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Dive into the research topics where Rosslyn Maybank is active.

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Featured researches published by Rosslyn Maybank.


Antimicrobial Agents and Chemotherapy | 2016

Escherichia coli Harboring mcr-1 and blaCTX-M on a Novel IncF Plasmid: First Report of mcr-1 in the United States

Patrick McGann; Erik Snesrud; Rosslyn Maybank; Brendan W. Corey; Ana C. Ong; Robert Clifford; Mary Hinkle; Timothy J. Whitman; Emil Lesho; Kurt E. Schaecher

The recent discovery of a plasmid-borne colistin resistance gene, mcr-1 , in China heralds the emergence of truly pan-drug-resistant bacteria ([1][1]). The gene has been found primarily in Escherichia coli but has also been identified in other members of the Enterobacteriaceae in human, animal, food


Genome Announcements | 2014

Complete Genome Sequence of the Quality Control Strain Staphylococcus aureus subsp. aureus ATCC 25923

Todd J. Treangen; Rosslyn Maybank; Sana Enke; Mary Beth Friss; Lynn F. Diviak; David Karaolis; Sergey Koren; Brian D. Ondov; Adam M. Phillippy; Nicholas H. Bergman; M. J. Rosovitz

ABSTRACT Staphylococcus aureus subsp. aureus ATCC 25923 is commonly used as a control strain for susceptibility testing to antibiotics and as a quality control strain for commercial products. We present the completed genome sequence for the strain, consisting of the chromosome and a 27.5-kb plasmid.


Diagnostic Microbiology and Infectious Disease | 2016

Real time application of whole genome sequencing for outbreak investigation – What is an achievable turnaround time?

Patrick McGann; Jessica L. Bunin; Erik Snesrud; Seema Singh; Rosslyn Maybank; Ana C. Ong; Yoon I. Kwak; Scott Seronello; Robert Clifford; Mary Hinkle; Stephen Yamada; Jason Barnhill; Emil Lesho

Whole genome sequencing (WGS) is increasingly employed in clinical settings, though few assessments of turnaround times (TAT) have been performed in real-time. In this study, WGS was used to investigate an unfolding outbreak of vancomycin resistant Enterococcus faecium (VRE) among 3 patients in the ICU of a tertiary care hospital. Including overnight culturing, a TAT of just 48.5 h for a comprehensive report was achievable using an Illumina Miseq benchtop sequencer. WGS revealed that isolates from patient 2 and 3 differed from that of patient 1 by a single nucleotide polymorphism (SNP), indicating nosocomial transmission. However, the unparalleled resolution provided by WGS suggested that nosocomial transmission involved two separate events from patient 1 to patient 2 and 3, and not a linear transmission suspected by the time line. Rapid TATs are achievable using WGS in the clinical setting and can provide an unprecedented level of resolution for outbreak investigations.


PLOS ONE | 2016

The Challenges of Implementing Next Generation Sequencing Across a Large Healthcare System, and the Molecular Epidemiology and Antibiotic Susceptibilities of Carbapenemase-Producing Bacteria in the Healthcare System of the U.S. Department of Defense

Emil Lesho; Robert Clifford; Fatma Onmus-Leone; Lakshmi Appalla; Erik Snesrud; Yoon I. Kwak; Ana Ong; Rosslyn Maybank; Paige Waterman; Patricia Rohrbeck; Michael Julius; Amanda L. Roth; Joshua Martinez; Lindsey Nielsen; Eric Steele; Patrick McGann; Mary Hinkle

