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Cost of whole genome sequencing for nontyphoidal Salmonella enterica

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Authors

Ford, Laura
Glass, Kathryn
Williamson, Deborah
Sintchenko, Vitali
Robson, Jennifer
Lancsar, Emily
Stafford, Russell
Kirk, Martyn

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Public Library of Science

Abstract

Background While whole genome sequencing (WGS) may be more expensive than traditional testing and polymerase chain reaction (PCR), simple cost comparisons ignore the potential for WGS to reduce the societal costs of non-typhoidal Salmonella enterica through public health action to prevent illness. Methods We determined how many cases the use of WGS data would need to prevent to be costequal to serotyping and MLVA, or culture independent testing based on PCR in Australia. We then examined the costs and cost-savings of current typing methods compared with WGS in outbreak scenarios. Results A median of 275 (90% CrI-55-775) or 1.9% (90% CrI-0.4%-5.4%) of notified serotyped Salmonella cases would need to be prevented for WGS to be cost-equal to current typing methods and 1,550 (90% CrI 820-2,725) or 9.6% of all notified Salmonella cases would need to be prevented to be cost-equal to PCR. WGS is likely to result in cost savings in prolonged outbreaks, where data can support earlier public health action. Conclusions Despite currently having a higher cost per isolate, routine WGS of Salmonella was no more expensive than existing typing methods or PCR where >2% of illness was averted.

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PLOS ONE (Public Library of Science)

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Open Access

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Creative Commons Attribution License

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