The morphological and cytochemical studies of peripheral blood cells of Schizothorax prenanti were studied by light and electron microscopy. Erythrocytes, thrombocytes and three types of leucocytes, lymphocytes, neutrophils and monocytes, were distinguished and characterized. In addition to mature erythrocytes, immature and dividing erythrocytes were observed. A few organelles such as mitochondria were distributed in the cytoplasm of erythrocytes. Lymphocytes with heavily clumped heterochromatic nucleus and minimal cytoplasm were classified into small and large lymphocytes. Three different populations of granules, with distinctive ultrastructural aspect, were observed in neutrophils. Monocytes were the fewest leucocytes possessing rich organelles, phagocytized materials and vacuoles. Thrombocytes with various types were the most abundant blood cells among leucocytes and contained a prominent nucleus with dense bands of heterochromatin and many cytoplasmic vacuoles. Periodic acid-Schiff staining was positive in neutrophils, monocytes, lymphocytes and thrombocytes, but not in erythrocytes. Peroxidase-positive staining was observed in neutrophils and monocytes, but not in erythrocytes, lymphocytes and thrombocytes. Only neutrophils were positive for oil red O. Except for erythrocytes, the other blood cells stained positively for acid phosphatase. Only neutrophils and monocytes were positive for α-naphthyl acetate esterase. None of the cells studied were positive for alkaline phosphatase. The morphologic and cytochemical features of blood cells of S. prenanti are similar to those of other fish. This investigation may be helpful as a tool to monitor the health status of cultured S. prenanti and will grant early detection of clinical pathology.

Aberrant autophagy is a major risk factor for inflammatory diseases and cancer. However, the genetic basis and underlying mechanisms are less established. UVRAG is a tumor suppressor candidate involved in autophagy, which is truncated in cancers by a frameshift (FS) mutation and expressed as a shortened UVRAGFS. To investigate the role of UVRAGFS in vivo, we generated mutant mice that inducibly express UVRAGFS (iUVRAGFS). These mice are normal in basal autophagy but deficient in starvation- and LPS-induced autophagy by disruption of the UVRAG-autophagy complex. iUVRAGFS mice display increased inflammatory response in sepsis, intestinal colitis, and colitis-associated cancer development through NLRP3-inflammasome hyperactivation. Moreover, iUVRAGFS mice show enhanced spontaneous tumorigenesis related to age-related autophagy suppression, resultant β-catenin stabilization, and centrosome amplification. Thus, UVRAG is a crucial autophagy regulator in vivo, and autophagy promotion may help prevent/treat inflammatory disease and cancer in susceptible individuals.

The objective of the study was to obtain baseline data on haematological parameters, blood cell sizes and morphology in cultured male and female Gymnocypris eckloni Herzenstein, 1891. Forty-eight healthy 3-year-old G. eckloni (26 males: 525.79 AE 48.56 g weight, 34.51 AE 1.88 cm total length; 22 females: 507.60 AE 54.48 g weight, 33.97 AE 1.84 cm total length) were used for this study. Both male and female gonadal maturity were at stage III (maturing). The fish were reared in 25-36 m 2 outdoor tanks at dissolved oxygen 6.86 AE 0.48 mg L À1 , pH 7.22 AE 0.58, temperature 12.40 AE 0.94°C and stocking density 50-80 fish m À3 during November 2014. The fish were fed commercial carp floating foods containing 35% crude protein three times daily. Haematological values were performed manually on heparin anticoagulated blood specimens using standard methods. The morphological features of blood cells and differential cell counts were done on WrightGiemsa stained blood smears with no anticoagulants. Erythrocytes, leucocytes (neutrophils, eosinophils, lymphocytes and monocytes) and thrombocytes were distinguished and characterized under light microscope. The percentage of the different leukocytes revealed predominance of small lymphocytes (male: 62.31 AE 2.06%; female: 63.00 AE 2.25%) and nurophiles (male: 23.85 AE 1.51%; female: 23.49 AE 1.67%) followed by fewer monocytes (male: 4.81 AE 0.68%; female: 4.80 AE 0.77%) and few eosinophils (male: 3.73 AE 0.82%; female: 3.52 AE 0.67%). The nurophile percentages of each stage showed that metamyelocyte accounted for the most (male: 13.29 AE 0.88%; female: 13.07 AE 0.98%), followed by banded ones (male: 7.18 AE 0.49%; female: 7.00 AE 0.58%). The microstructure of G. eckloni blood cells was similar to that of other fish. Sex-dependent differences for the erythrocyte counts, haemoglobin, haematocrit and mean corpuscular haemoglobin were found (P < 0.05 or P < 0.01); while differences in other haematological parameters (P > 0.05) and blood cell morphology between male and female fish were not significant. Hematologic parameters and knowledge of morphological characteristics of male and female G. eckloni blood cells could be utilized to evaluate the health status of this species in captivity.

Although many studies have confirmed that antimicrobial peptides (AMPs: PBD-mI and LUC-n) can be used as feed additives, there are few reports of their use in ruminants. The present study aimed to investigate the impact of AMPs on ameliorating rumen fermentation function and rumen microorganisms in goats. Eighteen 4-month-old Chuanzhong black goats were used in a 60-day experiment (6 goats per group). Group I was used as the control and was fed a basal diet, the group II were fed the basal diet supplemented with 2 g of AMPs [per goat/day] and group III were fed the basal diet supplemented 3 g of AMPs [per goat/day], respectively. Rumen fluid samples were collected at 0, 20 and 60 days. Bacterial 16S rRNA genes and ciliate protozoal 18S rRNA genes were amplified by PCR from DNA extracted from rumen samples. The amplicons were sequenced by Illumina MiSeq. Rumen fermentation parameters and digestive enzyme activities were also examined. Our results showed that dietary supplementation with AMPs increased the levels of the bacterial genera Fibrobacter , Anaerovibrio and Succiniclasticum and also increased the ciliates genus Ophryoscolex , but reduced the levels of the bacterial genera Selenomonas , Succinivibrio and Treponema , and the ciliate genera Polyplastron , Entodinium , Enoploplastron and Isotricha . Supplementation with AMPs increased the activities of xylanase, pectinase and lipase in the rumen, and also increased the concentrations of acetic acid, propionic acid and total volatile fatty acids. These changes were associated with improved growth performance in the goats. The results revealed that the goats fed AMPs showed improved rumen microbiota structures, altered ruminal fermentation, and improved efficiency regarding the utilization of feed; thereby indicating that AMPs can improve growth performance. AMPs are therefore suitable as feed additives in juvenile goats.

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