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1 involved in generating the helical shape of Campylobacter.
2 erotoxigenic Escherichia coli, Shigella, and Campylobacter.
3 ema, Selenomonas, Parvimonas, Dialister, and Campylobacter.
4 mer products rather than complete absence of Campylobacter.
5 uggested a new model of FeEnt acquisition in Campylobacter.
6 eneralist lineages of the zoonotic bacterium Campylobacter.
7 ng that two resistance mechanisms existed in Campylobacter.
8 adequate for protecting against exposure to Campylobacter.
9 ylobacter, indicating their functionality in Campylobacter.
10 of infection is an estimated 1 in 23500 for Campylobacter, 1 in 5050000 for Cryptosporidium, and 1 i
11 pathogens Shigella (36%), Giardia (33%), and Campylobacter (30%) predominated, but their presence was
12 753 pathogen-specific gastroenteritis cases (Campylobacter: 738, Salmonella: 624, Shigella: 376, Yers
14 e results identify a key virulence factor in Campylobacter and a potential target for the control of
15 erythromycin, a total of eight strains (four Campylobacter and four Enterococcus) obtained macrolide-
17 TM7, and 11 genera, including Anaeroplasma, Campylobacter, and Clostridium, were correlated with app
18 e for the detection of Salmonella, Shigella, Campylobacter, and Shiga toxin-producing enterohemorrhag
19 er in Actinomyces, Selenomonas, Veillonella, Campylobacter, and TM7 [G-1] than the Swedish groups.
21 STAT! Campy immunochromatographic assay for Campylobacter antigen was compared to culture for 500 cl
24 etected Salmonella, EHEC O157, Shigella, and Campylobacter at concentrations 1- to 2-log10 lower than
30 s, and provide improved resolution (i) among Campylobacter clonal complexes and (ii) between very clo
32 p., Shigella spp., Campylobacter jejuni, and Campylobacter coli and an EIA for Shiga toxins 1 and 2.
34 rolide-resistant mutants were induced in one Campylobacter coli and one Enterococcus faecium strain,
36 ry, clinical and environmental C. jejuni and Campylobacter coli contained genetic changes within the
38 diarrhoea-including Campylobacter jejuni and Campylobacter coli, Cryptosporidium spp, enteropathogeni
39 or the detection of Campylobacter jejuni and Campylobacter coli, leading global causes of bacterial g
41 n order to determine the natural patterns of Campylobacter colonization over a period of 63 weeks.
43 s of PglC, a prototypic dual domain PGT from Campylobacter concisus Using a luminescence-based assay,
44 Clostridium difficile, Campylobacter jejuni, Campylobacter concisus, and Salmonella enterica were rec
45 nocytophaga gingivalis, Eikenella corrodens, Campylobacter concisus, Porphyromonas gingivalis, Tanner
47 enterotoxigenic Escherichia coli, Shigella, Campylobacter, Cryptosporidium, norovirus GII, and adeno
50 s positively correlated with the presence of Campylobacter, Deinococcus, and Sulfurospirillum Finally
51 rch is required to better define whether the Campylobacter detectable in stormwater are pathogenic to
52 Factors associated with a reduced risk of Campylobacter detection included exclusive breastfeeding
53 ed excellent sensitivity and specificity for Campylobacter detection with low cross reactivity for ot
56 lts suggest that there is natural control of Campylobacter dynamics within a flock which could potent
58 he potentially deleterious implications of a Campylobacter enzyme immunoassay (EIA) result and the in
59 osis cases are acute and self-limiting, with Campylobacter excretion ceasing a few weeks after sympto
63 4 to December 2016, a cluster of 13 cases of Campylobacter fetus intestinal and extraintestinal infec
68 he substantial burden of apparently sporadic Campylobacter from cattle where transmission routes are
70 , Parvimonas micra, Eubacterium nodatum, and Campylobacter gracilis, a significant positive correlati
71 ture-independent detection tests (CIDTs) for Campylobacter have become an area of intense controversy
72 the FlgK junction onto the structure of the Campylobacter hook provides some clues about its diverge
73 uctural constraints, due to the structure of Campylobacter hook, causes divergence of one element of
74 new insights into the adaptive mechanisms of Campylobacter in animal food production environments.
