scholarly article | Q13442814 |
P356 | DOI | 10.3389/FMICB.2013.00375 |
P8608 | Fatcat ID | release_5ot43sd52bd2fp5gys3kapdlcq |
P932 | PMC publication ID | 3863721 |
P698 | PubMed publication ID | 24379807 |
P5875 | ResearchGate publication ID | 259500072 |
P50 | author | Shuyang Sun | Q58123489 |
Diane McDougald | Q30509891 | ||
P2093 | author name string | Carla Lutz | |
Martina Erken | |||
Parisa Noorian | |||
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The viable but non-culturable phenomenon explained? | Q74190266 | ||
Potentially pathogenic vibrios in brackish waters and mussels | Q74261816 | ||
Response and tolerance of toxigenic Vibro cholerae O1 to cold temperatures | Q77565143 | ||
Restoration of culturability of starvation-stressed and low-temperature-stressed Escherichia coli O157 cells by using H2O2-degrading compounds | Q77978505 | ||
Interaction of Vibrio cholerae O139 with an intestinal parasite, Entamoeba histolytica | Q79362946 | ||
Gene expression profile of Vibrio cholerae in the cold stress-induced viable but non-culturable state | Q79946965 | ||
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Viable but non-culturable Vibrio cholerae O1 revert to a cultivable state in the human intestine | Q87081108 | ||
Microscale nutrient patches in planktonic habitats shown by chemotactic bacteria | Q95442822 | ||
The viable but nonculturable state in bacteria | Q28239571 | ||
Widespread occurrence of norspermidine and norspermine in eukaryotic algae | Q28278493 | ||
Distinguishing between the extracellular DNases of Vibrio cholerae and development of a transformation system | Q28485705 | ||
Type VI secretion system translocates a phage tail spike-like protein into target cells where it cross-links actin | Q28485710 | ||
Vibrio cholerae in an Historically Cholera-Free Country | Q28710530 | ||
Integration of cyclic di-GMP and quorum sensing in the control of vpsT and aphA in Vibrio cholerae | Q29346624 | ||
Simple Sari Cloth Filtration of Water Is Sustainable and Continues To Protect Villagers from Cholera in Matlab, Bangladesh | Q29398228 | ||
Bacterial biofilms: from the natural environment to infectious diseases | Q29547677 | ||
A novel suicide vector and its use in construction of insertion mutations: osmoregulation of outer membrane proteins and virulence determinants in Vibrio cholerae requires toxR | Q29615324 | ||
Acanthamoeba polyphaga is a possible host for Vibrio cholerae in aquatic environments | Q30227507 | ||
Vibrio cholerae O139 requires neither capsule nor LPS O side chain to grow inside Acanthamoeba castellanii | Q30228374 | ||
The absence of a flagellum leads to altered colony morphology, biofilm development and virulence in Vibrio cholerae O139. | Q30327646 | ||
Vibrio cholerae O1 strains are facultative intracellular bacteria, able to survive and multiply symbiotically inside the aquatic free-living amoeba Acanthamoeba castellanii. | Q30360654 | ||
Waterfowl: the missing link in epidemic and pandemic cholera dissemination? | Q30373076 | ||
The Vibrio Cholerae Type VI Secretion System: Evaluating its Role in the Human Disease Cholera | Q30403083 | ||
Constitutive type VI secretion system expression gives Vibrio cholerae intra- and interspecific competitive advantages | Q30422970 | ||
Detection of Vibrio cholerae in environmental waters including drinking water reservoirs of Azerbaijan | Q30431766 | ||
Enhanced survival of Salmonella enterica in vesicles released by a soilborne Tetrahymena species | Q30475794 | ||
Relationships between Environmental Factors and Pathogenic Vibrios in the Northern Gulf of Mexico | Q30497309 | ||
Predictability of Vibrio cholerae in Chesapeake Bay. | Q30791141 | ||
Long-term effects of ocean warming on the prokaryotic community: evidence from the vibrios | Q31022948 | ||
