Abstract:Staphylococcus aureus is a pathogen important in causing human infections and intoxication. A sensitive fiber-optic that produces evanescent waves was developed for the detection of protein A, a product secreted only by S. aureus. In the immunosensor, a 40-mV argon-ion laser that generated laser light at 488 nm was used together with plastic optical fiber and antibodies to protein A were physically adsorbed onto the fiber. The principle of the detection involved a sandwich immunoassay with fluorescein isothioc… Show more
“…Rapid detection and identification of S. aureus bacteremia facilitates a prompt and adequate antibiotic therapy. Protein A is a potent virulence factor and can be taken as indicating the presence of S. aureus in clinical specimens [ 28 , 29 ]. Most S. aureus strains from clinical sources contained protein A associated with the cell wall or released extracellularly [ 30 ].…”
Bloodstream infection (BSI) is a major cause of mortality in hospitalized patients worldwide. Staphylococcus aureus is one of the most common pathogens found in BSI. The conventional workflow is time consuming. Therefore, we developed a lateral flow immunoassay (LFIA) for rapid detection of S. aureus-protein A in positive blood culture samples. A total of 90 clinical isolates including 58 S. aureus and 32 non-S. aureus were spiked in simulated blood samples. The antigens were extracted by a simple boiling method and diluted before being tested using the developed LFIA strips. The results were readable by naked eye within 15 min. The sensitivity of the developed LFIA was 87.9% (51/58) and the specificity was 93.8% (30/32). When bacterial colonies were used in the test, the LFIA provided higher sensitivity and specificity (94.8% and 100%, respectively). The detection limit of the LFIA was 107 CFU/mL. Initial evaluation of the LFIA in 20 positive blood culture bottles from hospitals showed 95% agreement with the routine methods. The LFIA is a rapid, simple and highly sensitive method. No sophisticated equipment is required. It has potential for routine detection particularly in low resource settings, contributing an early diagnosis that facilitates effective treatment and reduces disease progression.
“…Rapid detection and identification of S. aureus bacteremia facilitates a prompt and adequate antibiotic therapy. Protein A is a potent virulence factor and can be taken as indicating the presence of S. aureus in clinical specimens [ 28 , 29 ]. Most S. aureus strains from clinical sources contained protein A associated with the cell wall or released extracellularly [ 30 ].…”
Bloodstream infection (BSI) is a major cause of mortality in hospitalized patients worldwide. Staphylococcus aureus is one of the most common pathogens found in BSI. The conventional workflow is time consuming. Therefore, we developed a lateral flow immunoassay (LFIA) for rapid detection of S. aureus-protein A in positive blood culture samples. A total of 90 clinical isolates including 58 S. aureus and 32 non-S. aureus were spiked in simulated blood samples. The antigens were extracted by a simple boiling method and diluted before being tested using the developed LFIA strips. The results were readable by naked eye within 15 min. The sensitivity of the developed LFIA was 87.9% (51/58) and the specificity was 93.8% (30/32). When bacterial colonies were used in the test, the LFIA provided higher sensitivity and specificity (94.8% and 100%, respectively). The detection limit of the LFIA was 107 CFU/mL. Initial evaluation of the LFIA in 20 positive blood culture bottles from hospitals showed 95% agreement with the routine methods. The LFIA is a rapid, simple and highly sensitive method. No sophisticated equipment is required. It has potential for routine detection particularly in low resource settings, contributing an early diagnosis that facilitates effective treatment and reduces disease progression.
“…A similar LOD value of 1.56 pg/mL was only obtained with a chemiluminescence enzyme immunoassay (CLEIA) based system ( Fujimoto et al, 2008 ). The presented LSPCF fiber-optic biosensor presents many interesting and useful features, as it measures the fluorescence signal close to the reaction region resulting in a significant increase of the fluorescence efficiency ( Chang et al, 1996 ), showing also a high specificity, thanks to the sandwich immunoassay configuration.…”
This review summarizes the state of art of biosensor technology for Coronavirus (CoV) detection, the current challenges and the future perspectives. Three categories of affinity-based biosensors (ABBs) have been developed, depending on their transduction mechanism, namely electrochemical, optical and piezoelectric biosensors. The biorecognition elements include antibodies and DNA, which undergo important non-covalent binding interactions, with the formation of antigen-antibody and ssDNA/oligonucleotide-complementary strand complexes in immuno- and DNA-sensors, respectively. The analytical performances, the advantages and drawbacks of each type of biosensor are highlighted, discussed, and compared to traditional methods.
It is hoped that this review will encourage scientists and academics to design and develop new biosensing platforms for point-of-care (POC) diagnostics to manage the coronavirus disease 2019 (COVID-19) pandemic, providing interesting reference for future studies.
Biosensors
are chemical sensors in which the recognition system utilizes a biochemical mechanism. The term biosensor has been variously used to a number of devices either used to monitor living system or incorporating biotic elements. The current consensus is that this term should be reserved for sensors incorporating a biological element such as an enzyme, antibody, nucleic acid, microorganism, or eukariotic cell where the biological element is in intimate contact with the transducer. The main purpose of the recognition system is to provide specificity to the biosensor, thus creating a device able to detect either a specific molecular target or a related family of compounds. The ability of biosensors to detect trace and low levels of biologically active substances is the main characteristic of these systems, and for this reason they have applications in the fields of medicine, biotechnology, food, and environmental science.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.