Changes in soil carbon sequestration and soil respiration following afforestation on paddy fields in north subtropical China

Aims Although many studies have reported net gains of soil organic carbon (SOC) after afforestation on croplands, this is uncertain for Chinese paddy rice croplands. Here, we aimed to evaluate the effects of afforestation of paddy rice croplands on SOC sequestration and soil respiration (R s). Such knowledge would improve our understanding of the effectiveness of various land use options on greenhouse gas mitigation in China.Methods The investigation was conducted on the Chongming Island, north subtropical China. Field sites were reclaimed from coastal salt marshes in the 1960s, and soils were homogeneous with simple land use histories. SOC stocks and R s levels were monitored over one year in a paddy rice cropland, an evergreen and a deciduous broad-leaved plantation established on previous paddy fields and a reference fallow land site never cultivated. Laboratory incubation of soil under fast-changing temperatures was used to compare the temperature sensitivity (Q 10) of SOC decomposition across land uses.Important findings After 15–20 years of afforestation on paddy fields, SOC concentration only slightly increased at the depth of 0–5cm but decreased in deeper layers, which resulted in a net loss of SOC stock in the top 40cm. Seasonal increase of SOC was observed during the rice-growing period in croplands but not in afforested soils, suggesting a stronger SOC sequestration by paddy rice cropping. However, SOC sequestered under cropping was more labile, as indicated by its higher contents of dissolved organic carbon and microbial biomass. Also, paddy soils had higher annual R s than afforested soils; R s abruptly increased after paddy fields were drained and plowed and remained distinctively high throughout the dry farming period. Laboratory incubation revealed that paddy soils had a much higher Q 10 of SOC decomposition than afforested soils. Given that temperature was the primary controller of R s in this region, it was concluded that despite the stronger SOC sequestration by paddy rice cropping, its SOC was less stable than in afforested systems and might be more easily released into the atmosphere under global warming.     

近144年来秦岭太白山林线区3-6月平均气温的重建

秦岭太白山林线植被因海拔较高且受人为扰动较轻,对气候变化的响应尤为敏感,为获取过去气候变化信息提供了可靠代用资源。然而,结合树木年代学方法及Arcgis空间插值功能进行秦岭林线气候变化重建的工作至今仍处于空白。利用采自太白山林线地带太白红杉(Larix chinensis)所建立的树轮宽度资料,与提取自太白山保护区气温栅格数据中的采样点位置气象数据进行相关分析。结果表明,太白红杉与3—6月平均气温相关性最显著,采用线性回归建立了两者的拟合模型,剔除重建方程中的1997、1998年之后,方差解释量达57.2%(调整自由度后为55.5%);重建气温序列显示偏冷时段平均跨度(16年)较偏暖时段平均跨度(10.8年)长,偏冷时段有:1870—1881年、1903—1918年和1977—1996年;偏暖的时段有:1882—1892年、1919—1929年和1997—2013年;在1931—1978年这一时期,气温相对稳定,1988年之后升温强烈;周期分析显示近144年以来3—6月气温存在22—31 a,18—22 a以及10—13 a的3个振荡周期,可能与大尺度气候驱动及太阳活动存在联系。以上结果均得到历史记录以及周边重建结果的支持。     

Enhanced host immune responses in presence of HCV facilitate HBV clearance in coinfection

Hepatitis B virus (HBV)/Hepatitis C virus (HCV) coinfection is frequently observed because of the common infection routine. Despite the reciprocal inhibition exerted by HBV and HCV genomes, the coinfection of HBV and HCV is associated with more severe forms of liver diseases. However, the complexity of viral interference and underlying pathological mechanism is still unclarified. With the demonstration of absence of direct viral interplay, some in vitro studies suggest the indirect effects of viral-host interaction on viral dominance outcome. Here, we comprehensively investigated the viral replication and host immune responses which might mediate the interference between viruses in HBV/HCV coinfected Huh7-NTCP cells and immunocompetent HCV human receptors transgenic ICR mice. We found that presence of HCV significantly inhibited HBV replication in vitro and in vivo irrespective of the coinfection order, while HBV did not affect HCV replication. Pathological alteration was coincidently reproduced in coinfected mice. In addition to the participation of innate immune response, an involvement of HCV in up-regulating HBV-specific immune responses was described to facilitate HBV clearance. Our systems partially recapitulate HBV/HCV coinfection and unveil the uncharacterized adaptive anti-viral immune responses during coinfection, which renews the knowledge on the nature of indirect viral interaction during HBV/HCV coinfection.     

