Search bioRxiv⌕ Search

Biology subjects

Wang, X.-h.

Publications and source records attributed to Wang, X.-h..

2 recordsLinked to original sources

A revision of the African Russula radicans and allies in subgen. Heterophyllidiae provides an example of a clade that exhibits recent diversification and extensive phenotypic plasticity.

Russula subsection Radicantinae is described for R. radicans and allies, while subsection Aureotactinae is again restricted to R. aureotacta, the subsectional type species that has never been recollected since its original description. Russula radicans, originally described from Madagascar, as well as the Central African R. brunneoannulata, are epitypified. Russula xylophila is the first confirmed annulate species belonging to Sect. Ingratae and a close relative to R. oleifera. An ITS sequence has been obtained from the R. xylophila holotype collection made in 1928, but it is slightly different from those obtained from all new collections. For this reason and some minor morphological differences, we refrained from epitypification. Russula acriannulata, another species attributed to Aureotactinae in the past, is now also excluded from the subsection, but needs more sequencing to solve its systematic placement. The Malagasy Russula cibaensis and R. tapiae, as well as the Central African R. cameroonensis and R. afrovinacea are new species in Radicantinae.At least three more undescribed species are revealed by environmental sequences. The West African R. sankarae is reduced to a form of R. radicans. The latter species exhibits an impressive phenotypic plasticity in response to differences in habitat or host associations. It has a very wide distribution covering littoral rain forest in eastern Madagascar (forma radicans), Zambezian woodlands in Central and Eastern Africa (forma miomboensis fo. nov.) and gallery forests in West Africa (forma sankarae).

molecular biology↗

Proinflammatory and autoimmunogenic gut microbiome in systemic lupus erythematosus

Systemic lupus erythematosus (SLE), characterized by chronic inflammation and multi-organ damage, has been suggested to associate with gut dysbiosis, but knowledge is limited from small sample size and 16s rRNA-based studies. To shed new light on the role of microbiota in SLE development, we analyzed the fecal metagenome of 117 treatment-naive SLE patients and 115 sex- and age-matched healthy controls (HC) by deep-sequencing; in addition, 52 of the aforementioned patients have post-treatment fecal metagenome for comparison. We found significant differences in microbial composition and function between SLE and HC, revealing multiple plausible contributing bacterial species and metabolic pathways in SLE. In-depth SNP-based analysis revealed an oral-microbiome origin for two marker species, strengthening the importance of bacterial translocation in disease development. Lastly, we confirmed experimentally that peptides of SLE-enriched species mimicking autoantigens such as Sm and Fas could trigger autoimmune responses, suggesting a potential causal role of gut microbiota in SLE.

microbiology↗