Evaluation of the BD MAX™ MRSA XT Assay in a Clinical Laboratory

Slides:



Advertisements
Similar presentations
STABILITY OF SEEDED SWAB SPECIMENS FOR THE DETECTION OF CHLAMYDIA TRACHOMATIS IN THE GEN-PROBE APTIMA TEST J Schachter and J Moncada. University of California,
Advertisements

Figure 1. Trichomonas Assay Procedure
By Gracie Canales August 10, 2010
The Critical Challenge of Antibiotic Resistance: Are Wastewater Treatment Plants a Concern? Kourtney Brown 1, Stefan Walston 2, Channah Rock 2, & Jean.
Evaluation of the IMMY CrAg Lateral Flow Assay for Detection of Cryptococcal Antigen Susan Clarke and Robert Gibb Pathology Queensland – Central, Royal.
Utilizing a Non-Commercial Real- Time PCR to Detect HIV-1 RNA in HIV Antibody Negative Diagnostic Sera Submitted to The Maryland Public Health Laboratory.
Printed by Comparison of Primary Care and Clinical Laboratory Methods for the Diagnosis of Bacterial Vaginosis and Yeast Vaginitis.
Eye Spy: Microbial Growth on Contact Lenses Theresa Edson and Kyle Hilsabeck Introduction: Biofilms are “organized microbial systems consisting of layers.
NEW Product MAY 2006 STREPTO B ID NEW chromogenic media available ! STREPTO B ID NEW PRODUCT in the bMx offer SECOND in the NEW PREVENTION range dedicated.
Antimicrobial Susceptibility Testing – Part II
Seasonal Variation in the Prevalence of Coagulase-Positive Staphylococcus aureus Among College Students ( ) Megan Branche Dr. Carolyn Mathur, Mentor.
Diagnostic Microbiology and Immunology
Rapid and sensitive detection of MRSA by PCR-based methods in the environment and hospital patients. by Dr. Corinne Whitby Department of Biological Sciences,
The Use of Cefoxitin for the Determination of Methicillin Resistance in Staphylococci John D. Perry Microbiology Department Freeman Hospital Newcastle.
Mannitol Salt Agar-Cefoxitin Combination as a Screening Medium for MRSA SMYTH, RW and KAHLMETER, G Dept. of Clinical Microbiology, Central Hospital, S-351.
TITLE Mannitol Salt Agar-Cefoxitin Combination as a screening Medium for Methicillin-Resistant Staphylocuccus aureus.
Prevalence of Methicillin-resistant Staphylococcus aureus in El Oro Province, Ecuador Student Researchers: Christopher A. Monte, Beatrice R. Soderholm.
Methicillin-resistant Staphylococcus aureus in Loja Province, Ecuador Student Researcher: Sarah Hof Faculty Researcher: Daniel Herman, PhD Department of.
Is The Prevalence of Staphylococcus aureus Increasing Among York College Students? By: Angel Newson Department of Biological Sciences, York College of.
Prevalence of Methicillin-Resistant Staphylococcus aureus in Loja Province, Ecuador Student Researcher: Lauren Lamers, Faculty Researcher: Daniel Herman,
Julia Robbins August 11, Objectives Clinical Significance of MRSA in Healthcare Setting Principle of assay Assay Procedure Assay Perfomance.
Speciation of Methicillin-Resistant Staphylococci Isolated from Ecuadorian Hospitals and Communities Student Researcher: Beatrice R. Soderholm; Faculty.
Point of Care Testing for MRSA Nigel Brenwald Department of Microbiology Sandwell and West Birmingham Hospitals NHS Trust.
Combination of a microtiter plate method with the amplification of the icaA/aap genes is an effective tool to determine biofilm formation in Staphylococcus.
Copyright © 2015 Beck, Eric T. Eric T. Beck 1, Garrett C. Reymann 1, Blake W. Buchan 1,2, and Nathan A. Ledeboer 1,2 1 Department.
CONCLUSIONS Amended Abstract Detection of GBS Directly from ESwab Collected Samples Using the BD MAX™ GBS Assay Suzane Silbert, Talita T. Rocchetti, Alicia.
MALDI TOF analysis of Streptococcus pneumoniae from Cerebrospinal Fluid for the diagnosis of Acute Bacterial Meningitis Dr. R. Ravikumar, M.D., Professor.
