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  • 1
    Online Resource
    Online Resource
    Cambridge :Cambridge University Press,
    Keywords: Medical microbiology. ; Electronic books.
    Description / Table of Contents: Many bacteria survive infection of their host in a low growth state, including the classic persistent infectious bacteria, tuberculosis. This 2003 book will interest microbiologists, medical microbiologists and infectious disease clinicians who are interested in learning more about the fundamental science of bacterial dormancy in relation to disease.
    Type of Medium: Online Resource
    Pages: 1 online resource (291 pages)
    Edition: 1st ed.
    ISBN: 9780511203510
    Series Statement: Advances in Molecular and Cellular Microbiology Series ; v.Series Number 3
    DDC: 616.9201
    Language: English
    Note: Cover -- Half-title -- Series-title -- Title -- Copyright -- Contents -- Contributors -- Preface -- CHAPTER 1 Physiological and molecular aspects of growth, non-growth, culturability and viability in bacteria -- INTRODUCTION -- BACTERIAL GROWTH -- Molecular Information Related to Bacterial Growth -- Ribosomal RNA -- Chromosome Replication -- Cell Division -- Global Regulatory Proteins -- GROWTH AND STASIS -- Exponential Phase -- Stationary Phase -- Dormancy and Sporulation -- Exit from Dormant or Stationary Cellular States and Re-entry into Growth -- CULTURABILITY AND VIABILITY -- Culturability -- Viability -- The VBNC Controversy -- CONCLUSIONS -- REFERENCES -- CHAPTER 2 Survival of environmental and host-associated stress -- SPECIFIC AND GENERAL STRESS RESPONSES IN BACTERIA -- STATIONARY PHASE AND GENERAL STRESS SURVIVAL STRATEGIES -- Readily Reversible Stationary Phase Responses -- Sporulation -- High Cell Density Responses: Quorum Sensing -- THE Sigma-DEPENDENT STATIONARY-PHASE AND GENERAL STRESS RESPONSE -- Physiology -- Regulation of Sigma by Environmental Signals -- Regulation of Gene Expression by Sigma -- SURVIVAL STRATEGIES UNDER HOST-INDUCED STRESS CONDITIONS -- Counteracting Specific Host-Associated Stresses -- Oxidative Stress Response -- Acidic Stress Response -- Iron Deprivation -- General Defensive Strategies of Pathogens -- Expression of Specific Virulence Factors -- Adhesins and Invasins -- Toxins and Modulins -- Type III Secretion Systems-Effector Proteins -- REGULATION OF VIRULENCE GENES BY STRESS SIGNALS -- Induction of Virulence Gene Expression by Environmental Stress Conditions -- Specific Regulator Proteins of Virulence Factors -- Transcriptional Activators -- Two-Component Phosphorelay Signal Transduction -- General and Global Regulatory Mechanisms of Virulence Genes -- Alternative Sigma Factors. , DNA Supercoiling and Histone-Like Proteins -- CONCLUSIONS -- ACKNOWLEDGEMENTS -- REFERENCES -- CHAPTER 3 Surviving the immune response: an immunologist's perspective -- INTRODUCTION -- INTERFERENCE WITH PHAGOCYTOSIS -- LIMITATION OF CLEARANCE-THE RANULOMA -- GENETIC FACTORS -- HELMINTH SURVIVAL OF THE IMMUNE RESPONSE -- ANTIGENIC VARIATION -- VIRAL SURVIVAL OF THE IMMUNE RESPONSE: LATENCY -- SURVIVAL AND NEOPLASIA -- INTERFERENCE WITH MEDIATORS -- DICHOTOMY -- REFERENCES -- CHAPTER 4 Quantitative and qualitative changes in bacterial activity controlled by interbacterial signalling -- DEFINITIONS OF QUORUM SENSING -- SIGNALS AND SYNTHESIS, PERCEPTION AND RESPONSE -- PEPTIDE SIGNALLING IN BACILLUS SUBTILIS AND THE CONTROL OF ENDOSPORE FORMATION -- BACTERIAL CYTOKINES IN MICROCOCCUS AND MYCOBACTERIUM CONTROL THE EXIT FROM DORMANCY -- THE INHIBITION OF REPLICATION IN ESCHERICHIA COLI -- PATHOGENICALLY DORMANT BACTERIA -- Quorum Sensing is Essential for the Full Virulence of Pseudomonas aeruginosa -- Quorum Sensing is Essential for the Full Virulence of Staphylococcus aureus -- CONCLUDING REMARKS -- ACKNOWLEDGEMENTS -- REFERENCES -- CHAPTER 5 Mechanisms of stationary-phase mutagenesis in bacteria and their relevance to antibiotic resistance -- INTRODUCTION -- THE STATIONARY PHASE -- Signals for Entry into Stationary Phase -- Morphological and Physiological Manifestations -- DNA Damage and Metabolism in the Stationary Phase -- Mutations in Stationary Phase Cells -- ADAPTIVE EVOLUTION OF MUTATION RATES -- Heritable Global Mutators -- Heritable Local Mutators -- Environment-Dependent Mutators -- Error-Prone DNA Polymerases -- ADAPTIVE MUTAGENESIS -- Historical Perspective -- Adaptive Mutation in the E. coli FC40 Model System -- ADAPTIVE POINT MUTATIONS -- Transient Hypermutability of a Sub population -- Extrapolation to Other Systems. , ADAPTIVE