棉铃虫抗药性监测方法——浸叶法敏感毒力基线的建立及其应用

通过室内饲养的2个棉铃虫敏感品系,用浸叶法建立了11种常用药剂 (氯氰菊酯、溴氰菊酯、功夫菊酯、氰戊菊酯、久效磷、辛硫磷、甲基对硫磷、毒死蜱、灭多威、硫双灭多威、硫丹) 的敏感毒力基线,确定了它们的LC₅₀值和区分剂量。并用浸叶法监测了江苏、山东、河南、安徽4省棉田2代棉铃虫对氯氰菊酯、久效磷、灭多威和辛硫磷的抗性,结果表明用区分剂量监测抗性个体频率既快速简便,又适宜于进行早期抗性检测,因此这4种药剂的区分剂量可以推广应用于棉铃虫田间抗药性监测。     

辛硫磷-丙溴磷乳油防治棉铃虫药效试验

辛硫磷—丙溴磷乳油 (下简称辛·丙乳油 )是江苏省连云港华怡化工有限公司开发生产的新药剂 ,为明确其对棉铃虫Ｈｅｌｉｃｏｖｅｒｐａａｒｍｉｇｅｒａ的防治效果及使用技术 ,1 998年在 4代棉铃虫发生期间 ,进行了该药剂的田间和室内药效试验 ,现将结果报道如下。1　材料与方法1 1　供试药剂40 %辛·丙乳油 ,5 0 %辛·丙乳油 ,44 %氯·丙乳油 (瑞士汽巴嘉基有限公司 ) ,37 5 %硫双灭多威 (法国罗纳普朗克公司 ) ,2 5 %辛·氰乳油(辛硫磷 +氰戊菊酯 ) (中外合资盐城市丰山集团 )。1 2　试验方法1 2 1　田间不同用量试验　试验 1 998年在…     

棉铃虫核型多角体病毒与化学杀虫剂和卵磷脂混用的增效作用

棉铃虫核型多角体病毒(HaNPV)分别与三氟氯氰菊酯、溴氰菊酯、氰戊菊酯、灭净菊酯、灭多威、辛硫磷、甲基对硫磷和乙酰甲胺磷等化学杀虫剂混合饲喂棉铃虫幼虫,统计致死中浓度LC₅₀,计算增效比,测定虫体内与抗性有关的三种重要酶：多功能氧化酶(MFO)、羧酸酯酶(CarE)、乙酰胆碱酯酶(AChE)的活性。研究大豆卵磷脂对HaNPV致病性的影响。结果表明：HaNPV与化学杀虫剂混合饲喂抗性棉铃虫,生测统计增效比均大于1.0,特别是病毒与甲基对硫磷混用,增效比更是达到3.53,表现出良好的增效作用。混剂感染抗性棉铃虫,虫体内MFO的活性比化学杀虫剂单用时降低3～12倍,CarE和AChE的活性也比化学杀虫剂单用时低,HaNPV明显抑制了化学杀虫剂对MFO和CarE的诱导作用。HaNPV与大豆卵磷脂混用,提高了HaNPV对棉铃虫的感染致死率,缩短了致死中时间(LT₅₀)。     

SV1对4种杀虫剂的增效及延长残效期的研究

SV1是一种增效范围较广的农药增效剂,对多种杀虫剂具有增效作用。经室内毒力测定．与敌百虫混用对棉铃虫、粘虫和二化螟的增效比值分别为2．93倍、2．43倍和2．7倍;与氧化乐果、久效磷和氰戊菊酯混配对棉蚜、褐稻虱和萝卜蚜的增效比值分别为1．63—10．67倍。杀虫毒力随着加入SV1成分的增加而提高,一般常用农药与SV1混配之比需要1：3以上才明显增效。防治钵栽棉蚜通过系统观察,在防治效果相仿情况下,SV1可使氧化乐果药效延长9天,久效磷药效延长7天,氰戊菊酯药效延长6天以上。SV1可以成为生产上与有机磷及拟除虫菊酯类杀虫剂混用的增效剂优势品种。     

