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Francisella Marina Sp. Nov., Etiologic Agent of Systemic Disease in Cultured Spotted Rose Snapper (Lutjanus Guttatus) in Central America

Abstract

Historically, piscine francisellosis in various warm-, temperate-, and cold-water fish hosts has been attributed to From 2015 to 2016, an undescribed sp. was recovered during mortality events in cultured spotted rose snapper () off the Pacific coast of Central America. Despite high mortality and emaciation, limited gross findings were observed in affected fish. Histological examination revealed multifocal granulomatous lesions, with the presence of numerous small, pleomorphic coccobacilli, predominantly in the peritoneum, spleen, kidneys, liver, pancreas, heart, and intestine. Sequencing of an ∼1,400-bp fragment of the 16S rRNA gene demonstrated these isolates to be most similar (99.9% identity) to sp. isolate TX077308 cultured from seawater in the Gulf of Mexico, while sharing <99% similarity to other spp. Biochemical analysis, multilocus sequence comparisons of select housekeeping genes, repetitive extragenic palindromic PCR fingerprinting, matrix-assisted laser desorption ionization-time of flight mass spectrometry, and fatty acid methyl ester analysis revealed marked differences between these isolates and other described members of the genus. Koch's postulates were fulfilled by experimental intracoelomic injection and immersion trials using Nile () and blue () tilapia. Based on observed phenotypic and genotypic differences from recognized spp., the name sp. nov. (NRRL B-65518) is proposed to accommodate these novel strains. Finfish aquaculture is the fastest growing global food production sector. Infectious disease, particularly emergent pathogens, pose a significant threat to established and nascent aquaculture industries worldwide. Herein, we characterize a novel pathogen isolated from mortality events in cultured spotted rose snapper in Central America. The bacteria recovered from these outbreaks were genetically and phenotypically dissimilar from other known spp. from fish, representing a previously unrecognized member of the genus , for which the name sp. nov. is proposed.

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References
1.
Dahllof I, Baillie H, Kjelleberg S . rpoB-based microbial community analysis avoids limitations inherent in 16S rRNA gene intraspecies heterogeneity. Appl Environ Microbiol. 2000; 66(8):3376-80. PMC: 92158. DOI: 10.1128/AEM.66.8.3376-3380.2000. View

2.
Colquhoun D, Duodu S . Francisella infections in farmed and wild aquatic organisms. Vet Res. 2011; 42:47. PMC: 3060124. DOI: 10.1186/1297-9716-42-47. View

3.
Vojtech L, Sanders G, Conway C, Ostland V, Hansen J . Host immune response and acute disease in a zebrafish model of Francisella pathogenesis. Infect Immun. 2008; 77(2):914-25. PMC: 2632049. DOI: 10.1128/IAI.01201-08. View

4.
Kearse M, Moir R, Wilson A, Stones-Havas S, Cheung M, Sturrock S . Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics. 2012; 28(12):1647-9. PMC: 3371832. DOI: 10.1093/bioinformatics/bts199. View

5.
Reichley S, Ware C, Steadman J, Gaunt P, Garcia J, LaFrentz B . Comparative Phenotypic and Genotypic Analysis of Edwardsiella Isolates from Different Hosts and Geographic Origins, with Emphasis on Isolates Formerly Classified as E. tarda, and Evaluation of Diagnostic Methods. J Clin Microbiol. 2017; 55(12):3466-3491. PMC: 5703813. DOI: 10.1128/JCM.00970-17. View