Characterization of hapR, a positive regulator of the Vibrio cholerae HA/protease gene hap, and its identification as a functional homologue of the Vibrio harveyi luxR gene | Q32151390 | ||
Benthic ecology of Vibrio spp. and pathogenic Vibrio species in a coastal Mediterranean environment (La Spezia Gulf, Italy). | Q33471578 | ||
Quorum sensing regulation of the two hcp alleles in Vibrio cholerae O1 strains | Q33496132 | ||
Fish as reservoirs and vectors of Vibrio cholerae | Q33523276 | ||
Unexplored reservoirs of pathogenic bacteria: protozoa and biofilms | Q33539355 | ||
Quorum-regulated biofilms enhance the development of conditionally viable, environmental Vibrio cholerae | Q33667813 | ||
Self-limiting nature of seasonal cholera epidemics: Role of host-mediated amplification of phage | Q33771191 | ||
Inorganic polyphosphate in Vibrio cholerae: genetic, biochemical, and physiologic features | Q33792337 | ||
Quantification of Vibrio parahaemolyticus, Vibrio vulnificus and Vibrio cholerae in French Mediterranean coastal lagoons | Q33815379 | ||
vpsA- and luxO-independent biofilms of Vibrio cholerae. | Q50936016 | ||
The ecology of Vibrio vulnificus, Vibrio cholerae, and Vibrio parahaemolyticus in North Carolina estuaries. | Q51182932 | ||
Quantitative reverse transcription polymerase chain reaction analysis of Vibrio cholerae cells entering the viable but non-culturable state and starvation in response to cold shock. | Q51234974 | ||
Intracellular survival and replication of Vibrio cholerae O139 in aquatic free-living amoebae. | Q51439172 | ||
Sequence analyses of type IV pili from Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus. | Q51569741 | ||
Environmental reservoirs of Vibrio cholerae and their role in cholera. | Q51639008 | ||
Growth response of Vibrio cholerae and other Vibrio spp. to cyanobacterial dissolved organic matter and temperature in brackish water. | Q51711324 | ||
Viable but nonculturable bacteria: a survival strategy. | Q52545112 | ||
Dependent population dynamics between chironomids (nonbiting midges) and Vibrio cholerae. | Q52664277 | ||
Culturable and VBNC Vibrio cholerae: interactions with chironomid egg masses and their bacterial population. | Q52675355 | ||
Vibrios in association with sedimentary crustaceans in three beaches of the northern Adriatic Sea (Italy). | Q53126197 | ||
Characterization of a Vibrio cholerae phage isolated from the coastal water of Peru | Q53141242 | ||
Increased tolerance of Vibrio cholerae O1 to temperature, pH, or drying associated with colonization of shrimp carapaces. | Q53852705 | ||
Quantitative microbial risk assessment of pathogenic vibrios in marine recreational waters of southern california | Q36505982 | ||
Rapid growth of planktonic Vibrio cholerae non-O1/non-O139 strains in a large alkaline lake in Austria: dependence on temperature and dissolved organic carbon quality. | Q36538835 | ||
Cholera from raw seaweed transported from the Philippines to California | Q36542853 | ||
The Vibrio cholerae chitin utilization program | Q36602658 | ||
Genetic diversity and virulence potential of environmental Vibrio cholerae population in a cholera-endemic area | Q36604953 | ||
Indigenous Vibrio cholerae strains from a non-endemic region are pathogenic | Q36702416 | ||
Iron acquisition in Vibrio cholerae | Q36704725 | ||
Ecological relationships between Vibrio cholerae and planktonic crustacean copepods. | Q36710008 | ||
Occurrence of Vibrio cholerae serotype O1 in Maryland and Louisiana estuaries | Q36734068 | ||
Influence of salinity and organic nutrient concentration on survival and growth of Vibrio cholerae in aquatic microcosms | Q36740404 | ||
Vibrio cholerae CytR is a repressor of biofilm development | Q36835985 | ||
Cholera studies. 1. History of the disease. | Q36889179 | ||
Quorum-sensing autoinducers resuscitate dormant Vibrio cholerae in environmental water samples | Q36932411 | ||
Global impact of Vibrio cholerae interactions with chitin | Q37099108 | ||
