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Artykuły w czasopismach na temat "Phenotyping and genotyping of serratia marcescens"

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Zhang, Q., R. Weyant, A. G. Steigerwalt, et al. "Genotyping of Serratia marcescens Strains Associated with Cucurbit Yellow Vine Disease by Repetitive Elements-Based Polymerase Chain Reaction and DNA-DNA Hybridization." Phytopathology® 93, no. 10 (2003): 1240–46. http://dx.doi.org/10.1094/phyto.2003.93.10.1240.

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The bacterium that causes cucurbit yellow vine disease (CYVD) has been placed in the species Serratia marcescens based on 16S rDNA and groE sequence analysis. However, phenotypic comparison of the organism with S. marcescens strains isolated from a variety of ecological niches showed significant heterogeneity. In this study, we compared the genomic DNA of S. marcescens strains from different niches as well as type strains of other Serratia spp. through repetitive elements-based polymerase chain reaction (rep-PCR) and DNA-DNA hybridization. With the former, CYVD strains showed identical banding
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Garza-González, Elvira, Sandra Iveth Mendoza Ibarra, Jorge M. Llaca-Díaz та Gloria M. Gonzalez. "Molecular characterization and antimicrobial susceptibility of extended-spectrum β-lactamase-producing Enterobacteriaceae isolates at a tertiary-care centre in Monterrey, Mexico". Journal of Medical Microbiology 60, № 1 (2011): 84–90. http://dx.doi.org/10.1099/jmm.0.022970-0.

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Our objective was to analyse phenotypic and genetic data of extended-spectrum β-lactamase (ESBL)-producing Klebsiella pneumoniae, Enterobacter cloacae, Escherichia coli and Serratia marcescens that cause infections in our hospital. Over a 3 year period, 342 randomly selected clinical Enterobacteriaceae isolates were tested for ESBL production and evaluated for the presence of the β-lactamase genes bla SHV, bla TEM, bla CTX-M and bla TLA-1. The antibiotic susceptibilities of these isolates were also determined, and the clonality of the isolates was assessed by PFGE. Based on our analyses, 33/92
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Bhadra, Bhaskar, Pradosh Roy, and Ranadhir Chakraborty. "Serratia ureilytica sp. nov., a novel urea-utilizing species." International Journal of Systematic and Evolutionary Microbiology 55, no. 5 (2005): 2155–58. http://dx.doi.org/10.1099/ijs.0.63674-0.

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A Gram-negative, rod-shaped, urea-dissolving and non-spore-forming bacterium, designated strain NiVa 51T, was isolated from water of the River Torsa in Hasimara, Jalpaiguri district, West Bengal, India. On the basis of 16S rRNA gene sequence similarity, strain NiVa 51T was shown to belong to the γ-Proteobacteria and to be related to Serratia marcescens subsp. sakuensis (98·35 %) and S. marcescens subsp. marcescens (98·30 %); however, strain NiVa 51T exhibited only 43·7 % similarity to S. marcescens by DNA–DNA hybridization. The G+C content of the genomic DNA of the isolate was 60 mol%. Both bi
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Abid, Suhad Abbas, Israa M. S. Al-Kadmy, Sarah Naji Aziz, and Israa H. Hamzah. "The predominance of virulence genes associated with multidrug-resistant Serratia marcescens isolated from urinary tract infections." Reviews and Research in Medical Microbiology 35, no. 3 (2023): 160–66. http://dx.doi.org/10.1097/mrm.0000000000000343.

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Purpose: Serratia marcescens owns different virulence factors that contribute to their pathogenesis and result in bacterial invasion and resistance. Moreover, patients who suffer from urinary tract infections (UTIs) are at an increased risk of contracting different bacterial infections. This study aimed to detect and verify the occurrence of virulence genes in S. marcescens isolated from patients with UTIs in some hospitals in Iraq. Methodology: After bacterial collection, the identification was achieved by busing phenotypic and genotypic methods. The antibiotic susceptibility patterns were do
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Lima, Karla Valéria Batista, Raimundo Gladson Corrêa Carvalho, Irna Carla do Rosário Souza Carneiro, et al. "Outbreak of neonatal infection by an endemic clone of Serratia marcescens." Revista da Sociedade Brasileira de Medicina Tropical 44, no. 1 (2011): 106–9. http://dx.doi.org/10.1590/s0037-86822011000100024.