INTRODUCTION Assessment of a real-time PCR for the identification and characterisation of Verocytotoxigenic E. coli (VTEC) Claire Jenkins, Andy J. Lawson,
PREVALENCE AND CHARACTERIZATION OF MRSA IN A REGIONAL HOSPITAL IN CUENCA, ECUADOR Student Researchers: Annie Szmanda and Erin Leisen Faculty Researcher:
Carriage Rates of Methicillin-Resistant Staphylococcus aureus (MRSA) Among College Students Ryan Kitzinger, Leigh Nelson, Chad Sethman, Ph.D. ABSTRACT.
The Alarming Rise of CA-MRSA at UMass-Memorial Medical Center David M. Bebinger, M.D. Assistant Professor Division of Infectious Diseases UMass-Memorial.
Stethoscopes : Clinician’s Gift to Patients Titilayo Oluwabusi MD, Tochi Iroku-Malize MD MPH, Neubert Philippe MD, Oluwafunmilayo Fapohunda MD, Valeria.
1 SOFTWARE FOR VERIFICATION OF HOMOGENEITY RESULTS FROM AUTOMATED URINE ANALYZERS IN REAL TIME Waldemar Volanski Ademir Luiz do Prado Geraldo Picheth et.
 Bacterial strain typing: 1. understanding the epidemiology of MRSA 2. evaluating the effectiveness of infection control 3. evaluating.
S. aureus subtypes based on Methicillin resistance
Title of the Change Project
Comparison of the Focus Diagnostics Simplexa™ Flu A/B & RSV Direct Assay with the Prodesse® ProFlu™ + Assay for Detection of Influenza A Virus (FluA),
Comprised of Blood Agar and CHROMagarTM Orientation using WASPLabTM
Lytic phage in biosensing Vitaly Vodyanoy1, Iryna Sorokulova1, Rajesh Guntupalli1, Eric Olsen2, Ludmila Globa1, Oleg Pustovyy1 1Department of Anatomy,
PREMARKET EVALUATION OF THE BD MAXTM CLOSTRIDIUM DIFFICILE PCE ASSAY
HCV by PCR Neelam Gajjar 7/26/2009.
The Laboratory diagnosis and susceptibility testing of meticilline-resistant staphylococcus aureus By: Maj Anthere Murangwa, MSC Medical Microbiologist.
Objectives Methods Results Conclusions Contact 64
Table 1 Demographic and clinical characteristics of 758 admitted patients for whom cultures of nares were performed to assess methicillin-resistant Staphylococcus.
2011 American Society for Microbiology Meeting
Positive cultures for S. aureus
ASM 2017 Microbe Annual Meeting Sunday-507
Oduwole, K. O.; Hammerton, H.; Onayemi, O. D.; Mccormack, D. J.;
Screening for Methicillin-Resistant Staphylococcus spp
1Department of Esoteric Testing/R&D, Tampa General Hospital, Tampa, FL
Rainbow O157 Agar-Black colonies are E. coli O157
D th Interscience Conference on Antimicrobial Agents and Chemotherapy October 25-28, Washington, DC Evaluation of a Rapid PBP2’ Agglutination.
Reverse Complement PCR: fast, low cost amplicon based NGS
dentistry deintyddiaeth SCHOOL K-3364 ysgol
Clinical Pathology Quality Dashboard
Molecular characterisation of
Title Detection of HLA-B*58:01 with TaqMan assay and its association with allopurinol-induced sCADR.
Molecular characterization of methicillin-resistant Staphylococcus epidermidis strains from bacteraemic patients  S. Ibrahem, S. Salmenlinna, O. Lyytikäinen,
Clinical impact of a real-time PCR assay for rapid identification of Staphylococcus aureus and determination of methicillin resistance from positive blood.
Presented by: Ihsan Ullah M Imran Sharif
W. Witte, B. Pasemann, C. Cuny  Clinical Microbiology and Infection 
Molecular characterization and susceptibility of methicillin-resistant and methicillin- susceptible Staphylococcus aureus isolates from hospitals and the.
P. Moreillon, J.M. Entenza  Clinical Microbiology and Infection 
Spa typing directly from a mecA, spa and pvl multiplex PCR assay—a cost-effective improvement for methicillin-resistant Staphylococcus aureus surveillance 
Emergence of community-associated methicillin-resistant Staphylococcus aureus strains in the neonatal intensive care unit: an infection prevention and.
