Academic literature on the topic 'P. aeruginosa'

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Journal articles on the topic "P. aeruginosa"

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Gasink, Leanne B., Neil O. Fishman, Irving Nachamkin, Warren B. Bilker, and Ebbing Lautenbach. "Risk Factors for and Impact of Infection or Colonization With Aztreonam-Resistant Pseudomonas aeruginosa." Infection Control & Hospital Epidemiology 28, no. 10 (2007): 1175–80. http://dx.doi.org/10.1086/520740.

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Objective.To identify risk factors for infection or colonization with aztreonam-resistant Pseudomonas aeruginosa and examine the impact of this organism on mortality.Design.A case-control study was performed to identify risk factors for infection or colonization with aztreonam-resistant P. aeruginosa. A cohort study was subsequently performed to examine the impact of aztreonam resistance on outcomes.Setting.A tertiary referral center in southeastern Pennsylvania.Participants.Inpatients with a clinical culture positive for P. aeruginosa between January 1, 1999, and December 31, 2000.Results.Of
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Aguilera-Herce, Julia, Meritxell García-Quintanilla, Rocío Romero-Flores, Michael J. McConnell, and Francisco Ramos-Morales. "A Live Salmonella Vaccine Delivering PcrV through the Type III Secretion System Protects against Pseudomonas aeruginosa." mSphere 4, no. 2 (2019): e00116-19. https://doi.org/10.1128/mSphere.00116-19.

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<em>Pseudomonas aeruginosa</em> is a common Gram-negative opportunistic pathogen that is intrinsically resistant to a wide range of antibiotics. The development of a broadly protective vaccine against <em>P. aeruginosa</em> remains a major challenge. Here, we used an attenuated strain of <em>Salmonella enterica</em> serovar Typhimurium as a vehicle to express <em>P. aeruginosa</em> antigens. A fusion between the <em>S. enterica</em> type III secretion effector protein SseJ and the <em>P. aeruginosa</em> antigen PcrV expressed under the control of the <em>sseA</em> promoter was translocated by
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Ahmed, Faraz, Zulfiqar Ali Mirani, Ayaz Ahmed, et al. "Nanotubes Formation in P. aeruginosa." Cells 11, no. 21 (2022): 3374. http://dx.doi.org/10.3390/cells11213374.

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The present study discusses a biofilm-positive P. aeruginosa isolate that survives at pH levels ranging from 4.0 to 9.0. The biofilm consortia were colonized with different phenotypes i.e., planktonic, slow-growing and metabolically inactive small colony variants (SCVs). The lower base of the consortia was occupied by SCVs. These cells were strongly attached to solid surfaces and interconnected through a network of nanotubes. Nanotubes were observed at the stationary phase of biofilm indwellers and were more prominent after applying weight to the consortia. The scanning electron micrographs in
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Mohmed, Al-shahrani, Elhedmi Abdulkhaleg, Elkaib Hossam, Jrad Samira, and Alnaqib Shaymaa. "Determination and Study of Main Biological Features of Bacteriophages Active Against Bacteria Pseudomonas fluorescens and Pseudomonas aeruginosa." Alq J Med App Sci 6, no. 2 (2023): 507–10. https://doi.org/10.5281/zenodo.8280466.

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<strong>Background and aims</strong>. One of the significant areas of modern microbiology and biotechnology is the study of bacteriophages. This is due to the growing interest in terms of their practical application in various branches of medicine, agriculture, and the food industry. The purpose of our work was to isolate bacteriophages active against bacteria of the genus Pseudomonas and to study their biological properties. <strong>Methods</strong>. Bacteriophages isolated from spoiled poultry, beef and carp samples were the subjects of the study. 20 g of the weighed sample were inoculated w
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Worgall, Stefan, Toshiaki Kikuchi, Ravi Singh, Katherine Martushova, Leah Lande, and Ronald G. Crystal. "Protection against Pulmonary Infection with Pseudomonas aeruginosa following Immunization with P. aeruginosa-Pulsed Dendritic Cells." Infection and Immunity 69, no. 7 (2001): 4521–27. http://dx.doi.org/10.1128/iai.69.7.4521-4527.2001.

