Spatial abundance patterns and recruitment of a virus‐affected commercial mollusc fishery

Infectious pathogens figure prominently among those factors threatening marine wildlife. Mass mortality events caused by pathogens can fundamentally alter the structure of wild fish stocks and depress recruitment rates and yield. In the most severe instances, this can precipitate stock collapses resulting in dramatic economic losses to once valuable commercial fisheries. An outbreak of a herpes‐like virus among commercially fished abalone populations in the south‐west fishery of Victoria, Australia, during 2006–2007, has been associated with high mortality rates among all cohorts. Long‐term records from fishery‐independent surveys of blacklip abalone Haliotis rubra (Leach) enabled abundance from pre‐ and post‐viral periods to be analysed to estimate stock density and biomass. The spatial distribution of abundance in relation to physical habitat variables derived from high‐resolution bathymetric LiDAR data was investigated. Significant differences were observed in both measures between pre‐ and post‐viral periods. Although there was some limited evidence of gradual stock improvement in recent years, disease‐affected reefs have remained below productivity rates prior to the disease outbreak suggesting a reduction in larval availability or settlement success. This was corroborated by trends in sublegal sized blacklip abalone abundance that has yet to show substantial recovery post‐disease. Abundance data were modelled as a function of habitat variables using a generalised additive model (GAM) and indicated that high abundance was associated with complex reef structures of coastal waters (<15 m). This study highlights the importance of long‐term surveys to understand abalone recovery following mass mortality and the links between stock abundance and seafloor variability.     

PSB菌剂在淡水养殖中的研究现状分析

PSB菌剂 (即光合细菌制剂 )是一种营养丰富的环保型饲料添加剂 ,具有可净化水质 ,防治鱼病 ,维持生态平衡 ,减少二次污染等优点 ,颇受养殖业者的欢迎。合理使用该菌剂 ,将在水产养殖中发挥巨大作用。     

Influence of high dietary α-tocopherol intakes on specific immune response, nonspecific resistance factors and disease resistance of healthy and aflatoxin B1-induced immunocompromised Indian major carp, Labeo rohita (Hamilton)

The effect of aflatoxin treatment and/or feeding of a high level of α‐tocopherol on immune response and disease resistance was investigated in Indian major carp, Labeo rohita. Group A served as a healthy control, group B was treated with aflatoxin, group C was fed a high level of α‐tocopherol whereas group D was exposed both to aflatoxin and a high level of dietary α‐tocopherol for 60 days. Aflatoxin B₁ (AFB₁) was injected once intraperitoneally into fish on the first day of the experiment (groups B & D). High levels of DL‐α‐tocopherol (1000 mg kg^–1 feed) were provided to healthy as well as AFB₁‐treated immunocompromised fish for 60 days (groups C & D). At the end of the experiment blood samples were assayed for changes in nonspecific immunity and humoral protein levels. Disease resistance against two common bacterial pathogens viz., Aeromonas hydrophila and Edwardsiella tarda were evaluated in all groups. Significant (P < 0.05) suppression of specific immunity as measured through haemagglutination (HA) titre against sheep red blood cells (SRBCs) as well as bacterial (formalin‐killed E. tarda) agglutination titre; nonspecific resistance factors viz., globulin level, serum bactericidal and lysozyme activities, neutrophil activities, and disease resistance against two bacterial pathogens only in aflatoxin‐treated fish with respect to the control group, clearly indicated the immunosuppressive nature of aflatoxin. Feeding of a high level of α‐tocopherol to AFB₁‐treated immunocompromised fish significantly (P < 0.05) raised specific immunity, nonspecific resistance factors and disease resistance capacity when compared with aflatoxin‐exposed fish. Disease resistance and enhancement of immune status through feeding of high levels of α‐tocopherol to healthy as well as AFB₁‐treated immunocompromised fish confirmed the potential of α‐tocopherol in carp feed for prevention of disease and for combating natural/environmental immunosuppressants.     

洗卵—对虾育苗防病新技术

对虾能苗中采取洗卵措施，可减少受精卵表面携带的病毒和细菌，减轻疾病的发生与传播，提高孵化率。洗卵操作简便，很易在生产中实施。     

虾类肌肉白浊病病原和病理的研究进展

本文针对虾类肌肉白浊病易感染的罗氏沼虾、凡纳滨对虾、中国对虾进行了分析。从病毒、细菌、寄生虫和环境因素方面,总结了近十几年来虾类肌肉白浊病的病原和病理特征。归纳了虾类肌肉白浊病的流行病学、检测方法及综合防治。     

Study on the distribution and expression of a DNA vaccine against lymphocystis disease virus in Japanese flounder (Paralichthys olivaceus)

The distribution and expression of lymphocystis disease virus (LCDV) vaccine, on the basis of DNA vaccine (pEGFP-N2-LCDV0.6 kb) construction, were analyzed in tissues of the Japanese flounder by PCR, RT-PCR and fluorescent microscopy. Results from PCR studies indicated that the vaccine-containing plasmids were distributed in injected muscle, muscle located opposite the injection site, hind intestine, gill, spleen, head kidney, liver and gonad 7 days after vaccination. However, these vaccine-containing plasmids disappeared by 90 days following vaccination. Fluorescent microscopy observations revealed that green fluorescence appeared in muscle, muscle located at the opposite side of the injection site, hind intestine, gill, spleen, head kidney and liver of fish 36 h after vaccination, and that green fluorescence did not appear in control tissue. The green fluorescence became weaker at 60 days post-vaccination, however, it remained detectable in the spleen 90 days post-vaccination. Results from RT-PCR studies indicated that the Mcp gene is expressed in all tissues of vaccinated fish 7-20 days after vaccination. These results demonstrate that the DNA vaccine is distributed and expressed in different tissues of vaccinated fish, and therefore, may have provided an antigen producing specific immune response.     

