Complete genome analysis of bacteriochlorophyll acontaining Roseicitreum antarcticum ZS2-28T reveals its adaptation to Antarctic intertidal environment

Aerobic anoxygenic phototrophic bacteria (AAPB) are photoheterotrophic prokaryotes able to use both light and dissolved organic matter as energy sources. Roseicitreum antarcticum ZS2-28T was isolated from intertidal sediment in the Larsemann Hills, Princess Elizabeth Land, Antarctica, and was able to produce bacteriochlorophyll a. It is the type strain of the sole species within the genus Roseicitreum. The complete genome sequence of the bacterium was determined using Illumina HiSeq X and PacBio RSII systems. The genome of R. antarcticum ZS2-28T was 4253095 bp and consisted of one chromosome and four plasmids. A number of genes related to the bacteriochlorophyll a production, photosynthetic reaction, cold adaptation, salt adaptation, ultra-violet resistance and DNA damage repairing were found in the genome. In addition to genomic islands and type IV secretion systems, genes related to gene transfer agents were detected in the genome of R. antarcticum ZS2-28T, suggesting that this bacterium can adapt to its environment by acquiring exogenous nucleic acids. The annotated complete genome sequence provides genetic insights into the environmental adaptation and ecological function of R. antarcticum ZS2-28T in Antarctic coastal area

Genome-wide QTL mapping for three traits related to teat number in a White Duroc × Erhualian pig resource population

<p>Abstract</p> <p>Background</p> <p>Teat number is an important fertility trait for pig production, reflecting the mothering ability of sows. It is also a discrete and often canalized trait presenting bilateral symmetry with minor differences between the two sides, providing a potential power to evaluate fluctuating asymmetry and developmental instability. The knowledge of its genetic control is still limited. In this study, a genome-wide scan was performed with 183 microsatellites covering the pig genome to identify quantitative trait loci (QTL) for three traits related to teat number including the total teat number (TTN), the teat number at the left (LTN) and right (RTN) sides in a large scale White Duroc × Erhualian resource population.</p> <p>Results</p> <p>A sex-average linkage map with a total length of 2350.3 cM and an average marker interval of 12.84 cM was constructed. Eleven genome-wide significant QTL for TTN were detected on 8 autosomes including pig chromosomes (SSC) 1, 3, 4, 5, 6, 7, 8 and 12. Six suggestive QTL for this trait were detected on SSC6, 9, 13, 14 and 16. Eight chromosomal regions each on SSC1, 3, 4, 5, 6, 7, 8 and 12 showed significant associations with LTN. These regions were also evidenced as significant QTL for RTN except for those on SSC6 and SSC8. The most significant QTL for the 3 traits were all located on SSC7. Erhualian alleles at most of the identified QTL had positive additive effects except for three QTL on SSC1 and SSC7, at which White Duroc alleles increased teat numbers. On SSC1, 6, 9, 13 and 16, significant dominance effects were observed on TTN, and predominant imprinting effect on TTN was only detected on SSC12.</p> <p>Conclusion</p> <p>The results not only confirmed the QTL regions from previous experiments, but also identified five new QTL for the total teat number in swine. Minor differences between the QTL regions responsible for LTN and RTN were validated. Further fine mapping should be focused on consistently identified regions with small confidence intervals, such as those on SSC1, SSC7 and SSC12.</p

TfR1 binding with H-ferritin nanocarrier achieves prognostic diagnosis and enhances the therapeutic efficacy in clinical gastric cancer

H-ferritin (HFn) nanocarrier is emerging as a promising theranostic platform for tumor diagnosis and therapy, which can specifically target tumor cells via binding transferrin receptor 1 (TfR1). This led us to investigate the therapeutic function of TfR1 in GC. The clinical significance of TfR1 was assessed in 178 GC tissues by using a magneto-HFn nanoparticle-based immunohistochemistry method. The therapeutic effects of doxorubicin-loaded HFn nanocarriers (HFn-Dox) were evaluated on TfR1-positive GC patient-derived xenograft (GC-PDX) models. The biological function of TfR1 was investigated through in vitro and in vivo assays. TfR1 was upregulated (73.03%) in GC tissues, and reversely correlated with patient outcome. TfR1-negative sorted cells exhibited tumor-initiating features, which enhanced tumor formation and migration/invasion, whereas TfR1-positive sorted cells showed significant proliferation ability. Knockout of TfR1 in GC cells also enhanced cell invasion. TfR1-deficient cells displayed immune escape by upregulating PD-L1, CXCL9, and CXCL10, when disposed with IFN-γ. Western blot results demonstrated that TfR1-knockout GC cells upregulated Akt and STAT3 signaling. Moreover, in TfR1-positive GC-PDX models, the HFn-Dox group significantly inhibited tumor growth, and increased mouse survival, compared with that of free-Dox group. TfR1 could be a potential prognostic and therapeutic biomarker for GC: (i) TfR1 reversely correlated with patient outcome, and its negative cells possessed tumor-aggressive features; (ii) TfR1-positive cells can be killed by HFn drug nanocarrier. Given the heterogeneity of GC, HFn drug nanocarrier combined with other therapies toward TfR1-negative cells (such as small molecules or immunotherapy) will be a new option for GC treatment

Latexin expression is downregulated in human gastric carcinomas and exhibits tumor suppressor potential