77 t diminished the abundance of non-pathogenic Campylobacter in the juvenile gut, suggesting a potentia
79 ndings reveal the rising prevalence of FQ(R) Campylobacter in the U.S. and provide novel information
80 the TA systems, pVir was readily cured from Campylobacter, indicating their functionality in Campylo
81 rade 3]; diarrhoea and fever associated with Campylobacter infection [grade 3]; recurrence of abdomin
82 ntibiotic treatment may reduce the burden of Campylobacter infection and improve growth in children i
83 , we describe the epidemiology and impact of Campylobacter infection in the first 2 years of life.
87 oxacin, an antibiotic of choice for treating Campylobacter infection, through the pore of MOMP reveal
90 dentify risk factors for sporadic intestinal Campylobacter infections and to determine the relative i
94 ential for understanding the epidemiology of Campylobacter infections, a major worldwide cause of bac
100 macrolides, in the major foodborne pathogen Campylobacter is considered a serious threat to public h
102 , this 4-gene operon is only present in some Campylobacter isolates and other arsenic resistance mech
104 O157), shiga-toxin producing E. coli (stx2), Campylobacter jejuni (mapA), Shigella spp. (ipaH), and a
105 a patient with fecal specimens positive for Campylobacter jejuni (ST45) intermittently during a 10-y
107 rized two FeEnt receptors (CfrA and CfrB) in Campylobacter jejuni and C. coli, the enteric human path
109 athogens associated with diarrhoea-including Campylobacter jejuni and Campylobacter coli, Cryptospori
110 t targets mapA and ceuE for the detection of Campylobacter jejuni and Campylobacter coli, leading glo
111 Monomeric OTases, such as the PglBs from Campylobacter jejuni and Campylobacter lari, catalyze tr
112 genes with higher sequence diversity in the Campylobacter jejuni and Neisseria meningitidis genomes
113 says demonstrate that LpxJ and homologues in Campylobacter jejuni and Wolinella succinogenes can act
114 inked protein glycosylation (Pgl) pathway of Campylobacter jejuni are evaluated for their tolerance f
117 icated a moderate probability of illness for Campylobacter jejuni at the study beaches, especially wh
119 Here, we report the crystal structures of Campylobacter jejuni Cas9 (CjCas9), one of the smallest
122 Here the authors present the structure of Campylobacter jejuni CmeB pump combined with functional
124 acterial oligosaccharyltransferase, PglB, of Campylobacter jejuni favors acceptor proteins with conse
131 osphorylase (PNPase) facilitates survival of Campylobacter jejuni in low temperatures and favors swim
148 c acid cycle in the microaerophilic pathogen Campylobacter jejuni is potentially vulnerable, as it em
158 o-L-gluco-heptopyranose residue found in the Campylobacter jejuni NCTC11168 (HS:2) capsular polysacch
159 75-year-old man was diagnosed with probable Campylobacter jejuni prosthetic knee infection after a d
161 genetically diverse Campylobacter fetus and Campylobacter jejuni strains have been implicated in suc
162 n (strain VPI-5482) [PDB:3KZT], Cj0202c from Campylobacter jejuni subsp. jejuni serotype O:2 (strain
163 ber 2013, sexual transmission of 2 clades of Campylobacter jejuni subspecies jejuni isolates resulted
165 transfer of an N-glycosylation pathway from Campylobacter jejuni to Escherichia coli in 2002 can be
166 owth of the microaerophilic mucosal pathogen Campylobacter jejuni under oxygen-limited conditions was
167 The microaerophilic food-borne pathogen Campylobacter jejuni uses complex cytochrome-rich respir
172 detection of Salmonella spp., Shigella spp., Campylobacter jejuni, and Campylobacter coli and an EIA
173 classes of inhibitors of Bacillus anthracis, Campylobacter jejuni, and Clostridium perfringens IMPDHs