GENE AMPLIFICATION -- Adaptive Gene Amplification in the lac System -- ANTIBIOTIC RESISTANCE IN BACTERIA -- General Mechanisms -- Chromosomal Genes Conferring Antibiotic Resistance -- MUTATION TO ANTIBIOTIC RESISTANCE -- Antibiotic-Bacterium Interactions -- Fitness Cost of Resistance -- RATES OF MUTATION TO ANTIBIOTIC RESISTANCE -- Dependence on the Environment -- Stresses Encountered in vivo -- Antibiotic Concentration Gradients -- Stress-Induced Mutagenesis in the Evolution of Antibiotic Resistance? -- Stress-Induced Mutagenesis in Genotypic Switching Mechanisms? -- CONCLUDING COMMENTS -- ACKNOWLEDGEMENTS -- NOTE ADDED IN PROOF -- REFERENCES -- CHAPTER 6 Biofilms, dormancy and resistance -- INTRODUCTION -- Extent of the Problem in Medicine -- Surface Adhesion and Biofilm Formation -- Biofilm Models -- CONVENTIONAL CANDIDATES TO EXPLAIN RESISTANCE TO ANTIBIOTICS AND BIOCIDES: "THE USUAL SUSPECTS" -- Inability to Penetrate the Biofilm -- Enzyme Inactivation of Antimicrobials -- Efflux -- Repair -- SURVIVAL AND THE RESPONSE TO STRESS: WILL THE REAL CULPRIT PLEASE STAND UP? -- The General Stress Response (GSR) -- Biofilms and Quorum Sensing -- Potential Role of RpoS in Uptake/Adhesion -- SLOW/NO ROWTH-AN ACCOMPLICE TO DORMANCY? -- CONCLUDING COMMENTS -- REFERENCES -- CHAPTER 7 Tuberculosis -- INTRODUCTION -- THE QUIESCENT STATE OF M. TUBERCULOSIS -- Role of the Immune Response -- Quiescent Bacteria Associated with Antimicrobial Therapy -- Role of Oxygen -- ANTIBIOTIC TOLERANCE -- LOCATION OF PERSISTERS IN VIVO -- PHYSIOLOGICAL STATE IN VIVO -- THE MOLECULAR BASIS OF PERSISTENCE -- Global Gene Control -- Specific Proteins -- TUBERCULOSIS DISEASE CONTROL -- CONCLUSION -- REFERENCES -- CHAPTER 8 Gastritis and peptic ulceration -- THE DISCOVERY OF THE BACTERIAL CAUSE OF GASTRITIS -- From Campylobacter pyloridis to H. pylori. , H. pylori as a Cause of Gastritis and Peotic Ulceration -- HOW H. PYLORI CAUSES PEPTIC ULCERATION -- Why Duodenal Ulceration is Relatively Uncommon in the Developing World -- Other Causes of Peptic Ulceration -- Gastric Ulceration -- DORMANT PHASE OF H.PYLORI -"COCCOID FORMS " -- Introduction -- ATTACHMENT TO THE GASTRIC MUCOSA BY H. PYLORI -- The Two Methods of Attachment by H. Pylori to the Mucosa -- THE NATURAL HISTORY OF H.PYLORI INFECTION -- Method of Transmission of H. pylori -- COCCOID FORMS ARE PRESENT IN THE GASTRIC MUCOSA -- IN VITRO STUDIES OF COCCOID FORMS -- Culture Conditions Leading to H. pylori Coccoid Forms -- The Morphological and Other Changes That Occur When Spiral Forms Become Coccoid Forms -- Cell Culture -- COCCOID FORMS IN ANIMAL MODELS -- In the Gastric Mucosa -- Coccoid Forms Can Infect Mice -- COCCOID FORMS ARE VIABLE AND CAN CHANGE TO SPIRAL FORMS -- CHANGE TO THE COCCOID FORM DURING ANTIBIOTIC TREATMENT IN VITRO AND IN VIVO -- Treatment of H. pylori Infection and Coccoid Forms -- TRANSMISSION OF H. PYLORI -- Detection of Coccoid Forms in Faeces -- Survival of Coccoid Forms in Water, Milk and Disinfectants -- CONCLUSION -- REFERENCES -- CHAPTER 9 Resumption of yeast cell proliferation from stationary phase -- STATIONARY PHASE -- RESUMPTION OF YAST CELL PROLIFERATION -- VESICULAR TRANSPORT AND THE GCS1 PROTEIN -- ENDOSOMAL FUNCTION AND THE GCS1 PROTEIN -- ACKNOWLEDGEMENTS -- REFERENCES -- CHAPTER 10 Resting state in seeds of higher plants: dormancy,persistence and resilience to abiotic and biotic stresses -- INTRODUCTION -- DORMANCY IN HIGHER PLANTS -- Seed Dormancy Categories -- Seed Dormancy Induction -- Development of Primary Dormancy and Desiccation Tolerance -- Structural Features of Dormancy -- Overcoming Primary Dormancy in Seeds and Other Systems -- Chemical Effects -- Temperature Effects. , Secondary Dormancy in Seeds -- Overcoming Physical Dormancy in Seeds -- THE PERSISTENT STATE, RESISTANCE TO DISEASE AND HERBICIDES -- Persistence in the Dry and Wet State -- Dry Storage -- Wet Storage -- Depletion Rate in the Soil -- Defence Mechanisms -- Herbicide Resistance -- CONCLUSION -- REFERENCES -- Index.
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  • 2
    Book
    Book
    Miami Beach, Fla : Univ.
    Keywords: Report
    Type of Medium: Book
    Pages: VI,100 S , Ill., graph. Darst
    Series Statement: Sedimenta 10
    Language: English
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  • 3
    Publication Date: 2022-05-26
    Description: © The Author(s), 2016. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Science Advances 2 (2016): e1600883, doi:10.1126/sciadv.1600883.
