In Silico Serotyping Based on Whole-Genome Sequencing Improves the Accuracy of Shigella Identification

Author:

Wu Yun12,Lau Henry K.2,Lee Teresa2,Lau David K.2,Payne Justin3

Affiliation:

1. U.S. Food and Drug Administration, Office of Commissioner, Commissioner’s Fellowship Program, Silver Spring, Maryland, USA

2. U.S. Food and Drug Administration, Office of Regulatory Affairs, San Francisco Laboratory, Alameda, California, USA

3. U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, College Park, Maryland, USA

Abstract

Shigella causes diarrheal disease with serious public health implications. However, conventional Shigella identification methods are laborious and time-consuming and can be erroneous due to the high similarity between Shigella and enteroinvasive Escherichia coli (EIEC) and cross-reactivity between serotyping antisera. Further, serotype interpretation is complicated for inexperienced users. To develop an easier method with higher accuracy based on whole-genome sequencing (WGS) for Shigella serotyping, we systematically examined genomic information of Shigella isolates from 53 serotypes to define rules for differentiation and serotyping. We created ShigaTyper, an automated pipeline that accurately and rapidly excludes non- Shigella isolates and identifies 59 Shigella serotypes using Illumina paired-end WGS reads. A serotype can be unambiguously predicted at a data processing speed of 538 MB/min with 98.2% accuracy from a regular laptop. Once it is installed, training in bioinformatics analysis and Shigella genetics is not required. This pipeline is particularly useful to general microbiologists in field laboratories.

Funder

Food and Drug Administration

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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