Complete Genome Sequence of an H9N2 Avian Influenza Virus Isolated from Egret in Lake Dongting Wetland

We isolated a recombinant H9N2 avian influenza virus (AIV) from fresh egret feces in the Ardeidae protection region of the Dongting Lake wetland area in China, and it was designated A/Egret/Hunan/1/2012(H9N2). This is the first report of isolating H9N2 AIV from wild birds in the Dongting Lake wetland. Its eight gene segments are generated by reassortment of gene segments of different AIV subtypes. These results are helpful for understanding the epidemiology and evolution of AIV in wild birds during migration.     

基于价值评估的黄山市生境质量时空演变特征分析

评价与分析特定区域的生境质量及其时空变化对其生态安全格局构建、可持续发展意义重大。本文以典型旅游城市黄山市为研究区，综合生态系统服务价值评价模型、基于NPP与NDVI的生境质量指数评价、InVEST生境质量评价模型、空间分析等模型与方法对黄山市1987-2017年生境质量进行研究。结果表明：（1）1987-2007年，黄山市生境质量总值持续下降，2017出现回升，但生境受到的威胁仍增加，生境最优区为北部太平湖区域，生境质量低值主要分布在各县区主城区；生境质量栅格等级变化以4等级转变为3等级为主。（2）1987-2017年，黄山市105个乡镇（街道）中有84个乡镇（街道）生境质量有所下降，主要分布在东部区域；北部环太平湖区域的乡镇为生境质量"高高"型聚集区及热点区域，屯溪区、徽州区南部、歙县、休宁县主城区的各镇为生境质量"低低"型聚集区及冷点区域。（3）黄山市城市发展对生境质量影响较大，大体上距离城市中心点越近的圈层，生境质量越差；距离黄山市旅游中心点10-20、30-40、40-50 km的3个圈层形成生境质量低值点，为旅游与城区互助发展的结果；黄山市旅游与生境质量空间分布相关性较强，旅游设施、景区核密度越高，低等级生境质量占比越高。     

中国环境规制对旅游业碳排放强度影响的空间异质性

环境规制作为实现旅游低碳发展的重要动力之一,也是实现旅游业“碳达峰、碳中和”目标的有效路径。基于综合指数法和“自下而上”法,测度2005—2019年中国大陆30个省份(中国港澳台及西藏统计数据尚缺)的环境规制水平和旅游业碳排放强度,并借助面板回归模型和面板门槛模型探讨了环境规制对旅游业碳排放强度的影响及其区域异质性。结果表明：(1)研究期内,中国整体旅游业碳排放强度呈下降趋势;其中,中部地区下降趋势最为明显,其次分别为西部、东部和东北地区。(2)中国环境规制水平呈增长态势,其规制效应对胡焕庸线右侧的地区更为显著,并呈现出自东向西递减的梯度分布特征。(3)中国环境规制对旅游业碳排放强度存在明显的“倒逼减排”效应,但东北地区却存在一定的“绿色悖论”现象;环境规制对旅游业碳排放强度的影响存在单一阈值,当旅游能源强度小于阈值时,存在显著的“倒逼减排”效应,当旅游能源强度超过阈值时则存在“绿色悖论”效应。(4)东部地区环境规制未通过门槛效应检验;中部地区存在单个门槛值,环境规制有效促进旅游业碳排放强度的下降,不存在“绿色悖论”现象;西部和东北地区分别存在单、双门槛效应,环境规制对旅游业碳排放强度...     

Comprehensive in-silico analysis of deleterious SNPs in APOC2 and APOA5 and their differential expression in cancer and cardiovascular diseases conditions

Genetic variations in APOC2 and APOA5 genes involve activating lipoprotein lipase (LPL), responsible for the hydrolysis of triglycerides (TG) in blood and whose impaired functions affect the TG metabolism and are associated with metabolic diseases. In this study, we investigate the biological significance of genetic variations at the DNA sequence and structural level using various computational tools. Subsequently, 8 (APOC2) and 17 (APOA5) non-synonymous SNPs (nsSNPs) were identified as high-confidence deleterious SNPs based on the effects of the mutations on protein conservation, stability, and solvent accessibility. Furthermore, based on our docking results, the interaction of native and mutant forms of the corresponding proteins with LPL depicts differences in root mean square deviation (RMSD), and binding affinities suggest that these mutations may affect their function. Furthermore, in vivo, and in vitro studies have shown that differential expression of these genes in disease conditions due to the influence of nsSNPs abundance may be associated with promoting the development of cancer and cardiovascular diseases. Preliminary screening using computational methods can be a helpful start in understanding the effects of mutations in APOC2 and APOA5 on lipid metabolism; however, further wet-lab experiments would further strengthen the conclusions drawn from the computational study.     

