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1 rata, 2 coagulase-negative Staphylococcus, 1 Streptococcus pneumoniae).
2 icobacter pylori, Moraxella catarrhalis, and Streptococcus pneumoniae.
3 ntibiotic resistance in both V. cholerae and Streptococcus pneumoniae.
4 enzyme LicC, which is a virulence factor in Streptococcus pneumoniae.
5 ia meningitidis, Haemophilus influenzae, and Streptococcus pneumoniae.
6 were collected and cultured for isolation of Streptococcus pneumoniae.
7 (OVA) and then infected with M pneumoniae or Streptococcus pneumoniae.
8 ia, including the major respiratory pathogen Streptococcus pneumoniae.
9 cell wall biosynthesis and cell division of Streptococcus pneumoniae.
10 PD and challenged with opsonized serotype 14 Streptococcus pneumoniae.
11 so abrogating the virulence of the pathogen Streptococcus pneumoniae.
12 Th) 17 cells are important in the control of Streptococcus pneumoniae.
13 concept of this approach for 2 serotypes of Streptococcus pneumoniae.
14 logous stimulation with Escherichia coli and Streptococcus pneumoniae.
15 owth of the major human respiratory pathogen Streptococcus pneumoniae.
16 y erm(B) confer most macrolide resistance in Streptococcus pneumoniae.
17 es was correlated with relative abundance of Streptococcus pneumoniae.
18 e the agglutination of specific serotypes of Streptococcus pneumoniae.
19 man respiratory mucus and the human pathogen Streptococcus pneumoniae.
20 requently identified organism on culture was Streptococcus pneumoniae.
21 t transcription waves defining competence in Streptococcus pneumoniae.
22 mice, and the airway was then infected with Streptococcus pneumoniae.
23 gnificantly increased for nonneonates, while Streptococcus pneumoniae (1.07 to 0.26) and Enterococcus
24 an herpesvirus 6; 2 group B Streptococcus; 2 Streptococcus pneumoniae; 1 HSV; 1 parechovirus; 1 enter
25 were Staphylococcus aureus (34/37 [91.9%]), Streptococcus pneumoniae (10/11 [90.9%]), and Enterobact
26 re used to test 10 Staphylococcus aureus, 10 Streptococcus pneumoniae, 10 Haemophilus influenzae, and
27 operative bile and wound infection cultures (Streptococcus pneumoniae, 114 cultures [47.9%] in instit
29 uses were group B streptococcus 25% (16-33), Streptococcus pneumoniae 17% (9-6), and S aureus 12% (3-
30 ys, we estimate 40,600 pneumonia deaths from Streptococcus pneumoniae, 20,700 from RSV, 12,600 from i
31 The most common blood culture isolates were Streptococcus pneumoniae (24.9%), Staphylococcus aureus
33 ), whereas blood cultures most commonly grew Streptococcus pneumoniae (33%), followed by S. aureus (2
34 ogens were Klebsiella pneumoniae (86 [31%]), Streptococcus pneumoniae (54 [20%]), HIV (40 [15%]), and
36 detected among the 126 confirmed cases were Streptococcus pneumoniae (93 [73.8%]), Haemophilus influ
39 ryngeal infection by S. pyogenes, but not by Streptococcus pneumoniae, a bacterium that does not prod
40 ing on mitochondrial function in response to Streptococcus pneumoniae, a causative agent of bacterial
41 substantially reduced disease burden due to Streptococcus pneumoniae, a leading cause of childhood m
43 opportunistic pathogens Escherichia coli and Streptococcus pneumoniae across European countries and t
49 evolution, transmission and pathogenesis of Streptococcus pneumoniae, an opportunistic human-adapted
51 he pneumonococcal capsular polysaccharide of Streptococcus pneumoniae and against the AD-2S1 peptide
52 ureus in keratitis; Streptococcus viridians, Streptococcus pneumoniae and Coagulase negative Staphylo
