Complete Whole Genome Sequences of Escherichia coli Surrogate Strains and Comparison of Sequence Methods with Application to the Food Industry
In 2013, the U.S. Department of Agriculture Food Safety and Inspection Service (USDA-FSIS) began transitioning to whole genome sequencing (WGS) for foodborne disease outbreak- and recall-associated isolate identification of select bacterial species. While WGS offers greater precision, certain hurdle...
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Published in | Microorganisms (Basel) Vol. 9; no. 3; p. 608 |
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Abstract | In 2013, the U.S. Department of Agriculture Food Safety and Inspection Service (USDA-FSIS) began transitioning to whole genome sequencing (WGS) for foodborne disease outbreak- and recall-associated isolate identification of select bacterial species. While WGS offers greater precision, certain hurdles must be overcome before widespread application within the food industry is plausible. Challenges include diversity of sequencing platform outputs and lack of standardized bioinformatics workflows for data analyses. We sequenced DNA from USDA-FSIS approved, non-pathogenic
surrogates and a derivative group of rifampicin-resistant mutants (rif
) via both Oxford Nanopore MinION and Illumina MiSeq platforms to generate and annotate complete genomes. Genome sequences from each clone were assembled separately so long-read, short-read, and combined sequence assemblies could be directly compared. The combined sequence data approach provides more accurate completed genomes. The genomes from these isolates were verified to lack functional key
elements commonly associated with pathogenesis. Genetic alterations known to confer rif
were also identified. As the food industry adopts WGS within its food safety programs, these data provide completed genomes for commonly used surrogate strains, with a direct comparison of sequence platforms and assembly strategies relevant to research/testing workflows applicable for both processors and regulators. |
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AbstractList | In 2013, the U.S. Department of Agriculture Food Safety and Inspection Service (USDA-FSIS) began transitioning to whole genome sequencing (WGS) for foodborne disease outbreak- and recall-associated isolate identification of select bacterial species. While WGS offers greater precision, certain hurdles must be overcome before widespread application within the food industry is plausible. Challenges include diversity of sequencing platform outputs and lack of standardized bioinformatics workflows for data analyses. We sequenced DNA from USDA-FSIS approved, non-pathogenic
surrogates and a derivative group of rifampicin-resistant mutants (rif
) via both Oxford Nanopore MinION and Illumina MiSeq platforms to generate and annotate complete genomes. Genome sequences from each clone were assembled separately so long-read, short-read, and combined sequence assemblies could be directly compared. The combined sequence data approach provides more accurate completed genomes. The genomes from these isolates were verified to lack functional key
elements commonly associated with pathogenesis. Genetic alterations known to confer rif
were also identified. As the food industry adopts WGS within its food safety programs, these data provide completed genomes for commonly used surrogate strains, with a direct comparison of sequence platforms and assembly strategies relevant to research/testing workflows applicable for both processors and regulators. In 2013, the U.S. Department of Agriculture Food Safety and Inspection Service (USDA-FSIS) began transitioning to whole genome sequencing (WGS) for foodborne disease outbreak- and recall-associated isolate identification of select bacterial species. While WGS offers greater precision, certain hurdles must be overcome before widespread application within the food industry is plausible. Challenges include diversity of sequencing platform outputs and lack of standardized bioinformatics workflows for data analyses. We sequenced DNA from USDA-FSIS approved, non-pathogenic E. coli surrogates and a derivative group of rifampicin-resistant mutants (rifR) via both Oxford Nanopore MinION and Illumina MiSeq platforms to generate and annotate complete genomes. Genome sequences from each clone were assembled separately so long-read, short-read, and combined sequence assemblies could be directly compared. The combined sequence data approach provides more accurate completed genomes. The genomes from these isolates were verified to lack functional key E. coli elements commonly associated with pathogenesis. Genetic alterations known to confer rifR were also identified. As the food industry adopts WGS within its food safety programs, these data provide completed genomes for commonly used surrogate strains, with a direct comparison of sequence platforms and assembly strategies relevant to research/testing workflows applicable for both processors and regulators. In 2013, the U.S. Department of Agriculture Food Safety and Inspection Service (USDA-FSIS) began transitioning to whole genome sequencing (WGS) for foodborne disease outbreak- and recall-associated isolate identification of select bacterial species. While WGS offers greater precision, certain hurdles must be overcome before widespread application within the food industry is plausible. Challenges include diversity of sequencing platform