不同地区白颖苔草在热胁迫下的生理反应

通过光照培养箱模拟北京地区的高温高湿环境,将来源于黄骅、顺义、丰镇、乌海、海淀5个地区的白颖苔草(Carex rigescens)进行热胁迫21d,以胁迫第1d的数据作为对照,每隔4d对相对电导率、叶绿素含量、丙二醛(MDA)含量、脯氨酸(Pro)含量、保护性酶及可溶性蛋白7个生理指标进行分析比较.结果表明:随着热胁迫时间的延长,与对照相比各材料的过氧化物酶(POD)活性、MDA含量、Pro含量均显著上升之后下降,相对电导率显著增加,可溶性蛋白含量无明显变化,超氧化物歧化酶(SOD)活性及叶绿素含量变化趋势各不一致.通过隶属函数法综合分析可知,不同地区的白颖苔草耐热性高低顺序为:黄骅＞乌海＞丰镇＞海淀＞顺义.     

Oral vaccination of brushtail possums (Trichosurus vulpecula) with BCG: immune responses,persistence of BCG in lymphoid organs and excretion in faeces

AIMS: To determine immune responses, and the localisation and persistence of Mycobacterium bovis bacille Calmette-Guérin (BCG) in gut-associated lymphoid tissues (GALT) and other organs in possums vaccinated orally with lipid-formulated BCG vaccine. To determine the duration of excretion and longevity of survival of BCG in the faeces of vaccinated animals.

METHODS: Possums (n=28) were vaccinated with lipid-formulated BCG (1 x 10 ⁸ colony forming units (cfu) of formulated BCG) by the oral route. Control possums (n=17) were fed oral bait pellets containing formulation medium only. Possums were sacrificed at 3 days and at 1, 3, 6 and 8 weeks after vaccination or ingestion of bait. Proliferation responses to bovine purified protein derivative (PPD) were measured in lymphocytes from blood and mesenteric lymph nodes (MLN) and samples of lung, spleen, liver, MLN and Peyer's patches (PP) were cultured for the presence of BCG. The number of BCG organisms excreted in faeces and the duration of excretion were determined in eight vaccinated possums and eight control possums over a 3-week period. In a separate experiment, a further six possums were vaccinated with oral BCG vaccine (5–10 x 10 ⁸ cfu BCG/possum) and their faeces collected over 48–72 h, for culture of BCG. The longevity of survival of BCG in these faeces was determined by storing faecal samples (n=12) under three different conditions: in an incubator (22.5°C), and conditions which simulated the forest floor and open pasture. A proportion (1–2 g) of these faecal samples was collected after storage for 1, 3, 5, 8 or 20 weeks, and cultured for BCG.

RESULTS: Possums vaccinated orally with BCG vaccine showed strong proliferation responses to bovine PPD in peripheral blood lymphocytes at 6–8 weeks post-vaccination (p.v.). Positive lymphocyte proliferation assay (LPA) responses to bovine PPD were first evident in MLN at 3 weeks p.v. BCG was cultured from MLN and PP in a proportion of animals at 3–8 weeks p.v. BCG was not cultured from sections of spleen, lung or liver at any time p.v. BCG was recovered in low to moderate numbers from the faeces of vaccinated possums for up to 7 days, and maximal numbers were cultured in faeces collected 48–72 h p.v. After storage for 1 week, BCG was cultured from all faecal samples placed in the incubator and from a proportion of faeces exposed to conditions similar to those on the forest floor and pasture. With the exception of one faecal sample stored under forest floor conditions which was culture-positive for BCG at 3 and 5 weeks, BCG was not cultured from any other faecal sample stored for more than 1 week.

CONCLUSIONS: Ingestion of oral BCG vaccine by possums was associated with the development of strong cell-mediated immunity in both blood and MLN. Following oral vaccination with BCG, the organisms were localised and persisted in GALT but did not spread to the spleen, liver or lungs. BCG was shed in low to moderate numbers in the faeces for up to 7 days p.v. The viability of BCG excreted in faeces decreased rapidly, particularly when faeces were exposed to an open pasture environment. Oral vaccination of possums with formulated BCG is unlikely to result in undue contamination of the environment with BCG.     