Objective We sought to: 1) provide an overview of the genomic epidemiology of an extensive collection of carbapenemase-producing bacteria (CPB) collected in the U.S. Department of Defense health system; 2) increase awareness of the public availability of the sequences, isolates, and customized antimicrobial resistance database of that system; and 3) illustrate challenges and offer mitigations for implementing next generation sequencing (NGS) across large health systems. Design Prospective surveillance and system-wide implementation of NGS. Setting 288-hospital healthcare network. Methods All phenotypically carbapenem resistant bacteria underwent CarbaNP® testing and PCR, followed by NGS. Commercial (Newbler and Geneious), on-line (ResFinder), and open-source software (Btrim, FLASh, Bowtie2, an Samtools) were used for assembly, SNP detection and clustering. Laboratory capacity, throughput, and response time were assessed. Results From 2009 through 2015, 27,000 multidrug-resistant Gram-negative isolates were submitted. 225 contained carbapenemase-encoding genes (most commonly blaKPC, blaNDM, and blaOXA23). These were found in 15 species from 146 inpatients in 19 facilities. Genetically related CPB were found in more than one hospital. Other clusters or outbreaks were not clonal and involved genetically related plasmids, while some involved several unrelated plasmids. Relatedness depended on the clustering algorithm used. Transmission patterns of plasmids and other mobile genetic elements could not be determined without ultra-long read, single-molecule real-time sequencing. 80% of carbapenem-resistant phenotypes retained susceptibility to aminoglycosides, and 70% retained susceptibility to fluoroquinolones. However, among the CPB-confirmed genotypes, fewer than 25% retained susceptibility to aminoglycosides or fluoroquinolones. Conclusion Although NGS is increasingly acclaimed to revolutionize clinical practice, resource-constrained environments, large or geographically dispersed healthcare networks, and military or government-funded public health laboratories are likely to encounter constraints and challenges as they implement NGS across their health systems. These include lack of standardized definitions and quality control metrics, limitations of short-read sequencing, insufficient bandwidth, and the current limited availability of very expensive and scarcely available sequencing platforms. Possible solutions and mitigations are also proposed.


Antimicrobial Agents and Chemotherapy | 2016

Erratum for McGann et al., Escherichia coli Harboring mcr-1 and blaCTX-M on a Novel IncF Plasmid: First Report of mcr-1 in the United States

Patrick McGann; Erik Snesrud; Rosslyn Maybank; Brendan W. Corey; Ana C. Ong; Robert Clifford; Mary Hinkle; Timothy J. Whitman; Emil Lesho; Kurt E. Schaecher

Volume 60, no. 7, p. [4420–4421][1], 2016. Page 4420, right column, line 15: the correct reference for the sequence and description of plasmid pHNSHP45-2 is not reference 1 but is as follows. Zhi C, Lv L, Yu L-F, Doi Y, Liu J-H. 2016. Dissemination of the mcr-1 colistin resistance gene. Lancet


Infection Control and Hospital Epidemiology | 2018

Importation, Mitigation, and Genomic Epidemiology of Candida auris at a Large Teaching Hospital

Emil Lesho; Melissa Bronstein; Patrick McGann; Jason Stam; Yoon I. Kwak; Rosslyn Maybank; Jodi McNamara; Megan Callahan; Jean Campbell; Mary Hinkle; Edward E. Walsh

OBJECTIVE Candida auris (CA) is an emerging multidrug-resistant pathogen associated with increased mortality. The environment may play a role, but transmission dynamics remain poorly understood. We sought to limit environmental and patient CA contamination following a sustained unsuspected exposure. DESIGN Quasi-experimental observation. SETTING A 528-bed teaching hospital. PATIENTS The index case patient and 17 collocated ward mates. INTERVENTION Immediately after confirmation of CA in the bloodstream and urine of a patient admitted 6 days previously, active surveillance, enhanced transmission-based precautions, environmental cleaning with peracetic acid-hydrogen peroxide and ultraviolet light, and patient relocation were undertaken. Pre-existing agreements and foundational relationships among internal multidisciplinary teams and external partners were leveraged to bolster detection and mitigation efforts and to provide genomic epidemiology. RESULTS Candida auris was isolated from 3 of 132 surface samples on days 8, 9, and 15 of ward occupancy, and from no patient samples (0 of 48). Environmental and patient isolates were genetically identical (4-8 single-nucleotide polymorphisms [SNPs]) and most closely related to the 2013 India CA-6684 strain (~200 SNPs), supporting the epidemiological hypothesis that the source of environmental contamination was the index case patient, who probably acquired the South Asian strain from another New York hospital. All isolates contained a mutation associated with azole resistance (K163R) found in the India 2105 VPCI strain but not in CA-6684. The index patient remained colonized until death. No surfaces were CA-positive 1 month later. CONCLUSION Compared to previous descriptions, CA dissemination was minimal. Immediate access to rapid CA diagnostics facilitates early containment strategies and outbreak investigations. Infect Control Hosp Epidemiol 2018;39:53-57.


