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Narihiro, T.

Publications and source records attributed to Narihiro, T..

6 recordsLinked to original sources

Genetic variation in early-season leaf photosynthesis in sugar beet and its relationship with Cercospora leaf spot resistance

Improving photosynthesis is a promising approach to enhance sugar beet productivity. However, genetic variation in leaf photosynthesis and its relationship with disease resistance remain underexplored. We evaluated 98 sugar beet genotypes representing different breeding categories, including commercial F1 hybrids, seed-parent lines, and pollinator lines, in Hokkaido, northern Japan. Leaf gas exchange was measured during early growth under field conditions around the infection period of Cercospora leaf spot (CLS). To account for fluctuating irradiance during large-scale phenotyping, we applied a multilevel mixed-effects light-response model to estimate genotype-specific photosynthetic characteristics. Substantial genotypic variations in photosynthetic characteristics were detected. F1 hybrids exhibited higher photosynthetic capacity than breeding lines, whereas differences among breeding categories were unclear due to large within-category variation. Some breeding lines exhibited photosynthetic rates higher than those of hybrids, indicating exploitable genetic resources within the present genetic panel. We did not detect statistically significant trade-off between leaf photosynthesis and CLS resistance among 98 genotypes; in a subset of 19 genotypes analysed in detail, the relationship was even synergistic. Our results highlight the genetic diversity of leaf photosynthesis and its category-dependent structure, and suggest that selection for enhanced photosynthesis can proceed without substantial trade-off with CLS resistance. HighlightLeaf photosynthesis of 98 sugar beet genotypes showed significant genetic variation and dependence on breeding category. Active photosynthesis incurred minimal trade-off with Cercospora leaf spot resistance.

plant biology↗

The significance of sukumo (composted indigo leaves) as a microbial source for traditional Japanese indigo dyeing

A critical process in traditional Japanese indigo dyeing is the microbial reduction of indigo within the dye suspension, which consists solely of sukumo (fermented indigo leaves), wood ash lye, and microbial nutrients such as wheat bran. Although sukumo has long been recognized as a potential microbial source, the microbial community dynamics during its production is still largely unexplored, and its contribution to dyeing performance via microbial supply remains poorly characterized. In this study, we investigated the significance of sukumo as a microbial source, in addition to its established role as a pigment source. We conducted a time-series analysis of microbial communities throughout the four-month fermentation process of sukumo, using weekly samples collected from two geographically distinct indigo dyeing studios. Microbial profiling revealed similar successional patterns between the two sites. Notably, in the later stages of fermentation, known indigo-reducing bacteria, such as the genus Oceanobacillus and the family Tissierellaceae, emerged at both locations. Laboratory-scale dyeing experiments using immature sukumo demonstrated that supplementation with a small amount of mature sukumo restored dyeing activity and increased the abundance of Oceanobacillus and Tissierellaceae. Furthermore, the addition of the indigo-reducing isolate Tissierellaceae strain TU-1 to the immature sukumo-based dye suspension led to a marked enhancement in dyeing performance. These findings highlight the critical role of sukumo as a microbial source in traditional indigo dyeing and suggest that prolonged fermentation is essential for nurturing functional indigo-reducing bacteria. This insight provides a foundation for improving dye suspension performance through targeted microbial community management.

microbiology↗

Comparative metagenomic analysis provides novel insights into the ecophysiology of Myxococcota in activated sludge systems

Myxobacteria, belonging to the phylum Myxococcota, are ubiquitous in soil, marine, and other environments. Recent metagenomic sequencing analysis has shown that Myxococcota are predominant in activated sludge systems; however, their ecophysiological traits remain unclear. In this study, we evaluated the potential biological functions of 46 metagenomic bins of Myxococcota reconstructed from activated sludge samples from four municipal sewage treatment plants. The results showed that most Myxococcota bins had an almost complete set of genes associated with glycolysis and the TCA cycle. Palsa-1104 and Polyangiales bins contain glycoside hydrolase GH13 and peptidase M23, which are presumably involved in the lysis of the cell wall and cellular cytoplasm, indicating that part of the Myxococcota from activated sludge can prey on other microorganisms. The previously known cell contact-dependent predatory functions of Myxococcus xanthus are conserved in the family Myxococcaceae, though not in other families. Two bins belonging to Palsa-1104 had phototrophic gene clusters, suggesting that these bins may have both heterotrophic and autotrophic metabolisms. Assessment of the social behavior of the activated sludge Myxococcota, a FruA gene, and a C-signal gene involved in the regulation of fruiting body formation were lacking in Myxococcota bins, suggesting that they are incapable of fruiting body formation. In addition, multiple bins of Myxococcota had novel secondary metabolite biosynthesis gene clusters that may be used for the predation of other bacteria in the activated sludge. Our metagenome-based analyses provide novel insights into the microbial interactions associated with Myxococcota in activated sludge ecosystems.

microbiology↗

Microscopic and metatranscriptomic analyses revealed unique cross-domain symbiosis between Candidatus Patescibacteria/candidate phyla radiation (CPR) and methanogenic archaea in anaerobic ecosystems

