Detailed Information on Publication Record
2019
Utilization of Red Nonionogenic Tenside Labeling, Isoelectric Focusing, and Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry in the Identification of Uropathogens in the Presence of a High Level of Albumin
HORKA, Marie, Jiri SALPLACHTA, Filip RŮŽIČKA and Karel SLAISBasic information
Original name
Utilization of Red Nonionogenic Tenside Labeling, Isoelectric Focusing, and Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry in the Identification of Uropathogens in the Presence of a High Level of Albumin
Authors
HORKA, Marie (203 Czech Republic, guarantor), Jiri SALPLACHTA (203 Czech Republic), Filip RŮŽIČKA (203 Czech Republic, belonging to the institution) and Karel SLAIS (203 Czech Republic)
Edition
ACS INFECTIOUS DISEASES, WASHINGTON, AMER CHEMICAL SOC, 2019, 2373-8227
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10606 Microbiology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 4.614
RIV identification code
RIV/00216224:14110/19:00108321
Organization unit
Faculty of Medicine
UT WoS
000480672600009
Keywords in English
uropathogens; high level of albumin; red nonionogenic tenside; preconcentration and preseparation; isoelectric focusing; matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
Tags
International impact, Reviewed
Změněno: 29/4/2020 07:55, Mgr. Tereza Miškechová
Abstract
V originále
Cellulose-based preparative isoelectric focusing was used for preseparation and concentration of uropathogens Staphylococcus aureus, Escherichia coli, Enterococcus faecalis, Staphylococcus epidermidis, Candida albicans, and Candida parapsilosis in a urine sample containing a high concentration of human serum albumin. For the visibility of the colorless microbial zones in the separation medium, the microbial cells were labeled with red nonionogenic tenside (1-[[4-(phenylazo)-phenyl]azo]-2-hydroxy-3-naphthoic acid polyethylene glycol ester, PAPAN). A very short incubation time, about 2 min, was sufficient for the adsorption of 0.001% (w/v) PAPAN onto the cell surface at the optimized conditions. As low as 10(3) cells of E. coli (pI 4.6) resuspended in 100 mu L of urine sample and spiked with 0.1 mg mL(-1) of human serum albumin (pI 4.8) were successfully preseparated and concentrated using this method. Because the pI values of the labeled microorganisms remained unchanged, the focused red zones of microbial cells were collected from the separation media and further analyzed by either capillary isoelectric focusing or matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. The viability of the cells extracted from the collected zones was also confirmed. The proposed method provides reliable, relatively fast, and cost-effective identification of uropathogens in urine specimens with a high level of albumin.
Links
LQ1601, research and development project |
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MUNI/A/1189/2018, interní kód MU |
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NV16-29916A, research and development project |
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VI20172020069, research and development project |
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