Climate and infectious disease: use of remote sensing for detection of Vibrio cholerae by indirect measurement | Q37103393 | ||
Glycogen contributes to the environmental persistence and transmission of Vibrio cholerae | Q37248464 | ||
Positive transcriptional regulation of an iron-regulated virulence gene in Vibrio cholerae | Q37395794 | ||
Vibrio biofilms: so much the same yet so different | Q37397388 | ||
The PhoB regulatory system modulates biofilm formation and stress response in El Tor biotype Vibrio cholerae | Q37474004 | ||
A tangled web: regulatory connections between quorum sensing and cyclic Di-GMP. | Q38015806 | ||
Environmental occurrence and clinical impact of Vibrio vulnificus and Vibrio parahaemolyticus: a European perspective. | Q38114398 | ||
Molecular analysis of rugosity in a Vibrio cholerae O1 El Tor phase variant | Q38339427 | ||
Quorum Sensing-Dependent Biofilms Enhance Colonization in Vibrio cholerae | Q38349419 | ||
Vibrio cholerae requires the type VI secretion system virulence factor VasX to kill Dictyostelium discoideum | Q38686669 | ||
Water column dynamics of Vibrio in relation to phytoplankton community composition and environmental conditions in a tropical coastal area | Q38882220 | ||
An epidemiological study of Vibrio cholerae O1 in the Australian environment based on rRNA gene polymorphisms | Q38971020 | ||
Cholera in Lima, Peru, correlates with prior isolation of Vibrio cholerae from the environment | Q39010422 | ||
Attachment of toxigenic Vibrio cholerae 01 to various freshwater plants and survival with a filamentous green alga, Rhizoclonium fontanum | Q39096138 | ||
Environmental temperature, cholera, and acute diarrhoea in adults in Lima, Peru. | Q39158159 | ||
NspS, a predicted polyamine sensor, mediates activation of Vibrio cholerae biofilm formation by norspermidine | Q39362294 | ||
Marine biofilms on submerged surfaces are a reservoir for Escherichia coli and Vibrio cholerae. | Q39457577 | ||
The polar flagellar motor of Vibrio cholerae is driven by an Na+ motive force | Q39494772 | ||
VpsR, a Member of the Response Regulators of the Two-Component Regulatory Systems, Is Required for Expression of vps Biosynthesis Genes and EPS(ETr)-Associated Phenotypes in Vibrio cholerae O1 El Tor | Q39502809 | ||
Characterization of Vibrio cholerae O1 El tor galU and galE mutants: influence on lipopolysaccharide structure, colonization, and biofilm formation | Q39517916 | ||
Preliminary report on the pathogenicity of Legionella pneumophila for freshwater and soil amoebae | Q33848527 | ||
Characterization of a flagellar sheath protein of Vibrio cholerae. | Q33899685 | ||
Critical factors influencing the occurrence of Vibrio cholerae in the environment of Bangladesh | Q33913215 | ||
Warming oceans, phytoplankton, and river discharge: implications for cholera outbreaks | Q33981104 | ||
The mannose-sensitive hemagglutinin of Vibrio cholerae promotes adherence to zooplankton | Q33989901 | ||
A communal bacterial adhesin anchors biofilm and bystander cells to surfaces | Q34013625 | ||
Quorum-sensing regulators control virulence gene expression in Vibrio cholerae | Q34016637 | ||
Recent findings on the viable but nonculturable state in pathogenic bacteria | Q34020799 | ||
Algal blooms in the spread and persistence of cholera | Q34060601 | ||
Lysogenic conversion by a filamentous phage encoding cholera toxin | Q34062735 | ||
Adsorption and growth of Vibrio cholerae on chitin | Q34090913 | ||
Original involvement of antimicrobial peptides in mussel innate immunity. | Q34105854 | ||
ToxR of Vibrio cholerae affects biofilm, rugosity and survival with Acanthamoeba castellanii | Q34128649 | ||
Evolutionary and functional analyses of variants of the toxin-coregulated pilus protein TcpA from toxigenic Vibrio cholerae non-O1/non-O139 serogroup isolates | Q34132602 | ||