53 States for instance, Staphylococcus aureus, Streptococcus pneumoniae and Haemophilus influenzae are
54 ated killing enhanced pulmonary clearance of Streptococcus pneumoniae and Haemophilus influenzae in w
55 hood mortality and morbidity attributable to Streptococcus pneumoniae and Haemophilus influenzae type
57 between the opportunistic bacterial pathogen Streptococcus pneumoniae and its human host is its abili
59 that is also conserved in pathogens such as Streptococcus pneumoniae and Mycobacterium tuberculosis
61 nomic datasets of two major human pathogens, Streptococcus pneumoniae and Neisseria meningitidis, rev
63 us aureus, Coagulase negative Staphylococci, Streptococcus pneumoniae and Pseudomonas aeruginosa are
64 ng affects both susceptibility to subsequent Streptococcus pneumoniae and Staphylococcus aureus infec
65 were diagnosed with influenza or bacterial (Streptococcus pneumoniae and Staphylococcus aureus) etio
68 acillus subtilis, Listeria monocytogenes and Streptococcus pneumoniae) and suggest their importance f
69 dies, 19 met inclusion criteria (12 assessed Streptococcus pneumoniae) and were used for qualitative
70 lin (Ig) levels, specific antibodies against Streptococcus pneumoniae, and allergen-specific IgE, as
71 stillation of MS-WF, mice were infected with Streptococcus pneumoniae, and bronchoalveolar lavage flu
72 kin 17A (IL-17A) response against colonizing Streptococcus pneumoniae, and its transition to a pathog
73 coli derived lipopolysaccharide, heat-killed Streptococcus pneumoniae, and Mycobacterium tuberculosis
74 s agalactiae, Streptococcus anginosus group, Streptococcus pneumoniae, and Streptococcus pyogenes), p
75 histoplasmosis; pneumonia (viral, bacterial, Streptococcus pneumoniae, and unspecified pneumonia); in
76 e closely related Streptococcus pyogenes and Streptococcus pneumoniae, and while research on GBS TCSs
77 gate vaccine (PCV) antibiotic-nonsusceptible Streptococcus pneumoniae (ANSP) carriage: reduction of P
79 ify HAMLET's bacterial targets, here we used Streptococcus pneumoniae as a model organism and employe
80 terococcus faecalis ATCC 29212 (broth only), Streptococcus pneumoniae ATCC 49619 (disk and broth), an
81 chia coli ATCC 25922, 0.12 to 0.5 mug/ml for Streptococcus pneumoniae ATCC 49619, and 0.12 to 1 mug/m
82 methicillin-resistant Staphylococcus aureus, Streptococcus pneumoniae, beta-hemolytic streptococci, v
83 occus sp. was associated with qPCR levels of Streptococcus pneumoniae but dominance could not be pred
84 lla catarrhalis, Haemophilus influenzae, and Streptococcus pneumoniae, but not other bacterial pathog
85 ort in species such as Bacillus subtilis and Streptococcus pneumoniae, but whether this same mechanis
87 nce and vaccine escape in the human pathogen Streptococcus pneumoniae can be largely attributed to co
91 ral infections, but the impact of viruses on Streptococcus pneumoniae carriage prevalence and load re
94 screen for mutations affecting the growth of Streptococcus pneumoniae cells when the aPBP synthase PB
98 ens, Streptococcus sanguinis (ComGC(SS)) and Streptococcus pneumoniae (ComGC(SP)), revealing that thi
101 ring formation in the ovoid-shaped pathogen, Streptococcus pneumoniae Conventional and single-molecul
102 this study, we use glycoconjugates of type 3 Streptococcus pneumoniae CPS (Pn3P) to assess whether th
103 with positive UAT more often had a positive Streptococcus pneumoniae culture (25.4% vs 1.9%, P < .00
106 Listeria innocua, Pseudomonas aeruginosa and Streptococcus pneumoniae did not interfere the detection
