Structural and biochemical characterization of SADS‐CoV papain‐like protease 2

Swine acute diarrhea syndrome coronavirus (SADS‐CoV) is a novel coronavirus that is involved in severe diarrhea disease in piglets, causing considerable agricultural and economic loss in China. The emergence of this new coronavirus increases the importance of understanding SADS‐CoV as well as antivirals. Coronaviral proteases, including main proteases and papain‐like proteases (PLP), are attractive antiviral targets because of their essential roles in polyprotein processing and thus viral maturation. Here, we describe the biochemical and structural identification of recombinant SADS papain‐like protease 2 (PLP2) domain of nsp3. The SADS‐CoV PLP2 was shown to cleave nsp1 proteins and also peptides mimicking the nsp2|nsp3 cleavage site and also had deubiquitinating and deISGynating activity by in vitro assays. The crystal structure adopts an architecture resembling that of PLPs from other coronaviruses. We characterize both conserved and unique structural features likely directing the interaction of PLP2 with the substrates, including the tentative mapping of active site and other essential residues. These results provide a foundation for understanding the molecular basis of coronaviral PLPs' catalytic mechanism and for the screening and design of therapeutics to combat infection by SADS coronavirus.     

Alteration of protein homeostasis mediates the interaction of Pseudomonas aeruginosa with Staphylococcus aureus

Intracellular protein degradation is essential for the survival of all organisms, but its role in interspecies interaction is unknown. Here, we show that the ClpXP protease of Pseudomonas aeruginosa suppresses its antimicrobial activity against Staphylococcus aureus, a common pathogen co-isolated with P. aeruginosa from polymicrobial human infections. Using proteomic, biochemical, and molecular genetic approaches, we found that this effect is due to the inhibitory effects of ClpXP on the quorum sensing (QS) of P. aeruginosa, mainly by degrading proteins (e.g., PhnA, PhnB, PqsR, and RhlI) which are critical for the production of QS signal molecules PQS and C4-HSL. We provide evidence that co-culturing with S. aureus induces a decrease in the activity of ClpXP in P. aeruginosa, an effect which was also achieved by the treatment of P. aeruginosa with N-acetylglucosamine (GlcNAc), a widespread chemical present on the surface of diverse cell types from bacteria to humans. These findings extend the range of biological events governed by proteolytic machinery to microbial community structure, thus also suggesting that a chemical-induced alteration of protein homeostasis is a mechanism for interspecies interactions.     

Expansion of MIR482/2118 by a class‐II transposable element in cotton

Some plant microRNA (miRNA) families contain multiple members generating identical or highly similar mature miRNA variants. Mechanisms underlying the expansion of miRNA families remain elusive, although tandem and/or segmental duplications have been proposed. In this study of two tetraploid cottons, Gossypium hirsutum and Gossypium barbadense, and their extant diploid progenitors, Gossypium arboreum and Gossypium raimondii, we investigated the gain and loss of members of the miR482/2118 superfamily, which modulates the expression of nucleotide‐binding site leucine‐rich repeat (NBS‐LRR) disease resistance genes. We found significant expansion of MIR482/2118d in G. barbadense, G. hirsutum and G. raimondii, but not in G. arboreum. Several newly expanded MIR482/2118d loci have mutated to produce different miR482/2118 variants with altered target‐gene specificity. Based on detailed analysis of sequences flanking these MIR482/2118 loci, we found that this expansion of MIR482/2118d and its derivatives resulted from an initial capture of an MIR482/2118d by a class‐II DNA transposable element (TE) in G. raimondii prior to the tetraploidization event, followed by transposition to new genomic locations in G. barbadense, G. hirsutum and G. raimondii. The ‘GosTE’ involved in the capture and proliferation of MIR482/2118d and its derivatives belongs to the PIF/Harbinger superfamily, generating a 3‐bp target site duplication upon insertion at new locations. All orthologous MIR482/2118 loci in the two diploids were retained in the two tetraploids, but mutation(s) in miR482/2118 were observed across all four species as well as in different cultivars of both G. barbadense and G. hirsutum, suggesting a dynamic co‐evolution of miR482/2118 and its NBS‐LRR targets. Our results provide fresh insights into the mechanisms contributing to MIRNA proliferation and enrich our knowledge on TEs.     

古DNA捕获新技术与中国南方早期人群遗传研究新格局

古DNA捕获技术目前已获得极大的发展,能够从骨骼和环境沉积物等多种材料中获取到目的DNA片段,而且对于保存环境较差的低纬度地区,同样能够获取有效的内源DNA片段,极大地丰富了古DNA研究的材料来源。本文围绕这一新技术开展总结和讨论,主要分为两个方面：1）总结并介绍该技术应用前景;2）应用这一技术打开了中国南方早期人群研究的新局面,梳理该新技术的应用对史前中国南方人群古基因组研究所获得的新认识,并对中国南方早期人群古基因组深入分析;另外,利用古DNA捕获技术成功获取云南3446~3180 BP的大阴洞遗址4例高质量线粒体基因组信息,并开展了人群遗传历史的研究。     

有机类肥料对土壤养分含量的影响

绿色、可持续是我国发展现代农业的必然要求,肥料投入是关键之一。基于有机肥培肥土壤、生态友好的优势,发展和推广有机肥已经成为我国农业生产的一项基本国策。我国有机肥来源广泛、种类繁多,农业生产条件千差万别。本文分析了我国有机肥产品种类及标准现状、理化性质差异、碳氮矿化特性差异及影响因素,评述了施用有机肥对提高耕地基础地力的作用。因来源、制作工艺不同,不同有机肥的有机碳组分含量、全氮和活性氮含量、碳氮比等基本性质差异明显,这四者是影响有机肥碳氮矿化率、碳氮矿化量、碱解氮释放量等碳氮供应特性的主要内在因素;加之土壤环境等外界因素的影响,不同有机肥表现出不同的养分供应特性。总体上,有机肥一方面对提高土壤有机质含量,尤其是活性有机质含量和碳库管理指数效果明显,另一方面可增加土壤氮磷钾养分容量,减少作物生长消耗带来的土壤养分亏损,促进土壤质量良性发展。今后,应加强有机肥在耕地培肥中的应用,并加强有机肥肥效理论的基础研究和安全高效有机肥新产品的开发,促进有机肥资源的高效循环利用,使其成为重要的农业资源。     

退化高寒草甸狼毒发生区土壤真菌多样性的空间变异

狼毒是青藏高原危害最严重的毒草种类之一,其快速蔓延对高寒草甸生态系统的影响日益严重。选取祁连山中段退化高寒草甸为研究区,综合采用高通量测序技术、地统计学和GIS空间分析方法,分析狼毒发生区土壤真菌多样性的空间变异特征,研究狼毒群落与土壤真菌多样性的空间相关性。结果表明: 与非发生区相比,狼毒发生区土壤真菌群落物种丰富度下降而优势度显著增加,α多样性降低;土壤真菌群落物种构成差异增强,β多样性明显升高。狼毒入侵对土壤真菌多样性的空间格局有一定扰动,发生区各多样性指数的斑块破碎化程度增加,土壤真菌群落物种构成的空间异质性明显增强,α和β多样性的空间稳定性降低。狼毒盖度与土壤真菌α和β多样性指数呈现显著正相关及显著负相关的区域交错镶嵌分布,空间相关性规律不明显,表明狼毒入侵草甸土壤真菌多样性的空间变异可能受地上植被和土壤环境的共同作用。