Bright artificial light at night is associated with increased body mass,poor reproductive success and compromised disease tolerance in Australian budgerigars (Melopsittacus undulatus)

Artificial light at night (ALAN) can cause circadian disruption and result in adverse behavioral and ecological effects in free‐living birds, but studies on captive pet birds as companion animals have been infrequent. We studied the effects of exposure to bright ALAN on body mass, melatonin sulfate levels, reproduction and disease severity in Australian budgerigars (Melopsittacus undulatus) kept in captivity. During the experiment, birds were kept under outdoor temperature, humidity and natural photoperiod from September to December. A total of 48 birds were equally split into 4 groups (6 mating pairs each) and concurrently exposed to ALAN of 200 lux with different duration (0, 30, 60 and 90 min). Monthly observations were recorded for all dependent parameters. ALAN exposure increased mass gain and suppressed melatonin levels in a dose‐dependent manner, especially during December. In addition, ALAN exposure in all duration groups decreased egg production and reduced hatchability from 61% ± 14% in the ALAN‐unexposed control group to 0% in the ALAN‐exposed birds. Disease severity was also found to increase in line with the duration of ALAN exposure. In captive M. undulatus, ALAN exposure was demonstrated to affect photoperiodic regulation with subsequent excess mass gain and reproduction impairment, and increased susceptibility to infections plausibly through duration dose‐dependent suppression of melatonin. To the best of our knowledge, this is the first study to demonstrate a possible association between acute bright ALAN of increasing duration and both natural development of infections as well as reproductive cessation in captive birds. Our findings could be used to improve breeding conditions of captive birds.     

Response of apple trees to boron fertilization under conditions of low soil boron availability

The aim of the study was to examine the effect of boron (B) fertilization on the vegetative and the reproductive responses of apple (Malus domestica Borkh.) trees grown at low soil B availability. The experiment was carried out in 2005 under a greenhouse on 5-year-old ‘Jonagold’ apple trees/M.9 EMLA planted singly in 50-L containers filled with a sandy loam soil with hot water-soluble B concentration of 0.32 mg kg⁻¹. The trees were fertilized with B as foliar or soil application. Foliar B sprays were applied at the stage of pink bud, beginning of flowering, petal fall, and 10 days after flowering, at a solution concentration of 0.03%. Soil B fertilization was done at the bud break stage at a rate of 2 g per tree (27 mg B kg⁻¹ soil). The trees untreated with B served as the control. The results showed that soil B fertilization improved root development and tree vigor. Leaves of trees supplied with B to the soil had higher B concentration and chlorophyll, net photosynthetic rate, stomatal conductance, and activity of catalase and glutathione reductase than those of the control plants. Boron fertilization, regardless of application mode, increased fruit yield; the efficiency of foliar B sprays was higher than soil B application. Apple fruits of trees fertilized with B to the soil were bigger, more colored, richer in B, and had higher soluble solids concentration, and titratable acidity compared to those of the control trees.     

LRRK2/NF-κB signaling modulates inflammatory responses in BCG-infected RAW264.7 macrophages

AIM: To investigate the biological function and potential mechanism of leucine-rich repeat kinase 2 (LRRK2) in RAW264.7 macrophages during Mycobacterium tuberculosis infection. METHODS: The bacillus Calmette-Guerin (BCG)-infected RAW264.7 cell model was established. Colony-forming unit (CFU) analysis was used to determine the mycobacterial viability. The releases of interleukin (IL)-1β, IL-6 and interferon-γ (IFN-γ) in the RAW264.7 cells were detected by ELISA. qPCR and Western blot were used to measure the mRNA and protein expression levels, respectively. RESULTS: LRRK2 was robustly enhanced in the RAW264.7 cells in response to BCG infection. Additionally, silencing of LRRK2 suppressed intracellular growth of mycobacteria during BCG challenge. Moreover, silencing of LRRK2 dramatically attenuated the accumulation of inflammatory cytokines IL-1β, IL-6 and IFN-γ induced by BCG infection. More importantly, LRRK2 modulated BCG-induced inflammatory responses by positively regulating the nuclear factor-κB (NF-κB) signaling pathway. CONCLUSION: LRRK2/NF-κB signaling pathway positively modulates inflammatory responses during BCG infection, which may provide a better understanding of the pathogenesis of tuberculosis and useful information for developing potential therapeutic interventions against the disease.     