107 e question of whether the bacterial pathogen Streptococcus pneumoniae directly interferes with purine
109 m various pathogens (eg, influenza virus and Streptococcus pneumoniae), especially for pathogens whos
113 est and MALDI-TOF for the differentiation of Streptococcus pneumoniae from other mitis group streptoc
114 ve anaerobe and opportunistic human pathogen Streptococcus pneumoniae generates large amounts of hydr
115 ding proteins that Staphylococcus aureus and Streptococcus pneumoniae, Gram-positive bacterial pathog
116 uncil Unit The Gambia, for identification of Streptococcus pneumoniae, Haemophilus influenzae, and Ne
117 and Acanthamoeba), six bacterial pathogens (Streptococcus pneumoniae, Haemophilus influenzae, Neisse
119 vaccines against Haemophilus influenzae and Streptococcus pneumoniae has virtually eliminated the co
123 ies and provides a general strategy to block Streptococcus pneumoniae IgA1 protease activity to poten
124 copy single particle reconstructions how the Streptococcus pneumoniae IgA1 protease facilitates IgA1
127 g the efficacy of geOMVs as vaccines against Streptococcus pneumoniae in mice, and against Campylobac
129 ing of the spleen, we identify a tropism for Streptococcus pneumoniae in this organ mediated by tissu
131 ncoding the only PP2C Ser/Thr phosphatase in Streptococcus pneumoniae, indicating that GpsB plays a k
132 e vaccine (Prevnar-13) against the bacterium Streptococcus pneumoniae induced immune responses that w
134 of the alveolar barrier in a mouse model of Streptococcus pneumoniae-induced pneumonia, and ex vivo
136 th influenza, mice are better protected from Streptococcus pneumoniae infection due to a population o
140 re, we used a murine model of intrapulmonary Streptococcus pneumoniae infection to investigate the ro
142 es in cerebrospinal fluid from children with Streptococcus pneumoniae infection, compared with childr
147 Measures of the contribution of influenza to Streptococcus pneumoniae infections, both in the seasona
148 ia meningitidis, Haemophilus influenzae, and Streptococcus pneumoniae, inflicts a substantial burden
150 s in the pre-PCV period, 34% were mixed with Streptococcus pneumoniae IRRs (95% confidence interval)
172 at the activation of macrophage NF-kappaB by Streptococcus pneumoniae is highly diverse, with a prepo
182 cial cell wall constituent of the pathobiont Streptococcus pneumoniae, is bound to peptidoglycan (wal
183 We analyzed whole genome sequences of 1,680 Streptococcus pneumoniae isolates from four independent
184 phis infected with the common lung pathogens Streptococcus pneumoniae, Legionella pneumophila, or Myc
186 ith Escherichia coli, Klebsiella pneumoniae, Streptococcus pneumoniae, lipopolysaccharide (LPS), or a
188 age with blood culture-proven sepsis due to Streptococcus pneumoniae, meeting criteria for systemic
190 spine surgery was associated with increased Streptococcus pneumoniae meningitis outside of the posto
191 fection on bacterial carriage and density of Streptococcus pneumoniae, Moraxella catarrhalis, Haemoph
192 se bacterial species: Staphylococcus aureus, Streptococcus pneumoniae, Mycobacterium tuberculosis, Sa
195 ry identification and serotyping/grouping of Streptococcus pneumoniae, N. meningitidis, and H. influe
196 etermine a structural envelope of SpNOX, the Streptococcus pneumoniae NADPH oxidase (NOX), a prokaryo
200 ls were stimulated in vitro with heat-killed Streptococcus pneumoniae or CD3/CD28 antibodies and stai
201 ere was no change in colonization rates with Streptococcus pneumoniae or Neisseria meningitidis.