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ABSTRACT To develop a Pseudomonas aeruginosa vaccine that allows the host immune system to select the antigens, we hypothesized that dendritic cells (DC) pulsed with P. aeruginosa would induce protective immunity against pulmonary infections with P. aeruginosa. Incubation of murine bone marrow-derived DC with P. aeruginosa in vitro led to uptake of P. aeruginosa and activation of the DC. Spleen-derived CD4+ cells from mice immunized withP. aeruginosa-pulsed DC showed increased proliferation, demonstrating that DC pulsed with P. aeruginosa were capable of eliciting a P. aeruginosa-specific immu
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De Muynck, Benedicte, Anke Van Herck, Annelore Sacreas, et al. "Successful Pseudomonas aeruginosa eradication improves outcomes after lung transplantation: a retrospective cohort analysis." European Respiratory Journal 56, no. 4 (2020): 2001720. http://dx.doi.org/10.1183/13993003.01720-2020.

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Long-term survival after lung transplantation (LTx) is hampered by development of chronic lung allograft dysfunction (CLAD). Pseudomonas aeruginosa is an established risk factor for CLAD. Therefore, we investigated the effect of P. aeruginosa eradication on CLAD-free and graft survival.Patients who underwent first LTx between July, 1991, and February, 2016, and were free from CLAD, were retrospectively classified according to P. aeruginosa presence in respiratory samples between September, 2011, and September, 2016. P. aeruginosa-positive patients were subsequently stratified according to succ
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Aidah Abd Al-doori, Awatef Saber Jasem, and Adnan F. AL-Azzawie. "Effects of Nd:Yag Laser on some virulence factor genes of Pseudomonas aeruginosa bacteria." Tikrit Journal of Pure Science 25, no. 2 (2020): 86–92. http://dx.doi.org/10.25130/tjps.v25i2.240.

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The aim of this study was to assess effects of the 532nm Nd-yag laser on the genes of Tox A, Exo S, and Opr L, of Pseudomonas aeruginosa (P. aeruginosa) bacteria isolated from clinical (wounds, burns, otitis media) and environmental (water, soil) samples. Clinical samples were collected from patients coming to Saladdin General Hospital from wound, burns and middle ear infections while environmental samples were extracted from water and soil for Saladdin General Hospital . Bacterial samples irradiated by Nd-Yag laser with wavelength of 532 nm using energies (300mj,500mj) with (15 and 25 sec) an
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Chakraborty, Tamalika, Tushar Gupta, Nayana Verma, Zarin Parwez, Kaustav Deb, and Tamoghana Chakraborty. "PREVALENCE OF ANTIBIOTIC RESISTANCE IN PSEUDOMONAS AERUGINOSA." International Journal of Advanced Research 12, no. 01 (2024): 1249–60. http://dx.doi.org/10.21474/ijar01/18243.

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One of the main bacteria responsible for hospital-acquired illnesses is Pseudomonas aeruginosa. Through chromosomal changes or the horizontal acquisition of resistant determinants, antibiotic resistance can be easily developed it. High-risk clones, like ST175, are spreading together with the rising frequency of extensively-drug-resistant (XDR) or multi-drug-resistant (MDR) P. aeruginosa isolates. MDR/XDR infections should be taken seriously since they can make it difficult to choose the best empirical and conclusive antimicrobial therapies. New avenues for the treatment of MDR/XDR P. aeruginos
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Al-Hashimi, Omar, Ibrahim Omar Saeed, and Safaa Abed Lateef Al Meani. "Evaluating the qualitative characteristics and heavy elements of hospital water and their relationship with bioresistance in P. aeruginosa." Technium BioChemMed 8 (May 1, 2024): 64–75. http://dx.doi.org/10.47577/biochemmed.v8i.10934.

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ABSTRACT: Bacteria use the elements present in the environment to develop their vital defenses, trying to acquire genes from other strains or absorb heavy metals in order to adapt to them and increase their tolerance against high concentrations of heavy elements. Pseudomonas aeruginosa is an opportunistic bacterial pathogen that causes infections in hospitals and communities, including in humans and animals. P. aeruginosa's adaptability and endurance in therapeutic settings are cause for concern. Emerging pathogenic strains pose a global threat and cause significant concern. Biocides are commo
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Higgins, Gerard, Coral Fustero Torre, Jean Tyrrell, Paul McNally, Brian J. Harvey, and Valerie Urbach. "Lipoxin A4prevents tight junction disruption and delays the colonization of cystic fibrosis bronchial epithelial cells byPseudomonas aeruginosa." American Journal of Physiology-Lung Cellular and Molecular Physiology 310, no. 11 (2016): L1053—L1061. http://dx.doi.org/10.1152/ajplung.00368.2015.