棉铃虫对氰戊菊酯抗性和敏感品系的选育

用氰戊菊酯对来自阳谷的棉铃虫(YG)Heliothis armigera(Hubncr) 进行抗性晶系的筛选。在15代期间经过9代的室内选育,获得抗性品系(Fcn-R),抗性倍数高达2“3倍,筛选后F₁₅代LD₅₀值(24.1412μg/头)比筛选前F1代lD₅₀值(0.2020μg/头)提高了119.5倍。对来自偃师的棉铃虫(YS)进行了连续两代单对筛选,得到敏感品系(Fen-S),敏感晶系的LD50值为0.0116μg/头,接近1983年东台敏感晶系的LD₅₀值(0.0098μg/头)Fcn-R抗性晶系筛选前后分别测定了七种杀虫剂的剂量-死亡回归线,发现Fen-R抗性品系对溴氰菊酯[LD₅₀(Fen-R)/LD₅₀(YG)=5.2X] 和氯氰菊酯(2.5X)具有一定程度的交互抗性;而对功夫菊酯(0.66X),氯菊酯(0.89x)、灭多威(0.74X)及久效磷(1.5x)没有交互抗性。氰戊菊酯加Pb的增效试验结果表明棉铃虫对氰戊菊酯的抗性主要是由于多功能氧化酶的代谢作用。毒理学资料还暗示抗性为多因子(基因)的。     

磷酸酯酶与乙酰胆碱酯酶在棉铃虫对辛硫磷抗药性中的作用(英文)

利用人工选育的方法 ,获得了棉铃虫对辛硫磷的抗药性品系和相对敏感品系 ,其对辛硫磷的LD50分别为 1 1 .0 574μg/虫和 0 .9790 μg/虫。以生物测定与生化测定的方法 ,比较了两品系的差异。增效剂活体试验测定结果表明 ,磷酸三苯酯、增效磷对棉铃虫三龄幼虫均表现出一定的增效作用 ,但在两品系间的增效作用存在差异 ,对相对敏感品系的增效倍数分别为 2 .2 7倍、2 .1 3倍 ,对抗性品系的增效倍数分别为 6.93倍和 6.43倍。磷酸酯酶活性测定结果表明 ,抗性品系的酶活力分别是相对敏感品系的1 6.67倍 (碱性 )和 1 .89倍 (酸性 ) ,Km 和Vmax则分别为 0 .76倍、2 .64倍 (碱性 )和 1 .38倍、1 .78倍 (酸性 ) ;而羧酸酯酶的活性则差异不大。对靶标酶乙酰胆碱酯酶的活性测定表明 ,与相对敏感品系相比 ,抗性品系酶活性显著增强 ,并且对杀虫剂的亲和力降低 ,说明乙酰胆碱酯酶在棉铃虫对辛硫磷的抗药性中也有着重要的作用     

棉铃虫对氰戊菊酯-辛硫磷混剂的抗性演化及解毒酶活性变化

用氰戊菊酯-辛硫磷混剂（有效成分1∶10,简称氰-辛混剂）对棉铃虫Helicoverpa armigera室内品系(YS)进行16代的抗性选育,获得棉铃虫对氰-辛混剂的抗性品系（YS-FP）。YS-FP品系与YS品系相比,对氰-辛混剂的抗性为14.7倍,对其中的单剂氰戊菊酯和辛硫磷的抗性分别为2 170倍和3.1倍。随着筛选的进行,氰戊菊酯和辛硫磷之间的共毒系数在F₂代出现短暂的增加,然后逐渐降低,它们之间的互作由增效变为拮抗。交互抗性测定结果表明,YS-FP品系对氯氰菊酯、溴氰菊酯、三氟氯氰菊酯、三唑磷和灭多威产生了明显的交互抗性,对硫丹、多杀菌素和爱玛菌素没有产生交互抗性。YS-FP品系6龄幼虫中肠细胞色素P450氧化酶甲氧基香豆素O-脱甲基活性为YS品系的10倍,3龄幼虫谷胱甘肽S-转移酶和酯酶活性分别是YS品系的1.7倍（CDNB结合作用）和2.4倍（α-NA 酯酶水解作用）。氰-辛混剂的筛选导致了棉铃虫多种解毒酶活性的增加,特别是细胞色素P450氧化酶活性增强最为明显。本研究结果表明氰-辛混剂对棉铃虫的筛选导致了广谱的交互抗性和多种代谢抗性机理,并且两个单剂之间的互作由增效变为拮抗,因此氰 辛混剂在棉铃虫抗性治理中的作用是有限的和暂时的。     

