The peritrophic membrane in adult simuliids (Diptera) before and after feeding on blood and blood-sucrose mixtures

A peritrophic membrane formed in the posterior midgut of female simuliids of seven species within 30 min of feeding on blood of various avian or mammalian hosts, and 6–12 hr thereafter it displayed up to seven concentric laminae. Within the first 48 hr of blood digestion, the posterior part of the peritrophic membrane (where digestion was most advanced) began to decompose and PM disappearance was complete at the end of blood digestion. In different species blood digestion at 18°–20° required 120–180 hr which was increased to over 200 hr by microsporidan infection. If a blood-sucrose mixture went directly to the midgut, a thin membrane formed around it, but not if it went indirectly by way of the crop. A prefeeding secretion in the anterior midgut is considered to be the peritrophic membrane of the pharate adult surrounding a small, but variable, amount of material, the meconium.

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Résumé Sept espèces de simulies ont été étudiées: 5 ornithophiles, 2 mammalophiles. Trente minutes après un repas de sang sur divers oiseaux (poulet, canard) ou mammifères (homme, cerf, élan d'Amérique) on constate qu'une membrane péritrophique est sécrétée par toute le surface épithéliale dans la région moyenne de l'intestin moyen postérieur dilaté des femelles. Six à douze heures après le repas cette membrane comporte jusqu'à sept lamelles concentriques. Une sécrétion moins importante se forme autour de la petite quantité de sang que l'on trouve dans l'estomac antérieur, non dilaté et étroit; cette sécrétion glisse vers l'arrière et forme une capsule recouvrant le pôle antérieur du bol alimentaire sanguin dans la partie postérieure de l'intestin moyen, ceci pendant le premier jour. La digestion commence à la périphérie et à l'extrémité postérieure de la masse sanguine et se poursuit enfin à l'extrémité antérieure, où la membrane péritrophique conserve le plus longtemps sa structure en contact avec le sang non digéré. Dans les premières 48 heures de la digestion du sang, la région postértieure de la membrane péritrophique (là où la digestion est la plus avancée) commence à se décomposer, et sa disparition est complète quand la digestion du sang est achevée. Chez les différentes espèces étudiées, la digestion du sang à 18–20° exige 120–180 heures, pouvant demander plus de 200 heures chez des insectes atteints d'une infection par des microsporidies. Si un mélange de sang et sucrose parvient directement dans la région moyenne de l'intestin moyen, une membrane mince se forme autour, mais non si cet aliment passe par le jabot. Une sécrétion précédant l'alimentation s'observe dans l'intestin moyen antérieur des mouches non nourries et doit représenter, chez l'adulte venant d'éclore, la membrane péritrophique entourant le méconium: petite quantité de matière d'importance variable. Cette matière se retrouve souvent au centre de la masse sanguine après alimentation et est lente à digérer.

     

黑果山姜、舞花姜叶的显微鉴定

对黑果山姜Alpinia nigra(Gaertn.）Burtt和舞花姜Globba racemosa Smith叶进行了组织构造观察,为其原植物鉴定提供了依据。     

Inhibition of circular RNA CDR1as increases chemosensitivity of 5‐FU‐resistant BC cells through up‐regulating miR‐7