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The specialized proresolution lipid mediator lipoxin A4(LXA4) is abnormally produced in cystic fibrosis (CF) airways. LXA4increases the CF airway surface liquid height and stimulates airway epithelial repair and tight junction formation. We report here a protective effect of LXA4(1 nM) against tight junction disruption caused by Pseudomonas aeruginosa bacterial challenge together with a delaying action against bacterial invasion in CF airway epithelial cells from patients with CF and immortalized cell lines. Bacterial invasion and tight junction integrity were measured by gentamicin exclusion
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Dissertations / Theses on the topic "P. aeruginosa"

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Vieira, Anabela Carvalho. "Phage therapy to inactivate multidrug-resistant P. aeruginosa." Master's thesis, Universidade de Aveiro, 2011. http://hdl.handle.net/10773/6814.

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Mestrado em Microbiologia<br>With the increase in antibiotic resistance and after several years of abandonment, the use of bacteriophages (phages), as antimicrobial agents, to destroy bacteria began to arouse interest in the scientific community. This has led to a huge phage research in different fields and currently several studies are ongoing with animals and humans. Pseudomonas aeruginosa is an opportunistic pathogen, which frequently colonizes wounds infections. It has been estimated that a high number of deaths caused by wound infections results of bacterial infection, often by antibiotic
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Sousa, Juliana Rabelo de. "ProduÃÃo de biossurfactantes a partir da glicerina obtida da produÃÃo de biodiesel." Universidade Federal do CearÃ, 2008. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4635.

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Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico<br>O objetivo deste trabalho foi avaliar a glicerina resultante da transesterificaÃÃo do Ãleo de mamona como fonte de carbono e nutrientes para P. aeruginosa LAMI. O efeito da concentraÃÃo de nutrientes e de condiÃÃes ambientais foi avaliado de acordo com dois planejamentos fatoriais completos sobre o crescimento celular, produÃÃo de biossurfactante e propriedades tensoativas do surfactante produzido. A anÃlise estatÃstica dos dados foi realizada pelo software Statistica 6.0. Avaliou-se o efeito da concentraÃÃo de glicerina e de nit
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Smith, Eric Earl. "Genetic adaptation by Pseudomonas aeruginosa during chronic cystic fibrosis infections and genetic variation between strains of P. aeruginosa /." Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/5067.

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Bocelli, Marcio David. "Estudo da atividade de chalconas no controle de biofilmes bacterianos." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/75/75133/tde-17112016-141016/.

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Os biofilmes constituem uma forma de crescimento que permite a maior sobrevivência e resistência de microrganismos a agentes de controle como antibióticos e desinfetantes. Apesar da grande disponibilidade de agentes antimicrobianos no mercado, há escassez de produtos específicos e efetivos na erradicação/inibição de biofilmes. Existe atualmente grande interesse na seleção de moléculas capazes de inibir o crescimento dos biofilmes ou removê-los quando já estabelecidos. Doenças como fibrose cística (P. aeruginosa) e cárie dentária (S. mutans), são patologias intrinsecamente ligadas à formação de
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HALLE, FELIX. "Metabolisme du fer chez pseudomonas : etude d'une activite ferripyoverdine reductase chez p. fluorescens et p. aeruginosa." Université Louis Pasteur (Strasbourg) (1971-2008), 1993. http://www.theses.fr/1993STR13105.

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L'etude de la liberation intracellulaire du fer des complexes ferrisiderophore montre que chez p. Fluorescens et p. Aeruginosa le fer est libere de la ferripyoverdine par une activite de reduction enzymatique, appelee ferripyoverdine reductase (fpr). Cette activite est inhibee par de l'oxygene. En presence de nadh, le compose flavinique fmn stimule fortement l'activite. La purification de la fpr a conduit a une proteine de masse moleculaire de 28000. Apres obtention d'anticorps anti-fpr, il a ete constate par immunodetection que les enzymes responsables de l'activite fpr de differentes souches
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Cezairliyan, Brent (Brent O. ). "Regulation of the periplasmic stress responses in E. coli and P. aeruginosa." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/43224.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2008.<br>Includes bibliographical references.<br>The ability to adapt to changing environments is essential to survival. Bacteria have developed sophisticated means by which they sense and respond to stresses imposed by changes in the environment. I have undertaken the study of elements of the TE stress response pathway in the bacterium Escherichia coli and the orthologous pathway in the bacterium Pseudomonas aeruginosa. These pathways sense stress in the periplasm and relay the signal into the cytoplasm by a series of p
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Holland, Sinead. "Investigating azoreductases and NAD(P)H dependent quinone oxidoreductases in Pseudomonas aeruginosa." Thesis, Kingston University, 2017. http://eprints.kingston.ac.uk/40641/.

