria gonorrhoeae infection and probably involve an imbalance
148 Pre- and postmarketing safety reports of N. gonorrhoeae infection in patients receiving eculizumab w
150 atomic distribution of C. trachomatis and N. gonorrhoeae infection is needed to optimize future scree
151 considered for point-of-care diagnosis of N. gonorrhoeae infection or NGU in men, meatal swabs should
154 is infection, 0.56 [95% CI, .19-1.67] for N. gonorrhoeae infection, and 0.66 [95% CI, .38-1.15] for M
157 The majority of oropharyngeal Neisseria gonorrhoeae infections are asymptomatic, and many infect
159 iological investigation demonstrated that N. gonorrhoeae infections are dominated by relatively few s
160 ssed the positivity of C. trachomatis and N. gonorrhoeae infections at different anatomic sites in a
161 influence detection of C. trachomatis and N. gonorrhoeae infections at specific anatomic testing site
162 data on the burden of C. trachomatis and N. gonorrhoeae infections by anatomic site is lacking in ch
163 versal testing detected more oropharyngeal N.gonorrhoeae infections compared to selective testing, of
164 fication tests (NAATs) to diagnose Neisseria gonorrhoeae infections complicates the performance of a
165 g identified 92-100% of C. trachomatis or N. gonorrhoeae infections in participants assigned female a
167 that the prevalence of C. trachomatis and N. gonorrhoeae infections is much higher in extragenital so
168 ersal testing detected more oropharyngeal N. gonorrhoeae infections than selective testing, of which
169 ly more prevalent than C. trachomatis and N. gonorrhoeae infections, while the M. genitalium infectio
174 nding the evolutionary dynamics of Neisseria gonorrhoeae is a significant public and global health pr
175 he rise of antimicrobial-resistant Neisseria gonorrhoeae is a significant public health concern.
178 or public health concern globally is that N. gonorrhoeae is evolving high levels of antimicrobial res
180 The sexually transmitted pathogen Neisseria gonorrhoeae is regarded as being on the way to becoming
181 f colonization and pathogenesis of Neisseria gonorrhoeae is required to aid development of new treatm
182 Gonorrhea, caused by the bacterium Neisseria gonorrhoeae, is a globally prevalent sexually transmitte
184 losporin resistance-comprised 8.9% of all N. gonorrhoeae isolates and were primarily observed in male
186 n 1102 resistant and susceptible clinical N. gonorrhoeae isolates collected from 2000 to 2013 via the
191 ithromycin nonsusceptibility among Neisseria gonorrhoeae isolates threatens current treatment recomme
193 2018, the network tested 8,214 and 8,628 N. gonorrhoeae isolates, respectively, and the CDC received
196 dentify multilocus sequence types (MLST), N. gonorrhoeae multiantigen sequence types (NG-MAST), and m
197 currence of Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, and Trichomonas vagi
199 samples represent robust biospecimens for N. gonorrhoeae NAAT testing and may not require confirmatio
201 mmend the systematic screening for Neisseria gonorrhoeae (NG) and Chlamydia trachomatis (CT) infectio
202 y identify those with extragenital Neisseria gonorrhoeae (NG) and Chlamydia trachomatis (CT) so unive
205 c susceptibility testing (AST) for Neisseria gonorrhoeae (Ng) is critically needed to counter widespr
206 k-based mathematical model of HIV, Neisseria gonorrhoeae (NG), and Chlamydia trachomatis (CT) transmi
208 s As with N. meningitidis NspA (Nm-NspA), N. gonorrhoeae NspA (Ng-NspA) bound FH/FHL-1 through FH dom
210 tion, we assessed the cross-reactivity to N. gonorrhoeae of serum raised to the meningococcal vaccine
212 boratory isolation or detection of Neisseria gonorrhoeae only from a clinical specimen, and controls
214 ; 95% CI, 1.9-2.1), concurrent urogenital N. gonorrhoeae (OR, 2.4; 95% CI, 2.1-2.7), and concurrent a
216 nce of any bacterial STI (C. trachomatis, N. gonorrhoeae, or M. genitalium infection) was lower in th
218 OR2.0,95%CI1.9-2.1), concurrent urogenital N.gonorrhoeae (OR2.4,95%CI2.1-2.7), and concurrent anorect
220 prevalent among HIV-infected MSM (Neisseria gonorrhoeae, P = .03; Mycoplasma genitalium, P = .04; HS
221 transfer between bacteria, and in Neisseria gonorrhoeae plasmids can mediate high-level antimicrobia
225 c Chlamydia trachomatis Q(x) (CTQ)/Neisseria gonorrhoeae Q(x) (GCQ), Hologic Aptima Combo 2 (AC2) and
226 range for zoliflodacin against the Neisseria gonorrhoeae QC strain ATCC 49226 was defined as 0.06 to
227 rethral gonorrhea, >=92.8% coverage of an N. gonorrhoeae reference genome was achieved in all samples
233 . gonorrhoeae confirmation in over 13,000 N. gonorrhoeae screen-positive samples representing various
235 atis sensitivity 58.3%, specificity 44.7%; N gonorrhoeae sensitivity 66.0%, specificity 45.2%; T vagi
236 tis (sensitivity 71.7%, specificity 100%), N gonorrhoeae (sensitivity 76.0%, specificity 100%), and T
238 ous studies have demonstrated that Neisseria gonorrhoeae sialylates the terminal N-acetyllactosamine
240 mydia trachomatis AC2 also detects Neisseria gonorrhoeae Storage and temperature conditions may impac
241 pecies, Neisseria meningitidis and Neisseria gonorrhoeae, straddle the border between commensalism an
242 derived from the decreased-susceptibility N. gonorrhoeae strain 35/02 and ESC-resistant strain H041.
