中国水牛瘤胃纤毛虫分布与挥发性脂肪酸的研究

对中国广西西林水牛和摩拉水牛瘤胃纤毛虫种类分布进行了鉴定检测,并测定了其瘤胃液挥发性脂肪酸浓度,同时进行了比较研究。全部检出17属63种25型瘤胃纤毛虫,比以前进行的8种反刍动物瘤胃纤毛虫分布研究中出现的总数和每个宿主个体中出现的平均纤毛虫种数多,种类构成最复杂,其纤毛虫构成特点类似于东南亚地区水牛瘤胃纤毛虫构成特点。其中广西西林水牛中检出了Entodinium biconcavumsp n,是至今从未鉴定记载过的认为是新种的特殊种类。广西西林水牛检出13属54种20型、摩拉水牛检出16属45种11型瘤胃纤毛虫。广西西林水牛瘤胃纤毛虫平均密度为2.13×105/mL,摩拉水牛瘤胃纤毛虫密度为3.43×105/mL。中国水牛瘤胃纤毛虫属别构成中Entodinium属出现率最高,但两个水牛品种间存在明显差别,其他属别构成也不尽一致。这与不同品种原来的地理环境分布与饲养管理条件有关。广西西林水牛瘤胃总VFA浓度为75.60 mmol/mL,摩拉水牛的为58.74 mmol/mL。瘤胃总VFA含量中均为乙酸含量最高,属于典型的粗饲料发酵类型。     

胚泡着床前后母胎免疫调节的研究概况

母体容纳携带一半异体抗原的胎儿而成功妊娠,涉及母胎之间复杂的免疫调节,其中胚泡着床起着至关重要的作用,本文从着床期间激素、细胞因子以及一些免疫分子的角度,对近年来胚泡着床前后母胎界面免疫调节的研究情况进行了概述。     

微白黄链霉菌对红豆草壳二孢的拮抗效果评价

红豆草壳二孢叶斑黑茎病(Ascochyta onobrychidis)是红豆草(Onobrychis viciaefolia)最重要的病害之一,在分离此病菌的同时得到一种对此病菌具有较强抑制作用的微生物,为评价此拮抗菌的开发利用前景,本研究采用形态学、分子生物学和生物化学方法鉴定了其分类地位,并测定了其对红豆草壳二孢的抑菌效果。通过构建系统发育树并结合其形态特征和生理生化特性,将该拮抗菌鉴定为微白黄链霉菌(Streptomyces albidoflavu),在高氏一号培养基上菌落为黄白色,可产生黄白色水溶性色素,孢子丝钩状,顶端螺旋形;在平板对峙试验中该菌的菌落对红豆草壳二孢菌落的相对抑制率达74.33%,同时该菌发酵液对红豆草壳二孢菌丝生长和孢子萌发的抑制率分别为80.95%和93.87%。该菌具有生物防治红豆草壳二孢的开发和利用价值。     

新疆乌鲁木齐市犬布鲁氏菌病流行病学调查

为了解新疆乌鲁木齐市犬布鲁氏菌病流行特征,分析犬感染风险因素,初步掌握养犬人员对布鲁氏菌病的认知程度和行为特点,从而提出合理的预防对策和控制措施,采用流行病学横断面研究方法,通过估计流行率计算抽样数量,然后随机抽样,采用IELISA方法检测光滑型和粗糙型犬布鲁氏菌,同时结合调查问卷,获得乌鲁木齐市犬布鲁氏菌病流行率、感染风险因素和养犬人员对布鲁氏菌病认知情况,并对调查结果采用SPSS和Excel软件进行数据统计分析。结果显示:乌鲁木齐市犬布鲁氏菌病总流行率为25.5%(95%CI:20.9%~30.1%),且犬种和牛羊种并存,公共卫生威胁严重;从不同群体看,牧区流行率最高,为41.5%(95%CI:31.0%~52.0%);外购、散养、常接触牛羊、喂生肉、不处理犬粪便等行为是乌鲁木齐市犬布鲁氏菌感染的潜在风险因素,其中"常接触牛羊"(OR=1.97,95%CI:1.47~15.35)、"喂生肉"(OR=5.06,95%CI:1.69~20.74)是主要风险因素;乌鲁木齐市养犬人员对布鲁氏菌病的认知程度低,个人防护意识差。因此,应加强对犬感染牛羊种布鲁氏菌的公共卫生防控,减少犬与牛羊的直接接触,不喂生肉,定期开展犬布鲁氏菌病专项检测,同时加强宣传,提高养犬人员的布鲁氏菌病认知度。     

