review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0966-842X(97)01099-8 |
P698 | PubMed publication ID | 9294889 |
P2093 | author name string | Ochman H | |
Groisman EA | |||
P2860 | cites work | A Salmonella typhimurium virulence protein is similar to a Yersinia enterocolitica invasion protein and a bacteriophage lambda outer membrane protein | Q24681193 |
Molecular analysis of spv virulence genes of the salmonella virulence plasmids | Q29042112 | ||
Ethanolamine utilization in Salmonella typhimurium: nucleotide sequence, protein expression, and mutational analysis of the cchA cchB eutE eutJ eutG eutH gene cluster | Q34319376 | ||
Recombination-deficient mutants of Salmonella typhimurium are avirulent and sensitive to the oxidative burst of macrophages | Q34355873 | ||
Distribution of pathogenicity islands in Salmonella spp. | Q35532889 | ||
Characterization of the Salmonella typhimurium pagC/pagD chromosomal region. | Q35593631 | ||
Analysis of the boundaries of Salmonella pathogenicity island 2 and the corresponding chromosomal region of Escherichia coli K-12. | Q35619848 | ||
A PhoP-repressed gene promotes Salmonella typhimurium invasion of epithelial cells | Q36103190 | ||
Mutation of flgM attenuates virulence of Salmonella typhimurium, and mutation of fliA represses the attenuated phenotype | Q36104702 | ||
Salmonella typhimurium initiates murine infection by penetrating and destroying the specialized epithelial M cells of the Peyer's patches. | Q36363455 | ||
Involvement of a plasmid in the invasive ability of Shigella flexneri. | Q36437346 | ||
Identification of two previously unrecognized genes (guaA and argC) important for uropathogenesis | Q36833885 | ||
An unusual pagC::TnphoA mutation leads to an invasion- and virulence-defective phenotype in Salmonellae | Q36950718 | ||
Characterization and protective properties of attenuated mutants of Salmonella choleraesuis | Q36971527 | ||
Aromatic-dependent Salmonella typhimurium are non-virulent and effective as live vaccines | Q39513114 | ||
Magnesium metabolism. A review with special reference to the relationship between intracellular content and serum levels | Q39540258 | ||
Contribution of horizontal gene transfer and deletion events to development of distinctive patterns of fimbrial operons during evolution of Salmonella serotypes | Q39843989 | ||
Growth-phase regulation of plasmid virulence genes in Salmonella | Q40408622 | ||
Simultaneous identification of bacterial virulence genes by negative selection. | Q40682435 | ||
Cognate gene clusters govern invasion of host epithelial cells by Salmonella typhimurium and Shigella flexneri | Q40874006 | ||
A role for bacteriophages in the evolution and transfer of bacterial virulence determinants | Q41034498 | ||
Salmonellosis: host immune responses and bacterial virulence determinants. | Q41039744 | ||
Molecular genetic bases of Salmonella entry into host cells | Q41057366 | ||
Identification of a Salmonella virulence gene required for formation of filamentous structures containing lysosomal membrane glycoproteins within epithelial cells | Q41207631 | ||
Pathogenicity islands: bacterial evolution in quantum leaps | Q41245669 | ||
Functional analysis of ssaJ and the ssaK/U operon, 13 genes encoding components of the type III secretion apparatus of Salmonella Pathogenicity Island 2. | Q41488627 | ||
Ruffles induced by Salmonella and other stimuli direct macropinocytosis of bacteria | Q41502444 | ||
Characterization of the micro-environment of Salmonella typhimurium-containing vacuoles within MDCK epithelial cells | Q41594859 | ||
Resident Colonic Escherichia coli Strains Frequently Display Uropathogenic Characteristics | Q41645025 | ||
The virulence of trimethoprim-resistant thymine-requiring strains ofSalmonella | Q41766793 | ||
Role of hns in the virulence phenotype of pathogenic salmonellae | Q42595438 | ||
The role of a stress-response protein in Salmonella typhimurium virulence | Q42612990 | ||
A hemA mutation renders Salmonella typhimurium avirulent in mice, yet capable of eliciting protection against intravenous infection with S. typhimurium | Q44714478 | ||