243 The prevalence of mosaic PBP2 harboring N. gonorrhoeae strains highlight the ability for new N. gon
245 eae strains highlight the ability for new N. gonorrhoeae strains to spread and become established acr
247 ected to rise due to the spread of Neisseria gonorrhoeae strains with decreased susceptibility to ext
248 ne showed an additive effect against four N. gonorrhoeae strains, suggesting the possibility of using
250 ma genitalium, Mycoplasma hominis, Neisseria gonorrhoeae, Streptococcus agalactiae, Chlamydia trachom
253 cid amplification tests for C trachomatis, N gonorrhoeae, T vaginalis, bacterial vaginosis, and vulvo
254 ssociated with the unique function of the N. gonorrhoeae T4SS as well as generic features of F-type T
258 t antibiotics in 1,102 isolates of Neisseria gonorrhoeae that were confirmed in a second dataset of 4
259 ltidrug-resistant bacteria such as Neisseria gonorrhoeae The first structure of BamA, the central com
260 lement-inhibitory activity, also binds to N. gonorrhoeae The ligand for both FH and FHL-1 was identif
261 e clinical features of C. trachomatis and N. gonorrhoeae, the 2 organisms that drive research agendas
267 A, the central component of BAM, was from N. gonorrhoeae, the etiological agent of the sexually trans
268 those of Chlamydia trachomatis and Neisseria gonorrhoeae, the mechanisms by which this pathogen elici
272 pulations in the susceptibility of Neisseria gonorrhoeae to antimicrobials, and the reasons for this
273 or misS severely reduced the capacity of N. gonorrhoeae to colonize mice or maintain infection over
275 en mini kit provided the highest ratio of N. gonorrhoeae to human DNA and the most consistent results
276 highlights the role for NspA in enabling N. gonorrhoeae to subvert complement despite LOS phase vari
277 enterica, Haemophilus ducreyi and Neisseria gonorrhoeae, together with BamA's homolog, TamA from E.
278 platform using RNA signatures for Neisseria gonorrhoeae Transcriptome sequencing (RNA-seq) followed
279 genitalium, Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis, Mycoplasma hominis,
280 f the lipooligosaccharide (LOS) of Neisseria gonorrhoeae undergoes positive selection during human in
282 cimens were tested for C. trachomatis and N. gonorrhoeae using a Gen-Probe Aptima Combo 2 assay.
283 odel for the study of the pathogenesis of N. gonorrhoeae using a well-characterized DeltapilT mutant.
286 crobial resistance determinants in Neisseria gonorrhoeae was developed and is publicly accessible.
287 ction of Chlamydia trachomatis and Neisseria gonorrhoeae was established in a multisite, prospective
289 assay for detection of C. trachomatis or N. gonorrhoeae was observed, although some mailed swabs too
290 imulated infections, if >=10(4) CFU/ml of N. gonorrhoeae was present, sequencing of the large majorit
291 ependent velocity of DNA uptake by Neisseria gonorrhoeae We found that the DNA uptake velocity depend
292 ent risk factors for oropharyngeal Neisseria gonorrhoeae were assessed among MSM routinely universall
293 ndependent risk factors for oropharyngeal N. gonorrhoeae were assessed among MSM routinely universall
294 ctivatable photosensitizing porphyrins in N. gonorrhoeae were identified and quantified using ultrape
295 e transmission clusters (>=10 samples) of N. gonorrhoeae were susceptible to ciprofloxacin, ceftriaxo
296 the cervicovaginal microbiome can modify N. gonorrhoeae, which will enhance successful transmission
297 gnificantly decreased serum resistance of N. gonorrhoeae with either wild-type or truncated LOS.
300 etion of human DNA with saponin increased N. gonorrhoeae yields in simulated infections but decreased