    Description: The formation of the Isthmus of Panama stands as one of the greatest natural events of the Cenozoic, driving profound biotic transformations on land and in the oceans. Some recent studies suggest that the Isthmus formed many millions of years earlier than the widely recognized age of approximately 3 million years ago (Ma), a result that if true would revolutionize our understanding of environmental, ecological, and evolutionary change across the Americas. To bring clarity to the question of when the Isthmus of Panama formed, we provide an exhaustive review and reanalysis of geological, paleontological, and molecular records. These independent lines of evidence converge upon a cohesive narrative of gradually emerging land and constricting seaways, with formation of the Isthmus of Panama sensu stricto around 2.8 Ma. The evidence used to support an older isthmus is inconclusive, and we caution against the uncritical acceptance of an isthmus before the Pliocene.
    Description: This study was supported by the Smithsonian Tropical Research Institute to A.O., J.B.C.J., N.K., and H.A.L.; the NSF (EAR 1325683) to A.O., P.G.R.-D., and E.L.G.; the National System of Investigators to A.O.; the Secretaría Nacional de Ciencia, Tecnología e Innovación (Panamá) to A.O., H.A.L., and S.E.C.; the U.S. Geological Survey to R.F.S.; and the Consejo Nacional de Investigaciones Científicas y Técnicas (Argentina) to A.L.C., G.M.G., E.S., and L.S.
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 243 (2005), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Tolerance to antimicrobial agents is a universal phenomenon in bacteria which are no longer multiplying or whose growth rate slows. Since slowly multiplying bacteria occur in clinical infections, extended periods of antimicrobial chemotherapy are needed to eradicate these organisms and to achieve cure. In this study, the molecular basis of antibiotic tolerance was investigated using transposon mutagenesis. We screened 5000 Escherichia coli Tn10Cam mutants for reduction of kanamycin tolerance in late stationary phase and found that 4935 mutants were able to grow to late stationary phase. Reduced tolerance was observed in nine mutants which became sensitive to killing by kanamycin. The mutant KS639 was the most sensitive one to kanamycin, and its genome was disrupted in an intergenic region which lies between aldB and yiaW open reading frames. This mutant showed increased sensitivity not only to kanamycin but also to gentamicin, ciprofloxacin and rifampicin. Reduced tolerance of KS639 to kanamycin was also observed in a murine thigh infection model. P1 transduction to the wild type strains confirmed that the intergenic region was responsible for the tolerance of the bacterium to antibiotics. Using PCR-directed one-step gene replacement, we inactivated the genes aldB, yiaW and yiaV. We also deleted the intergenic region. There was no difference in kanamycin tolerance between each mutant (ΔaldB, ΔyiaW and ΔyiaV) and the parental strain. But the mutant lacking the intergenic region showed reduced tolerance to kanamycin. These data suggest that the intergenic region between aldB and yiaW genes may be involved in tolerance to antimicrobial agents in E. coli. Furthermore, they show that it is important in murine infection during antibiotic treatment and lead to a faster kill of the mutant bacteria.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 55 (1999), S. 910-914 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The Mycobacterium tuberculosis chaperonin 10 (Mtcpn10) has been crystallized by the sitting-drop vapour-diffusion method. The crystals belong to the monoclinic space group P21, with unit-cell parameters a = 76.5, b = 87.9, c = 124.4 Å, β = 106.8°. X-ray diffraction data were collected to 2.8 Å. The self-rotation function and the molecular-replacement solution show that the asymmetric unit contains a dimer of heptamers related by twofold non-crystallographic symmetry. The two heptamers interact through interleaving flexible loops in a similar fashion to M. leprae and Gp31 cpn10. In addition to its role in protein folding, Mtcpn10 has unique effects on the growth of host cells and is a major immunogen in tuberculosis infections. The structure determination will permit the analysis of the amino acids identified as important for the protein-folding and cell-signalling activity of Mtcpn10.