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1 anifestation and less on meningococcal CC or serogroup.
2 ent of septic shock was not related to CC or serogroup.
3 001) and not affected by comorbidity, CC, or serogroup.
4 pneumococcal disease changes by serotype and serogroup.
5 ), a naturally attenuated member of the TBEV serogroup.
6 ction with Vibrio cholerae of the O1 or O139 serogroup.
7 in survivors was comparable between the two serogroups.
8 train genotypes among vaccine and nonvaccine serogroups.
9 more resistant to human LL-37 than other GAS serogroups.
10 ted on plasmids found across diverse E. coli serogroups.
11 lassification into different orthobunyavirus serogroups.
12 te vaccine and 8 additional key serotypes or serogroups.
13 The assay will be expanded to 40 serotypes/serogroups.
14 nd are limited in their detection of various serogroups.
15 ngitidis reference genome sequences of known serogroups.
16 ns, with the prevalence varying widely among serogroups.
17 -helices was substantially different between serogroups.
18 rogroup 1, but not other clinically relevant serogroups.
19 ogroup (67%) and included a diverse array of serogroups.
20 caused by Vibrio cholerae of the O1 or O139 serogroups.
21 ing units/ml) for both toxigenic V. cholerae serogroups.
23 SBT) analysis of all incoming L. pneumophila serogroup 1 (Lp1) isolates to identify potential links b
24 nd 2013 L. pneumophila patient isolates were serogroup 1 and closely related to all 2013 hospital wat
26 the genus Legionella; Legionella pneumophila serogroup 1 is the causative agent of most cases in Euro
30 e sufficient for the detection of Legionella serogroup 1, but not other clinically relevant serogroup
33 alyses of 43 strains, including all known Lp serogroups 1-17 and 17 emergent LD-causing Legionella sp
35 tive structural studies of S. pneumoniae CPS serogroup 10 (CPS10) were extended to include geneticall
37 of the human pathogen Legionella pneumophila serogroup 12 strain 570-CO-H (ATCC 43290), a clinical is
38 sh Streptococcus pneumoniae serotypes within serogroup 18 from culturable/nonculturable pneumococcal
39 s fell into a single lineage associated with serogroup 23, which had an origin in 1908 as dated by co
43 ed a diverse data set of approximately 1,000 serogroup 6 genomes, assessed the prevalence and distrib
48 ype 6E, analyzed the genetic diversity among serogroup 6 pneumococci, and investigated whether pneumo
49 of protection against Neisseria meningitidis serogroup A (NmA) in Burkina Faso before the introductio
51 belt of sub-Saharan Africa, a meningococcal serogroup A conjugate vaccine (MACV) has been progressiv
52 e capsular polysaccharide (CPS), which in Nm serogroup A consists of N-acetyl-mannosamine-1-phosphate
55 PSA-TT was highly effective at prevention of serogroup A invasive meningococcal disease and carriage
56 s were conducted after introduction of a new serogroup A meningococcal conjugate vaccine (MenAfriVac)
57 e, highly immunogenic Neisseria meningitidis serogroup A meningococcal conjugate vaccine (PsA-TT) was
60 Despite enhanced surveillance, no case of serogroup A meningococcal meningitis was reported in the
62 months before vaccination, whereas only one serogroup A meningococcus was isolated in 5001 people li
64 provide population-level protection against serogroup A Neisseria meningitidis (MenA) are unknown.
66 critical for the replication and assembly of serogroup A rotavirus (RVA); however, the dramatic prima
68 s one such lineage of meningococci, known as serogroup A, clonal complex 5 (A:cc5), has caused three
70 ular polymerases from Neisseria meningitidis serogroups A (CsaB) and X (CsxA) were characterized.
76 ived from hydrolysis of mixtures of the four serogroups A, C, W, and Y reference polysaccharides.
