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1 pneumococcal disease changes by serotype and serogroup.
2 anifestation and less on meningococcal CC or serogroup.
3 ent of septic shock was not related to CC or serogroup.
4 001) and not affected by comorbidity, CC, or serogroup.
5 ), a naturally attenuated member of the TBEV serogroup.
6 revalence of 2.6-69.3% of positive swabs per serogroup.
7 d simultaneous detection of three Salmonella serogroups.
8 caused by Vibrio cholerae of the O1 or O139 serogroups.
9 rried by adulterant or nonadulterant E. coli serogroups.
10 ogroup (67%) and included a diverse array of serogroups.
11 ing units/ml) for both toxigenic V. cholerae serogroups.
12 in survivors was comparable between the two serogroups.
13 train genotypes among vaccine and nonvaccine serogroups.
14 more resistant to human LL-37 than other GAS serogroups.
15 de some protection against all meningococcal serogroups.
17 SBT) analysis of all incoming L. pneumophila serogroup 1 (Lp1) isolates to identify potential links b
18 nd 2013 L. pneumophila patient isolates were serogroup 1 and closely related to all 2013 hospital wat
20 the genus Legionella; Legionella pneumophila serogroup 1 is the causative agent of most cases in Euro
23 monly used laboratory strains: L pneumophila serogroup 1 Philadelphia (Phil-1)-derived strains JR32 a
24 alyses of 43 strains, including all known Lp serogroups 1-17 and 17 emergent LD-causing Legionella sp
28 sh Streptococcus pneumoniae serotypes within serogroup 18 from culturable/nonculturable pneumococcal
29 s fell into a single lineage associated with serogroup 23, which had an origin in 1908 as dated by co
32 of E. coli was 30% (n = 48) distributed in 8 serogroups (40/48, 83.3%), while 8 isolates (8/48, 16.6%
33 ed a diverse data set of approximately 1,000 serogroup 6 genomes, assessed the prevalence and distrib
36 ype 6E, analyzed the genetic diversity among serogroup 6 pneumococci, and investigated whether pneumo
39 ccal serogroup C vaccine in 2, meningococcal serogroup A and Haemophilus influenzae type b vaccine ea
43 belt of sub-Saharan Africa, a meningococcal serogroup A conjugate vaccine (MACV) has been progressiv
44 With the rollout of a novel meningococcal serogroup A conjugate vaccine (MACV) in the belt, the Wo
51 rogressive introduction of the meningococcal serogroup A conjugate vaccine within Africa's meningitis
52 introduction and rollout of a meningococcal serogroup A conjugate vaccine, MenAfriVac, in the Africa
54 e capsular polysaccharide (CPS), which in Nm serogroup A consists of N-acetyl-mannosamine-1-phosphate
56 meningitis belt where Neisseria meningitidis serogroup A historically caused large-scale epidemics.
57 eningitis belt, where Neisseria meningitidis serogroup A historically caused large-scale epidemics.
59 s were conducted after introduction of a new serogroup A meningococcal conjugate vaccine (MenAfriVac)
60 MACV impact, characterized the burden of non-serogroup A meningococcal disease (including the emergen
61 n the African meningitis belt has eliminated serogroup A meningococcal infections for >300 million Af
63 Despite enhanced surveillance, no case of serogroup A meningococcal meningitis was reported in the
65 months before vaccination, whereas only one serogroup A meningococcus was isolated in 5001 people li
67 although high coverage with MACV has reduced serogroup A outbreaks, large meningococcal meningitis ou
68 MenAfriVac vaccination against meningococcal serogroup A to prevent meningitis outbreaks in the north
70 rogroups were confirmed in 3917 (75%) cases: serogroup A was present in 4.7% of cases, B in 23.3%, C
72 s one such lineage of meningococci, known as serogroup A, clonal complex 5 (A:cc5), has caused three
73 gainst infection with Neisseria meningitidis serogroup A, we use an assumed SBA titre of 128 as a thr
74 ular polymerases from Neisseria meningitidis serogroups A (CsaB) and X (CsxA) were characterized.
79 ived from hydrolysis of mixtures of the four serogroups A, C, W, and Y reference polysaccharides.
