# Development, confirmation, and application of a seeded Escherichia coli process control organism to validate Salmonella enterica serovar Typhi environmental surveillance methods

**Authors:** Sarah E. Philo, Nicolette A. Zhou, Lorraine M. Lillis, Venkata Raghava, Dilip Abraham, Vinoth Kumar, Nirmal Kumar, Jonathan Rigby, Joanna Ciol Harrison, Christine S. Fagnant-Sperati, Alexandra L. Kossik, Angelo Q. W. Ong, Rachael Swanstrom, Elisabeth Burnor, Bethel Demeke, Nicola K. Beck, Jeffry H. Shirai, Stephen J. Libby, David S. Boyle, Nicholas Feasey, Gagandeep Kang, John Scott Meschke

PMC · DOI: 10.1371/journal.pone.0301624 · PLOS ONE · 2024-05-07

## TL;DR

Researchers developed a safe E. coli-based control organism to test and validate methods for detecting Typhoid-causing bacteria in water, especially in areas where the bacteria is rare.

## Contribution

A novel biosafe process control organism was created to validate S. Typhi environmental surveillance methods.

## Key findings

- The PCO mimics S. Typhi and was detected in 100% of replicates at 10 and 100 CFU/mL in lab experiments.
- The PCO was successfully detected in wastewater samples from Typhoid-endemic regions in India and Malawi.
- The PCO showed consistent quantification cycle values across different concentration methods.

## Abstract

Salmonella enterica serovar Typhi (S. Typhi) is the causative agent of Typhoid fever. Blood culture is the gold standard for clinical diagnosis, but this is often difficult to employ in resource limited settings. Environmental surveillance of waste-impacted waters is a promising supplement to clinical surveillance, however validating methods is challenging in regions where S. Typhi concentrations are low. To evaluate existing S. Typhi environmental surveillance methods, a novel process control organism (PCO) was created as a biosafe surrogate. Using a previous described qPCR assay, a modified PCR amplicon for the staG gene was cloned into E. coli. We developed a target region that was recognized by the Typhoid primers in addition to a non-coding internal probe sequence. A multiplex qPCR reaction was developed that differentiates between the typhoid and control targets, with no cross-reactivity or inhibition of the two probes. The PCO was shown to mimic S. Typhi in lab-based experiments with concentration methods using primary wastewater: filter cartridge, recirculating Moore swabs, membrane filtration, and differential centrifugation. Across all methods, the PCO seeded at 10 CFU/mL and 100 CFU/mL was detected in 100% of replicates. The PCO is detected at similar quantification cycle (Cq) values across all methods at 10 CFU/mL (Average = 32.4, STDEV = 1.62). The PCO was also seeded into wastewater at collection sites in Vellore (India) and Blantyre (Malawi) where S. Typhi is endemic. All methods tested in both countries were positive for the seeded PCO. The PCO is an effective way to validate performance of environmental surveillance methods targeting S. Typhi in surface water.

## Linked entities

- **Genes:** stag (small t antigen) [NCBI Gene 6373585]
- **Diseases:** Typhoid fever (MONDO:0005619)
- **Species:** Escherichia coli (taxon 562), Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** Typhoid (MESH:D014435)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Salmonella enterica subsp. enterica serovar Typhi (no rank) [taxon 90370]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11075847/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC11075847/full.md

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Source: https://tomesphere.com/paper/PMC11075847