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1 LC4 is induced by the intracellular pathogen Legionella pneumophila.
2 n is critical to the growth and virulence of Legionella pneumophila.
3 respectively, from the pathogenic bacterium Legionella pneumophila.
4 R amplicons derived from genomic DNA of live Legionella pneumophila.
5 core components of an orthologous system in Legionella pneumophila.
6 for assembly of macromolecular structures in Legionella pneumophila.
7 competence in the freshwater living pathogen Legionella pneumophila.
8 of five F-box-domain-containing proteins of Legionella pneumophila.
9 d by caspase-1 after macrophage infection by Legionella pneumophila.
10 S) with homology to the Dot/Icm apparatus of Legionella pneumophila.
11 sponsive to heat-killed Escherichia coli and Legionella pneumophila.
12 ne in the facultative intracellular pathogen Legionella pneumophila.
13 eviously identified competence regulators in Legionella pneumophila.
14 intracellular respiratory bacterial pathogen Legionella pneumophila.
15 ene, sciS, found to be homologous to icmF in Legionella pneumophila.
16 on with the intracellular bacterial pathogen Legionella pneumophila.
17 racellular iron acquisition strategy used by Legionella pneumophila.
18 ubsequent infection with Escherichia coli or Legionella pneumophila.
19 re form of pneumonia caused by the bacterium Legionella pneumophila.
20 ed with the Gram-negative bacterial pathogen Legionella pneumophila.
21 cteria, including the opportunistic pathogen Legionella pneumophila.
22 tor protein SidM from the bacterial pathogen Legionella pneumophila.
24 s of 9 different serogroups of the bacterium Legionella pneumophila, a common human pathogen responsi
27 Typhimurium, Pectobacterium carotovorum and Legionella pneumophila, also include global regulators t
35 ctivation of caspase-1 cleared unmanipulated Legionella pneumophila and Burkholderia thailandensis by
37 We found that the intracellular pathogens Legionella pneumophila and Coxiella burnetii use a type
38 eractions between the intracellular pathogen Legionella pneumophila and macrophages (Mphis), host and
39 inhibits axenic and intracellular growth of Legionella pneumophila and of 27 strains of wild-type an
40 eta induction by the intracellular bacterium Legionella pneumophila and promotes the bacterial growth
41 ssecting the interaction between a pathogen (Legionella pneumophila) and its host (cultured Drosophil
42 etecting and discriminating Legionella spp., Legionella pneumophila, and Legionella pneumophila serog
44 most strains of the gram-negative bacterium Legionella pneumophila are not competent under normal la
45 hough most Dot/Icm-translocated effectors of Legionella pneumophila are not required for intracellula
46 e early stages of intracellular infection by Legionella pneumophila are well established at the ultra
48 ave been identified using bioinformatics and Legionella pneumophila as a surrogate type IV delivery s
51 onfronted with metabolic stress, replicative Legionella pneumophila bacteria convert to resilient, in
52 uring infection of macrophages, the pathogen Legionella pneumophila bypasses the microbicidal endosom
53 femtomole levels of 16s rRNA from pathogenic Legionella pneumophila can be timely and effectively det
55 at a mono-ADP-ribosyltransferase, SdeA, from Legionella pneumophila catalyzes ADP-ribosylation of ubi
57 tion, the intracellular pathogenic bacterium Legionella pneumophila causes an extensive remodeling of
59 cleotides (oligos) generate mutations on the Legionella pneumophila chromosome by a mechanism that re
61 causative agent of Legionnaires' pneumonia, Legionella pneumophila, colonizes diverse environmental
62 he intracellularly replicating lung pathogen Legionella pneumophila consists of an extraordinary vari
67 re, we found that the intracellular pathogen Legionella pneumophila could interfere with autophagy by
77 Effectors delivered into host cells by the Legionella pneumophila Dot/Icm type IV transporter are e
81 cm-translocated ankyrin B (AnkB) effector of Legionella pneumophila exhibits molecular mimicry of euk
84 (29%) of 14 case patients showed evidence of Legionella pneumophila exposure, according to serologic
87 ria monocytogenes that ectopically expresses Legionella pneumophila flagellin, a potent activator of
88 he transition state mimetic structure of the Legionella pneumophila GAP LepB in complex with Rab1 and
91 irulence factors from the bacterial pathogen Legionella pneumophila has been discovered to modify hum
93 igation of legionellosis outbreaks caused by Legionella pneumophila However, as common sequence types
94 the PmrA/PmrB two-component system (TCS) of Legionella pneumophila in global gene regulation and in
97 at2, effectively suppress the replication of Legionella pneumophila in primary murine macrophages.