湖南郴州发现岭南两头蛇

2022年8月,于湖南省郴州市永兴县湘阴渡镇（113°01′18′′E,26°11′87′′N,海拔174 m）采集到两头蛇活体标本1号,通过形态测量比较,发现所采集标本与中国广东省分布的岭南两头蛇（Calamariaarcana）形态特征基本一致;后基于线粒体Cytb基因片段进行分子系统发育分析,结果显示该标本与岭南两头蛇形成高支持率单系群（后验概率PP为1.00,自举值BS为100）,所采集标本与岭南两头蛇的遗传距离为1%。综合形态学和分子生物学证据,最终确定该标本为两头蛇科（Calamariidae）两头蛇属的岭南两头蛇,系湖南省蛇类分布新记录种。     

有机磷农药对土壤动物群落结构的影响研究

本文研究了有机磷农药废水灌溉对土壤动物群落结构的影响,并探讨了影响机理,结果表明,土壤动物种类和数量随着农药影响程度的增加而减少,在农药污染影响严重的１、２区,计有土壤动物２１类和２２类,动物平均密度为２８５７１个／ｍ＾２和５１２６９个／ｍ＾２,受中度和轻蔗污染影响的３、４区分别有３５类和４７类,平均密度为５９２８５个／ｍ＾２,１５６５８７个／ｍ＾２。污染区土壤动物种类的减少主要由于常见类群和稀有     

毛细管水解及反相高效液相色谱分析蛋白质的氨基酸组成

 毛细管水解及反相高效液相色谱分析蛋白质的氨基酸组成陈平,梁宋平（湖南师范大学生物研究所,长沙４１０００６）氨基酸组成的分析是阐明蛋白质和多肽化学特性的基础,在蛋白质与多肽的氨基酸组成分析中,常采用对水解管反复充氮并抽真空的方法使蛋白质和多肽在隔绝氧气...     

Prognostic value and immune cell infiltration of hypoxic phenotype‐related gene signatures in glioblastoma microenvironment

Glioblastoma (GBM) is a malignant intracranial tumour with the highest proportion and lethality. It is characterized by invasiveness and heterogeneity. However, the currently available therapies are not curative. As an essential environmental cue that maintains glioma stem cells, hypoxia is considered the cause of tumour resistance to chemotherapy and radiation. Growing evidence shows that immunotherapy focusing on the tumour microenvironment is an effective treatment for GBM; however, the current clinicopathological features cannot predict the response to immunotherapy and provide accurate guidance for immunotherapy. Based on the ESTIMATE algorithm, GBM cases of The Cancer Genome Atlas (TCGA) data set were classified into high‐ and low‐immune/stromal score groups, and a four‐gene tumour environment‐related model was constructed. This model exhibited good efficiency at forecasting short‐ and long‐term prognosis and could also act as an independent prognostic biomarker. Additionally, this model and four of its genes (CLECL5A, SERPING1, CHI3L1 and C1R) were found to be associated with immune cell infiltration, and further study demonstrated that these four genes might drive the hypoxic phenotype of perinecrotic GBM, which affects hypoxia‐induced glioma stemness. Therefore, these might be important candidates for immunotherapy of GBM and deserve further exploration.     

Dihydromyricetin increases endothelial nitric oxide production and inhibits atherosclerosis through microRNA-21 in apolipoprotein E-deficient mice

Natural products were extracted from traditional Chinese herbal emerging as potential therapeutic drugs for treating cardiovascular diseases. This study examines the role and underlying mechanism of dihydromyricetin (DMY), a natural compound extracted from Ampelopsis grossedentata, in atherosclerosis. DMY treatment significantly inhibits atherosclerotic lesion formation, proinflammatory gene expression and the influx of lesional macrophages and CD4-positive T cells in the vessel wall and hepatic inflammation, whereas increases nitric oxide (NO) production and improves lipid metabolism in apolipoprotein E-deficient (Apoe^−/−) mice. Yet, those protective effects are abrogated by using NOS inhibitor L-NAME in Apoe^−/− mice received DMY. Mechanistically, DMY decreases microRNA-21 (miR-21) and increases its target gene dimethylarginine dimethylaminohydrolase-1 (DDAH1) expression, an effect that reduces asymmetric aimethlarginine (ADMA) levels, and increases endothelial NO synthase (eNOS) phosphorylation and NO production in cultured HUVECs, vascular endothelium of atherosclerotic lesions and liver. In contrast, systemic delivery of miR-21 in Apoe^−/− mice or miR-21 overexpression in cultured HUVECs abrogates those DMY-mediated protective effects. These data demonstrate that endothelial miR-21-inhibited DDAH1-ADMA-eNOS-NO pathway promotes the pathogenesis of atherosclerosis which can be rescued by DMY. Thus, DMY may represent a potential therapeutic adjuvant in atherosclerosis management.