<p>Abstract</p> <p>Background</p> <p>Latexin, also known as endogenous carboxypeptidase inhibitor (CPI), has been found to inhibit mouse stem cell populations and lymphoma cell proliferation, demonstrating its potential role as a tumor suppressor. Our previous study also suggested a correlation between latexin expression and malignant transformation of immortalized human gastric epithelial cells. Here, we examined latexin expression in human gastric carcinomas and investigated the effect of differential latexin expression on proliferation of gastric cancer cells <it>in vitro </it>and <it>in vivo</it>.</p> <p>Methods</p> <p>Monoclonal antibody against human latexin was prepared and immunohistochemical analysis was performed to detect latexin expression in 41 paired gastric carcinomas and adjacent normal control tissues. Human gastric cancer cells MGC803 (latexin negative) stably transfected with LXN gene and BGC823 cells (latexin positive) stably transfected with antisense LXN gene were established for anchorage-dependent colony formation assay and tumorigenesis assay in nude mice. Differentially expressed genes in response to exogeneous latexin expression were screened using microarray analysis and identified by RT-PCR. Bisulfite sequencing was performed to analyze the correlation of the methylation status of LXN promoter with latexin expression in cell lines.</p> <p>Results</p> <p>Immunohistochemical analysis showed significantly reduced latexin expression in gastric carcinomas (6/41, 14.6%) compared to control tissues (31/41, 75.6%) (<it>P </it>< 0.05). Overexpression of LXN gene in MGC803 cells inhibited colony formation and tumor growth in nude mice. Conversely, BGC823 cells transfected with antisense LXN gene exhibited enhanced tumor growth and colony formation. Additionally, several tumor related genes, including Maspin, WFDC1, SLPI, S100P, and PDGFRB, were shown to be differentially expressed in MGC803 cells in response to latexin expression. Differential expression of Maspin and S100P was also identified in BGC823 cells while latexin expression was downregulated. Further bisulfite sequencing of the LXN gene promoter indicated CpG hypermethylation was correlated with silencing of latexin expression in human cells.</p> <p>Conclusions</p> <p>Latexin expression was reduced in human gastric cancers compared with their normal control tissues. The cellular and molecular evidences demonstrated the inhibitory effect of latexin in human gastric cancer cell growth and tumorigenicity. These results strongly suggest the possible involvement of latexin expression in tumor suppression.</p

Research on the Internal Flow Field of Left Atrial Appendage and Stroke Risk Assessment with Different Blood Models

Extant clinical research has underscored that patients suffering from atrial fibrillation (AF) bear an elevated risk for stroke, predominantly driven by the formation of thrombus in the left atrial appendage (LAA). As such, accurately identifying those at an increased risk of thrombosis becomes paramount to facilitate timely and effective treatment. This study was designed to shed light on the mechanisms underlying thrombus formation in the LAA by employing three-dimensional (3D) left atrium (LA) models of AF patients, which were constructed based on Computed Tomography (CT) imaging. The distinct benefits of Computational Fluid Dynamics (CFD) were leveraged to simulate the blood flow field within the LA, using three distinct blood flow models, both under AF and sinus rhythm (SR) conditions. The potential risk of thrombus formation was evaluated by analyzing the Relative Residence Time (RRT) and Endothelial Cell Activation Potential (ECAP) values. The results gleaned from this study affirm that all three blood flow models align with extant clinical guidelines, thereby enabling an effective prediction of thrombosis risk. However, noteworthy differences emerged when comparing the intricacies of the flow field and thrombosis risk across the three models. The single-phase non-Newtonian blood flow model resulted in comparatively lower residence times for blood within the LA and lower values for the Oscillatory Shear Index (OSI), RRT, and ECAP within the LAA. These findings suggest a reduced thrombosis risk. Conversely, the two-phase non-Newtonian blood flow model exhibited a higher residence time for blood and elevated RRT value within the LAA, suggesting an increased risk for thrombosis

Molecular diversity of the microbial community in coloured snow from the Fildes Peninsula (King George Island, Maritime Antarctica)

Snow in Antarctica is a vast terrestrial ecosystem and plays a key role that has likely been underestimated. Algae are the key primary producers on the coloured snow surface, and they support a microbial community that includes bacteria, fungi and/or invertebrates. We analysed microbial communities that co-exist in green and red snow samples from the Fildes Peninsula by Illumina sequencing, Antarctica, as well as the influence of snow physicochemical properties. We detected several species of green algae from Chlorophyta and Ochrophyta as well as fungi and cercozoans. The three red snow samples (RS1, RS2 and RS3) were represented by mixed eukaryotic microalgae fromSanguina,Chloromonasand Trebouxiophyceae. The green snow sample GS5 exhibited lake-to-snow colonisation composed of Trebouxiophyceae, Ulvophyceae and Chrysophyta representatives. The red snow RS4, predominantly byChlainomonassp. from slush layers, which presented a different microbial community from the other red snow samples, was sampled close to green snow sample GS5 near Lake Changhu. The environmental parameters were involved into descriptive differences among these coloured snow samples. The two snow algaeChlainomonasandSanguinawere firstly reported from Antarctica, which indicates distinguished snow algae colonisation that is closely connected with the melting snow at the lake ice-cover. Meanwhile, consistent with previous bacterial community profiles, Proteobacteria and Bacteroidetes were mostly represented in all the coloured snow samples. Polaromonas(Betaproteobacteria) was the most abundant genus, and its presence was reportedly essential for the sustained growth of snow algae.Flavobacteriumfrom Bacteroidetes was the most frequently detected genera in GS5, but the Sphingobacteriia with only a few reads were an interestingly minority in GS5. The snow-algae-associated bacteria were closely related to psychrophilic strains or sequences from low-temperature environments. Many possible factors influence on the coloured snow microbial communities would require attentions, to help understand their occurrence mechanisms, their biogeographic distributions in polar regions