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Artykuły w czasopismach na temat "Biochemical identification of salmonella paratyphi"

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Kim, Gyu Ri, Si Hyun Kim, Eun-Young Kim, et al. "Performance of MALDI-TOF Mass Spectrometry (VITEK MS) in the Identification of Salmonella Species." Microorganisms 10, no. 10 (2022): 1974. http://dx.doi.org/10.3390/microorganisms10101974.

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Salmonella is a major pathogen causing foodborne infections in humans. Salmonella isolates are identified using biochemical and serological tests, including automated systems such as the VITEK2 system. However, there are few reports on Salmonella identification using VITEK MS. Therefore, we aimed to evaluate the usefulness of MALDI-TOF VITEK MS for Salmonella identification. A total of 1389 Salmonella isolates were identified using VITEK MS ver3.0 or ver3.2. All Salmonella isolates were confirmed by serotyping using the Kauffmann-White scheme, and the results were compared with the VITEK MS re
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Cordovana, Miriam, Norman Mauder, Markus Kostrzewa, et al. "Classification of Salmonella enterica of the (Para-)Typhoid Fever Group by Fourier-Transform Infrared (FTIR) Spectroscopy." Microorganisms 9, no. 4 (2021): 853. http://dx.doi.org/10.3390/microorganisms9040853.

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Typhoidal and para-typhoidal Salmonella are major causes of bacteraemia in resource-limited countries. Diagnostic alternatives to laborious and resource-demanding serotyping are essential. Fourier transform infrared spectroscopy (FTIRS) is a rapidly developing and simple bacterial typing technology. In this study, we assessed the discriminatory power of the FTIRS-based IR Biotyper (Bruker Daltonik GmbH, Bremen, Germany), for the rapid and reliable identification of biochemically confirmed typhoid and paratyphoid fever-associated Salmonella isolates. In total, 359 isolates, comprising 30 S. Typ
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Suman, Maiz-ul Ahad, Md Abdullah Siddique, S. M. Shamsuzzaman, et al. "Detection Of Mutated gyrA Gene From Nalidixic Acid Resistant Salmonella Typhi And Paratyphi A Isolated From Enteric Fever Patients In A Tertiary Care Hospital Of Bangladesh." Bangladesh Journal of Medical Microbiology 10, no. 1 (2017): 3–7. http://dx.doi.org/10.3329/bjmm.v10i1.31431.

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A cross sectional study for the detection of empirically used antibiotic resistant Salmonella was carried out in the department of microbiology of Rajshahi Medical College (RMC) and PCR and DNA sequencing were done in the department of microbiology of Dhaka Medical College during the period from August 2014 to July 2015.Total 323 blood samples were collected from suspected enteric fever patients from medicine and paediatric units of RMC hospital and cultured on brain heart infusion broth for isolation of Salmonella. Identification of Salmonella was done by biochemical tests and final identific
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Bakhrouf, Amina, Moncef Jeddi, and Michel J. Gauthier. "Modification des caractères culturaux et biochimiques du Salmonella paratyphi B après incubation dans l'eau de mer." Canadian Journal of Microbiology 38, no. 8 (1992): 871–74. http://dx.doi.org/10.1139/m92-142.

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After incubation in seawater Salmonella paratyphi B cells rapidly became unable to grow on bacteriological media. Previous adaptation to high osmolarity conditions greatly slowed down this process. Strains isolated from seawater microcosms after varying incubation periods were qualitatively different and showed changes in some of their growth (colony shape and size) and biochemical properties (acidification of some sugars, gelatinase activity, acetoin production, nitrate reduction). Because of these modifications, the bacteria showed atypical profiles and could not be identified as members of
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Chmel, Martin, Oldřich Bartoš, Ondřej Beran, et al. "Salmonella Paratyphi Infection: Use of Nanopore Sequencing as a Vivid Alternative for the Identification of Invading Bacteria." Prague Medical Report 122, no. 2 (2021): 96–105. http://dx.doi.org/10.14712/23362936.2021.10.

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In our study we present an overview of the use of Oxford Nanopore Technologies (ONT) sequencing technology on the background of Enteric fever. Unlike traditional methods (e.g., qPCR, serological tests), the nanopore sequencing technology enables virtually real-time data generation and highly accurate pathogen identification and characterization. Blood cultures were obtained from a 48-year-old female patient suffering from a high fever, headache and diarrhea. Nevertheless, both the initial serological tests and stool culture appeared to be negative. Therefore, the bacterial isolate from blood c
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Ijaz, Samia, Rifat Bibi, Nazia, et al. "Biochemical Characterization and Antibiotic Profile against Salmonella Species Isolated from Milk and Milk Products." Open Access Public Health and Health Administration Review 3, no. 2 (2025): 156–64. https://doi.org/10.59644/oaphhar.3(2).176.

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Salmonella species are among the most common foodborne pathogens associated with milk and dairy products. This study investigated the microbiological characteristics and antibiotic resistance patterns of Salmonella spp. in milk, ice cream, and cheese samples collected from August to December 2024 in Layyah District, Punjab, Pakistan. A total of 150 randomly selected samples (50 each of milk, ice cream, and cheese) were analyzed. Isolation and identification were performed using standard biochemical tests and further confirmed using the API 10S identification kit. Salmonella contamination was d
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Agrawal, P., R. Tuladhar, and N. Dahal. "Nalidixic Acid Susceptibility Test for Screening Salmonella Isolates of Reduced Susceptibility/Higher Minimum Inhibitory Concentration to Ciprofloxacin." Nepal Journal of Science and Technology 15, no. 2 (2015): 97–104. http://dx.doi.org/10.3126/njst.v15i2.12122.