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INTRODUCTION: The outbreak occurred between February and June 2006 and included identification of the cases, analysis of medical records, cultures from environmental sources, resistance analyses and genotyping profile of Serratia marcescens. METHODS: The cultures were composed of 13 blood isolates, 17 rectal and hand swabs and air sampling. RESULTS: The data obtained by pulsed-field gel electrophoresis exhibited three strains that contaminated 24 patients. Systemic infection was the most common in neonates with lower weight, long periods of hospitalization, premature delivery and the use of me
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Morandi, Stefano, Valentina Pica, Fabio Masotti, et al. "Proteolytic Traits of Psychrotrophic Bacteria Potentially Causative of Sterilized Milk Instability: Genotypic, Phenotypic and Peptidomic Insight." Foods 10, no. 5 (2021): 934. http://dx.doi.org/10.3390/foods10050934.

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The proteolytic traits of the psychrotrophic strains Pseudomonas poae LP5, Pseudomonas fluorescens LPF3, Chryseobacterium joostei LPR1, Pseudomonas fulva PS1, Citrobacter freundii PS37, Hafnia alvei PS46, and Serratia marcescens PS92 were initially investigated by phenotypic and genotypic approaches. Six strains elicited extracellular proteolytic activity, and five expressed the thermostable AprX or (likely) Ser1 enzymes. Then, the strains were inoculated (104 CFU/mL) in microfiltered pasteurized milk and kept at 4 °C for five days. All of the strains reached 108 CFU/mL at the end of storage a
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Cruz, Thalita PPS, Francisco KSF Azevedo, Marco A. Pepato, et al. "Whole-genome sequencing analysis of multidrug-resistant Serratia marcescens isolates in an intensive care unit in Brazil." Journal of Infection in Developing Countries 18, no. 05 (2024): 726–31. http://dx.doi.org/10.3855/jidc.18913.

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Introduction: Serratia marcescens is an opportunistic pathogen found ubiquitously in the environment and associated with a wide range of nosocomial infections. This multidrug-resistant bacterium has been a cause of concern for hospitals and healthcare facilities due to its ability to spread rapidly and cause outbreaks. Next generation sequencing genotyping of bacterial isolates has proven to be a valuable tool for tracking the spread and transmission of nosocomial infections. This has allowed for the identification of outbreaks and transmission chains, as well as determining whether cases are
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Prado, Gladys, Elisa Teixeira Mendes, Roberta Cristina Ruedas Martins, et al. "Phenotypic and genotypic characteristics of a carbapenem-resistant Serratia marcescens cohort and outbreak: describing an opportunistic pathogen." International Journal of Antimicrobial Agents 59, no. 1 (2022): 106463. http://dx.doi.org/10.1016/j.ijantimicag.2021.106463.

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Sarwar, Amna, Syeda Zahra Gillani, Rana Muhammad Shahbakht та ін. "Detection of Β-Lactamase OXA Genes and Biofilm Production in Carbapenem Resistant Gram-Negative Bacilli". Pakistan Journal of Medical and Health Sciences 17, № 4 (2023): 235–38. http://dx.doi.org/10.53350/pjmhs2023174235.

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Objectives: The emergence of carbapenem resistance in biofilm producer Gram-negative bacteria poses a substantial challenge to manage infections. This study aimed to evaluate biofilm production and molecular characterization of carbapenem resistance Gram-negative rods. Methods: Total of 46 bacteria were isolated from various clinical samples, including blood, CSF, urine, sputum, saliva, tracheal secretion, and pus. Following the standard guidelines for bacterial identification (CLSI), bacterial pathogens are isolated and identified. The antibiotic susceptibility profile was obtained against co
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Khalil, Nadim, Eleanor Powell, and Joel Mortensen. "663. Improved Detection of ESBL and AmpC Beta-Lactamase Producing Isolates of Enterobacteriaceae in Pediatric Patients with Bloodstream Infections Using Combined Genotypic and Phenotypic Antimicrobial Susceptibility Testing." Open Forum Infectious Diseases 7, Supplement_1 (2020): S387. http://dx.doi.org/10.1093/ofid/ofaa439.856.

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Abstract Background Infections secondary to pathogens resistant to third-generation cephalosporins (3GC), such as extended-spectrum (ESBL) and AmpC β-lactamase (AmpC) producing Enterobacteriaceae, are increasing. Currently, there are no recommendations regarding identification of AmpC in Citrobacter, Enterobacter, Morganella and Serratia spp. (CEMS organisms). This study’s aim was to increase the detection of AmpC and ESBL producing Enterobacteriaceae in blood cultures from pediatric population by combining genotypic with phenotypic antimicrobial susceptibility testing (AST). Methods All first
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Rozprawy doktorskie na temat "Phenotyping and genotyping of serratia marcescens"

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Beauman, Charlene Nichelle. "Evaluating the suitability of AFLP technology for genotyping strains of Serratia marcescens." 2007. http://digital.library.okstate.edu/etd/umi-okstate-2587.pdf.

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