174 Enterovirus, adenovirus A, Salmonella spp., Campylobacter jejuni, bovine polyomavirus, and bovine ro
175 ase 3, sequences from Clostridium difficile, Campylobacter jejuni, Campylobacter concisus, and Salmon
177 erial species (Bacteroides thetaiotaomicron, Campylobacter jejuni, Enterococcus faecalis, Escherichia
178 d to spray-irrigated dairy manure containing Campylobacter jejuni, enterohemorrhagic Escherichia coli
179 ty against Gram-negative bacteria, including Campylobacter jejuni, Escherichia coli O157:H7, and mult
182 d the highest antimicrobial activity against Campylobacter jejuni, L. monocytogenes, and Pseudomonas
183 The foodborne microaerophilic pathogen, Campylobacter jejuni, possesses a periplasmic formate de
184 eropathogenic E. coli (EPEC), Shigella spp., Campylobacter jejuni, Salmonella enterica, and Aeromonas
185 ae, Treponema pallidum, Helicobacter pylori, Campylobacter jejuni, Synechocystis sp., and Mycobacteri
189 previously identified in invasive strains of Campylobacter jejuni, the most prevalent cause of bacter
191 ugh frequent recombination with it, while in Campylobacter jejuni, we find a minority population we p
192 y and kinetic parameters of PglC, a PGT from Campylobacter jejuni, were quickly established using thi
193 that the periplasmic binding protein CeuE of Campylobacter jejuni, which was previously thought to bi
194 zation domain-containing protein 2 (NOD2) in Campylobacter jejuni-induced intestinal inflammation.
195 the contribution of PI3K-gamma signaling in Campylobacter jejuni-induced neutrophil accumulation and
202 IA (ProSpecT), and duplex PCR to distinguish Campylobacter jejuni/C. coli and non-jejuni/coli Campylo
204 us GII, rotavirus, and sapovirus), bacteria (Campylobacter jejuni/C. coli, Clostridium difficile, Sal
205 ure alone detected 80/89 (89.9% sensitivity) Campylobacter jejuni/Campylobacter coli-positive cases.
206 oli (STEC), Shigella spp. , Salmonella spp , Campylobacter jejuni/coli , and methicillin-resistant St
207 e 6 bacterial enteric pathogens tested, only Campylobacter jejuni/coli detection was significantly re
209 tructure of a single-subunit OST enzyme, the Campylobacter lari protein PglB, revealed a partially di
210 h as the PglBs from Campylobacter jejuni and Campylobacter lari, catalyze transfer of glycans from me
211 animals serve as a significant reservoir for Campylobacter, limited information is available on antib
215 to the pathogens concentration (particularly Campylobacter, Norovirus, and Legionella) and exposure f
217 ar polysaccharide (CP) biosynthesis, PglB (a Campylobacter oligosaccharyl transferase), and a protein
218 ylobacter jejuni/C. coli and non-jejuni/coli Campylobacter on 432 diarrheal and matched control stool
221 entative members of this superfamily are the Campylobacter PglCs, which initiate N-linked glycoprotei
223 al susceptibility testing suggested that the Campylobacter population developed resistance to several
224 consistently colonized with organisms from a Campylobacter population that adapted to the internal en
226 and the effect of antimicrobial treatment on Campylobacter populations in this unusual situation of l
227 e was a substantial reduction in predominant Campylobacter populations proposing that SUCRAM suppleme
228 ith most children (n = 1606; 84.9%) having a Campylobacter-positive stool sample by 1 year of age.
231 icola (94%/74%), Parvimonas micra (86%/62%), Campylobacter rectus (90%/76%), Eubacterium nodatum (64%
232 omitans (Aa), Porphyromonas gingivalis (Pg), Campylobacter rectus (Cr), and Tannerella forsythia (Tf)
233 lis, and Fusobacterium nucleatum, as well as Campylobacter rectus (except for amoxicillin alone).
236 th groups (both P = 0.043), as were those of Campylobacter rectus in the test group only (P = 0.028).
