To assess the dietary arginine requirement of Monopterus albus (21 ± 0.03 g), we compared six diets containing different arginine levels (2.03%, 2.58%, 3.16%, 3.63%, 4.24%, and 4.88%). The results revealed that dietary arginine content had a significant effect on weight gain (WG), specific growth rate (SGR), IL-1β, IL-10, lysozyme, and complement C3 activity in Monopterus albus ( ). The WG and SGR increased with increasing dietary arginine levels, and the regression analysis found that the optimum dietary arginine level for growth of rice field eel was 4.28–4.35% of the dry diet. However, the C3 and LZM activities peaked in the 2.58% arginine diet group ( ). The dietary arginine level had no significant effect on the viscerosomatic index, hepatosomatic index, condition factor, survival rate, nitric oxide, total nitric oxide synthase, insulin, growth hormone, trypsin, lipase, or amylase activities ( ). Arginine can significantly promote Monopterus albus growth; however, the immunity of Monopterus albus decreases as the arginine level exceeds 2.58%. A comprehensive assessment of growth and immunity recommends the optimum arginine level for Monopterus albus was 3.16–3.63% of the dry diet, corresponding to 6.58–7.70% of the dietary protein.

A pathogenic bacterium strain, LBK2, was isolated from giant spiny frog (Quasipaa spinosa) tadpoles infected with perforation disease in this study. Pathogenic strain LBK2, a Gram-negative bacterium with a certain degree of infectivity, was demonstrated to cause anorexia, lethargy, epidermal necrosis, and abdominal perforation in tadpoles in artificial infection experiments. The identification results of 16S rDNA gene sequencing showed that pathogenic strain LBK2 was identified as Pseudomonas sp. Virulence gene identification displayed that strain LBK2 carried three virulence genes: aer, epr, and fla. Finally, the antibiotic susceptibility testing of 11 antibiotics suggested that strain LBK2 was highly sensitive to nine antibiotics, including chloramphenicol, enrofloxacin, and rifampicin, but was resistant to erythromycin, sulfamethoxazole/trimethoprim, and low-concentration trichloroisocyanuric acid. This study determined the pathogenicity of Pseudomonas sp. to giant spiny frog tadpoles based on histopathological analysis and virulence factor carriage, and the drug susceptibility testing further provided a scientific basis for the selection of drugs in the prevention and treatment of abdominal perforation disease in giant spiny frog tadpoles.