神经敏感性的降低是棉铃虫对拟除虫菊酯抗药性的重要机制

用扫描电子显微镜和光学显微镜的染色观察,研究了棉铃虫Helicoverpa armigeraHubner 3龄幼虫腹部神经一肌肉的分布,表明其腹纵肌细胞适合于作电生理细胞内记录。用电生理细胞内微电极记录法研究了棉铃虫三个品系：对照品系、功夫菊酯抗性品系(Cy-R,抗性指数13.4)和氰戊菊酯抗性品系(Fn-R,抗性指数37.9)的3龄幼虫神经一肌肉材料对相应杀虫剂的神经敏感性。结果表明：用10^-6mol/L的功夫菊酯处理Cy-R,在30min内有40%的个体对药剂无反应,另外60%的个体产生反应所需的时间是对照品系的3.5倍。用10^-6mol/L的氰戊菊酯处理Fn-R,在30min内有47%的个体对药剂无反应,另外53%的个体产生反应所需的时间是对照品系的4.2倍。这些结果说明神经敏感性降低是棉铃虫对拟除虫菊酯抗药性的重要机制。     

辛硫磷防治棉铃虫试验简报

目前防治棉铃虫使用的药剂,防治三龄后幼虫的效果不够理想,因而在蛾、卵量较大的年份,常因防治不彻底而出现大量残虫,给棉花生产造成很大威胁。1973—1974年我们采用苏州化工厂“辛酯醇钠丙酮法”和连云港市综合化工厂“乙酯液碱法”(中间试验产品)生产的50％辛硫磷,作了些试验,结果表明辛硫磷具有以下特点: 1.具有强烈的触杀作用用浓度0.005—0.1％的辛硫磷稀释掖对三龄幼虫怍触杀试验,24、48小时后,杀虫率均为100％,显著优于当前常用的杀虫畏、双硫磷、杀虫脒、混灭威等农药。尤其对老龄幼虫是一     

棉铃虫对拟除虫菊酯抗性稳定性研究

研究棉铃虫Helicoverpa armigera (Hubner)对三种拟除虫菊醌（氰戊菊酯、溴氰菊酯、功夫菊酯)的抗性稳定性及敏感性恢复表明,即使棉铃虫对氰戊菊酯的抗性达到3166.3倍以上,抗性仍不稳定,经14代室内饲养后抗性下降为61.4倍;对一系列田间抗性种群的抗性稳定性研究后发现,棉铃虫对这三种拟除虫菊酯的抗性不稳定,在没有杀虫剂选择的情况下,开始几代抗性下降较快,当下降到一定水平(2～9倍)后,抗性比较稳定,很难完全恢复对拟除虫菊酯的敏感性。     

940. BULBOPHYLLUM ANKYLOCHELE

Bulbophyllum ankylochele, a native of New Guinea, is illustrated. Its ecology and pollination are explained, and it is compared with the superficially similar Masdevallia from South America. Suggestions for its successful cultivation are given.     