Biofilm formation and phenotypic variation enhance predation-driven persistence of Vibrio cholerae | Q34133215 | ||
Microbial scout hypothesis and microbial discovery | Q34172672 | ||
Predatory Bacteriovorax communities ordered by various prey species | Q34213857 | ||
The regulatory network of natural competence and transformation of Vibrio cholerae | Q34318274 | ||
The Vibrio cholerae type VI secretion system displays antimicrobial properties | Q34320269 | ||
Bacterial infections of free-living amoebae | Q34404920 | ||
Survival of Vibrio cholerae in nutrient-poor environments is associated with a novel "persister" phenotype | Q34428302 | ||
A colonization factor links Vibrio cholerae environmental survival and human infection | Q34474848 | ||
Trophic regulation of Vibrio cholerae in coastal marine waters | Q34475134 | ||
Evidence of a dominant lineage of Vibrio cholerae-specific lytic bacteriophages shed by cholera patients over a 10-year period in Dhaka, Bangladesh | Q34565895 | ||
Toxigenic Vibrio cholerae in the aquatic environment of Mathbaria, Bangladesh | Q34570460 | ||
Occurrence of Vibrio parahaemolyticus, V. cholerae, and V. vulnificus in Norwegian Blue Mussels (Mytilus edulis). | Q34570517 | ||
Diversity of Vibrio spp. isolated at ambient environmental temperature in the Eastern English Channel as determined by pyrH sequencing | Q34615274 | ||
A Vibrio cholerae protease needed for killing of Caenorhabditis elegans has a role in protection from natural predator grazing | Q34695043 | ||
Interaction of Legionella pneumophila with Acanthamoeba castellanii: uptake by coiling phagocytosis and inhibition of phagosome-lysosome fusion | Q34731994 | ||
Characterization of Vibrio cholerae bacteriophages isolated from the environmental waters of the Lake Victoria region of Kenya | Q34975231 | ||
Environmental influences on Vibrio populations in northern temperate and boreal coastal waters (Baltic and Skagerrak Seas) | Q35023465 | ||
Characterization of ferric and ferrous iron transport systems in Vibrio cholerae | Q35075619 | ||
Direct detection of Vibrio cholerae and ctxA in Peruvian coastal water and plankton by PCR | Q35097163 | ||
Polyphosphate stores enhance the ability of Vibrio cholerae to overcome environmental stresses in a low-phosphate environment | Q35129940 | ||
Vibrio cholerae hemagglutinin/protease degrades chironomid egg masses. | Q35154063 | ||
Entry into, and resuscitation from, the viable but nonculturable state by Vibrio vulnificus in an estuarine environment | Q35184918 | ||
Uptake and retention of Vibrio cholerae O1 in the Eastern oyster, Crassostrea virginica | Q35186485 | ||
Role of zooplankton diversity in Vibrio cholerae population dynamics and in the incidence of cholera in the Bangladesh Sundarbans | Q35191631 | ||
A simple filtration method to remove plankton-associated Vibrio cholerae in raw water supplies in developing countries. | Q35192100 | ||
Ecology and genetic structure of a northern temperate Vibrio cholerae population related to toxigenic isolates | Q35530718 | ||
Extracellular nucleases and extracellular DNA play important roles in Vibrio cholerae biofilm formation. | Q35539741 | ||
Indigenous bacteria in hemolymph and tissues of marine bivalves at low temperatures | Q35678569 | ||
Isolation of Vibrio cholerae from aquatic birds in Colorado and Utah | Q35731176 | ||
Attachment of Vibrio cholerae serogroup O1 to zooplankton and phytoplankton of Bangladesh waters. | Q35739157 | ||
Toxigenic Vibrio cholerae O1 in water and seafood, Haiti | Q35847257 | ||
Environmental determinants of Vibrio cholerae biofilm development | Q35942956 | ||
Persistence of vibrios in marine bivalves: the role of interactions with haemolymph components. | Q36126824 | ||
Viable but nonculturable Vibrio cholerae O1 in biofilms in the aquatic environment and their role in cholera transmission | Q36140742 | ||
Resuscitation of Vibrio vulnificus from the viable but nonculturable state | Q36150978 | ||
