Redefining piscine lactococcosis

Author:

Heckman Taylor I.1ORCID,Yazdi Zeinab1,Older Caitlin E.2,Griffin Matt J.3ORCID,Waldbieser Geoffrey C.2,Chow Alexander M.1,Medina Silva Isabella1,Anenson Kelsey M.1,García Julio C.4,LaFrentz Benjamin R.4ORCID,Slavic Durda5,Toohey-Kurth Kathy L.6,Yant Paula6,Fritz Heather M.6,Henderson Eileen E.6,McDowall Rebeccah5,Cai Hugh5,Adkison Mark7,Soto Esteban1ORCID

Affiliation:

1. Department of Medicine & Epidemiology, School of Veterinary Medicine, University of California, Davis, California, USA

2. USDA-ARS, Warmwater Aquaculture Research Unit, Stoneville, Mississippi, USA

3. College of Veterinary Medicine, Mississippi State University, Stoneville, Mississippi, USA

4. USDA-ARS, Aquatic Animal Health Research Unit, Auburn, Alabama, USA

5. Animal Health Laboratory, University of Guelph, Ontario, Canada

6. California Animal Health and Food Safety Laboratory, University of California, Davis, California, USA

7. California Department of Fish and Wildlife, Rancho Cordova, California, USA

Abstract

ABSTRACT Piscine lactococcosis is a significant threat to cultured and wild fish populations worldwide. The disease typically presents as a per-acute to acute hemorrhagic septicemia causing high morbidity and mortality, recalcitrant to antimicrobial treatment or management interventions. Historically, the disease was attributed to the gram-positive pathogen Lactococcus garvieae . However, recent work has revealed three distinct lactococcosis-causing bacteria (LCB)— L. garvieae, L. petauri, and L. formosensis— which are phenotypically and genetically similar, leading to widespread misidentification. An update on our understanding of lactococcosis and improved methods for identification are urgently needed. To this end, we used representative isolates from each of the three LCB species to compare currently available and recently developed molecular and phenotypic typing assays, including whole-genome sequencing (WGS), end-point and quantitative PCR (qPCR) assays, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), API 20 Strep and Biolog systems, fatty acid methyl ester analysis (FAME), and Sensititre antimicrobial profiling. Apart from WGS, sequencing of the gyrB gene was the only method capable of consistent and accurate identification to the species and strain level. A qPCR assay based on a putative glycosyltransferase gene was also able to distinguish L. petauri from L. garvieae/formosensis . Biochemical tests and MALDI-TOF MS showed some species-specific patterns in sugar and fatty acid metabolism or protein profiles but should be complemented by additional analyses. The LCB demonstrated overlap in host and geographic range, but there were relevant differences in host specificity, regional prevalence, and antimicrobial susceptibility impacting disease treatment and prevention. IMPORTANCE Lactococcosis affects a broad range of host species, including fish from cold, temperate, and warm freshwater or marine environments, as well as several terrestrial animals, including humans. As such, lactococcosis is a disease of concern for animal and ecosystem health. The disease is endemic in European and Asian aquaculture but is rapidly encroaching on ecologically and economically important fish populations across the Americas. Piscine lactococcosis is difficult to manage, with issues of vaccine escape, ineffective antimicrobial treatment, and the development of carrier fish or biofilms leading to recurrent outbreaks. Our understanding of the disease is also widely outdated. The accepted etiologic agent of lactococcosis is Lactococcus garvieae . However, historical misidentification has masked contributions from two additional species, L. petauri and L. formosensis , which are indistinguishable from L. garvieae by common diagnostic methods. This work is the first comprehensive characterization of all three agents and provides direct recommendations for species-specific diagnosis and management.

Funder

CNRA | California Department of Fish and Wildlife

Publisher

American Society for Microbiology

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