Plant species and microbial interactions have significant impacts on the diversity of bacterial communities. However, few studies have explored interactions among these factors, such the role of microbial interactions in regulating the effects of plant species on soil bacterial diversity. We assumed that plant species not only affect bacterial community diversity directly, but also influence bacterial community diversity indirectly through changing microbial interactions. Specifically, we collected soil samples associated with three different plant species, one evergreen shrub (Rhododendron simsii) and the other two deciduous shrubs (Dasiphora fruticosa and Salix oritrepha). Soil bacterial community composition and diversity were examined by high-throughput sequencing. Moreover, soil bacterial antagonistic interactions and soil edaphic characteristics were evaluated. We used structural equation modeling (SEM) to disentangle and compare the direct effect of different plant species on soil bacterial community diversity, and their indirect effects through influence on soil edaphic characteristics and microbial antagonistic interactions. The results showed that (1) Plant species effects on soil bacterial diversity were significant; (2) Plant species effects on soil microbial antagonistic interactions were significant; and (3) there was not only a significant direct plant species effect on bacterial diversity, but also a significant indirect effect on bacterial diversity through influence on microbial antagonistic interactions. Our study reveals the difference among plant species in their effects on soil microbial antagonistic interactions and highlights the vital role of microbial interactions on shaping soil microbial community diversity.
Lymphatic metastasis is the leading cause responsible for recurrence and progression in papillary thyroid cancer (PTC), where dysregulation of lncRNAs have been extensively demonstrated to be implicated. However, the specific lymphatic node metastatsis-related (LNM) lncRNAs remain not identified in PTC yet. LNM lncRNA, MFSD4A-AS1, were explored in PTC dataset from TCGA, and our clinical samples. The roles of MFSD4A-AS1 in lymphatic metastasis were investigated by in vitro, and in vivo. Bioinformatic analysis, Luciferase assay and RIP assay were performed to identify the potential targets and the underlying pathway of MFSD4A-AS1 in lymphatic metastasis of PTC. MFSD4A-AS1 was specifically upregulated in PTC tissues with lymphatic metastasis. Upregulating MFSD4A-AS1 promoted mesh formation and migration of HUVECs and invasion and migration of PTC cells. Importantly and consistently, MFSD4A-AS1 promoted lymphatic metastasis of PTC cells in vivo by inducing the lymphangiogenic formation and enhancing invasive capability of PTC cells. Mechanistic dissection further revealed that MFSD4A-AS1 functioned as ceRNA to sequester miR-30c-2-3p, miR-145-3p and miR-139-5p to disrupt the miRNAs-mediated inhibition of VEGFA and VEGFC, and further activated TGF-β signaling by sponging miR-30c-2-3p that targeted TGFBR2 and USP15, both of which synergistically promoted lymphangiogenesis and lymphatic metastasis of PTC. Our results unravel a novel dual mechanisms by which MFSD4A-AS1 promotes lymphatic metastasis of PTC, which will facilitate the development of anti-lymphatic metastatic therapeutic strategy in PTC.
Sacha inchi (Plukenetia volubilis L.) is a plant native to the rain forest of the Peruvian Amazon region. Because of its high protein and oil content as well as general nutritional quality, it is regarded as a promising new crop. Successfully introduced from South America in 2006, Sacha inchi has been cultivated in Xishuangbanna, in the southwestern region of Yunnan Province, China. During an investigation from August to October of 2012, severely stunted and withered Sacha inchi plants with rotted and galled root were observed in fields. Dissection of galled root tissue revealed mature root-knot nematode (Meloidogyne sp) females with body cavity filled with red color contents. The population was extracted and quantified from soil and root samples and identified to species by morphology, esterase (EST) isozyme phenotypes, and molecular characterization (3). Mean populations of 774 ± 251 Meloidogyne second stage juveniles (J2) per 100 cm3 of soil were extracted from the rhizosphere of symptomatic plants. These juveniles (n = 20) were characterized by length (410 to 480 μm) and hyaline tail terminus length (11 to 17 μm). Females (n = 20) were characterized by stylet length (14.1 to 17.3 μm) and the perineal pattern (rounded with fine striae, low to moderately high dorsal arch, and a distinct lateral field clearly demarcated from striae by parallel lines). The distinct lateral lines of the perineal pattern are diagnostic for this species (3). Gravid females were used for esterase (Est) isoenzyme analysis, and showed the J3 phenotype (relative migration rate [Rm] = 1.0, 1.25, and 1.4), typical of M. javanica, a species-specific phenotype used to differentiate this species from other members of Meloidogyne (1). Additionally, three single egg masses associated with red body females were extracted from the field-collected Sacha inchi roots and inoculated onto three potted tomato plants (Solanum lycopersicum ‘Rutgers’) and maintained in the greenhouse for 8 weeks until root galls and egg masses were visible. The observation of root-knot nematodes from tomato roots showed that all females' bodies were normal white, and the nematode species was also identified as M. javanica based on the esterase phenotype and the perineal pattern. It is suggested that the red body contents associated with females on Sacha inchi is the result of an unknown chemical compound acquired from that host. Although undetermined to species, Meloidogyne has been reported on Sacha inchi in Peru (2). To our knowledge, this is the first detection of M. javanica on this plant. Since M. javanica is widely distributed throughout the tropics, this root-knot nematode could be an important threat to the commercial cultivation of Sacha inchi. References: (1) R. M. Carneiro et al. Nematol. 2:645, 2000. (2) P. D. P. de Bienes. Sacha inchi (Plukenetia volubilis L.). Base de datos, 2010. (3) R. N. Perry et al. Root-Knot Nematodes. CABI. Wallingford, UK, 2009.
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