Evaluation of three chromogenic media (MRSA-ID, MRSA-Select and CHROMagar MRSA) and ORSAB for surveillance cultures of methicillin-resistant Staphylococcus.
PCR for the identification of methicillin-resistant Staphylococcus aureus (MRSA) strains using a single primer pair specific for SCCmec elements and the.
1.1.3 MI.
Use of broth enrichment and real-time PCR to exclude the presence of methicillin- resistant Staphylococcus aureus in clinical samples: a sensitive screening.
Evaluation of the BBL CrystalTM MRSA ID System for Rapid Detection of Methicillin Resistance in Staphylococcus aureus  Sylvie Dutka-Malen, Murielle Charles,
Presentation transcript:

Evaluation of the BD MAX™ MRSA XT Assay in a Clinical Laboratory Carly Kubasek, Faris Galambo, Elaine Vendrone, Suzane Silbert, Ray Widen Department of Esoteric Testing/R&D, Tampa General Hospital, Tampa, FL 2014 CVS Annual Meeting T80 Abstract Methods continued Results Background: The BD MAX™ MRSA XT assay (BD Diagnostics, Québec, Canada) performed on the BD MAX™ System (BD Diagnostics, Sparks, MD) is an FDA-cleared assay designed to detect methicillin-resistant Staphylococcus aureus (MRSA) specific DNA in nasal samples. Probes labeled with different fluorophores are used to detect a specific amplicon in the SCCmec right-extremity junction (MREJ), the genes for methicillin resistance mecA and mecC, and sample processing control (SPC) amplicons in three different optical channels of the BD MAX™ System. The objective of this study was to compare the new BD MAX™ MRSA XT assay with the standard PCR MRSA test used in our laboratory: the BD MAX™ MRSA 1st generation assay (BD Diagnostics). Methods: A total of 118 clinical samples were tested. Specimens were collected from the nares of each patient, using an NP ESwab (Copan Diagnostics Inc, USA). First, two aliquots of 200µL each of the same ESwab sample were transferred to two BD MAX Sample Buffer Tubes (SBT). Each SBT was tested separately by the BD MAX™ MRSA assay and by the BD MAX™ MRSA XT assay, according to manufacturer’s recommendations. This allowed direct comparison of results from the same patient. Direct cultures of the samples with discordant results were performed by pipetting 50µL of the remaining ESwab samples to each of the following media: TSA II, BBL™ CHROMagar™ Staph aureus, BBL CHROMagar MRSA II, and TSB w/ 6.5% NaCl (BD Diagnostics). Plates were examined for growth after 20-26h of incubation at 35°C. S. aureus identification was confirmed by latex agglutination tests and by an in-house validated mecA/femA specific PCR. Additionally, a challenge panel comprising multiple control strains was evaluated by the BD MAX™ MRSA XT assay to verify the ability of the assay to correctly identify a variety of MRSA strains and to exclude S. aureus strains with mecA gene dropouts, incorrectly identified as MRSA. Results: Out of 118 clinical samples tested, 34 were MRSA positive by both assays and 2 were MRSA positive by only the BD MAX™ MRSA 1st generation assay. Culture results from these 2 discordant samples revealed the presence of Staphylococcus epidermidis on the TSA II plate and in the TSB w/ 6.5% NaCl. No discordant results were obtained with the BD MAX™ MRSA XT assay for the challenge panel. Conclusion: Our results showed that the new BD MAX™ MRSA XT assay performed on the BD MAX™ System has excellent sensitivity and specificity. In addition to that, the new BD MAX™ MRSA XT assay appeared to have the ability to correctly identify a variety of MRSA strains and excludes the strains of S. aureus with mecA gene dropouts, incorrectly identified by the 1st generation assay as MRSA. Bacterial Culture: 50 µL of the remaining ESwab samples were plated into each of the following media: TSA II, BBL™ CHROMagar™ S. aureus, BBL CHROMagar MRSA II, and TSB w/ 6.5% NaCl (BD Diagnostics). Colony growth was observed after 20-26h of incubation at 35°C. S. aureus identification was confirmed by latex agglutination tests and by an in-house validated mecA/femA specific PCR. A challenge panel comprising multiple control strains was evaluated by the BD MAX™ MRSA XT and the Cepheid Xpert® MRSA