Effect of different purine auxotrophic mutations on mouse-virulence of a Vi-positive strain of Salmonella dublin and of two strains of Salmonella typhimurium | Q46564311 | ||
Salmonella enteritidis has a homologue of tolC that is required for virulence in BALB/c mice | Q46750415 | ||
Transcriptional activation of Salmonella typhimurium invasion genes by a member of the phosphorylated response-regulator superfamily. | Q48058213 | ||
Induction of haemolytic activity in Escherichia coli by the slyA gene product | Q48065031 | ||
Co-ordinate regulation of Salmonella typhimurium invasion genes by environmental and regulatory factors is mediated by control of hilA expression | Q50136962 | ||
Salmonella spp. are cytotoxic for cultured macrophages | Q50137708 | ||
Homocysteine antagonism of nitric oxide-related cytostasis in Salmonella typhimurium | Q50139335 | ||
Mg2+ as an extracellular signal: environmental regulation of Salmonella virulence | Q50140541 | ||
Mouse virulence gene A (mviA+) is a pleiotropic regulator of gene expression in Salmonella typhimurium | Q50147335 | ||
Selection of bacterial virulence genes that are specifically induced in host tissues | Q50167010 | ||
A Salmonella locus that controls resistance to microbicidal proteins from phagocytic cells | Q50195971 | ||
A cloned pathogenicity island from enteropathogenic Escherichia coli confers the attaching and effacing phenotype on E. coli K-12. | Q54574143 | ||
P433 | issue | 9 | |
P304 | page(s) | 343-349 | |
P577 | publication date | 1997-09-01 | |
P1433 | published in | Trends in Microbiology | Q15265732 |
P1476 | title | How Salmonella became a pathogen | |
P478 | volume | 5 |
Q50132938 | A green light for virulence gene expression |
Q35919194 | A multi-drug resistant Salmonella Typhimurium ST213 human-invasive strain (33676) containing the bla CMY-2 gene on an IncF plasmid is attenuated for virulence in BALB/c mice |
Q35421297 | A secreted Salmonella protein induces a proinflammatory response in epithelial cells, which promotes neutrophil migration |
Q40877432 | Adhesion and invasion of Escherichia coli from single and recurrent clinical cases of bovine mastitis in vitro |
Q33991294 | Analysis of the type 1 pilin gene cluster fim in Salmonella: its distinct evolutionary histories in the 5' and 3' regions. |
Q35047221 | Animal models paving the way for clinical trials of attenuated Salmonella enterica serovar Typhi live oral vaccines and live vectors |
Q40403972 | Association of Salmonella enterica serovar enteritidis yafD with resistance to chicken egg albumen |
Q33946964 | Bacteria are different: observations, interpretations, speculations, and opinions about the mechanisms of adaptive evolution in prokaryotes |
Q37346556 | Bacterial DNA topology and infectious disease. |
Q38997930 | Bacterial secretion systems and regulation of inflammasome activation |
Q33534366 | Batrachomyomachia: frogs 1, mice 0. |
Q34505359 | Biochemical analysis of SopE from Salmonella typhimurium, a highly efficient guanosine nucleotide exchange factor for RhoGTPases |
Q33594641 | Biological cost of AmpC production for Salmonella enterica serotype Typhimurium |
Q36651833 | ChIP-seq and transcriptome analysis of the OmpR regulon of Salmonella enterica serovars Typhi and Typhimurium reveals accessory genes implicated in host colonization. |
Q33725405 | Changes in membrane fluid state and heat shock response cause attenuation of virulence |
Q39656605 | Characterization of a novel intracellularly activated gene from Salmonella enterica serovar typhi |
Q37384964 | Chlamydia trachomatis diversity viewed as a tissue-specific coevolutionary arms race |
Q34751198 | Comparative genomics of Salmonella enterica serovars Derby and Mbandaka, two prevalent serovars associated with different livestock species in the UK |
Q38265217 | Complete Closed Genome Sequences of Salmonella enterica subsp. enterica Serotypes Anatum, Montevideo, Typhimurium, and Newport, Isolated from Beef, Cattle, and Humans |
Q50108063 | Conflicting needs for a Salmonella hypervirulence gene in host and non-host environments |
Q40861704 | Constitutively expressed phoP inhibits mouse-virulence of Salmonella typhimurium in an Spv-dependent manner |
Q39512031 | Contribution of Salmonella typhimurium virulence factors to diarrheal disease in calves |