A novel fluorescent assay for T-synthase activity

Loss of T-synthase (uridine diphosphate galactose:N-acetylgalactosaminyl-α1-Ser/Thr β3galactosyltransferase), a key enzyme required for the formation of mucin-type core 1 O-glycans, is observed in several human diseases, including cancer, Tn syndrome and IgA nephropathy, but current methods to assay the enzyme use radioactive substrates and complicated isolation of the product. Here we report the development of a novel fluorescent assay to measure its activity in a variety of tumor cell lines. Deficiencies in T-synthase activity correlate with mutations in the gene encoding the molecular chaperone Cosmc that is required for folding the T-synthase. This new high-throughput assay allows for facile screening of tumor specimens and other biological material for T-synthase activity and could be used diagnostically.     

Megakaryocyte polyploidy is inhibited by lysyl oxidase propeptide

Megakaryocytes (MKs), the platelet precursors, undergo an endomitotic cell cycle that leads to polyploidy. Lysyl oxidase propeptide (LOX-PP) is generated from lysyl oxidase (LOX) pro-enzyme after proteolytical cleavage. We recently reported that LOX, a known matrix cross-linking enzyme, contributes to MK lineage expansion. In addition, LOX expression levels are ploidy-dependent, with polyploidy MKs having minimal levels. This led us to test the effects of LOX-PP on the number and ploidy of primary MKs. LOX-PP significantly decreases mouse bone marrow MK ploidy coupled with a reduction in MK size. MK number is unchanged upon LOX-PP treatment. Analysis of LOX-PP- or vehicle-treated MKs by western blotting revealed a reduction in ERK1/2 phosphorylation and in the levels of its downstream targets, cyclin D3 and cyclin E, which are known to play a central role in MK endomitosis. Pull-down assays and immunochemistry staining indicated that LOX-PP interacts with α-tubulin and the mictotubules, which can contribute to decreased MK ploidy. Thus, our findings defined a role for LOX-PP in reducing MK ploidy. This suggests that high-level expression of LOX in aberrantly proliferating MKs could play a part in inhibiting their polyploidization via LOX-PP.     

RNA binding protein 24 regulates the translation and replication of hepatitis C virus

The secondary structures of hepatitis C virus (HCV) RNA and the cellular proteins that bind to them are important for modulating both translation and RNA replication. However, the sets of RNA-binding proteins involved in the regulation of HCV translation, replication and encapsidation remain unknown. Here, we identified RNA binding motif protein 24 (RBM24) as a host factor participated in HCV translation and replication. Knockdown of RBM24 reduced HCV propagation in Huh7.5.1 cells. An enhanced translation and delayed RNA synthesis during the early phase of infection was observed in RBM24 silencing cells. However, both overexpression of RBM24 and recombinant human RBM24 protein suppressed HCV IRES-mediated translation. Further analysis revealed that the assembly of the 80S ribosome on the HCV IRES was interrupted by RBM24 protein through binding to the 5′-UTR. RBM24 could also interact with HCV Core and enhance the interaction of Core and 5′-UTR, which suppresses the expression of HCV. Moreover, RBM24 enhanced the interaction between the 5′- and 3′-UTRs in the HCV genome, which probably explained its requirement in HCV genome replication. Therefore, RBM24 is a novel host factor involved in HCV replication and may function at the switch from translation to replication.     

Immunization of mice with vaccinia virus Tiantan strain yields antibodies cross-reactive with protective antigens of monkeypox virus

Highlights
1. The first study describing the cross-reactivity of antibodies elicited by a Chinese smallpox vaccine against monkeypox virus.
2. Mice immunized with vaccinia virus Tiantan strain yield antibodies cross-reactive with monkeypox virus protective antigens.
3. Cross-reactivities of VTT-elicited antibodies against monkeypox protective antigens are ranging from 33% to 94%.