84 nity-based outbreaks differed in predominant serogroup, age distribution of cases, and clinical syndr
85 eactivity with viruses belonging to the same serogroup and by long-lasting antibodies from prior infe
86 s closely related to CCHFV, sharing the same serogroup and many structural, biochemical, and cellular
87 servations highlight the difficulties in the serogrouping and capsular genogrouping of meningococcal
90 "top 7" Shiga toxin-producing E. coli (STEC) serogroups and were declared by the USDA as adulterants
91 of age, comorbidity, clinical manifestation, serogroup, and CC on disease course and outcome was asse
92 In Sweden, serogroup Y is now the dominating serogroup, and in 2012, the serogroup Y disease incidenc
93 thesis (cps) locus, classify N. meningitidis serogroups, and identify mechanisms for nongroupability
94 strains belonging to the hypervirulent M1T1 serogroup are more resistant to human LL-37 than other G
96 f the randomly selected STEC belonged to key serogroups associated with human disease and none encode
97 quadrivalent glycoconjugate (MenACWY-CRM) or serogroup B (4CMenB) vaccination on meningococcal carria
98 ecember 2013, a multicomponent meningococcal serogroup B (4CMenB) vaccine was used before licensure o
99 present with severe disease than those with serogroup B (aRRR 2.7, 95% CI 1.1-6.3); HIV coinfection
101 nsed vaccines against Neisseria meningitidis serogroup B (NmB) will depend partly on disease burden e
103 er milliliter (90 596 and 114 683 CFU/mL for serogroup B and C strains, respectively; P < .0001 compa
112 s regarding which vaccine to use in managing serogroup B IMD outbreaks require information about the
115 MenB-FHbp (factor H binding protein), a serogroup B meningococcal (MenB) vaccine, was used to co
117 ave been used for the prevention of invasive serogroup B meningococcal disease (IMD) since their lice
119 ination campaign in response to a university serogroup B meningococcal disease outbreak in 2015.
120 uced 4CMenB-a multicomponent vaccine against serogroup B meningococcal disease-into the national infa
130 Bexsero and Trumenba, against meningococcal serogroup B strains have been licensed; both vaccines co
132 mplement (hSBA) by use of four meningococcal serogroup B test strains expressing vaccine-heterologous
133 participants for three of four meningococcal serogroup B test strains representative of disease-causi
134 participants for three of four meningococcal serogroup B test strains representative of disease-causi
137 nsider the implementation of a meningococcal serogroup B vaccine for young children and/or serogroup
139 ble herd immunity effects with meningococcal serogroup B vaccines and the need for a booster dose to
141 the majority of university outbreaks due to serogroup B, and serogroup C is the primary cause of com
142 ity of IMD-W with IMD caused by meningococci serogroup B, Y, or C, adjusting for age, gender, and com
143 d genomes identified a diverse collection of serogroups (B, C1, C2 to C3, D1, E1, G, I, K, N, O, and
145 , the majority of studies have examined this serogroup, but there are 3 commonly used laboratory stra
146 am-negative Neisseria meningitidis, capsular serogroup C (MenC) or Gram-positive group B Streptococcu
148 tive specimens, 14 (88%) were N meningitidis serogroup C (NmC), 1 was NmW, and 1 was nongroupable.
154 of isolates from clonal complexes with high serogroup C capsule expression rate during carriage (seq
156 5 all provinces introduced the meningococcal serogroup C conjugate vaccine (MCCV) into their routine
157 lance data for meningococcal serogroup W and serogroup C disease in the Netherlands and England for t
158 meningococcal serogroup W with meningococcal serogroup C emergence, the rapid expansion of the MenW:c
159 MCCV dramatically reduced the incidence of serogroup C IMD in Canada through both direct and indire
160 university outbreaks due to serogroup B, and serogroup C is the primary cause of community-based outb
161 elong to a highly virulent and predominantly serogroup C lineage, including strains that are able to
164 erogroup B vaccine for young children and/or serogroup C or ACWY conjugate vaccine for adolescents.
165 rent serogroup W outbreak and the historical serogroup C outbreak, the increase in incidence started
168 ococcal vaccine in 9 patients, meningococcal serogroup C vaccine in 2, meningococcal serogroup A and
169 admissions decreased after the meningococcal serogroup C vaccine was introduced in 1999 and was 12.40
170 ing the emergence of a new epidemic clone of serogroup C), and documented the impact of pneumococcal
174 he clinical presentation of infection due to serogroups C/W/X includes nonmeningeal IMD, and there is
175 disease (IMD) isolates, which can be readily serogrouped, carriage isolates often lack capsule expres
177 rimean-Congo hemorrhagic fever virus (CCHFV) serogroup comprises sole members CCHFV and Hazara virus
178 uence-specific PCRs to identify 74 serotypes/serogroups covering all current vaccine types as well as
180 There was a significant change (P < .05) in serogroup distribution among all age groups between the
181 Core surveillance (ABCs) were characterized; serogroup distribution and molecular features of these i
184 nce of invasive meningococcal disease due to serogroup E in Queensland, Australia, in previously heal
185 lates was retained for all serogroups except serogroup E which has a synthetic requirement for UDP-Ga
187 meningococcal isolates was retained for all serogroups except serogroup E which has a synthetic requ