日光温室彩椒双干循环整枝栽培技术

采用双干循环整枝技术充分发挥了彩椒潜伏芽结果的能力,在其他管理措施相同的条件下每667 m2产量达12 000 kg以上,比常规双干整枝增产30%左右。     

‘紫罗兰’白菜叶片再生体系的建立

以‘紫罗兰’白菜无菌苗叶片为外植体,研究了不同6-BA和NAA浓度组合对白菜真叶不定芽再生的影响,同时采用不同生根培养基对再生芽进行生根诱导。结果表明:诱导‘紫罗兰’白菜真叶分化的适宜培养基为MS+2mg/L 6-BA+1mg/L NAA+4mg/L AgNO3,每个外植体平均再生芽数为1.42个;生根培养基以MS+0.5mg/L NAA最佳,平均每个不定芽诱导根数为16.54个。该试验结果为‘紫罗兰’白菜材料的快速繁殖提供了理论和技术参考。     

Identification of Suspected Stem/progenitor Cells in Bovine Mammary Epithelial Cells Culture System

To develop the potential function of dairy cow mammary stem cells (DCMECs) in regulation of lactation,we identify putative DCMECs which were BrdU label retaining epithelial cells,at the same time,analysis the location of two new mammary stem cells molecular marks FNDC3B and PROCR to verify the feasibility of them to indicate DCMECs.The mRNA levels of prolactin,growth hormone,insulin-like growth factor-1 and their receptors were detected along with cell passage by Real-time quantitative PCR.The results showed that the proportion of BrdU label-retaining epithelial cells was nearly 0.4% after 25 d continuous culture (passaged 4 times) and few cells were positive for FNDC3B or PROCR.Moreover,we observed the BrdU labelled epithelial cells by asymmetric division.The mRNA levels of prolactin,growth hormone,insulin-like growth factor-Ⅰ and their receptors in primary and passage cells were extremely significant difference(P<0.01).DCMECs would rapidly lose some physiological characteristics and the ability of milk synthesis when not under the condition of induction of lactation differentiation,but a certain percentage of mammary stem/progenitor cells will be retained,whose potential effects on the regulation of lactation and mammary acinar remodeling were worthy of attention.     

火龙果镰刀菌果腐病病原菌鉴定及生物学特性研究

采用形态学特征观察、rDNA-ITS序列、EF-1α序列比对和系统发育树分析的方法对引起火龙果镰刀菌果腐病病原菌进行鉴定,并初步研究其生物学特性。结果表明:引起火龙果镰刀菌果腐病是单隔镰刀菌(Fusarium dimerum Penzig in Saccardo),这是该菌引起火龙果果腐病在国内的首次报道。该菌菌丝生长的适宜温度25~35℃,最适温度30℃,适宜产孢温度25~35℃,最适产孢温度30~35℃,致死温度75℃(10 min);适宜pH5~9,最适pH7,最适产孢pH4;连续光照、D-果糖为碳源、牛肉膏和蛋白胨为氮源时最有利于该菌菌丝生长;完全黑暗、D-半乳糖为碳源、尿素为氮源时最有利于该菌产孢。综合分析认为,该菌耐高温,光照充足、弱酸和富含有机营养的环境有利于该菌的生长和繁殖。     

Improvements of TKC Technology Accelerate Isolation of Transgene-Free CRISPR/Cas9-Edited Rice Plants

Elimination of the CRISPR/Cas9 constructs in edited plants is a prerequisite for assessing genetic stability, conducting phenotypic characterization, and applying for commercialization of the plants. However, removal of the CRISPR/Cas9 transgenes by genetic segregation and by backcross is laborious and time consuming. We previously reported the development of the transgene killer CRISPR (TKC) technology that uses a pair of suicide genes to trigger self-elimination of the transgenes without compromising gene editing efficiency. The TKC technology enables isolation of transgene-free CRISPR-edited plants within a single generation, greatly accelerating crop improvements. Here, we presented two new TKC vectors that show great efficiency in both editing the target gene and in undergoing self-elimination of the transgenes. The new vectors replaced the CaMV35S promoter used in our previous TKC vector with two rice promoters to drive one of the suicide genes, providing advantages over our previous TKC vector under certain conditions. The vectors reported here offered more options and flexibility to conduct gene editing experiments in rice.