This study aims to explore the mechanism of Circular RNA CDR1as implicating in regulating 5‐fluorouracil (5‐FU) chemosensitivity in breast cancer (BC) by competitively inhibiting miR‐7 to regulate CCNE1. Expressions of CDR1as and miR‐7 in 5‐FU‐resistant BC cells were determined by RT‐PCR. CCK‐8, colony formation assay and flow cytometry were applied to measure half maximal inhibitory concentration (IC50), 5‐Fu chemosensitivity and cell apoptosis. Western blot was used to detect the expressions of apoptosis‐related factors. CDR1as was elevated while miR‐7 was inhibited in 5‐FU‐resistant BC cells. Cells transfected with si‐CDR1as or miR‐7 mimic had decreased IC50 and colony formation rate, increased expressions of Bax/Bcl2 and cleaved‐Caspase‐3/Caspase‐3, indicating inhibition of CDR1as and overexpression of miR‐7 enhances the chemosensitity of 5‐FU‐resistant BC cells. Targetscan software indicates a binding site of CDR1as and miR‐7 and that CCNE1 is a target gene of miR‐7. miR‐7 can gather CDR1as in BC cells and can inhibit CCNE1. In comparison to si‐CDR1as group, CCNE1 was increased and chemosensitivity to 5‐Fu was suppressed in si‐CDR1as + miR‐7 inhibitor group. When compared with miR‐7 mimic group, CDR1as + miR‐7 mimic group had increased CCNE1 and decreased chemosensitivity to 5‐Fu. Nude mouse model of BC demonstrated that the growth of xenotransplanted tumour in si‐CDR1as + miR‐7 inhibitor group was faster than that in si‐CDR1as group. The tumour growth in CDR1as + miR‐7 mimic group was faster than that in miR‐7 mimic group. CDR1as may regulate chemosensitivity of 5‐FU‐resistant BC cells by inhibiting miR‐7 to regulate CCNE1.     

Overexpression of <Emphasis Type="Italic">IrlVHA</Emphasis>-<Emphasis Type="Italic">c</Emphasis>, A Vacuolar-Type H<Superscript>+</Superscript>-ATPase c Subunit Gene from <Emphasis Type="Italic">Iris lactea</Emphasis>, Enhances Salt Tolerance in Tobacco

Vacuolar-type H⁺-ATPase (V-ATPase), a multi-subunit endomembrane proton pump, plays an important role in plant growth and response to environmental stresses. In the present study, transgenic tobacco that overexpressed the V-ATPase c subunit gene from Iris lactea (IrlVHA-c) was used to determine the function of IrlVHA-c. Quantitative PCR analysis showed that IrlVHA-c expression was induced by salt stress in I. lactea roots and leaves. Subcellular localization of green fluorescent protein (GFP) as marker combined with FM4-64 staining showed that the IrlVHA-c-GFP was localized to the endosomal compartment in tobacco cells. Compared with the wild-type, the IrlVHA-c transgenic tobacco plants exhibited greater seed germination rates, root length, fresh weight, and higher relative water content (RWC) of leaves under salt stress. Furthermore, the IrlVHA-c transgenic tobacco leaves have lower stomatal densities and larger stomatal apertures than wild-type. Under salt stress, superoxide dismutase (SOD) activity in the transgenic tobacco was significantly enhanced. Moreover, the level of malondialdehyde (MDA) in the transgenic tobacco was significantly lower than that in wild-type plants under salt stress. Taken together, these results suggested that the IrlVHA-c plays an important role in salt tolerance in transgenic tobacco by influencing stomatal movement and physiological changes.     

氮添加对湿地松林土壤水解酶和氧化酶活性的影响

通过3个水平野外氮添加控制试验(0、40、120 kg N·hm^-2·a^-1),研究氮添加对亚热带湿地松林土壤水解酶和氧化酶活性的影响.结果表明: 氮添加显著抑制了土壤有机质中碳、氮、磷水解酶和氧化酶的活性,导致β-1,4-葡糖苷酶(BG)、纤维素二糖水解酶(CBH)、β-1,4-乙酰基-葡糖胺糖苷酶(NAG)、过氧化物酶(PER)活性下降16.5%～51.1%,并且高水平氮添加对酶活性抑制效果更明显;氮添加导致α-1,4-葡糖苷酶(aG)、β-1,4-木糖苷酶(BX)、酸性磷酸酶(AP)、多酚氧化酶(PPO)活性降低14.5%～38.6%,不同水平氮添加处理间差异不显著.土壤酶活性存在明显的季节性差异,BG、NAG、BX、CBH、AP、PPO活性表现为3月>6月>10月,aG、PER活性表现为10月>3月>6月.多数土壤水解酶和氧化酶与pH呈显著正相关,与NO₃^--N含量呈显著负相关,表明氮添加导致pH降低和土壤中硝化作用增强,抑制了土壤水解酶和氧化酶活性.氮添加不利于亚热带土壤有机质的矿化和周转,并且随着氮添加量的增加,效果更明显.     

