Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Type of study
Language
Publication year range
1.
Viruses ; 13(8)2021 08 16.
Article in English | MEDLINE | ID: mdl-34452481

ABSTRACT

Scale drop disease virus (SDDV), an emerging piscine iridovirus prevalent in farmed Asian seabass Lates calcarifer in Southeast Asia, was firstly scientifically descripted in Singapore in 2015. Here, an SDDV isolate ZH-06/20 was isolated by inoculating filtered ascites from diseased juvenile yellowfin seabream into MFF-1 cell. Advanced cytopathic effects were observed 6 days post-inoculation. A transmission electron microscopy examination confirmed that numerous virion particles, about 140 nm in diameter, were observed in infected MFF-1 cell. ZH-06/20 was further purified and both whole genome and virion proteome were determined. The results showed that ZH-06/20 was composed of 131,122 bp with 135 putative viral proteins and 113 of them were further detected by virion proteome. Western blot analysis showed that no (or weak) cross-reaction was observed among several major viral proteins between ZH-06/20 and ISKNV-like megalocytivirus. An artificial challenge showed that ZH-06/20 could cause 100% death to juvenile yellowfin seabream. A typical sign was characterized by severe ascites, but not scale drop, which was considerably different from SDD syndrome in Asian seabass. Collectively, SDDV was confirmed, for the first time, as the causative agent of ascites diseases in farmed yellowfin seabream. Our study offers useful information to better understanding SDDV-associated diseases in farmed fish.


Subject(s)
DNA Virus Infections/veterinary , Fish Diseases/virology , Iridovirus/classification , Iridovirus/genetics , Sea Bream/virology , Animals , Ascites/pathology , China , Genome, Viral , Iridoviridae/genetics , Iridovirus/pathogenicity , Iridovirus/ultrastructure , Microscopy, Electron, Transmission , Phylogeny , Proteome , Viral Proteins/genetics , Virion/ultrastructure
2.
Article in English | MEDLINE | ID: mdl-31048018

ABSTRACT

Enrofloxacin (ENR) is the most commonly used antibiotic in crustacean farming in China. Diet supplementation with lactic acid (LA) may, however, affect the efficacy and safety of ENR-based drugs. The aims of this study were to investigate the effects of LA on drug residues and elimination of oral ENR in Chinese mitten crab (Eriocheir sinensis) and to determine ENR and gene expression levels of drug-metabolizing enzymes in the hepatopancreas. To this end, ENR was orally administered to the crabs at a dose of 10.0 mg kg-1 body weight on the eighth day after feeding diets supplemented with 0.3%LA. The results showed that ENR levels in the hepatopancreas were significantly different at 1 and 12 h between the ENR and ENR + 0.3% LA groups (P < 0.05). Lactic acid did not significantly affect the expression of CYP2A (phase I). However, the expressions of CYP3 (phase I) and GST (phase II) were significantly up-regulated by LA during the elimination process of ENR (6-24 h). At Tmax (1 h), the expression of phosphoenolpyruvate carboxykinase (PEPCK) was induced and expression of succinate dehydrogenase (SDH) was inhibited by LA. Both of these enzymes were significantly inhibited during the elimination process of ENR. The results suggest that LA contributes to the elimination of ENR, and thus, enhances hepatopancreas biotransformation and anti-injury capacity in E. sinensis.


Subject(s)
Brachyura/drug effects , Enrofloxacin/pharmacokinetics , Inactivation, Metabolic/drug effects , Lactic Acid/pharmacology , Administration, Oral , Animals , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/pharmacokinetics , Aquaculture , Aryl Hydrocarbon Hydroxylases/genetics , Aryl Hydrocarbon Hydroxylases/metabolism , Brachyura/enzymology , Cytochrome P450 Family 3/genetics , Cytochrome P450 Family 3/metabolism , Dietary Supplements , Energy Metabolism/drug effects , Energy Metabolism/genetics , Enrofloxacin/administration & dosage , Gene Expression Regulation/drug effects , Hepatopancreas/drug effects , Hepatopancreas/metabolism , Inactivation, Metabolic/genetics , Steroid Hydroxylases/genetics , Steroid Hydroxylases/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...