190 The commercial vaccine, containing nine serogroups, has low efficacy compared with bivalent vacc
192 e-fatality ratio associated with these non-A serogroups; however, data on the nonmeningeal IMD burden
193 bodies were directed most frequently against serogroups Icterohaemorrhagiae (22.0%) and Autumnalis (1
196 against footrot and, with 50 combinations of serogroups in flocks, flock-specific vaccines are necess
198 ribution, and annual changes in serotype and serogroup, including changes in vaccine-type Spn meningi
199 s compared with controls and group B and all serogroup invasive meningococcal disease in cases compar
201 ]; OR, 0.18 [95% CI, 0.08-0.44]) and for all serogroup invasive meningococcal disease, 11 of 98 cases
205 Vibrio cholerae belonging to the O1 and O139 serogroups is commonly associated with epidemic diarrhea
206 ethods were evaluated for their abilities to serogroup isolates and were compared with two genotyping
209 hysiologically less relevant N. meningitidis serogroup L, is one of the smallest known Stealth protei
210 ingococcal meningitis outbreaks due to other serogroups may continue to occur; effective multivalent
214 the classical and El Tor biotype strains of serogroup O1 that is most frequently associated with epi
215 holerae O139 isolates are closely related to serogroup O1, biotype El Tor V. cholerae, and comprise a
219 h the detection of toxigenic Vibrio cholerae serogroups O1 and O139, which are associated with choler
220 cytotoxic P. aeruginosa strains 6077, 6206 (serogroup O11), and PA14 (serogroup 010) were less sensi
221 higa toxin-producing Escherichia coli (STEC) serogroup O121 and O26 infections linked to contaminated
223 ile the invasive P. aeruginosa strains PAO1 (serogroup O5) and 6294 (serogroup O6) were trapped by NE
225 ginosa strains PAO1 (serogroup O5) and 6294 (serogroup O6) were trapped by NETs, the cytotoxic P. aer
227 vestigate the prevalence and distribution of serogroups of D. nodosus in England to elucidate whether
229 Twenty adults were enrolled in each of 3 serogroups of individuals: those negative for both HSV1
232 trains (P = .014) and severe disease with O7 serogroup (P = .034) and PapGII adhesin (OR, 2.3 [95% CI
238 The differences between IMD-W and other serogroups remained after adjusting for age, gender, and
241 irmed and N. meningitidis/H. influenzae were serogrouped/serotyped by real-time polymerase chain reac
242 be used to detect and associate the E. coli serogroup-specific gene with major virulence genes and d
246 w insights into the biology of a V. cholerae serogroup that, from a genomic perspective, is poorly un
250 and H. influenzae belonged to meningococcus serogroup W (45.5%) and H. influenzae type b (54.5%), re
251 ease in invasive meningococcal disease (IMD) serogroup W (IMD-W) cases caused by sequence type-11 clo
252 has been found in the Neisseria meningitidis serogroup W (NmW) capsular polysaccharide (CPS) and is a
254 annual relative increase in the incidence of serogroup W and serogroup C between both countries.
255 national surveillance data for meningococcal serogroup W and serogroup C disease in the Netherlands a
260 Since 2009, the incidence of meningococcal serogroup W disease has increased rapidly in the UK beca
261 Netherlands, the incidence of meningococcal serogroup W disease increased substantially in 2015-16 c
262 me multilocus sequence typing (1546 loci) on serogroup W disease isolates from both countries for sur
265 al and phylogenetic associations between the serogroup W outbreaks in the Netherlands and England, an
266 o a sublineage of the Neisseria meningitidis serogroup W ST-11 clonal complex (hereafter, the "origin
268 the historical similarities of meningococcal serogroup W with meningococcal serogroup C emergence, th
273 ence genes carried by each of the top 7 STEC serogroups were detected by dPCR with appropriately dilu
277 d SASG were in 91% to 100% agreement for all serogroups, while the results of WGS and RT-PCR showed 9
278 was defined as >=2 primary cases of the same serogroup within <3 months in an organization, or a >=2-
279 ntly, a bivalent vaccine targeting these two serogroups would protect 27% of flocks fully (if only H
281 w the dominating serogroup, and in 2012, the serogroup Y disease incidence was 0.46/100,000 populatio
282 jective of this study was to investigate the serogroup Y emergence by whole-genome sequencing and com
284 sease (IMD) caused by Neisseria meningitidis serogroup Y has increased in Europe, especially in Scand
287 to 2012 (n = 143), which had relatively low serogroup Y incidence, and two isolates obtained in 1999
289 -genome sequencing was performed on invasive serogroup Y isolates from 1995 to 2012 in Sweden (n = 18
290 olecule real-time (SMRT) sequencing on eight serogroup Y isolates from different sublineages to unrav
291 se isolates were compared to a collection of serogroup Y isolates from England, Wales, and Northern I
293 cture of these isolates was similar to other serogroup Y isolates internationally, a distinct strain
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 Invasive meningococcal disease (IMD) due to serogroup Y Neisseria meningitidis emerged in Europe dur
298 obtained in 1999 in the United States, where serogroup Y remains one of the major causes of IMD.
299 There were only 5 observed acquisitions of serogroup Y strains during the study; therefore, the imp
300 cal population structure of Swedish invasive serogroup Y strains to those of other countries with dif