Ruicheng Wang

Hopanoids are a series of important lipid biomarkers in the bacterial cellular membranes that are found ubiquitously in different spatial and temporal environments. Squalene-hopane cyclase, a key and prerequisite molecular component of the hopanoid biosynthesis pathway, is encoded by the sqhC gene. To investigate the composition, niche, and distribution of microbial sqhC-containing communities, we analyzed hopanoid producer data and environmental parameters across different ecosystems on the basis of sequencing reads of peat samples from increasing gradient depths across peatland profile C in the Dajiuhu Peatland, as well as data collected from available published papers. The results indicated that the acidic Dajiuhu Peatland harbored mainly Acidobacteria (59.16%) among its sqhC-containing groups. The main composition of hopanoid producers in the peatland was different from that in other ecosystems, with Alphaproteobacteria found in soil (37.78%), cave (48.21%), hypersaline lagoon (34.04%), and marine (32.59%) ecosystems; Betaproteobacteria, Gammaproteobacteria, and Deltaproteobacteria found in reef (100%), acid mine drainage (55.00%), and estuary, mangrove, and harbor (39.66%) ecosystems; and an unknown cluster found in freshwater (29.43%) and hot spring (89.58%) ecosystems. Compared with other phyla or sub-phyla, Alphaproteobacteria, Betaproteobacteria, and Gammaproteobacteria were the most widespread, occurring in eight ecosystems. Peatland was significantly separated from the other nine ecosystem modules in the occurrence network, and the marine ecosystem had the greatest impact on the eco-network of sqhC microbes. An RDA indicated that pH, DO, salinity, and TOC had significant impacts on sqhC-containing microbial communities across the different ecosystems. Our results will be helpful to understanding the diversity, composition, and distribution of the sqhC community and its response to multiple environmental factors across different ecosystems.

Pyrene is a pollutant in the environment and affects the health of living organisms. It is important to understand microbial-mediated pyrene resistance and the related molecular mechanisms due to its toxicity and biodegradability. Due to the unclear response mechanisms of bacteria to PAHs, this study detected the transcriptional changes in Escherichia coli under different pyrene concentrations using transcriptome sequencing technology. Global transcriptome analysis showed that the number of differentially expressed genes (DEGs) in multiple metabolic pathways increased with increasing concentrations of pyrene. In addition, the effects and toxicity of pyrene on Escherichia coli mainly included the up-regulation and inhibition of genes related to carbohydrate metabolism, membrane transport, sulfate reduction, various oxidoreductases, and multidrug efflux pumps. Moreover, we also constructed an association network between significantly differentially expressed sRNAs and key genes and determined the regulatory relationship and key genes of Escherichia coli under pyrene stress. Our study utilized pyrene as an exogenous stress substance to investigate the possible pathways of the bacterial stress response. In addition, this study provides a reference for other related research and serves as a foundation for future research.

Thiomicrorhabdus species, belonging to the family Piscirickettsiaceae in the phylum Pseudomonadotav are usually detected in various sulfur-rich marine environments. However, only a few bacteria of Thiomicrorhabdus have been isolated, and their ecological roles and environmental adaptations still require further understanding. Here, we report a novel strain, XGS-01^T, isolated from a coastal sediment, which belongs to genus Thiomicrorhabdus and is most closely related to Thiomicrorhabdus hydrogeniphila MAS2^T, with a sequence similarity of 97.8%. Phenotypic characterization showed that XGS-01^T is a mesophilic, sulfur-oxidizing, obligate chemolithoautotrophy, with carbon dioxide as its sole carbon source and oxygen as its sole electron acceptor. During thiosulfate oxidation, strain XGS-01^T can produce extracellular sulfur of elemental α-S₈, as confirmed via scanning electron microscopy and Raman spectromicroscopy. Polyphasic taxonomy results indicate that strain XGS-01^T represents a novel species of the genus Thiomicrorhabdus, named Thiomicrorhabdus lithotrophica sp. nov. Genomic analysis confirmed that XGS-01^T performed thiosulfate oxidation through a sox multienzyme complex, and harbored fcc and sqr genes for sulfide oxidation. Comparative genomics analysis among five available genomes from Thiomicrorhabdus species revealed that carbon fixation via the oxidation of reduced-sulfur compounds coupled with oxygen reduction is conserved metabolic pathways among members of genus Thiomicrorhabdus.