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1 ress and virulence by the bacterial pathogen Francisella tularensis.
2 ent of tularemia and category A select agent Francisella tularensis.
3 a category A intracellular mucosal pathogen, Francisella tularensis.
4 el organism for the study of highly virulent Francisella tularensis.
5 ellular pathogens Listeria monocytogenes and Francisella tularensis.
6 he highly infectious intracellular bacterium Francisella tularensis.
7 ss caused by the category A biodefense agent Francisella tularensis.
8 the highly infectious and zoonotic pathogen Francisella tularensis.
9 (EHEC and UPEC), Salmonella typhimurium, and Francisella tularensis.
10 mulation would protect the host from inhaled Francisella tularensis.
11 TLR2-activating human intracellular pathogen Francisella tularensis.
12 cated in the O-antigen biosynthetic locus of Francisella tularensis.
13 is caused by the category A biodefense agent Francisella tularensis.
14 on of T helper 1 (Th1) cell immunity against Francisella tularensis.
15 in the protective innate immune response to Francisella tularensis.
16 in Bacillus anthracis, Yersinia pestis, and Francisella tularensis.
17 r the intramacrophage growth and survival of Francisella tularensis.
18 with the facultative intracellular bacterium Francisella tularensis.
19 with Gram-negative Salmonella typhimurium or Francisella tularensis.
20 er vacuolar pathogens, Coxiella burnetii and Francisella tularensis.
21 llenge with the live vaccine strain (LVS) of Francisella tularensis.
22 _1680/FTT_0166c as a new virulence factor in Francisella tularensis.
23 ed by a Gram-negative coccoid rod bacterium, Francisella tularensis.
24 been reported with Dichelobacter nodosus and Francisella tularensis.
25 uivalent but highly divergent sequences from Francisella tularensis.
26 on by using the live vaccine strain (LVS) of Francisella tularensis.
27 0) in cutaneous and pulmonary infection with Francisella tularensis.
28 by infection by the gram-negative bacterium, Francisella tularensis.
29 infections using Rift Valley fever virus and Francisella tularensis.
30 from individuals infected with the bacteria Francisella tularensis, a category A biodefense pathogen
31 th the Gram-negative intracellular bacterium Francisella tularensis, a category A biological threat a
32 rticularly good antibacterial effect against Francisella tularensis, a Category A biowarfare pathogen
36 e attenuated vaccine is needed for combating Francisella tularensis, a highly infectious bacterial pa
37 macrophages the intracellular life cycle of Francisella tularensis, a highly infectious bacterium th
38 of genes that contribute to the virulence of Francisella tularensis, a highly infectious pathogen and
43 chanisms by which virulent type A strains of Francisella tularensis accomplish this evasion are not u
44 ion of the lipid A 1-phosphatase, LpxE, from Francisella tularensis allowed us to construct recombina
45 However, a comparative genome analysis of Francisella tularensis allowed us to predict the existen
49 aureus (MRSA) and priority pathogens such as Francisella tularensis and Burkholderia pseudomallei.
50 cted in membranes of Helicobacter pylori and Francisella tularensis and may be responsible for the re
51 and Prevention Category A bioterrorism agent Francisella tularensis and prototype of a superfamily of
54 agilis, Bacillus anthracis, Yersinia pestis, Francisella tularensis, and Brucella abortus), the last
55 spp., Toxoplasma gondii, Coxiella burnetii, Francisella tularensis, and Neospora caninum, estimate c
58 dentified the two major lipid A species from Francisella tularensis as asymmetric tetraacylated struc
59 hances murine susceptibility to infection by Francisella tularensis as indicated by accelerated morta
60 lian pathogens such as Coxiella burnetii and Francisella tularensis, as well as Coxiella-like and Fra
62 r nodosus and FtPilE from the human pathogen Francisella tularensis at 2.3 and 1 A resolution, respec
63 ae, Pseudomonas aeruginosa, Yersinia pestis, Francisella tularensis, Bacillus anthracis and Vibrio ch
64 O-antigen of the lipopolysaccharide (LPS) of Francisella tularensis bacteria, a Tier 1 Select Agent o
66 racis, Yersinia pestis, Burkholderia mallei, Francisella tularensis, Brucella abortus, and ricin.
67 ned for Bacillus anthracis, Yersinia pestis, Francisella tularensis, Brucella melitensis, Clostridium
68 anisms (Bacillus anthracis, Yersinia pestis, Francisella tularensis, Brucella spp., Burkholderia spp.
69 ains of Bacillus anthracis, Yersinia pestis, Francisella tularensis, Burkholderia mallei, Burkholderi
70 protection against infection with attenuated Francisella tularensis, but their role in infection medi
71 Schu S4 strain of the intracellular pathogen Francisella tularensis by host macrophages involves CR3/
72 urface exposed and required for virulence of Francisella tularensis by subverting the host innate imm
75 egative, facultative intracellular bacterium Francisella tularensis causes acute, lethal pneumonic di
82 R recruitment, we evaluated Escherichia coli-Francisella tularensis chimeric variants of tmRNA and Sm
85 pectrum efficacy against Bacillus anthracis; Francisella tularensis; Coxiella burnetii; and Ebola, Ma
90 chanisms by which the intracellular pathogen Francisella tularensis evades innate immunity are not we
91 VS and Schu S4 strains of the human pathogen Francisella tularensis express a siderophore when grown
92 es of the Gram-negative facultative anaerobe Francisella tularensis: F. tularensis subsp. tularensis
94 se appears to contribute to the virulence of Francisella tularensis following pulmonary infection.