高寒草场主要牧草对黄帚橐吾水浸液化感胁迫的生理响应

用不同浓度的黄帚橐吾叶水浸液处理高寒草场4种常见牧草中华羊茅、大雀麦、垂穗披碱草和早熟禾后,测定了受体植物叶片内超氧化物歧化酶、过氧化物酶和过氧化氢酶的活性,及丙二醛、可溶性糖和脯氨酸的含量以及相对电导率等生理指标,旨在探讨受试植物对黄帚橐吾化感作用的生理响应。结果显示,游离脯氨酸的变化在所有处理中均达到显著或极显著差异,且明显的依赖浓度,可能与降低渗透势,保证组织在化感物质胁迫引起水势下降时细胞膨压得以维持有关。其余指标变化不同,反应出不同受体植物对相同化感胁迫的生理响应是不同的。     

小地老虎雄蛾对性信息素的行为反应

为深入了解小地老虎性信息素通讯系统,利用风洞技术测定了小地老虎雄蛾对性信息素各组分及其不同组合的行为反应.结果表明,5种单一组分Z7-12:Ac(A)、Z9-14:Ac(B)、Z11-16:Ac(C)、Z5-10:Ac(D)、Z8-12:Ac(E)只能引起雄蛾兴奋,均不能引起雄蛾向性信息素源定向飞行;当性信息素释放源为二元混合物AB时,能引起15.71%的雄蛾完成从兴奋到搜索释放源,并表现出预交尾的完整行为反应;在同等使用剂量下,三元混合物ABC的引诱效果最好,有40.58%的雄蛾能搜索释放源,26.15%的雄蛾表现预交尾行为.三元混合物ABC在最佳比例(3:1:1)下,制成不同剂量的诱芯进行风洞试验,结果发现剂量为100μg时雄蛾反应最强烈,有29.87%的雄蛾表现预交尾行为,50μg次之,二者间差异不显著(P≥0.05).     

The effects of diet supplemented with Lactobacillus rhamnosus on tissue parameters of rainbow trout,Oncorhynchus mykiss (Walbaum)

This study was carried out to establish the effects of a 6 week treatment with the diet supplemented with L. rhamnosus in concentrations of 10⁷ CFU g^?1 (G1 group) and 10⁸ CFU g^?1 (G2 group) on the condition expressed by condition factors (Fulton's, Clark's and B), intestinal microbiology, haematological, histological and selected antioxidative parameters of rainbow trout. A significantly higher condition factors were found in G1 group indicating that higher concentration of probiotic (10⁸ CFU g^?1) did not result in the better condition. Cholesterol and urea levels were significantly higher in both G1 and G2 groups, albumin in G1 and creatinine in G2 group with respect to control. A significantly higher liver TBARS level was observed in G2 group. The feeding with supplemented probiont apparently changed the resident microbiota. Three weeks after withdrawal of the supplemented feed, the microflora mostly reverted to the control composition, although L. rhamnosus in faecal matter of fish remained inherent. The epithelial structure of the proximal and distal intestine revealed the increased absorptive area in both treated groups, as well as the increase in the mucin‐secreting goblet cells. The L. rhamnosus‐treated groups demonstrated the capacity for the augmentation of the innate host defence.     

Effects of dietary pyridoxine on disease resistance,immune responses and intestinal microflora in juvenile Jian carp (Cyprinus carpio var. Jian)

This experiment was conducted to evaluate the effects of dietary pyridoxine on disease resistance, immune responses and intestinal microflora of fish. A total of 1050 Jian carp (11.71 ± 0.05 g) were randomly distributed into seven groups, feeding diets containing graded levels of pyridoxine (0.2, 1.7, 3.2, 5.0, 6.3, 8.6 and 12.4 mg kg^?1 diet). After 80 days of feeding, a challenge trial was conducted by injection of Aeromonas hydrophila for 17 days. Results indicated that with increasing dietary pyridoxine concentration up to 5.0 mg kg^?1 diet, survival rate after challenge with A.hydrophila and phagocytic activity of leukocyte were improved (P < 0.05), and plateaued thereafter (P > 0.05). Red blood cell and white blood cell counts were lowest when fed the diet containing 1.7 mg pyridoxine kg^?1 diet. Haemagglutination titre, lysozyme activity, acid phosphatase activity, total iron‐binding capacity, antibody titre and immunoglobulin M content followed the similar pattern to that observed with survival rate. Aeromonas hydrophila, Escherichia coli and Lactobacillus counts in intestine were not affected by dietary pyridoxine concentration (P > 0.05). These results suggested that pyridoxine could enhance immune response of fish.