The largest database of trusted experimental protocols

Vitek 2 ast card

Manufactured by bioMérieux
Sourced in France

VITEK-2 AST cards are lab equipment used for antibiotic susceptibility testing (AST). They provide automated identification and antimicrobial susceptibility results for a wide range of microorganisms.

Automatically generated - may contain errors

9 protocols using vitek 2 ast card

1

Identification and Antibiotic Susceptibility Testing for S. aureus

Check if the same lab product or an alternative is used in the 5 most similar protocols
Initial identification and antibiotic susceptibility testing (AST) for S. aureus were performed by the CMWH laboratory as per their standard procedures. Clinical samples were plated onto 5% sheep blood agar. Identification was performed using the deoxyribonuclease test and the staphylococcus latex agglutination test, and AST was performed for first-line laboratory antimicrobials using the disk-diffusion method with CLSI breakpoints.26 Alternatively, if an isolate was either identified as MRSA or was growing repeatedly from blood cultures, identification and AST were performed using the VITEK-2 GP ID and VITEK-2 AST cards (bioMérieux, Marcy-Étoile, France; version 9.01), respectively.
Where possible, the index S. aureus isolate from each patient was sub-cultured, stored at -80⁰C, and shipped to Melbourne, Australia for confirmatory testing. Confirmatory identification was performed using MALDI-TOF (Bruker, Hanau, Germany) and confirmatory AST was performed using VITEK-2 AST cards (bioMérieux, version 8.01) on all available isolates.
+ Open protocol
+ Expand
2

Antimicrobial Susceptibility of S. aureus

Check if the same lab product or an alternative is used in the 5 most similar protocols
All clinical specimens for isolation and cultivation were processed according to the National Operating Procedures for Clinical Laboratory Testing. Antimicrobial susceptibility of the 504 strains of S. aureus was tested against 16 drugs using VITEK-2 AST cards (bioMérieux, France) based on the manufacturer’s standard protocol. The tested antibiotics were: cefoxitin, benzylpenicillin, oxacillin, linezolid, gentamicin, ciprofloxacin, levofloxacin, moxifloxacin, erythromycin, clindamycin, quinupristin, vancomycin, tetracycline, tigecycline, nitrofurantoin, and rifampicin. The minimum inhibitory concentration (MIC) breakpoints of antimicrobials for S. aureus using VITEK-2 COMPACT system can be referred to in Supplementary Table S2. The criteria for antimicrobial susceptibility determination and quality control were based on the 2017 Clinical and Laboratory Standards Institute (CLSI) guidelines. The MRSA phenotype was determined using the cefoxitin disk diffusion method [28 ]. Further details can be found in the Supplementary Material/Methods section.
+ Open protocol
+ Expand
3

Antibiotic Resistance Gene Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Antibiotic resistance genes were identified using Resfinder version 2.1 with a threshold of 98% identity and 60% query coverage [23 (link)]. A manual search for known mutations in parC, gyrA, folA and folP was performed. Minimal inhibitory concentration for each isolate was determined using VITEK® 2 AST Cards (Biomérieux, France).
+ Open protocol
+ Expand
4

Bacterial Identification and Antimicrobial Susceptibility

Check if the same lab product or an alternative is used in the 5 most similar protocols
Wound and pus samples were inoculated on chocolate agar, MacConkey agar, and blood agar and incubated at 37°C for 24–48 hours. After the incubation period, the plates were examined for the presence of pathogenic bacteria according to the standard microbiological identification techniques, in accordance with the guidelines of Clinical and Laboratory Standards Institute (CLSI). All isolates were confirmed using the VITEK 2 system (bioMérieux) for identification of Gram-negative and Gram-positive bacteria (GN and GP ID card), whereas VITEK® 2 AST Cards were used for antimicrobial susceptibility testing.
+ Open protocol
+ Expand
5

Antibiotic Susceptibility Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Antibiotic susceptibility to extended-spectrum β-lactam and carbapenem antibiotics was evaluated using a VITEK 2 Compact (bioMérieux) with VITEK® 2 AST cards (bioMérieux). The test was run according to the manufacturer’s instructions. Furthermore, for isolates defined as “pathogenic/sensitive” a minimum inhibitory concentration (MIC) test was conducted for the following antibiotics: tetracycline, streptomycin, polymyxin B, gentamycin, nitrofurantoin, chloramphenicol, trimethoprim, cefuroxime, cefaclor, cefazolin, and amikacin. The tests were conducted using the E-Test (Liofilchem) according to the manufacturer’s instruction. Briefly, for each strain, 0.5 McFarland was spread on Mueller Hinton agar (Merck, Darmstadt, Germany) plates and exposed to a strip of varying antibiotic concentrations. The plates were incubated for 24 h in 37 °C, and the zone of growth inhibition was assessed visually to determine the MIC.
+ Open protocol
+ Expand
6