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Enteric fever is the major diagnosis among febrile patients in Nepal with yearly increase in nalidixic acid resistance and reduced ciprofloxacin susceptibility among Salmonella isolates. This study was carried out to evaluate the validity of nalidixic acid resistance as an indicator of reduced susceptibility of Salmonella isolates to ciprofloxacin. In this study, 999 blood specimens collected from suspected enteric fever patients visiting B&B Hospital were processed by standard microbiological techniques. Isolates were identified by biochemical tests and serotyping. Antibiotic susceptibili
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Niroula, Dhirendra, Jyotsna Shrestha, Supriya Sharma, and Anjana Singh. "Antibiotic Susceptibility Pattern of Salmonella Enterica serovars Typhi and Paratyphi A Isolated From Patients Suspected of Enteric Fever." Tribhuvan University Journal of Microbiology 7 (December 26, 2020): 31–36. http://dx.doi.org/10.3126/tujm.v7i0.33791.

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Objectives: The study aimed to assess the antibiotic susceptibility profile of Salmonella spp isolated from patients suspected of enteric fever.
 Methods: This cross-sectional prospective study was carried out from April to June, 2014among 484 patients clinically suspected of enteric fever visiting Bir Hospital, Kathmandu, Nepal. Blood sample collected from each patient was processed for culture in bile broth. Identification of Salmonella spp was done by conventional microbiological techniques including colony characteristics, Gram's staining and biochemical tests. Antibiotic susceptibili
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Olorunsola, R. A., D. Eruvbetine, O. M. Idowu, O. Oyekunle, and I. M. Ogunade. "Salmonella organism transmission in hatching broiler egggs." Nigerian Journal of Animal Production 41, no. 1 (2021): 230–34. http://dx.doi.org/10.51791/njap.v41i1.2729.

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The vertical transmission of Salmonella organism in hatching broiler eggs were investigated in selected states in South-Western Nigeria. Hatching eggs were obtained from fifteen major hatcheries. five (hatchery A, B, C, D and E from each State [Lagos (LA), Oyo (OY) and Ogun (OG)]. A total of 300 hatchable eggs of 20 eggs from each hatchery were collected. Individual egg was broken and separated into Shell, albumin and yolk. The samples were incubated into buffer peptone water and incubated at 37°C for 24 hours. Typical colonies of salmonella grown on Xylose lysine deoxycholate agar were seen a
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Fahima Akter and Md Shamimuzzaman. "DETECTION OF INVA GENE BY PCR AND IDENTIFICATION WITH SUSCEPTIBILITY PATTERN EVALUATION BY VITEK 2 OF SALMONELLA ISOLATES." Journal of Applied Biological Sciences 18, no. 3 (2024): 235–52. https://doi.org/10.71336/jabs.1313.

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This study aims to identify and antimicrobial susceptibility of hospital wastewater in Dhaka city. Total 134 Salmonella isolates were identified using cultural characteristics, automated biochemical test, and PCR for invA gene detection. Biochemical identification and Antimicrobial Susceptibility Test (AST) were performed through VITEK 2. Essential Agreement (EA) and Categorical Agreement (CA) were worked out according to the CLSI breakpoint. We also measured Very Major Error (VME), Major Error (ME), and Minor Error (mE). Seven Salmonella serotypes were identified through VITEK 2 ID-GN card an
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Części książek na temat "Biochemical identification of salmonella paratyphi"

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Mishra, Rohit, Yong Chiang Tan, Amr Adel Ahmed Abd El-Aal, and Chandrajit Lahiri. "Computational Identification of the Plausible Molecular Vaccine Candidates of Multidrug-Resistant Salmonella enterica." In Salmonella - a Challenge From Farm to Fork [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.95856.

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Salmonella enterica serovars are responsible for the life-threatening, fatal, invasive diseases that are common in children and young adults. According to the most recent estimates, globally, there are approximately 11–20 million cases of morbidity and between 128,000 and 161,000 mortality per year. The high incidence rates of diseases like typhoid, caused by the serovars Typhi and Paratyphi, and gastroenteritis, caused by the non-typhoidal Salmonellae, have become worse, with the ever-increasing pathogenic strains being resistant to fluoroquinolones or almost even the third generation cephalo
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Kabir, Abdul, Momin Khan, and Anees Ur Rahman. "Accurate Identification of Salmonella enterica in Calves." In Salmonella - Current Trends and Perspectives in Detection and Control. IntechOpen, 2024. http://dx.doi.org/10.5772/intechopen.1004932.

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Salmonella enterica is a bacterium that can cause serious infections in humans and animals, especially cattle. The identification and differentiation of S. enterica serotypes in cattle is important for epidemiological surveillance, disease prevention and control, and public health protection. However, the current methods and techniques for S. enterica detection have various challenges and limitations, such as low sensitivity and specificity, high cost and complexity, and the need for viable and pure bacterial cultures. Therefore, there is a need for further research and development of novel an
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