To verify the parasitic lifestyle of Candidatus Patescibacteria in the enrichment cultures derived from a methanogenic bioreactor, we applied multifaceted approaches combining cultivation, microscopy, metatranscriptomic, and protein structure prediction analyses. Cultivation experiments with the addition of exogenous methanogenic archaea with acetate, amino acids, and nucleoside monophosphates and 16S rRNA gene sequencing confirmed the increase in the relative abundance of Ca. Patescibacteria and methanogens. The predominant Ca. Patescibacteria were Ca. Yanofskybacteria and 32-520 lineages (to which belongs to class Ca. Paceibacteria) and positive linear relationships (r2 [≥] 0.70) between the relative abundance of Ca. Yanofskybacteria and Methanothrix, suggesting that the tendency of the growth rate is similar to that of the host. By fluorescence in situ hybridization (FISH) observations, the FISH signals of Methanothrix and Methanospirillum cells with Ca. Yanofskybacteria and with 32-520 lineages, respectively, were significantly lower than those of the methanogens without Ca. Patescibacteria, suggesting their parasitic interaction. The TEM and SEM observations also support parasitism in that the cell walls and plugs of these methanogens associated with submicron cells were often deformed. In particular, some Methanothrix-like filamentous cells were dented where the submicron cells were attached. Metatranscriptomic and protein structure prediction analyses identified highly expressed secreted genes from the genomes of Ca. Yanofskybacteria and 32-520, and these genes contain adhesion-related domains to the host cells. Considering the results through the combination of microscopic observations, gene expression, and computational protein modeling, we propose that the interactions between Ca. Yanofskybacteria and 32-520 belonging to class Ca. Paceibacteria and methanogenic archaea are parasitism.

microbiology↗

Unique episymbiotic relationship between Gracilibacteria and Zoogloea in activated sludge flocs in a municipal wastewater treatment plant

Among the various bacteria present in activated sludge, uncultivated Patescibacteria (also known as the Candidate Phyla Radiation/CPR superphylum) are ubiquitous at the class or phylum level. Patescibacteria have a highly restricted metabolic capacity and are thought to be episymbiotic/endosymbiotic or predatory. However, only a limited number of Patescibacteria and their hosts have been identified. Therefore, many Patescibacteria have not been (co-)cultured and identified by fluorescence in situ hybridization (FISH) or electron microscopy. Little is known about the morphology, metabolic potential, and hosts of Gracilibacteria (formerly GN02 or BD1-5) which belong to Patescibacteria. In our previous study, we confirmed the presence of Gracilibacteria in activated sludge and successfully recovered its high-quality genome. In this study, we designed new probes to visualize members of Gracilibacteria in activated sludge and identified its host using FISH. The FISH observations revealed that Gracilibacteria, which formed loosely associated clusters, were located within dense clusters of Zoogloea, which were dominant in the activated sludge. The metagenome-assembled genomes (MAGs) of Zoogloea possessed genes related to extracellular polymeric substance (EPS) biosynthesis, floc formation, and nutrient removal, including a polyhydroxyalkanoate (PHA) accumulation pathway. The MAGs of Gracilibacteria possessed genes associated with type IV pili, competence protein EC (ComEC), and PHA degradation, which suggests that they have a Zoogloea-dependent lifestyle in activated sludge flocs. These findings clearly indicate a new symbiotic relationship between Gracilibacteria and Zoogloea, and to the best of our knowledge, this is the first study to show this interaction.

microbiology↗

Symbiosis between Patescibacteria and Archaea discovered in wastewater-treating bioreactors

Each prokaryotic domain, Bacteria and Archaea, contains a large and diverse group of organisms characterized with ultrasmall cell size and symbiotic lifestyles - Patescibacteria (also known as Candidate Phyla Radiation/CPR) and DPANN archaea. Cultivation-based approaches have revealed that Patesibacteria and DPANN symbiotically interact with bacterial and archaeal partners/hosts respectively, but cross-domain symbiosis/parasitism has never been observed. Here, we discovered physical interaction between ultramicrobacterial Patescibacteria and methanogenic archaea using cultures from anaerobic wastewater treatment sludge. In the cultures, we observed physical attachment of ultramicrobial cells to cells resembling Methanothrix and Methanospirillum using transmission electron microscopy and successfully detected physical association of Ca. Yanofskybacteria and Methanothrix using fluorescence in situ hybridization (FISH) (other ultramicrosized bacterial cells, presumably Patescibacteria, were also observed to attach on Methanospirillum). This was further confirmed to be a symbiosis rather than simple aggregation based on the observation that most ultramicrobacterial cells attached to Methanothrix were Ca. Yanofskybacteria and positive correlation (p < 0.05) between the relative abundance of Patescibacteria lineages and methanogenic archaea (e.g., Ca. Yanofskybacteria-Methanothrix and uncultured clade 32-520-Methanospirillum). The results shed light on a novel cross-domain symbiosis and inspire potential strategies for culturing CPR/DPANN.

microbiology↗