Q33801543 | Contribution of genomics to bacterial pathogenesis |
Q36098329 | Control regions for chromosome replication are conserved with respect to sequence and location among Escherichia coli strains |
Q36483666 | Coordinate regulation of Salmonella pathogenicity island 1 (SPI1) and SPI4 in Salmonella enterica serovar Typhimurium |
Q34146148 | Crosstalk between virulence loci: regulation of Salmonella enterica pathogenicity island 1 (SPI-1) by products of the std fimbrial operon |
Q50043862 | DNA supercoiling is differentially regulated by environmental factors and FIS in Escherichia coli and Salmonella enterica |
Q34466495 | Diarrhoeagenic Escherichia coli--an emerging problem? |
Q28067316 | Ecological Opportunity, Evolution, and the Emergence of Flea-Borne Plague |
Q30984469 | Effect of constitutively expressed phoP gene on the localization of Salmonella typhimurium within Mac-1 positive phagocytes |
Q44202161 | Effect of peroral anti-bacterial antiserum treatment on intestinal immune parameters of germ-free piglets intragastrically infected with virulent Salmonella typhimurium or enteropathogenic E. coli |
Q56783570 | Emerging pathogens: the epidemiology and evolution of species jumps |
Q50126816 | Environmental regulation of Salmonella pathogenicity island 2 gene expression |
Q34129328 | Evasion of host cell defense mechanisms by pathogenic bacteria. |
Q21558786 | Evolution of Salmonella enterica virulence via point mutations in the fimbrial adhesin |
Q42369791 | Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome |
Q39504407 | Evolution of an autotransporter: domain shuffling and lateral transfer from pathogenic Haemophilus to Neisseria |
Q42354965 | Evolution of bopA Gene in Burkholderia: A Case of Convergent Evolution as a Mechanism for Bacterial Autophagy Evasion. |
Q34465580 | Evolution of rhizobia by acquisition of a 500-kb symbiosis island that integrates into a phe-tRNA gene |
Q33762702 | Evolution of the linear chromosomal DNA in Streptomyces: is genomic variability developmentally modulated? |
Q34240776 | Evolution of variation in presence and absence of genes in bacterial pathways |
Q30828698 | Examination of Salmonella gene expression in an infected mammalian host using the green fluorescent protein and two-colour flow cytometry |
Q50068958 | Expression of the Fis protein is sustained in late-exponential- and stationary-phase cultures of Salmonella enterica serovar Typhimurium grown in the absence of aeration |
Q33984672 | Ferrioxamine-mediated Iron(III) utilization by Salmonella enterica |
Q34757086 | Flagella and chemotaxis are required for efficient induction of Salmonella enterica serovar Typhimurium colitis in streptomycin-pretreated mice |
Q56169293 | Foodborne Pathogens and Host Predilection |
Q58697525 | Formation of phenotypic lineages in Salmonella enterica by a pleiotropic fimbrial switch |
Q33836599 | Functional and evolutionary roles of long repeats in prokaryotes. |
Q36362734 | Functional heterogeneity of the UpaH autotransporter protein from uropathogenic Escherichia coli |
Q39089838 | Gene expression analysis of Salmonella enterica SPI in macrophages indicates differences between serovars that induce systemic disease from those normally causing enteritis |
Q33745256 | Gene transfer, speciation, and the evolution of bacterial genomes |
Q91694504 | Genetic boundaries delineate the potential human pathogen Salmonella bongori into discrete lineages: divergence and speciation |
Q50129052 | Genetic dynamics of Salmonella typhi--diversity in clonality |
Q86523950 | Genome architecture and global gene regulation in bacteria: making progress towards a unified model? |
Q34121384 | Genome-based identification of chromosomal regions specific for Salmonella spp. |
Q25257713 | Genome-wide screen for Salmonella genes required for long-term systemic infection of the mouse |
Q50042692 | Genomic fingerprinting and serotyping of Salmonella from Galápagos iguanas demonstrates island differences in strain diversity |
Q50074672 | H-NS, the genome sentinel |
Q55255691 | HilD and PhoP independently regulate the expression of grhD1, a novel gene required for Salmonella Typhimurium invasion of host cells. |