Retrospective Study of Infective Endocarditis

Check if the same lab product or an alternative is used in the 5 most similar protocols
This retrospective study was conducted between Jan 2011 to Dec 2016 (for a period of five years). Data collection was based on the systematic review of all-patient charts from medical records department in order to determine the clinical and microbiological pectrum, 191 patients records, definitely diagnosed with IE, based on modified Dukes criteria were re-viewed and included. Demographic details such as age, sex, clinical findings, and antibiotic usage were analysed from these cases. Three sets of blood cultures, BacT/Alert FNaerobic and SN aerobic bottles per set (bioMerieux, Marcy l’Etoile, France), were submitted to the microbiology lab, within 24 hours of admission and immediately loaded into BACT/ALERT 3D system. Gram staining was performed on all the positive flagged bottles and further sub-cultured on Blood (COS bioMerieux, Marcy l’Etoile, France) and Chrome agar (COS bioMerieux, Marcy l’Etoile, France) plates and incubated at 37°C for 24h. The Vitek 2 (bioMérieux, Marcy l’Etoile, France) GN cards (ID GN panel) were used, for accurate identification of Gram-negative pathogens and Vitek 2 AST Cards (N281 panel), for antimicrobial susceptibility testing.
The Vitek 2 GP cards (ID GP) were used, for accurate identification of Gram-positive pathogens, and Vitek 2 AST cards for antimicrobial susceptibility testing.
+ Open protocol
+ Expand
7

Antimicrobial Susceptibility Testing of Clinical Isolates

Check if the same lab product or an alternative is used in the 5 most similar protocols
Antimicrobial susceptibility testing (AST) of the clinical isolates was performed using the gram-negative and gram-positive Vitek2® AST cards (N280, N281, and P628) (bioMérieux, Inc., Durham, NC), as per the manufacturer's instructions. The minimum inhibitory concentration for colistin was determined by the Clinical and Laboratory Standards Institute (CLSI) broth microdilution method.12 The antibacterial drugs tested against gram-negative pathogens included amikacin, cefepime, cefoperazone/sulbactam, ceftazidime, ciprofloxacin, levofloxacin, imipenem, meropenem, piperacillin/tazobactam, and chloramphenicol. The antibacterial drugs tested against gram-positive organisms included vancomycin, teicoplanin, ciprofloxacin, linezolid, erythromycin, clindamycin, and doxycycline. Multidrug resistance was defined as resistance to two or more different classes of antimicrobials.13 After processing, the samples were discarded as per the COVID-19 biomedical waste management guidelines.14
+ Open protocol
+ Expand
8

Carbapenem-resistant A. baumannii Bloodstream Isolates

Check if the same lab product or an alternative is used in the 5 most similar protocols
Carbapenem-resistant A. baumannii bloodstream isolates from patients with CRAB between June 2016 and December 2019 at Chonnam National University Hospital (a 1,000-bed tertiary care hospital with eight ICUs in Gwangju, Korea) were stored at −80°C. Species identification was performed initially by matrix-assisted laser desorption ionization-time of flight mass spectrometry-based VITEK MS (bioMérieux, France) and VITEK 2 (bioMérieux) and was confirmed by using MLST-based identification as previously described (Gaiarsa et al., 2019 (link)). Carbapenem resistance was initially determined using the VITEK 2 AST Card (bioMérieux) and confirmed by broth microdilution test (Clinical and Laboratory Standards Institute, 2020 ). Duplicate CRAB isolates from the same patient were excluded.
+ Open protocol
+ Expand
9

Hospital-Acquired E. coli and Enterococcus Infections: Resistance Profiles

Check if the same lab product or an alternative is used in the 5 most similar protocols
All hospitalised cases with confirmed E. coli or enterococcal infection during the 8-weeks study period were reviewed to investigate possible hospital-acquired (HAI) infection and relationship with environmental contamination. The resistance profile of isolates from hospitalised cases was analysed by VITEK®2 AST Card and VITEK® 2 Systems Version: 08.02 (bioMérieux, France). The VITEK®2 cards used for testing enterococcal isolates do not include vancomycin analysis. The VITEK®2 GN97 cards for E. coli isolates analyse resistance to 19 antimicrobials and test for presumptive extended-spectrum beta-lactamase (ESBL) production. The cards used for Enterococcus species analyse resistance to 19 antimicrobials. The resistance profiles of suspected HAI cases were compared to those of faecal bacteria isolated from the environment. In our study, we used 6 antimicrobials for E. coli and 4 for Enterococcus species in the disc diffusion test (resources for the project did not allow testing using the VITEK® 2 System).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!