940株血培养分离菌的临床分布及抗菌药物敏感性分析

目的定期对医院血流感染分离菌的分布和抗菌药物敏感性进行分析,为菌血症的治疗提供可靠的药敏结果,提高治愈率。方法对大连市中心医院2010年1月至2013年12月8 277份血标本采用全自动血培养仪Bac T/Alert3D和Micro Scan Walk Away-40全自动细菌鉴定仪进行细菌培养、鉴定和抗生素敏感性试验。结果 8 277份血标本中检出病原菌940株,阳性率为11.4%。940株病原菌中革兰阳性菌441株,占46.9%;以金黄色葡萄球菌、凝固酶阴性葡萄球菌、屎肠球菌、粪肠球菌和肺炎链球菌为主;革兰阴性杆菌486株,占51.7%,以大肠埃希菌、肺炎克雷伯菌、阴沟肠杆菌、鲍曼不动杆菌和铜绿假单胞菌为主;真菌13株,占1.4%。大肠埃希菌、肺炎克雷伯菌对亚胺培南、美洛培南高度敏感;鲍曼不动杆菌对头孢哌酮/舒巴坦、米诺环素高度敏感;粪肠球菌、屎肠球菌、葡萄球菌对达托霉素、万古霉素、利奈唑胺、奎奴普丁/达福普汀高度敏感。结论血液培养意义重大,病原菌分布呈多样化趋势,且表现为多重耐药。     

miRNA‐940 reduction contributes to human Tetralogy of Fallot development

Tetralogy of Fallot (TOF) is a complex congenital heart defect and the microRNAs regulation in TOF development is largely unknown. Herein, we explored the role of miRNAs in TOF. Among 75 dysregulated miRNAs identified from human heart tissues, miRNA‐940 was the most down‐regulated one. Interestingly, miRNA‐940 was most highly expressed in normal human right ventricular out‐flow tract comparing to other heart chambers. As TOF is caused by altered proliferation, migration and/or differentiation of the progenitor cells of the secondary heart field, we isolated Sca‐1⁺ human cardiomyocyte progenitor cells (hCMPC) for miRNA‐940 function analysis. miRNA‐940 reduction significantly promoted hCMPCs proliferation and inhibited hCMPCs migration. We found that JARID2 is an endogenous target regulated by miRNA‐940. Functional analyses showed that JARID2 also affected hCMPCs proliferation and migration. Thus, decreased miRNA‐940 affects the proliferation and migration of the progenitor cells of the secondary heart field by targeting JARID2 and potentially leads to TOF development.     

miR-940 regulates the inflammatory response of chondrocytes by targeting MyD88 in osteoarthritis

Molecular and Cellular Biochemistry - Osteoarthritis (OA) has been identified to be one of the most prevalent forms of joint disorders, marked with inflammatory immune response that may give rise...     

Cannabinoid receptor-independent suppression of the superoxide generation of human neutrophils (PMN) by CP55 940, but not by anandamide

Cannabinoids have been shown to affect various immune functions. To date, almost no data exist on PMN, which provide the first line antimicrobial defense. The objective of the present study was to investigate the effects of the synthetic dibenzopyrane ligand CP55 940, the endogenous cannabinoid anandamide and methanandamide on the "respiratory burst" of isolated human PMN in vitro. After preincubation with high micromolar concentrations of CP55 940, fMLP-stimulated PMN showed a reduction in superoxide production, whereas the spontaneous burst activity of resting PMN remained unaffected. This inhibitory effect of CP55 940 was not CB-receptor-mediated. In contrast, anandamide and methanandamide did not alter the oxidative microbicidal PMN function.     