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 237 (2004), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Sigma factors are important global regulators which control bacterial gene expression during growth and in response to stress. Previous work showed that mRNA of the sigJ gene was up-regulated in late stationary-phase and after rifampicin treatment. In order to verify the function of SigJ, we constructed a Mycobacterium tuberculosis mutant lacking the sigJ gene. In a microaerophilic stationary-phase model, the sigJ mutant showed the same growth pattern as the wild-type strain. In an immune stasis murine model in which the bacterial number plateaued between the second and the 15th week, the mutant showed a similar growth curve to the wild-type strain. However, the sigJ mutant was more susceptible to killing by H2O2 than its parental strain. The parental level of sensitivity to H2O2 was recovered in the sigJ complemented strain. These data suggest that the SigJ protein is not essential for survival in long-term stationary phase or in bacterial stasis in mice. However, the sigJ gene may control an alternative H2O2 resistance pathway.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 202 (2001), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: In order to determine which genes are involved in maintaining viability of 100-day stationary-phase bacteria and persistent bacteria after antibiotic treatment, we used a mini-DNA array to examine the transcription of 82 genes of M. tuberculosis in the 100-day stationary-phase cultures before and after rifampicin treatment. We found that the mRNA level of a sigma factor gene, sigJ, was strongly up-regulated in the late stationary-phase cultures. Other genes were also up-regulated, although to a lesser extent than sigJ. Surprisingly, after rifampicin treatment there was no significant change in sigJ expression, and most of the other 82 genes in the mini-DNA array also maintained expression, some at relatively high levels. These results suggest that SigJ may control gene expression in the quiescent state and may be an important component in the mechanisms by which M. tuberculosis survives prolonged stationary phase even in the presence of sterilising antibiotics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature medicine 4 (1998), S. 537-538 
    ISSN: 1546-170X
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] To the editor—Soldan et al. report an increased IgM response to HHV-6 early antigen (p41/38) and detection of serum HHV-6 DNA in relapsing-remitting MS1 and, confirming the work of Challoner et al.2, propose an association between HHV-6 and the etiology and pathogenesis of MS. We urge caution ...
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 326 (1987), S. 549-550 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] SIR-Although most of the attempts to develop vaccines against AIDS (acquired immune deficiency syndrome) have focused on the B-lymphocyte defined epi-topes of the envelope (env) protein of the human immunodeficiency virus (HIV-1) (see refs 1 and 2) there is a growing interest in other proteins of ...
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1075-2617
    Keywords: p24 ; HIV ; synthetic proteins ; CD spectroscopy ; secondary-structure prediction ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aggregation and structural properties of the synthetic C-terminal half [Ala330, Ala350)270-373; 104-mer)] polypeptide from HIV-1 p24gag were studied. In concentrated solutions the synthetic polypeptide aggregated to tetramers which, upon dilution, gave a mixture of monomeric and dimeric species. These results correlated well with the in vitro aggregation properties of recombinant p24. The tetrameric form of the synthetic polypeptide had a pI which differed by about four units from that of the mixture of monomeric and dimeric species. CD studies indicated that the latter contained, in aqueous solutions, a compact molecule lacking, however, a defined tertiary structure. Addition of MeOH to aqueous solutions of both tetramer and monomer/dimer mixture induced a more defined structure, which was assigned to that of an α+β protein in agreement with secondary structure predictions. A model of the dimeric form of the 104-mer, which takes into account the results presented here and those from a study on the specificity of a set of anti-104-mer MoAbs, is presented.Finally, the results indicated that the structure of the 104-mer in its dimeric form is similar to that adopted by the same sequence when part of full-length p24. © 1997 European Peptide Society and John Wiley & Sons, Ltd.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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