237 ing association of Prevotella intermedia and Campylobacter rectus with the etiology of peri-implantit
238 terium nucleatum, Prevotella intermedia, and Campylobacter rectus), two red-complex periodontal patho
240 nomycetemcomitans, Porphyromonas gingivalis, Campylobacter rectus, and Tannerella forsythia) in vascu
241 romonas gingivalis, Treponema denticola, and Campylobacter rectus, were highest in patients with GAgP
243 forsythia, as well as Actinomyces viscosus, Campylobacter rectus/showae, Prevotella intermedia, Parv
245 n various C. jejuni strains, suggesting that Campylobacter requires at least one of the two genes for
246 untry settings, the ProSpecT EIA and PCR for Campylobacter reveal extremely high rates of positivity.
247 were only 19/196 (10%) positive cultures for Campylobacter, Salmonella, or Shigella entero-pathogens
248 of 16S rRNA from 53 of these non-jejuni/coli Campylobacter samples showed that it most closely matche
249 ss with the following methods: four types of Campylobacter selective media, four commercial stool ant
252 lus, Corynebacterium, Cellulosimicrobium and Campylobacter showed lower abundances in OLP patients, a
254 imental model for the study of diarrheagenic Campylobacter species and will be useful in exploring th
256 lphia region were prospectively analyzed for Campylobacter species other than C. jejuni and C. coli u
257 tool spiked with each of the above-mentioned Campylobacter species revealed reactivity with EIA.
258 vasion, and intracellular survival, emerging Campylobacter species should be investigated as etiologi
259 at least one additional non-jejuni and -coli Campylobacter species that may be missed by routine cult
261 ent isolation of C. concisus The majority of Campylobacter species were not clinically significant.
262 Of 225 samples tested, 13 (5.8%) yielded Campylobacter species, with frequent isolation of C. con
267 95% CI 3.0-7.1), rotavirus (4.8%, 4.5-5.0), Campylobacter spp (3.5%, 0.4-6.3), astrovirus (2.7%, 2.2
268 th diarrhoea in the second year of life were Campylobacter spp (7.9%, 3.1-12.1), norovirus GII (5.4%,
269 oody diarrhoea was primarily associated with Campylobacter spp and Shigella spp, fever and vomiting w
272 bacter pylori, and fluoroquinolone-resistant Campylobacter spp, Neisseria gonorrhoeae, and Salmonella
276 erichia coli (OR: 1.39; 95% CI: 1.05, 1.83), Campylobacter spp. (OR: 1.46; 95% CI: 1.11, 1.91), heat-
278 ed for the concentrations of PCR amplicon of Campylobacter spp. between 1 and 25 nM with a limit of d
279 million (95% UI 70-251 million) cases, while Campylobacter spp. caused 96 million (95% UI 52-177 mill
281 , intestinal enterococci, and thermotolerant Campylobacter spp. in surface waters than that of rDNA-b
282 lmonella (nontyphoidal) spp., Shigella spp., Campylobacter spp. or Yersinia enterocolitica and matche
283 s pathogenic strains of Escherichia coli and Campylobacter spp. that declined in prevalence based on
284 ric pathogens directly from stool specimens: Campylobacter spp., Clostridium difficile (toxin A/B), P
285 llected and tested by enzyme immunoassay for Campylobacter Stool and blood samples were assayed for m
286 port comprehensive performance data for four Campylobacter stool antigen CIDTs versus culture and mol
287 pecificity, and positive predictive value of Campylobacter stool antigen tests were highly variable.
291 nserved DNA methyltransferase, which we term Campylobacter transformation system methyltransferase (c
292 restingly, the OSTs from Campylobacter coli, Campylobacter upsaliensis, Desulfovibrio desulfuricans,
293 ne copies/swab, respectively; P < .001), and Campylobacter ureolyticus (1.7 x 10(5) and 1.6 x 10(7)16
296 26 267 nondiarrheal stool samples tested for Campylobacter We describe a high prevalence of infection
297 Contigs were deposited at the pubMLST.org/campylobacter website and automatically annotated for 1,
299 health risks associated with the exposure to Campylobacter when harvesting urban stormwater for toile
300 sor would help in the sensitive detection of Campylobacter which can result in reducing pre-enrichmen
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