一种快速、无损大豆种子DNA提取方法的建立和应用

基因分型是进行植物基因功能的遗传分析和分子标记辅助育种的重要环节。该研究以大豆(Glycine max)成熟种子为材料, 建立了通过钻孔采集样品、快速提取DNA进行基因型鉴定的方法。用此方法, 一个熟练的工作人员可以在1个小时内完成120个样品的采集和DNA提取; 同时种子钻孔取样后, 不会对大豆种子的萌发造成影响。利用该方法获得的DNA可满足PCR扩增的要求。实验重复性好, 成功率在98%以上。这种快速且无损的大豆种子基因型鉴定方法可以用于鉴定杂交种子、品种纯度以及遗传分析等研究工作。     

Combining Untargeted and Targeted Proteomic Strategies for Discrimination and Quantification of Cashmere Fibers

Cashmere is regarded as a specialty and luxury fiber due to its scarcity and high economic value. For fiber quality assessment, it is technically very challenging to distinguish and quantify the cashmere fiber from yak or wool fibers because of their highly similar physical appearance and substantial protein sequence homology. To address this issue, we propose a workflow combining untargeted and targeted proteomics strategies for selecting, verifying and quantifying biomarkers for cashmere textile authentication. Untargeted proteomic surveys were first applied to identify 174, 157, and 156 proteins from cashmere, wool and yak fibers, respectively. After marker selection at different levels, peptides turned out to afford much higher selectivity than proteins for fiber species discrimination. Subsequently, parallel reaction monitoring (PRM) methods were developed for ten selected peptide markers. The PRM-based targeted analysis of peptide markers enabled accurate determination of fiber species and cashmere percentages in different fiber mixtures. Furthermore, collective use of these peptide makers allowed us to discriminate and quantify cashmere fibers in commercial finished fabrics that have undergone heavy chemical treatments. Cashmere proportion measurement in fabric samples using our proteomic approach was in good agreement with results from traditional light microscopy, yet our method can be more readily standardized to become an objective and robust assay for assessing authenticity of fibers and textiles. We anticipate that the proteomic strategies presented in our study could be further implicated in discovery of quality trait markers for other products containing highly homologous proteomes.     

Impacts on Sirtuin Function and Bioavailability of the Dietary Bioactive Compound Dihydrocoumarin

The plant secondary metabolite and common food additive dihydrocoumarin (DHC) is an inhibitor of the Sirtuin family of NAD⁺-dependent deacetylases. Sirtuins are key regulators of epigenetic processes that maintain silent chromatin in yeast and have been linked to gene expression, metabolism, apoptosis, tumorogenesis and age-related processes in multiple organisms, including humans. Here we report that exposure to the polyphenol DHC led to defects in several Sirtuin-regulated processes in budding yeast including the establishment and maintenance of Sir2p-dependent silencing by causing disassembly of silent chromatin, Hst1p-dependent repression of meiotic-specific genes during the mitotic cell cycle. As both transient and prolonged exposure to environmental and dietary factors have the potential to lead to heritable alterations in epigenetic states and to modulate additional Sirtuin-dependent phenotypes, we examined the bioavailability and digestive stability of DHC using an in vivo rat model and in vitro digestive simulator. Our analyses revealed that DHC was unstable during digestion and could be converted to melilotic acid (MA), which also caused epigenetic defects, albeit less efficiently. Upon ingestion, DHC was observed primarily in intestinal tissues, but did not accumulate over time and was readily cleared from the animals. MA displayed a wider tissue distribution and, in contrast to DHC, was also detected in the blood plasma, interstitial fluid, and urine, implying that the conversion of DHC to the less bioactive compound, MA, occurred efficiently in vivo.