outputs and lack of standardized bioinformatics workflows for data analyses. We sequenced DNA from USDA-FSIS approved, non-pathogenic E. coli surrogates and a derivative group of rifampicin-resistant mutants (rif R ) via both Oxford Nanopore MinION and Illumina MiSeq platforms to generate and annotate complete genomes. Genome sequences from each clone were assembled separately so long-read, short-read, and combined sequence assemblies could be directly compared. The combined sequence data approach provides more accurate completed genomes. The genomes from these isolates were verified to lack functional key E. coli elements commonly associated with pathogenesis. Genetic alterations known to confer rif R were also identified. As the food industry adopts WGS within its food safety programs, these data provide completed genomes for commonly used surrogate strains, with a direct comparison of sequence platforms and assembly strategies relevant to research/testing workflows applicable for both processors and regulators. |
Author | Gill, Jason J Taylor, Thomas M Smith, Gary C Riggs, Penny K Konganti, Kranti Davis, Brian W Hillhouse, Andrew E Michalik, Jordyn Therrien, Dustin A Cross, H Russell |
AuthorAffiliation | 3 Department of Veterinary Integrated Biosciences, Texas A&M University, College Station, TX 77843-4461, USA; bdavis@cvm.tamu.edu 2 Texas A&M Institute for Genome Sciences and Society, MS 2470, College Station, TX 77843-2470, USA; k.kranti.neu@gmail.com (K.K.); hillhouse@tamu.edu (A.E.H.) 1 Department of Animal Science, Texas A&M University, College Station, TX 77843-2471, USA; therrienda@gmail.com (D.A.T.); jason.gill@tamu.edu (J.J.G.); jordyn.michalik@tamu.edu (J.M.); hrcross@tamu.edu (H.R.C.); gary.smith@tamu.edu (G.C.S.) |
AuthorAffiliation_xml | – name: 1 Department of Animal Science, Texas A&M University, College Station, TX 77843-2471, USA; therrienda@gmail.com (D.A.T.); jason.gill@tamu.edu (J.J.G.); jordyn.michalik@tamu.edu (J.M.); hrcross@tamu.edu (H.R.C.); gary.smith@tamu.edu (G.C.S.) – name: 3 Department of Veterinary Integrated Biosciences, Texas A&M University, College Station, TX 77843-4461, USA; bdavis@cvm.tamu.edu – name: 2 Texas A&M Institute for Genome Sciences and Society, MS 2470, College Station, TX 77843-2470, USA; k.kranti.neu@gmail.com (K.K.); hillhouse@tamu.edu (A.E.H.) |
Author_xml | – sequence: 1 givenname: Dustin A surname: Therrien fullname: Therrien, Dustin A organization: Department of Animal Science, Texas A&M University, College Station, TX 77843-2471, USA – sequence: 2 givenname: Kranti surname: Konganti fullname: Konganti, Kranti organization: Texas A&M Institute for Genome Sciences and Society, MS 2470, College Station, TX 77843-2470, USA – sequence: 3 givenname: Jason J orcidid: 0000-0002-9494-6053 surname: Gill fullname: Gill, Jason J organization: Department of Animal Science, Texas A&M University, College Station, TX 77843-2471, USA – sequence: 4 givenname: Brian W orcidid: 0000-0002-6121-135X surname: Davis fullname: Davis, Brian W organization: Department of Veterinary Integrated Biosciences, Texas A&M University, College Station, TX 77843-4461, USA – sequence: 5 givenname: Andrew E orcidid: 0000-0003-4874-7077 surname: Hillhouse fullname: Hillhouse, Andrew E organization: Texas A&M Institute for Genome Sciences and Society, MS 2470, College Station, TX 77843-2470, USA – sequence: 6 givenname: Jordyn surname: Michalik fullname: Michalik, Jordyn organization: Department of Animal Science, Texas A&M University, College Station, TX 77843-2471, USA – sequence: 7 givenname: H Russell surname: Cross fullname: Cross, H Russell organization: Department of Animal Science, Texas A&M University, College Station, TX 77843-2471, USA – sequence: 8 givenname: Gary C surname: Smith fullname: Smith, Gary C organization: Department of Animal Science, Texas A&M University, College Station, TX 77843-2471, USA – sequence: 9 givenname: Thomas M orcidid: 0000-0003-4191-5285 surname: Taylor fullname: Taylor, Thomas M organization: Department of Animal Science, Texas A&M University, College Station, TX 77843-2471, USA – sequence: 10 givenname: Penny K orcidid: 0000-0003-3296-320X surname: Riggs fullname: Riggs, Penny K organization: Department of Animal Science, Texas A&M University, College Station, TX 77843-2471, USA |
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CitedBy_id | crossref_primary_10_1093_fqsafe_fyac040 crossref_primary_10_3390_microorganisms10030619 crossref_primary_10_1111_1541_4337_13153 |
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Keywords | short reads long reads Escherichia coli bacterial surrogate whole genome sequence high throughput sequencing closed genome |
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SubjectTerms | Antibiotics bacterial surrogate Bioinformatics closed genome Deoxyribonucleic acid DNA Drug resistance E coli Escherichia coli Food industry Food processing industry Food safety Foodborne diseases Gene sequencing Genes Genomes Genomics Inspection long reads Nucleotide sequence Organisms Pathogenesis Pathogens Platforms Porosity Resistant mutant Rifampin Safety programs short reads Strains (organisms) Surveillance Virulence whole genome sequence Whole genome sequencing |
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Title | Complete Whole Genome Sequences of Escherichia coli Surrogate Strains and Comparison of Sequence Methods with Application to the Food Industry |
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