Q93106825 | HilD induces expression of a novel Salmonella Typhimurium invasion factor, YobH, through a regulatory cascade involving SprB |
Q33996250 | HreP, an in vivo-expressed protease of Yersinia enterocolitica, is a new member of the family of subtilisin/kexin-like proteases |
Q33955487 | Identification and analysis of bacterial virulence genes in vivo |
Q47937820 | Identification and molecular characterization of a novel Salmonella enteritidis pathogenicity islet encoding an ABC transporter |
Q33756666 | Identification and sequence analysis of a 27-kilobase chromosomal fragment containing a Salmonella pathogenicity island located at 92 minutes on the chromosome map of Salmonella enterica serovar typhimurium LT2 |
Q34002724 | Identification of a putative Salmonella enterica serotype typhimurium host range factor with homology to IpaH and YopM by signature-tagged mutagenesis |
Q45252292 | Identification of genes that are dispensable for animal infection by Salmonella typhimurium |
Q34009658 | Identification, characterization, and variable expression of a naturally occurring inhibitor protein of IS1106 transposase in clinical isolates of Neisseria meningitidis |
Q34009568 | In vivo genetic analysis indicates that PhoP-PhoQ and the Salmonella pathogenicity island 2 type III secretion system contribute independently to Salmonella enterica serovar Typhimurium virulence |
Q38741409 | Influence of Salmonella enterica serovar Pullorum pathogenicity island 2 on type III secretion system effector gene expression in chicken macrophage HD11 cells |
Q33999966 | Influence of the Salmonella typhimurium pathogenicity island 2 type III secretion system on bacterial growth in the mouse. |
Q37763020 | Innate immune response in the gut against Salmonella - review |
Q35070419 | Integrated circuits: how transcriptional silencing and counter-silencing facilitate bacterial evolution |
Q35049823 | Integration of a complex regulatory cascade involving the SirA/BarA and Csr global regulatory systems that controls expression of the Salmonella SPI-1 and SPI-2 virulence regulons through HilD |
Q36437267 | Isolation of a temperate bacteriophage encoding the type III effector protein SopE from an epidemic Salmonella typhimurium strain |
Q33783262 | Isolation, propagation and characterisation of Cryptosporidium. |
Q22122396 | Lateral gene transfer and the nature of bacterial innovation |
Q52923446 | Lifestyle evolution in symbiotic bacteria: insights from genomics. |
Q34790534 | Limited boundaries for extensive horizontal gene transfer among Salmonella pathogens |
Q39538602 | Living in stools is not as dumb as you think |
Q34581241 | Lon, a stress-induced ATP-dependent protease, is critically important for systemic Salmonella enterica serovar typhimurium infection of mice. |
Q27976514 | Macrophage-dependent induction of the Salmonella pathogenicity island 2 type III secretion system and its role in intracellular survival |
Q39535813 | Mining Bacillus subtilis chromosome heterogeneities using hidden Markov models |
Q36489643 | Mobile effector proteins on phage genomes |
Q33786879 | Molecular Characterization of Salmonella from Human and Animal Origins in Uganda |
Q51761554 | Molecular and Conventional Analysis of Acute Diarrheal Isolates Identifies Epidemiological Trends, Antibiotic Resistance and Virulence Profiles of Common Enteropathogens in Shanghai. |
Q47986494 | Molecular and functional analysis indicates a mosaic structure of Salmonella pathogenicity island 2. |
Q33752670 | Molecular characterization of the fragilysin pathogenicity islet of enterotoxigenic Bacteroides fragilis. |
Q50109676 | Morphologic and molecular characterization of Salmonella typhimurium infection in neonatal calves |
Q42587342 | Multiple insertional events, restricted by the genetic background, have led to acquisition of pathogenicity island IIJ96-like domains among Escherichia coli strains of different clinical origins |
Q44708860 | Multiple insertions of fimbrial operons correlate with the evolution of Salmonella serovars responsible for human disease |
Q36637862 | PCR-based subtractive hybridization and differences in gene content among strains of Helicobacter pylori |