Infection Control and Hospital Epidemiology | 2018

Got GAS? Ease the Bloat with Real-Time Whole-Genome Sequencing

Emil Lesho; Erik Snesrud; Melissa Bronstein; Margaret Pettis; Ana Ong; Rosslyn Maybank; Yoon I. Kwak; Anthony Jones; Kelly Vore; Patrick McGann; Mary Hinkle

Financial support: Support for this study was received from the German Research Foundation (grant no.WO 1746/1-2 toM.W. and grant no. KA 4199/ 1-1 to T.H.). Additional funding was received from the Innovative Medicines Initiative Joint Undertaking (grant no. 115737-2 to K.K., Combatting bacterial resistance in Europe—molecules against gram-negative infections [COMBACTE-MAGNET]). The funders had no role in the preparation of this manuscript. Potential conflicts of interest: All authors report no conflicts of interest relevant to this article.


Genome Announcements | 2017

Complete genome sequence of Staphylococcus epidermidis 1457

Madeline R. Galac; Jason Stam; Rosslyn Maybank; Mary Hinkle; Dietrich Mack; Holger Rohde; Amanda L. Roth; Paul D. Fey

ABSTRACT Staphylococcus epidermidis 1457 is a frequently utilized strain that is amenable to genetic manipulation and has been widely used for biofilm-related research. We report here the whole-genome sequence of this strain, which encodes 2,277 protein-coding genes and 81 RNAs within its 2.4-Mb genome and plasmid.


Military Medicine | 2016

From the Battlefield to the Bedside: Supporting Warfighter and Civilian Health With the “ART” of Whole Genome Sequencing for Antibiotic Resistance and Outbreak Investigations

Emil Lesho; Xiaoxu Lin; Robert Clifford; Erik Snesrud; Fatma Onmus-Leone; Lakshmi Appalla; Ana Ong; Rosslyn Maybank; Lindsey Nielsen; Yoon I. Kwak; Mary Hinkle; John Turco; Juan A. Marin; Sally Hooks; Stacy Matthews; Stephen Hyland; Jered Little; Paige Waterman; Patrick McGann

Awareness, responsiveness, and throughput characterize an approach for enhancing the clinical impact of whole genome sequencing for austere environments and for large geographically dispersed health systems. This Department of Defense approach is informing interagency efforts linking antibiograms of multidrug-resistant organisms to their genome sequences in a public database.


Journal of Clinical Microbiology | 2016

Detecting 16S rRNA Methyltransferases in Enterobacteriaceae by Use of Arbekacin.

Patrick McGann; Sarah Chahine; Darius Okafor; Ana C. Ong; Rosslyn Maybank; Yoon I. Kwak; Kerry Wilson; Michael Zapor; Emil Lesho; Mary Hinkle

ABSTRACT 16S rRNA methyltransferases confer resistance to most aminoglycosides, but discriminating their activity from that of aminoglycoside-modifying enzymes (AMEs) is challenging using phenotypic methods. We demonstrate that arbekacin, an aminoglycoside refractory to most AMEs, can rapidly detect 16S methyltransferase activity in Enterobacteriaceae with high specificity using the standard disk susceptibility test.

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Mary Hinkle

Walter Reed Army Institute of Research

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Emil Lesho

Walter Reed Army Institute of Research

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Erik Snesrud

J. Craig Venter Institute

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Yoon I. Kwak

Walter Reed Army Institute of Research

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Patrick McGann

Walter Reed Army Institute of Research

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Ana Ong

Walter Reed Army Institute of Research

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Robert Clifford

Walter Reed Army Institute of Research

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Ana C. Ong

Walter Reed Army Institute of Research

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Anthony Jones

Walter Reed Army Institute of Research

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Fatma Onmus-Leone

Walter Reed Army Institute of Research

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