79 oniae lytA (NHS assay); (ii) N. meningitidis serogroups A, W135, and X (AWX assay); and (iii) N. meni
81 servations highlight the difficulties in the serogrouping and capsular genogrouping of meningococcal
84 of age, comorbidity, clinical manifestation, serogroup, and CC on disease course and outcome was asse
85 In Sweden, serogroup Y is now the dominating serogroup, and in 2012, the serogroup Y disease incidenc
86 ecific for detecting its target organisms or serogroups, and the LLD was similar to that for the sing
87 strains belonging to the hypervirulent M1T1 serogroup are more resistant to human LL-37 than other G
90 to uncover the genomic basis of conflicting serogroup assay results for an isolate (M16917) from a p
91 f the randomly selected STEC belonged to key serogroups associated with human disease and none encode
92 quadrivalent glycoconjugate (MenACWY-CRM) or serogroup B (4CMenB) vaccination on meningococcal carria
93 ecember 2013, a multicomponent meningococcal serogroup B (4CMenB) vaccine was used before licensure o
95 nsed vaccines against Neisseria meningitidis serogroup B (NmB) will depend partly on disease burden e
96 er milliliter (90 596 and 114 683 CFU/mL for serogroup B and C strains, respectively; P < .0001 compa
108 disease in developed countries is caused by serogroup B infection, against which there is no univers
110 MenB-FHbp (factor H binding protein), a serogroup B meningococcal (MenB) vaccine, was used to co
112 identified in 87 (36%) of 244 children with serogroup B meningococcal disease and 49 (15%) of 328 co
113 age was 6.5 (SD 2.8) years in children with serogroup B meningococcal disease and 6.9 (2.9) in contr
117 noted in three (1%) of 239 children who had serogroup B meningococcal disease compared with none of
118 Eligible children were survivors who had had serogroup B meningococcal disease confirmed by culture o
119 ines, public health response to outbreaks of serogroup B meningococcal disease is limited by lack of
121 ination campaign in response to a university serogroup B meningococcal disease outbreak in 2015.
122 w vaccines and suggest that all survivors of serogroup B meningococcal disease should be screened for
125 uced 4CMenB-a multicomponent vaccine against serogroup B meningococcal disease-into the national infa
131 duce mortality and morbidity associated with serogroup B meningococci infections, but uncertainty rem
133 the vaccine might induce against the diverse serogroup B meningococci strains that cause disease.
134 ra from individuals colonized long term with serogroup B meningococci were also upregulated during pr
137 In this study, the transcriptome of adherent serogroup B N. meningitidis strain MC58 was determined a
142 to the introduction of an approximately 2-kb serogroup B sequence cassette into the serogroup C genom
144 The outbreak was associated with a novel serogroup B strain (CC269) and risk factors were indicat
146 Bexsero and Trumenba, against meningococcal serogroup B strains have been licensed; both vaccines co
147 there is no currently available vaccine for serogroup B strains of N. meningitidis, this kind capsul
148 meningitidis species, with high sensitivity (serogroup B synD, 99% [75/76]; W135 synG, 97% [38/39]; a
149 (LLD) were 9, 43, and 10 copies/reaction for serogroup B synD, W135 synG, and Y synF assays, respecti
150 New singleplex real-time PCR assays for serogroup B synD, W135 synG, and Y synF showed 100% spec
151 mplement (hSBA) by use of four meningococcal serogroup B test strains expressing vaccine-heterologous
152 participants for three of four meningococcal serogroup B test strains representative of disease-causi
153 participants for three of four meningococcal serogroup B test strains representative of disease-causi
157 nsider the implementation of a meningococcal serogroup B vaccine for young children and/or serogroup
159 ble herd immunity effects with meningococcal serogroup B vaccines and the need for a booster dose to
160 e and other settings will help inform use of serogroup B vaccines currently under consideration for l
161 ease seen in the Southern cone was caused by serogroup B, but serogroup W135 strains have increased i
162 steria monocytogenes, Neisseria meningitidis serogroup B, Candida albicans, and P. berghei ANKA, and
165 xico, Central America and Caribbean regions, serogroups B and C were equally present, and serogroup Y
169 am-negative Neisseria meningitidis, capsular serogroup C (MenC) or Gram-positive group B Streptococcu
173 of isolates from clonal complexes with high serogroup C capsule expression rate during carriage (seq
175 5 all provinces introduced the meningococcal serogroup C conjugate vaccine (MCCV) into their routine
177 lance data for meningococcal serogroup W and serogroup C disease in the Netherlands and England for t
179 meningococcal serogroup W with meningococcal serogroup C emergence, the rapid expansion of the MenW:c
181 MCCV dramatically reduced the incidence of serogroup C IMD in Canada through both direct and indire
182 ells were measured before a booster of a Hib-serogroup C meningococcal (MenC) conjugate vaccine and a
183 We measured the frequency of circulating serogroup C meningococcal (MenC)-specific memory B cells
186 ases caused by clonal complex ST-11 and ST-8 serogroup C meningococci decreased from 251 of 268 (94%)
187 erogroup B vaccine for young children and/or serogroup C or ACWY conjugate vaccine for adolescents.