Q34290188 | Pathogenicity islands in bacterial pathogenesis |
Q37693828 | Phenotypic differences between Salmonella and Escherichia coli resulting from the disparate regulation of homologous genes |
Q34586205 | Phylogenetics and differentiation of Salmonella Newport lineages by whole genome sequencing |
Q34334253 | Polynucleotide phosphorylase negatively controls spv virulence gene expression in Salmonella enterica. |
Q50867088 | Postgenomic analysis of bacterial pathogens repertoire reveals genome reduction rather than virulence factors. |
Q39144745 | Potassium transport of Salmonella is important for type III secretion and pathogenesis |
Q48379907 | Prevalence and polymorphism of genes encoding translocated effector proteins among clinical isolates of Salmonella enterica. |
Q39234350 | Prevalence of virulence and antimicrobial resistance genes in Salmonella spp. isolated from commercial chickens and human clinical isolates from South Africa and Brazil |
Q40062098 | Protein Acetylation Is Involved in Salmonella enterica Serovar Typhimurium Virulence |
Q64105572 | Proteotyping as alternate typing method to differentiate Campylobacter coli clades |
Q34261274 | Punicalagin inhibits Salmonella virulence factors and has anti-quorum-sensing potential |
Q36227773 | Role of neutrophils in murine salmonellosis |
Q40173901 | Role of the Salmonella pathogenicity island 1 (SPI-1) protein InvB in type III secretion of SopE and SopE2, two Salmonella effector proteins encoded outside of SPI-1. |
Q35549925 | Role of the Salmonella pathogenicity island 1 effector proteins SipA, SopB, SopE, and SopE2 in Salmonella enterica subspecies 1 serovar Typhimurium colitis in streptomycin-pretreated mice |
Q40153848 | Salmonella Pathogenicity Island 4 encodes a giant non-fimbrial adhesin and the cognate type 1 secretion system |
Q50127381 | Salmonella SirA is a global regulator of genes mediating enteropathogenesis |
Q50120790 | Salmonella SsrB activates a global regulon of horizontally acquired genes |
Q47875866 | Salmonella enterica serovar Choleraesuis derivatives harbouring deletions in rpoS and phoP regulatory genes are attenuated in pigs, and survive and multiply in porcine intestinal macrophages and fibroblasts, respectively. |
Q39522566 | Salmonella enterica serovar Typhimurium response involved in attenuation of pathogen intracellular proliferation |
Q39503254 | Salmonella host cell invasion emerged by acquisition of a mosaic of separate genetic elements, including Salmonella pathogenicity island 1 (SPI1), SPI5, and sopE2. |
Q33955493 | Salmonella interactions with host cells: in vitro to in vivo |
Q35114802 | Salmonella maintains the integrity of its intracellular vacuole through the action of SifA. |
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Q36370147 | Salmonella pathogenicity island 2 mediates protection of intracellular Salmonella from reactive nitrogen intermediates |
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Q34288964 | Salmonella pathogenicity islands encoding type III secretion systems |
Q33878633 | Salmonella pathogenicity islands: big virulence in small packages. |
Q34277949 | Salmonella strains isolated from Galápagos iguanas show spatial structuring of serovar and genomic diversity |
Q39509891 | Salmonella typhimurium and lipopolysaccharide stimulate extracellularly regulated kinase activation in macrophages by a mechanism involving phosphatidylinositol 3-kinase and phospholipase D as novel intermediates. |
Q41882234 | Salmonella-induced caspase-2 activation in macrophages: a novel mechanism in pathogen-mediated apoptosis |
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Q33957069 | Sulphur islands in the Escherichia coli genome: markers of the cell's architecture? |
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Q37340611 | The fate of new bacterial genes. |
Q38314825 | The integration host factor (IHF) integrates stationary-phase and virulence gene expression in Salmonella enterica serovar Typhimurium. |
Q35044792 | The interplay between Salmonella typhimurium and its macrophage host--what can it teach us about innate immunity? |
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