Analysis of the Borrelia burgdorferi cyclic-di-GMP-binding protein PlzA reveals a role in motility and virulence
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Interaction of the Lyme disease spirochete with its tick vectorThe diguanylate cyclase, Rrp1, regulates critical steps in the enzootic cycle of the Lyme disease spirochetes.The unique paradigm of spirochete motility and chemotaxis.PilZ Domain Protein FlgZ Mediates Cyclic Di-GMP-Dependent Swarming Motility Control in Pseudomonas aeruginosa.The cyclic-di-GMP signaling pathway in the Lyme disease spirochete, Borrelia burgdorferiGenome stability of Lyme disease spirochetes: comparative genomics of Borrelia burgdorferi plasmids.Of ticks, mice and men: understanding the dual-host lifestyle of Lyme disease spirochaetes.Spirochetal motility and chemotaxis in the natural enzootic cycle and development of Lyme diseaseCyclic di-GMP riboswitch-regulated type IV pili contribute to aggregation of Clostridium difficile.Analysis of the HD-GYP domain cyclic dimeric GMP phosphodiesterase reveals a role in motility and the enzootic life cycle of Borrelia burgdorferi.Motor rotation is essential for the formation of the periplasmic flagellar ribbon, cellular morphology, and Borrelia burgdorferi persistence within Ixodes scapularis tick and murine hosts.The Xanthomonas oryzae pv. oryzae PilZ Domain Proteins Function Differentially in Cyclic di-GMP Binding and Regulation of Virulence and MotilityThe Borrelia burgdorferi RelA/SpoT Homolog and Stringent Response Regulate Survival in the Tick Vector and Global Gene Expression during StarvationCyclic di-GMP modulates gene expression in Lyme disease spirochetes at the tick-mammal interface to promote spirochete survival during the blood meal and tick-to-mammal transmissionEffect of levels of acetate on the mevalonate pathway of Borrelia burgdorferiBorrelia burgdorferi and tick proteins supporting pathogen persistence in the vector.Motility is crucial for the infectious life cycle of Borrelia burgdorferi.Understanding barriers to Borrelia burgdorferi dissemination during infection using massively parallel sequencingBorrelia burgdorferi CheD Promotes Various Functions in Chemotaxis and the Pathogenic Life Cycle of the SpirocheteSecond messenger regulation of biofilm formation: breakthroughs in understanding c-di-GMP effector systems.Inactivation of cyclic Di-GMP binding protein TDE0214 affects the motility, biofilm formation, and virulence of Treponema denticola.Borrelia burgdorferi CheY2 Is Dispensable for Chemotaxis or Motility but Crucial for the Infectious Life Cycle of the Spirochete.Cyclic Di-GMP receptor PlzA controls virulence gene expression through RpoS in Borrelia burgdorferi.Cyclic di-GMP, an established secondary messenger still speeding up.Klebsiella pneumoniae and type 3 fimbriae: nosocomial infection, regulation and biofilm formation.The bacterial second messenger c-di-GMP: probing interactions with protein and RNA binding partners using cyclic dinucleotide analogsSpirochetes flagellar collar protein FlbB has astounding effects in orientation of periplasmic flagella, bacterial shape, motility, and assembly of motors in Borrelia burgdorferi.The Borrelia burgdorferi CheY3 response regulator is essential for chemotaxis and completion of its natural infection cycle.Cyclic-di-GMP binding induces structural rearrangements in the PlzA and PlzC proteins of the Lyme disease and relapsing fever spirochetes: a possible switch mechanism for c-di-GMP-mediated effector functions.RNA-mediated signal perception in pathogenic bacteria.Cyclic Di-GMP Regulates Multiple Cellular Functions in the Symbiotic Alphaproteobacterium Sinorhizobium meliloti.A Cyclic di-GMP-binding Adaptor Protein Interacts with Histidine Kinase to Regulate Two-component Signaling.Coordinated cyclic-di-GMP repression of Salmonella motility through YcgR and cellulose.Gene Regulation, Two Component Regulatory Systems, and Adaptive Responses in Treponema Denticola.Genome reduction of Borrelia burgdorferi: two TCS signaling pathways for two distinct host habitats.Structural analyses unravel the molecular mechanism of cyclic di-GMP regulation of bacterial chemotaxis via a PilZ adaptor protein.Cyclic-di-GMP regulation of virulence in bacterial pathogens.Immune escape strategies of Borrelia burgdorferi.A cyclic di-GMP-binding adaptor protein interacts with a chemotaxis methyltransferase to control flagellar motor switching.Borrelia host adaptation Protein (BadP) is required for the colonization of a mammalian host by the agent of Lyme disease.
P2860
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P2860
Analysis of the Borrelia burgdorferi cyclic-di-GMP-binding protein PlzA reveals a role in motility and virulence
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Analysis of the Borrelia burgd ...... role in motility and virulence
@ast
Analysis of the Borrelia burgd ...... role in motility and virulence
@en
Analysis of the Borrelia burgd ...... role in motility and virulence
@nl
type
label
Analysis of the Borrelia burgd ...... role in motility and virulence
@ast
Analysis of the Borrelia burgd ...... role in motility and virulence
@en
Analysis of the Borrelia burgd ...... role in motility and virulence
@nl
prefLabel
Analysis of the Borrelia burgd ...... role in motility and virulence
@ast
Analysis of the Borrelia burgd ...... role in motility and virulence
@en
Analysis of the Borrelia burgd ...... role in motility and virulence
@nl
P2093
P2860
P356
P1476
Analysis of the Borrelia burgd ...... role in motility and virulence
@en
P2093
Gerry Hobbs
Joshua E Pitzer
Md A Motaleb
Michael R Miller
Syed Z Sultan
Yoshihiro Hayakawa
P2860
P304
P356
10.1128/IAI.00075-11
P407
P577
2011-05-01T00:00:00Z