Search

Entomopathogenic fungi are one of the key regulators of insect populations in nature. Some species such as Beauveria bassianawith a wide host range have been developed as promising alternatives to chemical insecticides for the biocontrol of insect pests. However, the long-term persistence of the released strains, the effect on non-target hosts and local fungal populations remains elusive, but they are considerable concerns with respect to environmental safety. Here we report the temporal features of the Beauveriapopulation genomics and evolution over 20 years after releasing exotic strains to control pine caterpillar pests. We found that the isolates within the biocontrol site were mostly of clonal origins. The released strains could persist in the environment for a long time but with low recovery rates. Similar to the reoccurrence of host jumping by local isolates, the infection of non-target insects by the released strains was evident to endemically occur in association with host seasonality. No obvious dilution effect on local population structure was evident by the releases. However, the population was largely replaced by genetically divergent isolates once per decade but evolved with a pattern of balancing selection and towards expansion through adaptation, non-random outcrossing and isolate migration. This study not only unveils the real-time features of entomopathogenic fungal population genomics and evolution but also provides added values to alleviate the concerns of environmental safety regarding the biocontrol application of mycoinsecticides.

Entomopathogenic fungi are one of the key regulators of insect populations in nature. Some species such as Beauveria bassianawith a wide host range have been developed as promising alternatives to chemical insecticides for the biocontrol of insect pests. However, the long-term persistence of the released strains, the effect on non-target hosts and local fungal populations remains elusive, but they are considerable concerns with respect to environmental safety. Here we report the temporal features of the Beauveriapopulation genomics and evolution over 20 years after releasing exotic strains to control pine caterpillar pests. We found that the isolates within the biocontrol site were mostly of clonal origins. The released strains could persist in the environment for a long time but with low recovery rates. Similar to the reoccurrence of host jumping by local isolates, the infection of non-target insects by the released strains was evident to endemically occur in association with host seasonality. No obvious dilution effect on local population structure was evident by the releases. However, the population was largely replaced by genetically divergent isolates once per decade but evolved with a pattern of balancing selection and towards expansion through adaptation, non-random outcrossing and isolate migration. This study not only unveils the real-time features of entomopathogenic fungal population genomics and evolution but also provides added values to alleviate the concerns of environmental safety regarding the biocontrol application of mycoinsecticides.

An imbalance in osteogenesis and osteoclastogenesis is a crucial pathological factor in the development of osteoporosis. Osteoclasts (OCs) play a pivotal role in osteoporosis, whose new therapy exploration has been focused on the suppression of OC formation. Sophoridine is found from the Chinese traditional food sophora flower to exhibit anti-osteoporosis capacity by screening. This study is focused on its anti-osteoporosis mechanism evaluation. The anti-osteoporosis effect of sophoridine, (15 mg kg–1body), was evaluated in ovariectomized (OVX) mice by monitoring changes in bone histomorphometry index, formation of osteoclasts from blood-derived mononuclear cells, and changes in the synthesis of pro-osteoclastogenic cytokines. Signal pathways were investigated by QPCR, Western blot, and immunofluorescence. Sophoridine has a significant anti-osteoporosis effect in vivo, which can inhibit RANKL-induced OC formation, the appearance of OC-specific marker genes, and OC marker protein in vitro. Mechanistically, sophoridine dose- and time-dependently blocks the RANKL-induced OC formation and the activation of ERK and c-Fos as well as the induction and nucleus translocation of NFATc1. Sophora flower might be a useful alternative functional food in preventing or treating osteoporosis.

Two-dimensional preparative high-performance liquid chromatography (HPLC) was used on the non-aqueous mobile phase in the separation of weakly polar compounds from Capsicum annuum L.The resulting silica column, coupled with an amide column, showed good orthogonality with the non-aqueous mobile phase, and two separate compounds were efficiently isolated in purity above 97%. The relative antioxidant activities of the purified compounds were assessed by a unique cellular antioxidant activity (CAA) model using an anti-oxidative response element (ARE) to regulate the expression level of the luciferase reporter gene, with tert-butyl hydroquinone (TBHQ) as positive control. A luciferase cellular antioxidant activity unit (LCAA) for the measurement of antioxidant capacity has been defined by the antioxidant capacity of 1.5 μg mL−1TBHQ, and the relative antioxidant capacities of two active compounds of interest, Fraction 5-4 and Fraction 5-5, were found to be 0.397 LCAA and 0.523 LCAA, respectively. The protocols described will be of considerable assistance in the development of functional foodstuffs.