189 rent serogroup W outbreak and the historical serogroup C outbreak, the increase in incidence started
191 ic BMEM induced in humans by a meningococcal serogroup C PS (Men C)-TT conjugate vaccine conform to t
193 admissions decreased after the meningococcal serogroup C vaccine was introduced in 1999 and was 12.40
197 hypertension, coronary arterial disease, and serogroup C1 infections-were each assigned +1 point to f
198 e scheme, 39 pairs of serovars in Salmonella serogroup C2 differ only by the minor antigen O:6(1).
200 disease (IMD) isolates, which can be readily serogrouped, carriage isolates often lack capsule expres
201 rimean-Congo hemorrhagic fever virus (CCHFV) serogroup comprises sole members CCHFV and Hazara virus
202 Y) unambiguously is complex since all these serogroups contribute to the sialic acid monosaccharide
203 uence-specific PCRs to identify 74 serotypes/serogroups covering all current vaccine types as well as
205 Y (29.6% [8.1-46.0] carriage reduction), and serogroups CWY (28.5% [2.8-47.5] carriage reduction) com
206 ns and phylogenetic analysis showed that the serogroup diagnostic capsule polymerase gene (synD) of M
207 There was a significant change (P < .05) in serogroup distribution among all age groups between the
208 Core surveillance (ABCs) were characterized; serogroup distribution and molecular features of these i
211 lates was retained for all serogroups except serogroup E which has a synthetic requirement for UDP-Ga
212 meningococcal isolates was retained for all serogroups except serogroup E which has a synthetic requ
215 adapted for the monitoring of L. pneumophila serogroups in clinical and environmental samples in a fe
217 Vibrio cholerae belonging to the O1 and O139 serogroups is commonly associated with epidemic diarrhea
218 ethods were evaluated for their abilities to serogroup isolates and were compared with two genotyping
219 melon silver mottle virus (WSMoV, tospovirus serogroup IV) and melon yellow spot virus (MYSV, tospovi
220 melon silver mottle virus (WSMoV, tospovirus serogroup IV), and Melon yellow spot virus (MYSV, tospov
223 hysiologically less relevant N. meningitidis serogroup L, is one of the smallest known Stealth protei
224 %) were identified correctly at least to the serogroup level, including all of the 13-valent conjugat
225 sms, including expression of capsule (select serogroups), Neisserial surface protein A (NspA), factor
226 cing of a multilocus sequence type 95 (ST95) serogroup O1 strain previously indicated that APEC resem
227 the classical and El Tor biotype strains of serogroup O1 that is most frequently associated with epi
230 h the detection of toxigenic Vibrio cholerae serogroups O1 and O139, which are associated with choler
232 cytotoxic P. aeruginosa strains 6077, 6206 (serogroup O11), and PA14 (serogroup 010) were less sensi
233 higa toxin-producing Escherichia coli (STEC) serogroup O121 and O26 infections linked to contaminated
234 detection for seven STEC strains of various serogroups (O26, O45, O103, O111, O121, O145, and O157)
235 V. parahaemolyticus RIMD2210633, a clinical serogroup O3:K6 isolate, and examined the effects in viv
236 ile the invasive P. aeruginosa strains PAO1 (serogroup O5) and 6294 (serogroup O6) were trapped by NE
238 ginosa strains PAO1 (serogroup O5) and 6294 (serogroup O6) were trapped by NETs, the cytotoxic P. aer
240 rains of another dominant APEC lineage (ST23 serogroup O78 strains chi7122 and IMT2125) and compared
243 demonstrated for the analysis of 9 different serogroups of the bacterium Legionella pneumophila, a co
245 trains (P = .014) and severe disease with O7 serogroup (P = .034) and PapGII adhesin (OR, 2.3 [95% CI
246 ction using multivariable analysis were D+R- serogroup (P</=0.0001), donor age >50 years (P=0.013), a
247 nation of the different ExPEC subpathotypes, serogroups, phylogenetic types, and sequence types.