Residue Leu940 Has a Crucial Role in the Linkage and Reaction Specificity of the Glucansucrase GTF180 of the Probiotic Bacterium Lactobacillus reuteri 180

Highly conserved glycoside hydrolase family 70 glucansucrases are able to catalyze the synthesis of α-glucans with different structure from sucrose. The structural determinants of glucansucrase specificity have remained unclear. Residue Leu⁹⁴⁰ in domain B of GTF180, the glucansucrase of the probiotic bacterium Lactobacillus reuteri 180, was shown to vary in different glucansucrases and is close to the +1 glucosyl unit in the crystal structure of GTF180-ΔN in complex with maltose. Herein, we show that mutations in Leu⁹⁴⁰ of wild-type GTF180-ΔN all caused an increased percentage of (α1→6) linkages and a decreased percentage of (α1→3) linkages in the products. α-Glucans with potential different physicochemical properties (containing 67–100% of (α1→6) linkages) were produced by GTF180 and its Leu⁹⁴⁰ mutants. Mutant L940W was unable to form (α1→3) linkages and synthesized a smaller and linear glucan polysaccharide with only (α1→6) linkages. Docking studies revealed that the introduction of the large aromatic amino acid residue tryptophan at position 940 partially blocked the binding groove, preventing the isomalto-oligosaccharide acceptor to bind in an favorable orientation for the formation of (α1→3) linkages. Our data showed that the reaction specificity of GTF180 mutant was shifted either to increased polysaccharide synthesis (L940A, L940S, L940E, and L940F) or increased oligosaccharide synthesis (L940W). The L940W mutant is capable of producing a large amount of isomalto-oligosaccharides using released glucose from sucrose as acceptors. Thus, residue Leu⁹⁴⁰ in domain B is crucial for linkage and reaction specificity of GTF180. This study provides clear and novel insights into the structure-function relationships of glucansucrase enzymes.     

Depletion of intermediate filament protein Nestin,a target of microRNA-940, suppresses tumorigenesis by inducing spontaneous DNA damage accumulation in human nasopharyngeal carcinoma