Little information is available on the roles of earthworms in N transformation and biological activities in heavy metal-contaminated soils. The purpose of the present paper is to examine the effects of earthworm on nitrifying and denitrifying enzyme activities of Zn-treated soils. ZnCl2solution was added to soils at rates ranging from 0 to 400 mg Zn kg–1and was allowed to fractionate and stabilize for 60 days. The Zn-tolerant earthwormPheretimasp., which had been previously screened, was then introduced into Zn-treated soils and allowed to work for 40 days. Original soils without the addition of Zn and introduction of earthworms but incubated under the same conditions were used as controls. Zn-treated soils without the introduction of earthworms were also used as controls. Results showed that earthworm activity increased both nitrifying and denitrifying enzyme activities of the soils. These beneficial effects of earthworms were particularly evident in the treatments where Zn had an adverse effect. Zn added at a rate ≤200 mg Zn kg–1generally had a stimulating effect on the enzyme activities measured. However, Zn added at a rate >200 mg Zn kg–1had an adverse effect on nitrifying and denitrifying enzyme activities, which could be alleviated or even completely eliminated by earthworm activities.Little information is available on the roles of earthworms in N transformation and biological activities in heavy metal-contaminated soils. The purpose of the present paper is to examine the effects of earthworm on nitrifying and denitrifying enzyme activities of Zn-treated soils. ZnCl2solution was added to soils at rates ranging from 0 to 400 mg Zn kg–1and was allowed to fractionate and stabilize for 60 days. The Zn-tolerant earthwormPheretimasp., which had been previously screened, was then introduced into Zn-treated soils and allowed to work for 40 days. Original soils without the addition of Zn and introduction of earthworms but incubated under the same conditions were used as controls. Zn-treated soils without the introduction of earthworms were also used as controls. Results showed that earthworm activity increased both nitrifying and denitrifying enzyme activities of the soils. These beneficial effects of earthworms were particularly evident in the treatments where Zn had an adverse effect. Zn added at a rate ≤200 mg Zn kg–1generally had a stimulating effect on the enzyme activities measured. However, Zn added at a rate >200 mg Zn kg–1had an adverse effect on nitrifying and denitrifying enzyme activities, which could be alleviated or even completely eliminated by earthworm activities.

The Src family tyrosine kinase, Fyn, can facilitate regulation of cell proliferation and differentiation. Mice with mutations in the fyngene have defects in the brain, immune system, and epidermal differentiation. To identify molecules that may interact with Fyn in the epidermis, we performed a yeast two-hybrid interaction screen of a murine keratinocyte library. A novel adaptor-like molecule was isolated and termed Srcasm for Srcactivating andsignaling molecule. Murine Srcasm is a 52.7-kDa protein that contains a VHS membrane association domain and a number of tyrosine motifs suggesting that it may be a substrate for Src family kinases and serve as an adaptor protein. Northern blot analysis of murine tissues demonstrates that Srcasm expression is highest in brain and kidney. In situhybridization analysis reveals that srcasmmRNA is expressed in regions of the epidermis and hair follicle where keratinocyte differentiation occurs. In the brain, srcasmmRNA distribution correlates with that of fyn, with both being highly expressed in the hippocampal and cerebellar Purkinje neurons. Fyn can phosphorylate Srcasm, and association of these molecules relies on cooperative binding between the SH2 and SH3 domains of Fyn and corresponding canonical binding sites in Srcasm. Srcasm is capable of interacting with Grb2 and the regulatory subunit of phosphoinositide 3-kinase, p85, in a phosphorylation-dependent manner. The evidence suggests that Srcasm may help promote Src family kinase signaling in cells.

In preliminary experiments we noted developmental (i.e., embryonic and neonatal) myosin heavy chains (MHCs) in the diaphragms of patients with severe chronic obstructive pulmonary disease (COPD). We hypothesized that this finding represented new fiber formation secondary to injury associated with the mechanical stress of COPD or previously undescribed MHCs in the human diaphragm. To distinguish between these possibilities, we analyzed diaphragmatic biopsies obtained from 9 patients with severe COPD (forced expiratory volume in 1 s = 21 ± 2% predicted, residual volume = 283 ± 22% predicted) and 10 age-matched controls. First, using immunocytochemistry with specific monoclonal antibodies, we noted that control diaphragms had greater proportions of fibers expressing embryonic (50 ± 2 vs. 28 ± 3%, P< 0.0001) and neonatal (52 ± 2 vs. 32 ± 3%, P< 0.001) MHCs than COPD diaphragms. Second, SDS-PAGE demonstrated that these developmental MHCs represented only a very small fraction of the diaphragmatic MHC content. Third, the RT-PCR demonstrated mRNA coding for embryonic and neonatal MHCs in COPD and control diaphragms. Last, COPD and control diaphragms exhibited normal histology on light microscopy. We conclude that the presence of developmental MHC isoforms does not indicate new fiber formation in diaphragms of patients with severe COPD. Although these results represent the first systematic description of embryonic and neonatal MHCs in normal adult human diaphragms, their function remains to be elucidated.

By altering IP3receptor gating, presenilin mutations associated with familial Alzheimer’s disease increase Ca2+release from the endoplasmic reticulum.