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. 2024 Jul 23;58(29):13065-13075.
doi: 10.1021/acs.est.4c01358. Epub 2024 Jul 11.

Occurrence, Sources and Virulence Potential of Arcobacter butzleri in Urban Municipal Stormwater Systems

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Occurrence, Sources and Virulence Potential of Arcobacter butzleri in Urban Municipal Stormwater Systems

Liam R Carson et al. Environ Sci Technol. .

Abstract

A. butzleri is an underappreciated emerging global pathogen, despite growing evidence that it is a major contributor of diarrheal illness. Few studies have investigated the occurrence and public health risks that this organism possesses from waterborne exposure routes including through stormwater use. In this study, we assessed the prevalence, virulence potential, and primary sources of stormwater-isolated A. butzleri in fecally contaminated urban stormwater systems. Based on qPCR, A. butzleri was the most common enteric bacterial pathogen [25%] found in stormwater among a panel of pathogens surveyed, including Shiga-toxin producing Escherichia coli (STEC) [6%], Campylobacter spp. [4%], and Salmonella spp. [<1%]. Concentrations of the bacteria, based on qPCR amplification of the single copy gene hsp60, were as high as 6.2 log10 copies/100 mL, suggesting significant loading of this pathogen in some stormwater systems. Importantly, out of 73 unique stormwater culture isolates, 90% were positive for the putative virulence genes cadF, ciaB, tlyA, cjl349, pldA, and mviN, while 50-75% of isolates also possessed the virulence genes irgA, hecA, and hecB. Occurrence of A. butzleri was most often associated with the human fecal pollution marker HF183 in stormwater samples. These results suggest that A. butzleri may be an important bacterial pathogen in stormwater, warranting further study on the risks it represents to public health during stormwater use.

Keywords: Arcobacter; enteric bacterial pathogens; microbial contamination; stormwater; urban drainage; water pollution; water quality.

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Conflict of interest statement

The authors declare no competing financial interest.

Figures

Figure 1
Figure 1
Proportion of samples that were positive for each source tracking marker, out of a pool of samples positive for A. butzleri and also positive for at least one source-tracking marker (i.e., excluding all A. butzleri-negative and source tracking-negative samples [n = 86]). Note that MuBac was only tested in Calgary samples (n = 64).

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