Journal
AQUACULTURE REPORTS
Volume 33, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.aqrep.2023.101813
Keywords
Aptamer; Affinity constant; Temperature-sensitive site; Binding protein; Secondary structure; Conditional pathogenicity
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In this study, five aptamers with high affinities for temperature-sensitive Pseudomonas plecoglossicida were selected using SELEX. The binding proteins of these aptamers were identified as ribosomal proteins. The findings provide insights into the temperature-sensitive pathogenic mechanism of P. plecoglossicida in P. crocea.
Pseudomonas plecoglossicida can infect Pseudosciaena crocea and cause visceral white spot disease, resulting in substantial economic losses to the P. crocea industry. Pseudomonas plecoglossicida is a temperate-sensitive bacterium and only infects P. crocea below 22 degree celsius. Aptamers are oligonucleotide molecules selected by the systematic evolution of ligands by exponential enrichment (SELEX) and can identify all kinds of targets. In the present study, five aptamers (M17, M19, M48, M56 and M81) for P. plecoglossicida cultured at 18 degree celsius were selected by SELEX and based on comparative analysis of the high frequency sequences. The five aptamers had significantly higher affinities for the pathogenic P. plecoglossicida at 18 degree celsius than for the nonpathogenic P. plecoglossicida at 28 degree celsius and the other six bacteria (Escherichia coli, Edwardsiella tarda, Aeromonas hydrophila, Vibiro harveryi, Vibiro alginolyticus, Pseudomonas aeruginosa) (P < 0.01). The affinity constants (K-d) and maximum affinity (A(m)) of these aptamers for P. plecoglossicida were determined, with K-d values of M17 (23.35 +/- 6.40), M19 (66.37 +/- 14.73), M48 (105.91 +/- 21.41), M56 (31.16 +/- 5.03) and M81 (52.63 +/- 13.82) nmol/L and with A(m) values of M17 (1041.26 +/- 57.08), M19 (2291.76 +/- 171.96), M48 (1258.51 +/- 21.41), M56 (1307.70 +/- 54.01) and M81 (543.27 +/- 44.16) nmol/L, respectively. The secondary structures of the aptamers were analyzed, and the aptamer binding proteins of the pathogenic P. plecoglossicida were isolated by magnetic separation and purified by polyacrylamide gel electrophoresis. Mass spectrometry revealed ribosomal proteins to be the main aptamer binding proteins. The secondary and tertiary structures and subcellular localization of these aptamer binding proteins were also studied and analyzed. These findings provide a foundation for the temperature-sensitive pathogenic mechanism of P. plecoglossicida in P. crocea. This is the first report on aptamers that recognize temperature-sensitive sites in P. plecoglossicida.
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