98 r the recovery of a standardized inoculum of Legionella pneumophila in respiratory specimens (sputum
99 Based on the crystal structure of LapG of Legionella pneumophila in the accompanying report by Cha
100 es intracellular infection of macrophages by Legionella pneumophila In the present study, we identifi
101 infection mouse model of influenza virus and Legionella pneumophila in which we can separate resistan
104 Type II protein secretion is critical for Legionella pneumophila infection of amoebae, macrophages
106 the present study, we examined the effect of Legionella pneumophila infection on the expression of th
110 cultured in broth to the transmissive phase, Legionella pneumophila infects macrophages by inhibiting
111 The Dot/Icm type IV secretion system of Legionella pneumophila injects into host cells the F-box
119 AnkB effector of the intravacuolar pathogen Legionella pneumophila is a bona fide F-box protein, whi
143 evious studies established that the pathogen Legionella pneumophila is capable of hijacking Rab1 func
144 e Dot/Icm type IV secretion system (T4SS) of Legionella pneumophila is crucial for the pathogen to su
145 Dot/Icm type IVb secretion system (T4SS) of Legionella pneumophila is dependent on correct disulfide
149 owth of Chlamydia psittaci, trachomatis, and Legionella pneumophila is regulated by the levels of int
158 le genome sequence analysis was performed on Legionella pneumophila isolates from the infected patien
159 he performance of laboratories in genotyping Legionella pneumophila isolates using the standard Europ
160 rsistence and associated risks of pathogenic Legionella pneumophila (L. pneumophila), thus raising hu
161 cloned and characterized, two proteins from Legionella pneumophila (L1 H-NOX and L2 H-NOX) and one f
162 Previously, we reported that mutants of Legionella pneumophila lacking a type II secretion (T2S)
163 experimental validation of 20 effectors from Legionella pneumophila, Legionella longbeachae, and Coxi
164 plasma pneumoniae, Chlamydophila pneumoniae, Legionella pneumophila, Legionella micdadei, Bordetella
166 model for Mtb), Pseudomonas aeruginosa (Pa), Legionella pneumophila (Lp), and Enterococcus faecalis (
167 from Escherichia coli (EcFAAL) and FAAL from Legionella pneumophila (LpFAAL) bound to acyl adenylate,
175 dentify amoeba isolates, and the presence of Legionella pneumophila , Mycobacterium spp., Pseudomonas
176 ersistence of three opportunistic pathogens (Legionella pneumophila, Mycobacterium avium, and Pseudom
178 tive for at least one OPPP (Legionella spp., Legionella pneumophila, Mycobacterium avium, Mycobacteri
181 tospira interrogans, Mesorhizobium loti, and Legionella pneumophila, one or both glucosamine residues
182 rulent strain of the intracellular bacterium Legionella pneumophila or a nonpathogenic mutant of L. p
183 Bartonella henselae, Listeria monocytogenes, Legionella pneumophila, or adenovirus type 5, promoted a
184 mon lung pathogens Streptococcus pneumoniae, Legionella pneumophila, or Mycobacterium tuberculosis-in
191 lination of Rab35, which is catalyzed by the Legionella pneumophila protein AnkX, interferes with the
192 study provides detailed understanding of the Legionella pneumophila protein DrrA and of AMP-transfer
194 resses translation of the hupA mRNA, and the Legionella pneumophila protein RocC binds the RocR sRNA,
195 gen testing for Streptococcus pneumoniae and Legionella pneumophila provide direction for the clinici
196 sional structure of the protein lpg2210 from Legionella pneumophila provides the first structural inf
197 her lethal (Yersinia pestis) and non-lethal (Legionella pneumophila, Pseudomonas aeruginosa) pulmonar
198 lytes of three pathogenic bacterial strains: Legionella pneumophila, Pseudomonas aeruginosa, and Salm
199 is, Escherichia coli, Klebsiella pneumoniae, Legionella pneumophila, Pseudomonas aeruginosa, Stenotro
206 se-11 was dispensable for the restriction of Legionella pneumophila replication in macrophages and in
208 onnaires' disease, the gamma-proteobacterium Legionella pneumophila, resides and replicates within a
209 ) and 26GUmicroL(-1) for Legionella spp. and Legionella pneumophila, respectively, were achieved.
