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Identification, virulence, and mass spectrometry of toxic ECP fractions of West Alabama isolates of Aeromonas hydrophila obtained from a 2010 disease outbreak

Author:
Pridgeon, Julia W., Klesius, Phillip H., Song, Lin, Zhang, Dunhua, Kojima, Kyoko, Mobley, James A.
Source:
Veterinary microbiology 2013 v.164 no.3-4 pp. 336
ISSN:
0378-1135
Subject:
Aeromonas hydrophila, Ictalurus punctatus, catfish, chromatography, disease outbreaks, elastase, fingerlings, gills, hemolysis, intraperitoneal injection, kidneys, marketing channels, mass spectrometry, nucleotide sequences, proteins, ribosomal RNA, toxicity, virulence, Alabama
Abstract:
In West Alabama, disease outbreaks in 2009 caused by Aeromonas hydrophila have led to an estimated loss of more than $3 million. In 2010, disease outbreak occurred again in West Alabama, causing losses of hundreds of thousands of pounds of market size channel catfish. During the 2010 disease outbreak in West Alabama, four isolates of A. hydrophila were cultured from the kidney tissues of diseased channel catfish. Both analytical profile index (API) 20 E biochemical tests and 16S–23S rRNA sequencing results confirmed the four isolates as A. hydrophila. Virulence studies revealed that the four isolates were highly virulent to channel catfish by intraperitoneal injection, with LD50 value of ∼1.3×105CFU/fish. Extracellular proteins (ECPs) of A. hydrophila are well known to be toxic to fish. Therefore, ECPs of the four 2010 West Alabama isolates of A. hydrophila were characterized in this study. The ECPs of the four 2010 isolates were found to be toxic to channel catfish fingerlings, with LD50 value of 16μg/fish. Thirty ECP fractions were obtained from the ECPs of the 2010 isolates of A. hydrophila by cation-exchange chromatography, of which nine fractions were found to be toxic to catfish gill cells and channel catfish fingerlings. Mass spectrometry identified 228 proteins from the nine toxic fractions, of which 23 were shared by toxic fractions, including well known virulence factors such as hemolysin, aerolysin, elastase (metalloprotease), nuclease, and 5′-nucleotidase. Hemolytic activity, protease activity, and nuclease activity of the four isolates were found to be significantly (P<0.05) higher than that of a reference A. hydrophila strain AL98-C1B. Our results might shed light on the possible virulence factors of the highly virulent West Alabama isolates of A. hydrophila.
Handle:
10113/56860