2018
DOI: 10.1016/j.fsi.2017.10.043
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Oral immunization with recombinant Lactobacillus casei expressing OmpAI confers protection against Aeromonas veronii challenge in common carp, Cyprinus carpio

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Cited by 59 publications
(45 citation statements)
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“…Recent reports of infection in diverse aquatic species have prompted investigation into the bacterial pathogenesis in humans, animals, and fish [24,25]. Previously, research has shown that isolates could infect fish in the laboratory [26]. We investigated the burden of A. veronii infection in commercially available fish, including Carassius auratus, Cyprinus carpio, Ctenopharyngodon idella, and Silurus asotus.…”
Section: Discussionmentioning
confidence: 99%
“…Recent reports of infection in diverse aquatic species have prompted investigation into the bacterial pathogenesis in humans, animals, and fish [24,25]. Previously, research has shown that isolates could infect fish in the laboratory [26]. We investigated the burden of A. veronii infection in commercially available fish, including Carassius auratus, Cyprinus carpio, Ctenopharyngodon idella, and Silurus asotus.…”
Section: Discussionmentioning
confidence: 99%
“…2019). Similarly, Zhang et al (2018) generated two recombinant Lactobacillus casei (surface‐displayed or secretory) expressing the OmpAI of A. veronii . The recombinant L. casei strains were directly delivered and could survive throughout the intestinal tract, and treated common carp showed an effective immune response and obtained 66.7% survival rate (Zhang et al .…”
Section: Application In Aquaculturementioning
confidence: 99%
“…Lactobacillus casei CC16 was isolated from the intestine of common carp, and grown in De Man, Rogosa and Sharpe (MRS) medium (Thermo Fisher Scientific, Oxoid, UK) at 30 • C without shaking. The Escherichia coli-Lactobacillus shuttle vector pPG-1 and pPG-2 have been described in our previous study [44]. The competent cells, Escherichia coli MC1061, were grown in Luria-Bertani (LB) medium for cloning of the plasmids at 37 • C with shaking.…”
Section: Bacterial Strains Plasmids and Growth Conditionsmentioning
confidence: 99%
“…Xylose was added to the culture medium to a final concentration of 10 g/L to induce antigen expression. After induction at 30 • C for 10 h, bacterial cells or supernate (a 10-fold concentration) were examined by SDS-PAGE and transferred to nitrocellulose membrane as in our previous study [44].…”
Section: Western Blotting Assaymentioning
confidence: 99%