Replacement of fish meal in juvenile channel catfish,Ictalurus punctatus,diets using a yeast‐derived protein source: the effects on weight gain,food conversion ratio,body composition and survival of catfish challenged with Edwardsiella ictaluri

We examined the effects of a yeast‐derived protein source (NuPro^®) as a replacement for menhaden fish meal on weight gain, specific growth rate (SGR), food conversion ratio (FCR), whole‐body composition and disease resistance in juvenile channel catfish (9.9 ± 0.2 g fish^?1). NuPro^® replaced fish meal at six levels (0, 25, 50, 75, 100 and 125 g kg^?1 diet). Catfish were sampled for whole‐body composition and then challenged with the bacterium Edwardsiella ictaluri. Growth performance was negatively affected (P < 0.01) when NuPro^® was added at 125 g kg^?1 diet. The amount of whole‐body fat decreased (P < 0.05) when NuPro^® was added at 75 g kg^?1 or more of the diet. Regardless of the amount of NuPro^® added, survival after challenge with E. ictaluri was similar among treatments. Results indicate that up to 100 g kg^?1 of NuPro^® can be added without negatively affecting growth performance. The yeast‐derived protein source used in this study is a sustainable protein alternative that could be used as a partial replacement for fish meal in juvenile channel catfish diets.     

校园绿化病虫害生态防治探讨

以中国矿业大学南湖校区校园绿化病虫害发生情况为例,分析说明校园绿化病虫害的发生原因,提出以"生态防治"为主的理念,即以可持续发展为目标,通过加强校园绿化养护、绿地抚育管理,采取以物理防治和生物防治为主、化学防治为辅、多种措施相结合的综合防治措施,积极进行生态植保,逐步建立一个和谐、稳定、相对平衡的生态型校园。     

Beneficial effects of dietary exogenous protease on the growth,intestinal health and immunity of GIFT (Oreochromis niloticus) fed plant‐based diets

This study investigated the effects of dietary exogenous protease on the growth performance, intestinal health, immune parameters and disease resistance of genetically improved farmed tilapia (GIFT, Oreochromis niloticus). Five test diets with commercial protease at the levels of 0, 1.38, 2.76, 5.52 and 11.04 U/g (named PE0, PE1, PE2, PE5 and PE11, respectively) were administered to triplicate tanks with 30 fish for 60 days, and then, the fish were challenged with Streptococcus agalactiae for 14 days. The results indicated that weight gain increased as exogenous protease increased from 0 to 5.52 U protease/g diet and then decreased significantly (p < .05) with a further increase in exogenous protease supplementation (p < .05). The height of the villi in the proximal intestine and distal intestine, the width of the villi in three segments of the intestine, and the thickness of the muscle layer in the proximal intestine and mid‐intestine (p < .05) were increased in the fish fed the PE5 diet. Immune and antioxidant indices (except malondialdehyde), and survival after challenged with S. agalactiae were higher in fish fed PE5 diets than in those fed other diets (p < .05). In conclusion, 5.52 U/g protease supplementation in a plant‐based diet could promote the growth performance, intestinal physical barrier function, innate immunity and S. agalactiae resistance of GIFT.     

Non‐permissive C6/36 cell culture for the Australian isolate of Macrobrachium rosenbergii nodavirus

Macrobrachium rosenbergii nodavirus (MrNV) that causes white tail disease (WTD) is an emerging disease that contributes to serious production losses in Macrobrachium hatcheries worldwide. Mosquito cell lines (C6/36) have been reported to support the growth of MrNV and used to observe the cytopathic effects (CPE) in infected cells. This study determined the susceptibility of C6/36 mosquito cells to the Australian isolate of MrNV in order to use fewer animals in further investigations. Different staining methods were used to observe MrNV viral activity in C6/36 cells. Typical cytopathic effects such as vacuolation and viral inclusion bodies were observed in infected C6/36 cells with H&E and Giemsa staining. With acridine orange, it was easier to detect presumptive MrNV messenger ribonucleic acid in the infected cells. Using neutral red staining to measure mitochondrial activity showed light absorption of infected cells maximized at day 4 (O.D. = 0.6) but was significantly lower (chi‐square = 41.265, df = 1, P < 0.05) than control groups (O.D. = 2) which maximized at day 12. Using trypan blue staining to count the number of cells with disrupted cell membranes, the maximum number of presumptively dead cells at day 8 (4 × 10⁵ cells) in infected treatments was higher than the control treatment at day 10 (1.8 × 10⁵ cells). However, TaqMan real‐time PCR did not confirm the replication of MrNV in the cells over 14 days. The mean viral copies and mean cycle times of positive samples were stable at 2.07 × 10⁴ and 24.12, respectively. Limited evidence of viral replication was observed during four serial passages. This study determined the mortality of the C6/36 cell line to the Australian isolate of MrNV but suggests limited patent replication was occurring. Trying different cell lines or adapting the virus to the C6/36 cells may be necessary to successfully replicate Australian MrNV in cell lines.