Abstract

Pathogen surveillance must be part of any population supplementation or reintroduction program for the conservation of threatened and endangered species. The unintended transmission of pathogens can have devastating effects on these already at-risk populations or the natural ecosystem at large. In the San Francisco Estuary (estuary), abundance of the endemic Delta Smelt (Hypomesus transpacificus) has declined to the point where regulatory managers are preparing to augment the wild population using fish propagated in a hatchery to prevent species extinction. Although disease is not an overt cause of population decline, comprehensive pathogen presence and prevalence data are lacking. Here, we performed a pilot study that applied molecular assays originally developed in salmonids to assess the presence of a wide variety of pathogens in the gill tissue of cultured and wild Delta Smelt—as well as cultured fish—deployed in enclosures in the estuary. We found the assays to be highly sensitive, and observed positive detections of a single pathogen, Ichthyophthirius multifiliis, in 13% of cultured Delta Smelt. We also detected ten other pathogens at very low levels in cultured, enclosure-deployed, and wild Delta Smelt that likely represent the ambient pathogen composition in the estuary (as opposed to actual infection). Our results corroborate previous work that cultured Delta Smelt do not appear to present a high risk for pathogen transmission during population supplementation or reintroduction. However, the molecular pathogen screening assays tested here have great utility as an early warning system indicator of when further diagnostic testing might be necessary to limit the extent and frequency of disease outbreaks; their utility will be further increased once they are customized for Delta Smelt.

Highlights

  • Pathogen screening is an integral component of any population supplementation or reintroduction program (Viggers et al 1993; Leighton 2002; Kock et al 2010)

  • All quantitative PCR (qPCR) efficiencies ranged between 80 and 120%, except for the Moritella viscosa assay from plate 1, which had a qPCR efficiency of 74.4% (Figure A1)

  • We report the results of the first effort to conduct pathogen screening of cultured and wild Delta Smelt using high-throughput qPCR and assays developed for salmonid pathogen screening by Miller at al. (2016)

Read more

Summary

Introduction

Pathogen screening is an integral component of any population supplementation or reintroduction program (Viggers et al 1993; Leighton 2002; Kock et al 2010). Before release into the wild, source individuals must be tested to confirm that they do not carry infectious pathogens which may be transmitted into naïve recipient populations or to other susceptible sympatric taxa. Released individuals may be vulnerable to pathogens in the wild environment; native populations and putative release sites should be screened to prevent population supplementation or reintroduction failure due to disease. Pathogen screening tests may not capture novel or emerging pathogens For these reasons, instances of disease in wild populations are often under-reported or may rely on anecdotal evidence (Naish et al 2007; Kock et al 2010), but with supplementation and reintroduction the potential for pathogen transmission to wild populations should not be underestimated

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call