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Wang, F.-Q.

Publications and source records attributed to Wang, F.-Q..

4 recordsLinked to original sources

Bacteriophages of the predominant coral symbiont Endozoicomonas: novel models for coral holobiont interactions

Phages are important symbionts in corals that modulate the community and functions of other symbiotic bacteria. Although phages infecting coral pathogens have been reported, no phage targeting beneficial microorganisms in corals has been isolated to date. From seawater near Acropora and Stylophora corals, we isolated the first bacteriophages (designated EmPhiA and EmPhiS) that infect Endozoicomonas montiporae CL-33, a model strain of the coral-prevalent and predominant Endozoicomonas bacteria. Electron microscopic observations of both phages showed Myovirus-like morphology and head sizes characteristic of jumbophages, with cryo-electron microscopy reveals long whiskers unprecedent in known phages. Genetically, these phages shared 99.21% genome similarity and are distant from known prokaryotic viruses, suggesting that they represent a novel viral species, which we name Encorevirus taiwanensis, in a novel family Encoreviridae. The small burst sizes of these phages (13.14 PFU/cell for EmPhiA and 21.4 PFU/cell for EmPhiS) potentially enable continuous coexistence of them with host bacteria within corals, making them putative core members of coral holobionts. Furthermore, host range test showed that EmPhiA and EmPhiS infect both Endozoicomonas bacteria isolated from stony and soft corals, implying their presence in a broad spectrum of host marine invertebrates. Using EmPhiS, we also investigated phage-bacterium interaction during its infection of E. montiporae CL-33. Interestingly, in addition to modulation of host cellular machinery, we found expression of several tellurium resistance proteins by EmPhiS during infection, which may provide the host additional stress resistance. These phages provide a novel model that will greatly advance our understanding of coral-Endozoicomonas-phage interactions.

microbiology↗

Genomic insights into polysaccharide substrate utilization and novel genera resource mining in macroalgal epiphytic bacteria

Marine macroalgae, among the fastest photosynthesizing organisms, play a crucial role in the ocean carbon cycle by converting fixed carbon dioxide into polysaccharides. Macroalgal epiphytic bacteria possessing specific polysaccharide utilization loci (PULs) have a generalized polysaccharide degradation potential that facilitates their growth and colonization. In this study, we conducted extensive research on their polysaccharide degradation potential. Through sampled and purified epiphytic bacteria and metagenomic analysis revealed a high prevalence of novel genera and species. Two novel genera, 1117T and 3-347T, were taxonomically characterized and conducted detailed functional analyses. The results demonstrated that these genera possess abundant PULs and strong capabilities for synthesizing secondary metabolites. Furthermore, their high relative abundance on macroalgal surfaces aligns with global ecological distribution patterns. These traits facilitate their colonization, growth, and environmental adaptation on macroalgal surfaces. We further performed in-depth annotation of a large number of PULs and CAZyme genes of macroalgal epiphytic bacteria. Potential polysaccharide substrates for their degradation can be predicted and focused on. Additionally, we conducted growth curve analyses by starch, xylan, {beta}-1,3-glucan, and carboxymethyl cellulose substrates to validate the genomic predictions. In summary, our findings demonstrate that macroalgal epiphytic bacteria possess significant potential for degrading algal polysaccharides. This capability may enhance their competitiveness and survival probability on macroalgal surfaces. These bacteria, originating from different sources and genera, possess similar PULs, which may result from horizontal gene transfer or evolutionary relationships. ImportanceMacroalgae are major primary producers in coastal areas and their carbon sequestration capacity per unit area far exceeds that of terrestrial forests. In this work, we extensively studied macroalgal epiphytic bacteria with polysaccharide degradation potential. We found that epiphytic bacteria from different macroalgal sources and genera share similar PULs to degrade the same polysaccharide, which may be the result of horizontal gene transfer or evolutionary relationships. Core taxa on the macroalgal surface have gradually evolved polysaccharide-degrading abilities of different marine macroalgae in order to expand their colonization and survival chances. We also identified a large number of uncultivated algal biosphere species and unreported new genera and species for expansion of macroalgal epiphytic bacteria studies. These studies have thus highlighted the important ecological and research value of macroalgal epiphytic bacteria, especially in influencing polysaccharide carbon storage and marine carbon cycling.

microbiology↗

Surface-mediated Bacteriophage Defense Incurs Fitness Tradeoffs for Interbacterial Antagonism

Bacteria in polymicrobial habitats are constantly exposed to biotic threats from bacteriophages (or "phages"), antagonistic bacteria, and predatory eukaryotes. These antagonistic interactions play crucial roles in shaping the evolution and physiology of bacteria. To survive, bacteria have evolved mechanisms to protect themselves from such attacks, but the fitness costs of resisting one threat and rendering bacteria susceptible to others remain unappreciated. Here, we examined the fitness consequences of phage resistance in Salmonella enterica, revealing that phage-resistant variants exhibited significant fitness loss upon co-culture with competitor bacteria. These phage-resistant strains display varying degrees of lipopolysaccharide (LPS) deficiency and increased susceptibility to contact-dependent interbacterial antagonism, such as the type VI secretion system (T6SS). Utilizing mutational analyses and atomic force microscopy, we show that the long-modal length O-antigen of LPS serves as a protective barrier against T6SS-mediated intoxication. Notably, this competitive disadvantage can also be triggered independently by phages possessing LPS-targeting endoglycosidase in their tail spike proteins, which actively cleave the O- antigen upon infection. Our findings reveal two distinct mechanisms of phage-mediated LPS modifications that modulate interbacterial competition, shedding light on the dynamic microbial interplay within mixed populations.

microbiology↗

A CRISPR-Cas assisted shotgun mutagenesis method for evolutionary genome engineering

Genome mutagenesis drives the evolution of organisms. Here, we developed a CRISPR-Cas assisted random mutation (CARM) technology for whole genome mutagenesis. The method leverages an entirely random gRNA library and SpCas9-NG to randomly damage genomes in a controllable shotgun-like manner that then triggers diverse and abundant mutations via low-fidelity repair. As a proof-of-principle, CARM was applied to evolve the capacity of Saccharomyces cerevisiae BY4741 to produce {beta}-carotene. After seven rounds of iterative evolution over two months, a {beta}-carotene hyper-producing strain, C7-143, was isolated with a 10.5-fold increase in {beta}-carotene production and 857 diverse genomic mutants that comprised indels, duplications, inversions, and chromosomal rearrangements. Transcriptomic analysis revealed that the expression of 2,541 genes of strain C7-143 were significantly altered, suggesting that the metabolic landscape of the strain was deeply reconstructed. In addition, CARM was applied to evolve the industrially relevant Saccharomyces cerevisiae CEN.PK2-1C, the S-adenosyl-L-methionine production of which was increased to 2.28 times after just one round. Thus, CARM is a user-friendly and practical strategy for genetic remodeling and reverse engineering to investigate complicated organismal metabolism.

evolutionary biology↗