249 primary sequence divergence of NSP4s across serogroups raises the possibility that viroporin activit
251 entify 11 individual serotypes plus 10 small serogroups representing the majority of disease-causing
253 . influenzae hpd, and S. pneumoniae lytA and serogroup-specific genes in the cap locus for N. meningi
254 each NSP4 tested had viroporin activity, but serogroup-specific viroporin phenotypes were identified.
255 , we performed deep RNA sequencing using O39 serogroup strain AM-19226 and derivatives carrying delet
259 rotection is effective across L. pneumophila serogroups, suggesting that Abs specific for conserved p
261 able to protect against four N. meningitidis serogroups, there is currently no commercial vaccine to
263 , the public health importance of the Bhanja serogroup viruses remains unclear, due in part to the la
264 annual relative increase in the incidence of serogroup W and serogroup C between both countries.
265 national surveillance data for meningococcal serogroup W and serogroup C disease in the Netherlands a
268 Since 2009, the incidence of meningococcal serogroup W disease has increased rapidly in the UK beca
269 Netherlands, the incidence of meningococcal serogroup W disease increased substantially in 2015-16 c
270 me multilocus sequence typing (1546 loci) on serogroup W disease isolates from both countries for sur
273 al and phylogenetic associations between the serogroup W outbreaks in the Netherlands and England, an
274 the historical similarities of meningococcal serogroup W with meningococcal serogroup C emergence, th
276 Southern cone was caused by serogroup B, but serogroup W135 strains have increased in recent years.
278 attenuated viral vaccine candidates for this serogroup, we have generated a recombinant LACV expressi
281 belong to the California encephalitis virus serogroup, which causes 70 to 100 cases of encephalitis
283 t among isolates belonging to the O1 and O18 serogroups within phylogenetic group B2, which are impli
286 0% (95% CI 17.3-55.0) carriage reduction for serogroup Y and 36.2% (15.6-51.7) carriage reduction for
287 w the dominating serogroup, and in 2012, the serogroup Y disease incidence was 0.46/100,000 populatio
288 jective of this study was to investigate the serogroup Y emergence by whole-genome sequencing and com
289 sease (IMD) caused by Neisseria meningitidis serogroup Y has increased in Europe, especially in Scand
290 to 2012 (n = 143), which had relatively low serogroup Y incidence, and two isolates obtained in 1999
292 -genome sequencing was performed on invasive serogroup Y isolates from 1995 to 2012 in Sweden (n = 18
293 se isolates were compared to a collection of serogroup Y isolates from England, Wales, and Northern I
294 pact of a meningococcal conjugate vaccine on serogroup Y meningococcal carriage and to define the dyn
295 d to reveal additional genes associated with serogroup Y meningococcal disease, and this work would b
297 obtained in 1999 in the United States, where serogroup Y remains one of the major causes of IMD.
298 There were only 5 observed acquisitions of serogroup Y strains during the study; therefore, the imp
299 cal population structure of Swedish invasive serogroup Y strains to those of other countries with dif
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