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Oral Presentation <strong>Abstracts</strong><br />

laboratories in the states and internationally to<br />

build applications to extract information about<br />

genus, species, lineage, serotype, pathotype,<br />

virulence profile and antimicrobial resistance<br />

markers and subtyping using gene by gene approaches<br />

(whole genome multi-locus sequence<br />

typing, wgMLST) from the genome sequences.<br />

The PulseNet foodborne disease surveillance<br />

network infrastructure and analytical platform<br />

(BioNumerics, Applied Maths) and database<br />

will be used because of its versatility and<br />

because the public health laboratories have<br />

worked with it for > 15 years. Additionally,<br />

the use of this analytic software does not require<br />

extensive bioinformatics skills or local<br />

high performance computing capacity. The<br />

method will also be validated and will replace<br />

conventional CLIA related reference identification<br />

activities in the branch and public health<br />

laboratories. Results: WGS has successfully<br />

been tested for the US national surveillance<br />

of listeriosis since September 2013 and the<br />

wgMLST analysis has been implemented in<br />

the daily routine. The technology has proven<br />

its power supplementing traditional methods in<br />

outbreak investigations by adding phylogenetic<br />

relevance and increased resolution compared<br />

with current methods thereby enhancing case<br />

definitions and source tracking. The wgMLST<br />

method is currently being piloted in-house<br />

for surveillance of Campylobacteraceae,<br />

Shiga toxin-producing E. coli, and Salmonella<br />

with the remainder of foodborne bacteria to<br />

be added over the next three years. A betatesting<br />

pilot with the PulseNet public health<br />

laboratory partners will start in summer 2015.<br />

Conclusion: WGS will revolutionize the surveillance<br />

of both sporadic and outbreak related<br />

foodborne infections by replacing and enhancing<br />

current laboratory methods in use in public<br />

health laboratories.<br />

n S4:4<br />

SALMONELLA SEROTYPE DETERMINATION<br />

UTILIZING HIGH-THROUGHPUT GENOME<br />

SEQUENCING DATA<br />

S. Zhang 1 , Y. Yin 2 , M. Jones 3 , Z. Zhang 4 , B.<br />

Deatherage Kaiser 5 , B. Dinsmore 6 , C. Fitzgerald<br />

6 , P. Fields 6 , X. Deng 1 ;<br />

1<br />

University of Georgia, Griffin, GA, 2 Illinois<br />

Institute of Technology, Chicago, IL, 3 J. Craig<br />

Venter Institute, Rockville, MD, 4 University of<br />

Michigan, Ann Arbor, MI, 5 Pacific Northwest<br />

National Laboratory, Richard, WA, 6 Centers<br />

for Disease Control and Prevention, Atlanta,<br />

GA.<br />

Serotyping forms the basis of national and<br />

international surveillance networks for Salmonella,<br />

one of the most prevalent foodborne<br />

pathogens worldwide. Public health microbiology<br />

is currently being transformed by whole<br />

genome sequencing (WGS) which opens the<br />

door to serotype determination using WGS<br />

data. SeqSero (www.denglab.info/SeqSero)<br />

is a novel web-based tool for determining<br />

Salmonella serotypes using high-throughput<br />

genome sequencing data. SeqSero is based<br />

on curated databases of Salmonella serotype<br />

determinants (rfb gene cluster, fliC and fljB<br />

alleles) and is predicted to determine serotype<br />

rapidly and accurately for nearly the full spectrum<br />

of Salmonella serotypes (more than 2,300<br />

serotypes), from both raw sequencing reads<br />

and genome assemblies. The performance of<br />

SeqSero was evaluated by testing: 1) raw reads<br />

from genomes of 308 Salmonella isolates of<br />

known serotype; 2) raw reads from genomes<br />

of 3,306 Salmonella isolates sequenced and<br />

made publicly available by GenomeTrakr, a<br />

U.S. national monitoring network operated<br />

by the Food and Drug Administration; and 3)<br />

354 other publicly available draft or complete<br />

Salmonella genomes. We also demonstrated<br />

Salmonella serotype determination from raw<br />

sequencing reads of fecal metagenomes from<br />

mice orally infected with this pathogen. Seq-<br />

Sero can help to maintain the well-established<br />

ASM Conference on Rapid Next-Generation Sequencing and Bioinformatic<br />

Pipelines for Enhanced Molecular Epidemiologic Investigation of Pathogens<br />

21

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