Nasopharyngeal carcinoma (NPC) is a major malignant tumor of the head and neck region in southern China. The understanding of its underlying etiology is essential for the development of novel effective therapies. We report for the first time that microRNA-940 (miR-940) significantly suppresses the proliferation of a variety of cancer cell lines, arrests cells cycle, induces caspase-3/7-dependent apoptosis and inhibits the formation of NPC xenograft tumors in mice. We further show that miR-940 directly binds to the 3′-untranslated regions of Nestin mRNA and promotes its degradation. Likewise, depletion of Nestin inhibits tumor cell proliferation, arrest cells at G2/M, induces apoptosis and suppresses xenograft tumor formation in vivo. These functions of miR-940 can be reversed by ectopic expression of Nestin, suggesting that miR-940 regulates cell proliferation and survival through Nestin. Notably, we observed reduced miR-940 and increased Nestin levels in NPC patient samples. Protein microarray revealed that knockdown of Nestin in 5-8F NPC cells alters the phosphorylation of proteins involved in the DNA damage response, suggesting a mechanism for the miR-940/Nestin axis. Consistently, depletion of Nestin induced spontaneous DNA damage accumulation, delayed the DNA damage repair process and increased the sensitivity to irradiation and the chemotherapeutic agent doxorubicin. Collectively, our findings indicate that Nestin, which is downregulated by miR-940, can promote tumorigenesis in NPC cells through involvement in the DNA damage response. The levels of microRNA-940 and Nestin may serve as indicators of cancer status and prognosis.Nasopharyngeal carcinoma (NPC), a major malignant tumor of the head and neck region, is endemic to Southeast Asia, southern China, the Arctic, the Middle East and North Africa.¹ Low differentiation and high metastatic potential and recurrence rates are major pathologic features of NPC. The incidence of NPC in southern China has remained very high, with a 5-year overall survival rate of approximately 70%.² Within 4 years after radiation therapy, about 30–40% of NPC patients develop distant metastasis, which is associated with poor prognosis.³ Therefore, an understanding of the underlying etiology is essential for the development of novel effective therapies for NPC.MicroRNAs (miRNAs), a class of small (∼22 nucleotides) noncoding RNAs, reduce mRNA stability and/or suppress translation by binding to the 3′-untranslated regions (3′-UTRs) or coding sequences of target mRNAs.⁴ As such, miRNAs are involved in the majority of basic biologic processes, including cell proliferation, apoptosis, differentiation and development.⁵ Cumulative evidence also suggests that miRNAs can function as potential oncogenes or tumor suppressor genes.^{6, 7} Abnormal expression of miRNAs and mutations of their genes have been documented in various types of tumors.⁸ Recently, a growing number of miRNAs have been implicated in the development of NPC. For instance, the decreased expression of miR-100 has been reported to cause Plk1 overexpression, which in turn contributes to NPC progression.⁹ MiR-200a upregulation in the undifferentiated cell line C666-1 inhibits cell growth, migration and invasion by targeting ZEB2 and CTNNB1.¹⁰ Inhibition of miR-141, which is upregulated in NPC specimens, may affect cell cycle, apoptosis, cell growth, migration and invasion through targeting of BRD3, UBAP1 and PTEN.¹¹ In addition, reduced levels of let-7 in NPC might have a role in the proliferation through DNA methylation.¹² In view of the roles of miRNAs in tumorigenesis, identification of key miRNAs and their targets that contribute to NPC progression may provide novel targets for NPC diagnosis and treatment.Nestin, a member of the type VI intermediate filament protein family, is widely expressed in mammalian nervous tissue, some immortalized mammalian stem cell lines¹³ and precursor cells of some tissues, for which expression is decreased with differentiation.^{14, 15, 16} As a stem cell/progenitor cell marker,¹⁷ Nestin is essential for mitogen-stimulated proliferation of neural progenitor cells,¹⁸ and loss of Nestin leads to apoptosis of neural progenitor cells in zebrafish.¹⁹ Recently, Nestin has been detected in various cell lines established from human solid tumors²⁰ and has been associated with aggressive nervous system tumors.²¹ All of these findings suggest that Nestin is associated with tumorigenesis; however, the precise role of Nestin and the relationship between Nestin and NPC progression are still unknown.In this study, we screen 350 different miRNAs and determined that miR-940 inhibits the proliferation of the NPC cell lines 5-8F and CNE2. Furthermore, miR-940 expression induces G2/M arrest, promotes apoptosis and suppresses xenograft tumor growth. Bioinformatic and luciferase reporter assays revealed that miR-940 targets two putative binding sites in the Nestin 3′-UTR region. A physiologic role for miR-940 was suggested by its common downregulation in NPC tissues, whereas Nestin showed a converse pattern of upregulation. Knockdown of Nestin in 5-8F and CNE2 cells induces G2/M arrest and apoptosis and inhibits cell proliferation and xenograft tumor growth; conversely, ectopic expression of Nestin partially reverses the effects of miR-940 on cell proliferation, cell cycle and apoptosis. Interestingly, knockdown of Nestin induces spontaneous DNA damage accumulation, delays DNA damage repair and enhances sensitivity to ionizing radiation (IR) of 5-8F cells both in vitro and in vivo. These results elucidate a pathway by which miR-940 regulates tumor progression in NPC by targeting Nestin.     

Possible implication of the Golgi apparatus casein kinase in the phosphorylation of vesicle docking protein p115 Ser-940: a study with peptide substrates

Phosphorylation of human vescicle docking protein p115 at Ser-942 (homologous to Ser-940 in rat p115) promotes its dissociation from the Golgi membrane. Here we show that a peptide encompassing the 934--950 sequence of p115 is unaffected or poorly phosphorylated by a variety of Ser/Thr protein kinases with the notable exception of the Golgi apparatus casein kinase (G-CK) which phosphorylates it with an efficiency comparable to that of its optimal peptide substrates. In contrast phosphorylation of the p115 peptide by protein kinase CK2 is negligible compared to that of the specific peptide substrates of this kinase. Phosphorylation by G-CK is abolished if a conserved cluster of acidic residues at position between n + 4 and n + 9 (EDDDDE) is replaced by a neutral stretch (GAGAGA). These data strongly support the view that G-CK but not the other two classes of ubiquitous "casein kinases" (CK1 and CK2) is the natural phosphorylating agent of p115.