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'Psedomonas aeruginosa' is a prevalent nosocmial pathogen predominantly associated with infections in immune compromised individuals and long term colonisation and pathogenesis in the lungs of Cystic Fibrosis patients. With multi-drug resistant strains increasingly common, the discovery of novel targets for antimicrobial chemotherapy is of utmost importance and expansion of data on 'P. aeruginosa's' complex genome could facilitate this. Azoreductases are a group of enzymes mainly noted for their reductive capacity against azo and quinone compounds. Ubiquitous amongst many classes of organism i
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LORE', NICOLA IVAN. "DISSECTION OF P. AERUGINOSA / HOST INTERACTION DURING ACUTE AND CHRONIC AIRWAYS INFECTION." Doctoral thesis, Università degli Studi di Milano, 2012. http://hdl.handle.net/2434/173425.

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Cystic fibrosis (CF) lung disease is characterized by transient airway P. aeruginosa infections and excessive neutrophil-dominated inflammation early in life followed by permanent chronic infection leading to the decline in lung functions. In CF disease, strong selective pressures in the airways lead to P. aeruginosa genotypic and phenotypic adaptation. Thus, colonization is maintained by P. aeruginosa pathoadaptive lineages, which are clonal with the initially acquired strain. The main aim of this thesis is to dissect the strategies through which the P. aeruginosa patho-adaptive strain
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Nusair, Arwa Y. "Comparison of Aspartate Transcarbamoylase Activity Between Pseudomonas Aeruginosa Which Has One Chromosome and Burkholderia Cepacia Which Has Three Chromosomes." Thesis, University of North Texas, 2012. https://digital.library.unt.edu/ark:/67531/metadc149646/.

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The pyrimidine biosynthetic pathway is essential and similar in all bacteria. The pathway from Pseudomonas is regulated by nucleotides which bind to the upstream region of the pyrBC’ gene complex. Work in our lab mapped the genes and showed that the pyrB and pyrC’ were part of an overlap complex. The Pseudomonas aeruginosa has one circular chromosome. A former Pseudomonas now called Burkholderia cepacia is similar to P. aeruginosa except that it contains three circular chromosomes (CI, CII, CIII) and one large plasmid. The primary chromosome named CI contains the pyrBC’. To our knowledge
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Besson, Christine. "Conception, synthèse et évaluation de substrats et d'inhibiteurs de l'élastase de P. Aeruginosa." Lyon 1, 1993. http://www.theses.fr/1993LYO10160.

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Dans le but de developper un dosage specifique, sensible et selectif de l'elastase de pseudomonas aeruginosa, nous avons synthetise par voie chimique ou enzymatique des derives peptidiques. Ceux-ci ont ensuite ete evalues comme substrats de l'elastase en utilisant la methode conductimetrique. Nous avons aussi evalue trois inhibiteurs potentiels de l'enzyme. Enfin, nous avons effectue des modifications chimiques de l'enzyme et evalue sa stabilisation vis-a-vis de la temperature
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Books on the topic "P. aeruginosa"

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Gunnulfsen, Helena Maria. How Can P. Aeruginosa Infections Be Treated More Efficiently? GRIN Verlag GmbH, 2019.

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Kubesch, Peter. Membranständige Pathomechanismen von pseudomonas Aeruginosa: Studie zur Pathogenese der Lungeninfektion mit P. Aeruginosa bei Patienten mit cystischer Fibrose. 1988.

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Schneider, Christian Matthias. DNA-Fingerprinting von P. aeruginosa: Etablierung und Evaluierung neuer Methoden zur molekularen Speziesbestimmung und Subtypisierung. 1996.

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Govan, John, and Andrew Jones. Microbiology of CF lung disease. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780198702948.003.0003.