97 The macrophage proinflammatory response to Francisella tularensis (Ft) live vaccine strain (LVS) wa
102 cid phosphatase from the category A pathogen Francisella tularensis (FtHAP) has been implicated in in
103 ymbionts (FLEs) with significant homology to Francisella tularensis (gamma-proteobacteria) have been
106 accinations with the intracellular bacterium Francisella tularensis have been studied using the live
108 the comparison between the genome of LVS and Francisella tularensis holarctica strain FSC200, which d
109 onstrated that targeting fixed (inactivated) Francisella tularensis (iFT) organisms to FcR in mice i.
110 w-derived macrophages (BMDMs) to inactivated Francisella tularensis (iFt)-containing immune complexes
113 ion of the lipid A 1-phosphatase, LpxE, from Francisella tularensis in Y. pestis yields predominantly
116 used by the Gram-negative bacterial pathogen Francisella tularensis Infection of macrophages and thei
117 ocked Th17 cell generation in the lung after Francisella tularensis infection, and inhibited the incr
171 A fundamental step in the life cycle of Francisella tularensis is bacterial entry into host cell
172 The facultative intracellular bacterium Francisella tularensis is capable of causing systemic in
177 the highly infectious intracellular pathogen Francisella tularensis is directly related with the abil
198 any other gram-negative bacteria, the LPS of Francisella tularensis isolated from in vitro cultures i
199 tularemia, a zoonose caused by the bacterium Francisella tularensis, largely refer to Parinaud's ocul
200 .) and intradermal (i.d.) inoculation of the Francisella tularensis live vaccine strain (Ft-LVS).
201 IKKs in myeloid cells in vivo in response to Francisella tularensis Live Vaccine Strain (Ft. LVS) inf
202 teria Mycobacterium tuberculosis (M. tb.) or Francisella tularensis Live Vaccine Strain (LVS) in macr
203 subset in the lungs of mice during pulmonary Francisella tularensis live vaccine strain (LVS) infecti
208 ammation, priming with glycolipid (FtL) from Francisella tularensis live vaccine strain induces splen
210 hown that priming with glycolipid (FtL) from Francisella tularensis live-vaccine strain (i) induces F
211 and public health pathogens-Influenza virus, Francisella tularensis, Mycobacterium tuberculosis, Micr
212 eumonic tularemia is caused by inhalation of Francisella tularensis, one of the most infectious micro
217 s, successful protective immune responses to Francisella tularensis require rapid and efficient induc
218 to various assemblies of the loblolly pine, Francisella tularensis, rice and budgerigar genomes.
220 study, we describe novel inhibitors against Francisella tularensis SchuS4 FabI identified from struc
225 gions of two slightly more distantly related Francisella tularensis strains were also compared agains
226 shown to be associated with highly virulent Francisella tularensis strains, including Schu S4, while
228 nd illustrate its use on three datasets from Francisella tularensis, Streptococcus pyogenes, and Esch
229 F. novicida protected against challenge with Francisella tularensis subsp. holarctica and F. novicida
231 ble to the live attenuated vaccine strain of Francisella tularensis subsp. holarctica in their abilit
232 -flight (MALDI-TOF) mass spectrometry on the Francisella tularensis subsp. holarctica LVS defined thr
233 eral highly pathogenic subspecies, including Francisella tularensis subsp. holarctica, whose distribu
241 b O-PS gene cluster from the highly virulent Francisella tularensis subsp. tularensis (type A) strain
242 Comparative genome hybridization of the Francisella tularensis subsp. tularensis and F. tularens
243 n Francisella philomiragia ATCC 25015 and on Francisella tularensis subsp. tularensis CCUG 2112, the
248 Clinical isolates of highly virulent type A Francisella tularensis subsp. tularensis organisms were
249 n of the virulent prototypical type A strain Francisella tularensis subsp. tularensis Schu S4 affects
250 Inactivation of both copies of iglE rendered Francisella tularensis subsp. tularensis Schu S4 avirule
252 scribe the isolation and characterization of Francisella tularensis subsp. tularensis strain Schu S4
253 dings concerning the four subspecies and two Francisella tularensis subsp. tularensis subpopulations
256 AIM2 inflammasome during infection with the Francisella tularensis subspecies novicida (F. novicida)
258 onal exposure to lethal doses of aerosolized Francisella tularensis subspecies tularensis, strain SCH
271 istinct lack of activation of these cells by Francisella tularensis, the causative agent of tularemia
275 ased, whole-genome resequencing platform for Francisella tularensis, the causative agent of tularemia
288 including virulent strains of the bacterium Francisella tularensis, to enable colonization and infec
289 ogens, such as the highly virulent bacterium Francisella tularensis, to ensure their replication and
291 ts ortholog FTT_0166c in the highly virulent Francisella tularensis type A strain SchuS4 are required
292 elates of vaccine-induced protection against Francisella tularensis using murine splenocytes and furt
294 l for inflammasome activation in response to Francisella tularensis, vaccinia virus and mouse cytomeg
297 of animals as early as 4 hrs post-exposure, Francisella tularensis was associated with an almost com
300 ctions with the live vaccine strain (LVS) of Francisella tularensis within the mouse liver are the fo
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