Off the hook--how bacteria survive protozoan grazing | Q36151453 | ||
CTX genetic element encodes a site-specific recombination system and an intestinal colonization factor. | Q36262564 | ||
Ecology of Vibrio parahaemolyticus and Vibrio vulnificus in the coastal and estuarine waters of Louisiana, Maryland, Mississippi, and Washington (United States). | Q36276091 | ||
Association of Vibrio cholerae O1 El Tor and O139 Bengal with the Copepods Acartia tonsa and Eurytemora affinis | Q36313557 | ||
A novel role for enzyme I of the Vibrio cholerae phosphoenolpyruvate phosphotransferase system in regulation of growth in a biofilm. | Q36422242 | ||
Role of chemotaxis in the association of motile bacteria with intestinal mucosa: chemotactic responses of Vibrio cholerae and description of motile nonchemotactic mutants | Q36429310 | ||
Ecology and physics of bacterial chemotaxis in the ocean | Q36435157 | ||
Molecular architecture and assembly principles of Vibrio cholerae biofilms | Q36441854 | ||
Vibrio cholerae O1 El Tor: identification of a gene cluster required for the rugose colony type, exopolysaccharide production, chlorine resistance, and biofilm formation | Q36456326 | ||
Association of Vibrio cholerae with fresh water amoebae | Q39521127 | ||
Salinity-induced survival strategy of Vibrio cholerae associated with copepods in Cochin backwaters | Q39521464 | ||
Vibrio cholerae O1 strain TSI-4 produces the exopolysaccharide materials that determine colony morphology, stress resistance, and biofilm formation | Q39562123 | ||
Conversion of viable but nonculturable Vibrio cholerae to the culturable state by co‐culture with eukaryotic cells | Q39656052 | ||
High-frequency rugose exopolysaccharide production by Vibrio cholerae | Q39661876 | ||
Analyses of the roles of the three cheA homologs in chemotaxis of Vibrio cholerae | Q39678554 | ||
In situ analysis of nucleic acids in cold-induced nonculturable Vibrio vulnificus | Q39802551 | ||
Environmental Vibrio spp., isolated in Mozambique, contain a polymorphic group of integrative conjugative elements and class 1 integrons | Q39837521 | ||
Isolation of Vibrio cholerae O139 synonym Bengal from the aquatic environment in Bangladesh: implications for disease transmission | Q39914947 | ||
Growth of Vibrio cholerae O1 in red tide waters off California. | Q40171953 | ||
Steps in the development of a Vibrio cholerae El Tor biofilm | Q40225093 | ||
VpsT is a transcriptional regulator required for expression of vps biosynthesis genes and the development of rugose colonial morphology in Vibrio cholerae O1 El Tor. | Q40584757 | ||
Viable but nonculturable Vibrio cholerae O1 in the aquatic environment of Argentina | Q40621463 | ||
Molecular biology and regulatory aspects of glycogen biosynthesis in bacteria | Q40663905 | ||
Ferric uptake regulation protein acts as a repressor, employing iron (II) as a cofactor to bind the operator of an iron transport operon in Escherichia coli | Q41332825 | ||
Occurrence of Vibrio cholerae in municipal and natural waters and incidence of cholera in Azerbaijan | Q41416671 | ||
Genetic evidence that the Vibrio cholerae monolayer is a distinct stage in biofilm development | Q41466889 | ||
Identification and characterization of RbmA, a novel protein required for the development of rugose colony morphology and biofilm structure in Vibrio cholerae | Q41819957 | ||
Induction of melanin biosynthesis in Vibrio cholerae | Q41827978 | ||
PhoB regulates motility, biofilms, and cyclic di-GMP in Vibrio cholerae | Q41839121 | ||
Role of melanin pigment in expression of Vibrio cholerae virulence factors | Q41865177 | ||
Cyclic dimeric GMP signaling and regulation of surface-associated developmental programs | Q41911376 | ||
The phosphoenolpyruvate phosphotransferase system regulates Vibrio cholerae biofilm formation through multiple independent pathways. | Q41987646 | ||