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This chapter presents the microbiology of CF and describes the classical bacterial pathogens including Staphylococcus aureus, Haemophilus influenza, Pseudomonas aeruginosa and organisms of the Burkholderia cepacia complex. The dominant of these is P. aeruginosa. Infections with other opportunistic pathogens including non-tuberculous mycobacteria, Stenotrophomonas maltophila, and Achromobacter (Alcaligenes) xylosoxidans are also encountered. This chapter details measures to prevent the onset of chronic infection with these organisms include regular screening of respiratory tract samples for bac
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Book chapters on the topic "P. aeruginosa"

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Pier, Gerald B. "Acquired Resistance to P. aeruginosa." In Pseudomonas aeruginosa as an Opportunistic Pathogen. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3036-7_15.

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Holder, Ian Alan. "P. aeruginosa Burn Infections: Pathogenesis and Treatment." In Pseudomonas aeruginosa as an Opportunistic Pathogen. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3036-7_14.

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Galloway, Darrell R. "Role of Exotoxins in the Pathogenesis of P. aeruginosa Infections." In Pseudomonas aeruginosa as an Opportunistic Pathogen. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3036-7_6.

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Casabona, María-Guillermina, Sylvie Elsen, Valentina Cogoni, and Ina Attrée. "P. aeruginosa Type VI Secretion Machinery: Another Deadly Syringe." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_4.

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Estin, M. L., D. A. Stoltz, and J. Zabner. "Paraoxonase 1, Quorum Sensing, and P. aeruginosa Infection: A Novel Model." In Advances in Experimental Medicine and Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60761-350-3_17.

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Parvez, Noushad, Leena Pathak, Ankit Patel, et al. "Chitinase Expressed as an Inducible Trait in Pseudomonas aeruginosa Schröter P-15." In New Horizons in Insect Science: Towards Sustainable Pest Management. Springer India, 2015. http://dx.doi.org/10.1007/978-81-322-2089-3_8.

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AL-Kamali, Marwan F. S. H., Andrei A. Boika, Dmitry V. Tapalski, Dmitry Kovalenko, and Hamdan A. S. AL-Shamiri. "Bactericidal Activity of Mesoporous SiO2 Matrices Inlaid with Cu° and CuO Nanoparticles Against P. Aeruginosa." In Recent Advances in Technology Research and Education. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-54450-7_16.

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Benz, Roland. "Mechanism of Anion Transport Through the Phosphate-Starvation-Inducible Outer Membrane Protein P of Pseudomonas Aeruginosa." In The Jerusalem Symposia on Quantum Chemistry and Biochemistry. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-3075-9_30.

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Hazlett, Linda D., and Sharon Masinick. "Binding of a Cytopathic or an Invasive Strain of p. Aeruginosa to Cytoskeletal, Basement Membrane, or Matrix Proteins of Wounded Cornea is Similar and does not Rely on Interaction with Actin Filaments." In Lacrimal Gland, Tear Film, and Dry Eye Syndromes 2. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5359-5_80.

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"P. aeruginosa ATCC 15442." In Encyclopedia of Green Materials. Springer Nature Singapore, 2024. https://doi.org/10.1007/978-981-97-4618-7_300611.

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Conference papers on the topic "P. aeruginosa"

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Zhou, Enze, Huabing Li, Dake Xu, and Jianjun Wang. "Accelerated Corrosion of 2304 Duplex Stainless Steel by Marine Pseudomonas Aeruginosa Biofilm." In CORROSION 2017. NACE International, 2017. https://doi.org/10.5006/c2017-09326.

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Abstract Microbiologically Influenced Corrosion (MIC) in the marine environment has caused a serious threat to the safety of marine materials. The corrosion rate of MIC is usually much faster than the general corrosion process. The 2304 duplex stainless steel (DSS) is an excellent alternative to 316L SS in marine applications, while its MIC behavior is barely known. In this work, surface analysis and electrochemical techniques were used to study the corrosion behavior of 2304 DSS caused by the marine aerobe Pseudomonas aeruginosa. Compared with the abiotic control, the largest pit depth showed
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Xu, Dake, Tong Xi, Jin Xia Liaoning, Chunguang Yang, Qi Li, and Ke Yang. "The Microbiologically Influenced Corrosion (MIC) Resistance Behavior of 2205 Cu-bearing Duplex Stainless Steel in the Presence of Aerobic Marine Pseudomonas Aeruginosa Biofilm." In CORROSION 2016. NACE International, 2016. https://doi.org/10.5006/c2016-07357.