assays to verify the ability of the assays to correctly identify MRSA. Table 1. BD MAX™ MRSA 1st Generation, BD MAX™ MRSA XT and Direct Culture Results: Table 2. Discrepant Results Analysis Among BD MAX™ MRSA 1st Generation, BD MAX™ MRSA XT and MRSA Culture: Results BD MAX MRSA 1st G. BD MAX MRSA XT Direct Culture MRSA Positive 36 34 33 Negative 82 84 85 Tests/ Samples MRSA 1st G. PCR MRSA XT PCR Direct Culture Enrichment Culture femA PCR mecA PCR Sample 14 + - Sample 27* Sample 29* Figure 1. BD MAX™ Instrument Operation One manual pipetting step – 200 µL aliquot from ESwab sample transferred to a Sample Buffer Tube *Samples 27 (Ct=36) and 29 (Ct=35) were negative for MRSA by direct and enriched culture, positive for mecA gene but negative for femA. Possibly cassette dropouts from a MRSA mixed with a MRCONS. Table 3. Challenge Panel Results: CONCLUSIONS Load reagents and specimens onto the BD MAX™ rack ID Strain Description MREJ Type BD MAX MRSA XT Cepheid Xpert MRSA 3097 MSSA (mecA dropout) ii - + 1 MRSA i 2800 9 iii 11 iv 16 v 2937 vi 19 vii 131 ix 2952 xiii 797 xiv ATCC BAA- 2312 (mecC) xxi ATCC 29213 NA ATCC 14990 MSSE The BD MAX™ MRSA XT is a new automated real-time PCR assay that is able to detect MRSA in nares samples in a single walk away sample in – answer out test. The first generation BD MAX™ MRSA and the BD MAX™ MRSA XT assay displayed 98.3% overall agreement. Two samples were positive on the first generation BD MAX™ MRSA and negative on the BD MAX™ MRSA XT. Direct and enriched cultures, and femA PCR were negative for MRSA as well. Positive results for mecA gene were detected suggesting the possibility of a mecA dropout. The resolved sensitivity and specificity for the BD MAX™ MRSA XT were 100%. The BD MAX™ MRSA XT assay correctly identified all the targets in a challenge panel that include a variety of MREJ types, along with an isolate that contained mecC rather than mecA. Importantly the BD MAX™ MRSA XT correctly excluded a mecA dropout MSSA isolate. The data indicates that the BD MAX™ MRSA XT assay provides highly accurate and rapid detection of MRSA in nares samples used in screening patients for colonization with MRSA. The BD MAX MRSA XT assay can potentially assist with isolation steps to help reduce post procedure or nosocomial infections. Introduction Create worklist Methicillin-resistant Staphylococcus aureus (MRSA) is a leading cause of healthcare-associated infections. MRSA colonization is associated with increased risk of disease, high cost and poor clinical outcomes. Early identification of patients colonized with MRSA and subsequent prevention of patient-to-patient spread through infection control measures are considered important interventions to control MRSA. Traditional culture-based methods for detecting MRSA depend on isolation of pure colonies, followed by identification of S. aureus and confirmation of methicillin resistance either by oxacillin susceptibility testing, detection of the mecA gene or detection of penicillin binding protein PBP2a encoded by the mecA gene. The BD MAX™ MRSA XT assay is a new automated molecular assay that detects the SCCmec right-extremity junction (MREJ) and the mecA and mecC methicillin resistance genes. Place racks and cartridges on BD MAX™ Methods A total 118 clinical samples were collected from the nares of patients for routine MRSA testing, using a NP ESwab (Copan Diagnostics). Note* Use of the ESwab with the BD MAX MRSA XT and BD MAX MRSA assay is outside of package insert claims; however, it’s use was validated at Tampa General Hospital. BD MAX™ MRSA XT and MRSA Assay (1st Generation) 200 µL of ESwab sample were transferred to two BD MAX Sample Buffer Tubes (SBT) The Sample Buffer Tubes were vortexed on a multi-tube vortexer for 60 seconds. The SBTs were transferred to two BD MAX racks, one for each assay. Unitized Reagent Strips containing assay-specific reagent tubes were placed in BD MAX racks. The entire assembly was placed in the BD MAX instrument along with BD MAX PCR cartridges. Close door to initiate run then release results through LIS interface This study was supported by BD Diagnostics (Sparks, MD).