205 al [CI] = 3.27-5.37; n = 2432 participants), Streptococcus pneumoniae otitis media (OR = 2.51; 95% CI
206 a three-dimensional structure of the related Streptococcus pneumoniae PBP2X suggests that some substi
207 eumolysin (PLY), a major virulence factor of Streptococcus pneumoniae, perforates cholesterol-rich li
216 n Abidjan, targeting the main causes of PBM: Streptococcus pneumoniae (pneumococcus), Haemophilus inf
219 etwork, Togo conducts surveillance targeting Streptococcus pneumoniae (pneumococcus), Neisseria menin
223 e-wall like) peptidoglycan (PG) synthesis in Streptococcus pneumoniae (pneumococcus); yet, mechanisms
224 These studies tested the role of Nrf2 during Streptococcus pneumoniae pneumonia and identified Nrf2-d
226 ediated hemolysis of ES PspCN, a CFH-binding Streptococcus pneumoniae protein domain, binds CFH tight
230 exposure was shortened in PCT subjects with Streptococcus pneumoniae respiratory infection and those
231 on of infant rats with increasing inocula of Streptococcus pneumoniae resulted in a dose-dependent in
232 hepatitis B, Haemophilus influenzae type b, Streptococcus pneumoniae, rotavirus, measles, meningitis
233 The lowest IE prevalence was found with Streptococcus pneumoniae (S pneumoniae) 1.2% (0.8-1.6) a
234 Neisseria meningitidis (N. meningitidis), Streptococcus pneumoniae (S. pneumoniae), and Haemophilu
235 tion of Staphylococcus aureus (S. aureus) or Streptococcus pneumoniae (S. pneumoniae), respectively;
238 In addition, they show high efficiency in Streptococcus pneumoniae septicemia mouse model and neut
241 verified here for Shigella sonnei O-antigen, Streptococcus pneumoniae serotype 12F, and Staphylococcu
242 nvasive pneumococcal disease (IPD) caused by Streptococcus pneumoniae serotype 2 (Sp2) is infrequent.
246 eak was due to multiple pathogens, including Streptococcus pneumoniae serotype 5 and influenza viruse
248 ble PCR primers were designed to distinguish Streptococcus pneumoniae serotypes within serogroup 18 f
250 ting invasive pneumococcal disease caused by Streptococcus pneumoniae Some components of the S. pneum
251 cations for urinary antigen tests (UATs) for Streptococcus pneumoniae (SP) and Legionella pneumophila
254 ly cover only 13 of the over 90 serotypes of Streptococcus pneumoniae (Sp), so nonvaccine serotypes a
257 onfirmed: Neisseria meningitidis ([Nm] 85%), Streptococcus pneumoniae ([Sp] 13%), and Haemophilus inf
263 ibe the epidemiology of laboratory-confirmed Streptococcus pneumoniae (Spn), Neisseria meningitidis,
265 mycin did not significantly affect levels of Streptococcus pneumoniae, Staphylococcus aureus, Pseudom
266 teria monocytogenes, Neisseria meningitidis, Streptococcus pneumoniae, Streptococcus agalactiae, cyto
267 nsed vaccines against the common otopathogen Streptococcus pneumoniae target the bacterial capsular p
273 s is a prerequisite for the human pathobiont Streptococcus pneumoniae (the pneumococcus) to cause sev
274 he case for the opportunistic human pathogen Streptococcus pneumoniae (the pneumococcus)(6), which la
277 e show that sublethal infection of mice with Streptococcus pneumoniae, the most common pathogen of co
278 In a number of bacterial species, including Streptococcus pneumoniae, the prevalence of resistance h
279 erotyping assay that uses culture lysates of Streptococcus pneumoniae This study describes the develo
280 n of asymptomatic nasopharyngeal carriage of Streptococcus pneumoniae to invasive pneumococcal diseas
282 ative data for the pattern of disease due to Streptococcus pneumoniae, trends in the serotype of inva
283 related to the capsular polysaccharide from Streptococcus pneumoniae type 37, which consists of a be
286 er vaccination with the 13-valent-conjugated Streptococcus pneumoniae vaccine were assessed in a MAIT
287 n sub-Saharan Africa sub-optimally interrupt Streptococcus pneumoniae vaccine-serotype (VT) carriage
288 MRSA and 22 (1.0%) with MSSA; 115 (5.1%) had Streptococcus pneumoniae Vancomycin or linezolid was adm
289 orescently labeled Haemophilus influenzae or Streptococcus pneumoniae was assessed by fluorimetry.
290 he commensal genus Neisseria and the species Streptococcus pneumoniae was associated with lower EAC r
292 cost-effective assay to detect serotypes of Streptococcus pneumoniae, we developed a novel loop-medi
298 subtilis and the heterodimer PatA/PatB from Streptococcus pneumoniae, when produced in several E. co
299 beta-lactam and co-trimoxazole resistance in Streptococcus pneumoniae with accuracies ranging from 88
300 ccus pyogenes, Streptococcus agalactiae, and Streptococcus pneumoniae with K(d) values of 0.6-4.6 uM.