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Abstract Recently, more and more reports indicated that microbiologically influenced corrosion (MIC) severely influences the safety of petroleum installations and marine infrastructures. Conventional MIC mitigation methods are physical scrubbing, coatings, and biological or biocide treatments to inhibit the corrosive biofilm. A novel antibacterial 2205-Cu duplex stainless steel (DSS) was developed from the material aspect to mitigate the corrosive marine biofilm by the release of Cu2+ and copper-rich phases on the antibacterial DSS surface. In this study, the MIC resistance behavior of a 2205
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Tanji, Yasunori, Hirofumi Kawai, Ryosuke Terashi, and Kazuhiko Miyanaga. "Effect of Cathodic Protection on Biofilm Formation and Maturation." In CORROSION 2007. NACE International, 2007. https://doi.org/10.5006/c2007-07513.

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Abstract Cathodic protection (CP) is known as a reliable method to protect steel from corrosion. However, the influence of CP on biofilm formation and maturation is not well known. There are three possible effects of CP on biofilm formation and maturation. Those are: 1) deprivation of anchorage sites for bacterial adhesion, 2) increase of electrostatic repulsion between the steel surface and negatively charged bacteria, 3) elimination of bacteria in the biofilm by increasing pH. To investigate these possible effects of CP on biofilm, carbon steel coupons were immersed in artificial seawater wi
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Федоров, Нікіта. "СУЧАСНІ МЕТОДИ ВИДІЛЕННЯ P. AERUGINOSA". У THEORETICAL AND PRACTICAL ASPECTS OF MODERN SCIENTIFIC RESEARCH, chair Аліна Стасенко. European Scientific Platform, 2025. https://doi.org/10.36074/logos-24.01.2025.090.

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Silva, Leidyanne Karolaine Barbosa da, Esaú Simões Da Silva, Rhana Cavalcanti Do Nascimento, and Maria Joanellys dos Santos Lima. "RESISTÊNCIA ANTIMICROBIANA DE PSEUDOMONAS AERUGINOSA EM AMBIENTE HOSPITALAR." In Anais do II Congresso Brasileiro de Saúde On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1971.

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Introdução: Pseudomonas aeruginosa é uma bactéria gram negativa que causa principalmente pneumonias, a mesma está associada a grande parte das infecções intra-hospitalares que podem ocorrer em um período de 48h após a entrada na unidade de saúde, ou até 10 dias após a alta médica. Raramente causa problemas em pacientes saudáveis, entretanto, é uma das responsáveis por morbidade e mortalidade nos imunocomprometidos, como os portadores de fibrose cística. Objetivo: Este trabalho possui como objetivo realizar uma breve revisão sobre a resistência da P. aeruginosa a antimicrobianos em ambiente hos
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Liimatta, K., S. A. Riquelme, C. Lozano, et al. "Metabolic Reprogramming Drives P. Aeruginosa Airway Infection." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a6158.

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Argyraki, A., M. Markvart, Anne Nielsen, T. Bjarnsholt, L. Bjørndal, and P. M. Petersen. "Comparison of UVB and UVC irradiation disinfection efficacies on Pseudomonas Aeruginosa (P. aeruginosa) biofilm." In SPIE Photonics Europe, edited by Jürgen Popp, Valery V. Tuchin, Dennis L. Matthews, and Francesco S. Pavone. SPIE, 2016. http://dx.doi.org/10.1117/12.2225597.

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Bhavsar, TM, D. Hardej, and JO Cantor. "Aerosolized Lysozyme Mitigates P. Aeruginosa Pneumonia in Hamsters." In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a5947.

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Henriquez, Tania, Ismael Castañón, Silvia Scali, and Chiara Falciani. "Peptide-based vesicle isolation method for P. aeruginosa." In 37th European Peptide Symposium. The European Peptide Society, 2024. http://dx.doi.org/10.17952/37eps.2024.p1162.

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Pires, D. P., S. Sillankorva, and J. Azeredo. "The use of bacteriophages for P. aeruginosa biofilm control." In 2011 1st Portuguese Meeting in Bioengineering ¿ The Challenge of the XXI Century (ENBENG). IEEE, 2011. http://dx.doi.org/10.1109/enbeng.2011.6026045.

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Reports on the topic "P. aeruginosa"

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Sauer, Karin. Regulation of Initial Attachment of P. aeruginosa. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada545997.

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2

ชวนชื่น, รุ่งทิพย์, та ชาญวิทย์ ตรีพุทธรัตน์. การศึกษาอินทริกรอนส์ใน Pseudomonas aeruginosa และ Acinetobacter baumannii : รายงานวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2011. https://doi.org/10.58837/chula.res.2011.105.