Microbial scout hypothesis, stochastic exit from dormancy, and the nature of slow growers | Q42027974 | ||
The rbmBCDEF gene cluster modulates development of rugose colony morphology and biofilm formation in Vibrio cholerae | Q42039844 | ||
Virulence and the environment: a novel role for Vibrio cholerae toxin-coregulated pili in biofilm formation on chitin | Q42092038 | ||
Vibrio cholerae non-O1 isolated from ayu fish (Plecoglossus altivelis) in Japan | Q42125349 | ||
Role of Vibrio polysaccharide (vps) genes in VPS production, biofilm formation and Vibrio cholerae pathogenesis | Q42185441 | ||
Relative contributions of Vibrio polysaccharide and quorum sensing to the resistance of Vibrio cholerae to predation by heterotrophic protists | Q42225939 | ||
Mannitol and the mannitol-specific enzyme IIB subunit activate Vibrio cholerae biofilm formation | Q42260607 | ||
Vibrio cholerae O1 from superficial water of the Tucunduba Stream, Brazilian Amazon | Q42594150 | ||
Effect of fatty acids and cholesterol present in bile on expression of virulence factors and motility of Vibrio cholerae | Q42800298 | ||
Temporal quorum-sensing induction regulates Vibrio cholerae biofilm architecture | Q42913652 | ||
Virulence genes in halophilic Vibrio spp. isolated in common mussels. | Q43029865 | ||
Detection of toxigenic Vibrio cholerae O1 in freshwater lakes of the former Soviet Republic of Georgia | Q43926374 | ||
Plankton composition and environmental factors contribute to Vibrio seasonality | Q44103173 | ||
Association of Vibrio cholerae with plankton in coastal areas of Mexico. | Q44243959 | ||
The population and evolutionary dynamics of Vibrio cholerae and its bacteriophage: conditions for maintaining phage-limited communities | Q44360238 | ||
Persistence of adhesive properties in Vibrio cholerae after long‐term exposure to sea water | Q44597035 | ||
Chironomid egg masses as a natural reservoir of Vibrio cholerae non-O1 and non-O139 in freshwater habitats | Q44697534 | ||
Grazing of protozoa and its effect on populations of aquatic bacteria | Q45135793 | ||
Detection and diversity of pathogenic Vibrio from Fiji. | Q45293608 | ||
Temporal and spatial distribution patterns of potentially pathogenic Vibrio spp. at recreational beaches of the German north sea. | Q45343184 | ||
Temperature affects Vibrio cholerae O1 El Tor persistence in the aquatic environment via an enhanced expression of GbpA and MSHA adhesins | Q45817338 | ||
A molecular survey on virulence associated genotypes of non-O1 non-O139 Vibrio cholerae in aquatic environment of Tehran, Iran. | Q46154684 | ||
Quorum sensing controls biofilm formation in Vibrio cholerae | Q47608536 | ||
The cadA gene of Vibrio cholerae is induced during infection and plays a role in acid tolerance | Q47910947 | ||
Proteome comparison of Vibrio cholerae cultured in aerobic and anaerobic conditions | Q47924538 | ||
Role of catalase and oxyR in the viable but nonculturable state of Vibrio vulnificus | Q48166264 | ||
Pathogen reservoirs. Chironomid egg masses and Vibrio cholerae | Q49167489 | ||
Factors influencing survival of enterotoxigenic Escherichia coli, Salmonella enterica (serovar Typhimurium) and Vibrio parahaemolyticus in marine environments | Q50052084 | ||
Occurrence and potential pathogenesis of Vibrio cholerae, Vibrio parahaemolyticus and Vibrio vulnificus on the South Coast of Sweden | Q50275639 | ||
Adult non-biting midges: possible windborne carriers of Vibrio cholerae non-O1 non-O139. | Q50772353 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | Vibrio cholerae | Q160821 |
P304 | page(s) | 375 | |
P577 | publication date | 2013-01-01 | |
P1433 | published in | Frontiers in Microbiology | Q27723481 |
P1476 | title | Environmental reservoirs and mechanisms of persistence of Vibrio cholerae | |
P478 | volume | 4 |
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