210 oazide (PMA) to simultaneously detect viable Legionella pneumophila, Salmonella typhimurium, and Stap
212 ion of macrophages, the pathogenic bacterium Legionella pneumophila secretes effector proteins that i
216 Legionella spp., Legionella pneumophila, and Legionella pneumophila serogroup 1 in primary specimens.
217 bacteria belonging to the genus Legionella; Legionella pneumophila serogroup 1 is the causative agen
220 t the genomic sequence of the human pathogen Legionella pneumophila serogroup 12 strain 570-CO-H (ATC
223 ows: for Bordetella pertussis, 2 CFU/ml; for Legionella pneumophila (serotypes 1 to 15) and Legionell
224 In this report, we found that members of the Legionella pneumophila SidE effector family harbor a DUB
232 stem (T4SS) highly similar to the Dot/Icm of Legionella pneumophila that is believed to be essential
233 In some instances, such as infection with Legionella pneumophila, the activation of the NLRC4 infl
238 fer protection from secondary infection with Legionella pneumophila, the causative agent of a severe
239 thal infection by the intracellular pathogen Legionella pneumophila, the causative agent of a severe
240 ip5 restricts intracellular proliferation of Legionella pneumophila, the causative agent of a severe
241 cal protection from pulmonary infection with Legionella pneumophila, the causative agent of a severe
249 is a previously uncharacterized effector of Legionella pneumophila, the causative agent of Legionnai
250 mune response to bacterial pathogens such as Legionella pneumophila, the causative agent of Legionnai
253 The genome of the Philadelphia-1 strain of Legionella pneumophila, the causative organism of Legion
258 as the gold standard for DNA-based typing of Legionella pneumophila, the Legionella laboratory at the
259 scovery protocol by targeting this enzyme in Legionella pneumophila, the major causative agent of Leg
263 Naip5 is involved in host resistance to Legionella pneumophila through cell autonomous mechanism
264 The ability of the intracellular bacterium Legionella pneumophila to cause disease is totally depen
266 ls by the Dot/Icm injection apparatus allows Legionella pneumophila to establish a niche called the L
268 ystem is a type IVb secretion system used by Legionella pneumophila to modulate vesicular transport i
269 etwork of proteins secreted by the bacterium Legionella pneumophila to promote intracellular growth,
271 To transit between hosts, intracellular Legionella pneumophila transform into a motile, infectio
272 vacuole that supports bacterial replication, Legionella pneumophila translocates a large number of ba
274 The Dot/Icm type IV secretion system of Legionella pneumophila translocates numerous bacterial e
277 al host organism Acanthamoeba castellanii to Legionella pneumophila under in vivo (LCV) conditions.
278 igated the role of RNase R in the biology of Legionella pneumophila under various conditions and perf
288 this list are the sialylated human pathogens Legionella pneumophila, Vibrio parahemeolyticus, Pseudom
293 the DNA uptake system in the human pathogen Legionella pneumophila We found that a repressor of this
294 ddition, during coinfection experiments with Legionella pneumophila, we found that defective intracel
295 g homogenates from guinea pigs infected with Legionella pneumophila were plated monthly onto differen
296 ologs encoded by the Philadelphia isolate of Legionella pneumophila were toxic to yeast, and SidJ sup
297 increased survival of the bacterial pathogen Legionella pneumophila when present inside its protozoan
298 rucella melitensis, Bartonella henselae, and Legionella pneumophila, which are also able to persist w
300 n, and infection in mouse models compared to Legionella pneumophila, yet these two species have indis
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