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ศึกษา class 1 integrons ในเชื้อ Pseudomonas aeruginosa (n=101) และ Acinetobacter baumannii (n=176) ที่แยกได้จากผู้ป่วยในโรงพยาบาล พบว่า เชื้อทุกตัวดื้อต่อยาปฏิชีวนะหลายชนิดพร้อมกัน เชื้อ P. aeruginosa จำนวน 96 isolates (95%) ให้ผลบวกต่อยีน intl1 โดยในเชื้อเหล่านี้เชื้อจำนวน 70 isolates (73%) มี gene cassette จัดรูปแบบ integron profile ได้ 12 รูปแบบ ซึ่งที่พบมากที่สุดคือ aadB-cmlA-aadA1 และมีเชื้อเพียง 1 isolate ที่สามารถถ่ายทอด class 1 integrons แบบขวางได้ ส่วน A. baumannii จำนวน 69 isolates (39%) ที่พบว่ามียีน intl1 โดยเชื้อจำนวน 42 isolates (61%) มี gene cassette จัดรูปแบบ integron profile ไ
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พงษ์สามารถ, สุนันท์, วิมลมาศ ลิปิพันธ์ та พนิดา วยัมหสุวรรณ. ศึกษาสารสกัดโพลีแซคคาไรด์จากเปลือกของผลทุเรียนเพื่อใช้ประโยชน์ทางการแพทย์. จุฬาลงกรณ์มหาวิทยาลัย, 2003. https://doi.org/10.58837/chula.res.2003.28.

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แยกสารโพลีแซคคาไรด์ได้ 2 ชนิด จากเปลือกแห้งของผลทุเรียน (Durio zibethinus L.) เตรียมในรูปผงแห้งของ polysaccharide gel (PG) และ polysaccharide fiber (PF) องค์ประกอบธาตุหลักของโพลีแซคคาไรด์ประกอบด้วย Carbon (C) Hydrogen (H) และ Oxygen (O) ในสัดส่วนอะตอมของ C:H:O เท่ากับ 2.9:5.3:3.1 และ 3.5:6.4:3.1 ใน PG และ PF ตามลำดับ PG มีองค์ประกอบของ acidic sugar ได้แก่ galacturonic acid มากกว่าห้าสิบเปอร์เซนต์ ของน้ำหนัก PG และมีน้ำตาล neutral sugar ได้แก่ glucose fructose rhamnose และ arabinose ใน PF มีองค์ประกอบของน้ำตาล glucose เพียงชนิดเดียว ทำการตรวจวิเคราะห์น้ำตาลโดยวิธี colorimetric method TLC และ HP
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เร่งพิพัฒน์, ศิริรัตน์, ฐิติพงศ์ ธนะรัชติการนนท์ та ปัญชลี ประคองศิลป์. การใช้แลคติกแอซิดแบคทีเรียเป็นโพรไบโอติกเพื่อเสริมในอาหารไก่ : รายงานการวิจัยฉบับสมบูรณ์. จุฬาลงกรณ์์มหาวิทยาลัย, 1998. https://doi.org/10.58837/chula.res.1998.33.

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การแยกแลคติกแอซิดแบคทีเรียจากลำไส้ไก่ที่มีสุขภาพแข็งแรงจากตลาดสดแหล่งต่างๆ ในกรุงเทพมหานคร จำนวน 54 ตัวอย่าง ได้เชื้อแลคติกแอซิดแบคทีเรีย จำนวนทั้งสิ้น 28 สายพันธุ์ และเมื่อนำมาทดสอบความสามารถในการยับยั้งเชื้อทดสอบ Bordetella avium, Listeria monocytogenes, Pasteurella multocida, Proteus vugalis, Pseudomonas aeruginose, Salmonella enteritidis, Salmonella typhimurium และ Staphylococcus aureus พบว่าส่วนน้ำเลี้ยงเชื้อของแลคติกแอซิดแบคทีเรียจำนวน 6 สายพันธุ์ สามารถยับยั้งเชื้อทดสอบบนอาหารเลี้ยงเชื้อแข็ง โดยดูความกว้างของบริเวณยับยั้ง และเมื่อนำเชื้อทั้ง 6 สายพันธุ์ มาทำการจัดกลุ่มตามหลักอนุกรมวิธาน
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