Publications

4358

Abstract Axenic cultures are essential for studying microbial ecology, evolution, and genomics. Despite the importance of pure cultures, public culture collections are biased towards fast-growing copiotrophs, while many abundant aquatic prokaryotes remain uncultured due to uncharacterized growth requirements and oligotrophic lifestyles. Here, we applied high-throughput dilution-to-extinction cultivation using defined media that mimic natural conditions to samples from 14 Central European lakes, yielding 627 axenic strains. These cultures include 15 genera among the 30 most abundant freshwater bacteria identified via metagenomics, collectively representing up to 72% of genera detected in the original samples (average 40%) and are widespread in freshwater systems globally. Genome-sequenced strains are closely related to metagenome-assembled genomes (MAGs) from the same samples, many of which remain undescribed. We propose a classification of several novel families, genera, and species, including many slowly growing, genome-streamlined oligotrophs that are notoriously underrepresented in public repositories. Our large-scale initiative to cultivate the “uncultivated microbial majority” has yielded a valuable collection of abundant freshwater microbes, characterized by diverse metabolic pathways and lifestyles. This culture collection includes promising candidates for oligotrophic model organisms, suitable for a wide array of ecological studies aimed at advancing our ecological and functional understanding of dominant, yet previously uncultured, taxa.

Buckwheat (Fagopyrum esculentum Moench) is a fast-growing, low-input crop in the Polygonaceae family, cultivated on about 2 million hectares worldwide, mainly in Russia, China, and Ukraine by FAO (2023). In Taiwan, it is grown as a winter cover crop during fallow periods and is valued for improving soil health, suppressing weeds, and supporting sustainable farming systems. It is also utilized in various food products due to its rich fiber content and gluten-free properties. In May 2024, 147 out of 3000 plants (Taichung No. 5) corresponding to an incidence rate of approximately 5% exhibiting floral abnormalities, including phyllody, virescence, and flower sterility, were observed in Xinshe District in Taichung, central Taiwan (Fig. 1). These symptoms were indicative of possible phytoplasma infection. For further investigation, floral and leaf tissues were randomly collected from 10 symptomatic and 10 asymptomatic buckwheat plants. Plant total DNA was extracted using the DNeasy Plant Mini Kit, and PCR was performed targeting the 16S rRNA gene using universal phytoplasma primers P1A/P7A, followed by a semi-nested reaction with P1A/16S-SR (Lee et al. 2004). All PCR amplicons of approximately 1.5 kb were obtained only from symptomatic samples. PCR amplicons were sequenced by Sanger sequencing, and sequences were assembled by BioEdit. All symptomatic samples yielded identical sequences and a representative sequence (1,543 bp, nearly full-length 16S rRNA gene) was deposited in GenBank (Accession no. PV487329). Based on virtual RFLP analysis using iPhyClassifier (Zhao et al. 2009), the phytoplasma strain detected in diseased buckwheat plants was identified as a ‘Candidatus Phytoplasma aurantifolia/citri’-related strain, sharing 98.27% sequence identity with the reference strain (witches broom disease of lime, WBDL, Accession no. U15442). The strain, designated as Buckwheat Phyllody (BWP) TSIPS 3-1, was classified within the 16SrII-A subgroup, with a similarity coefficient of 1.00 when compared to the reference strain of subgroup 16SrII-A (Accession no. L33765). A BLASTn search against the NCBI database revealed that BWP-TSIPS 3-1 shared 99.94% identity with the 16S rRNA gene of potato purple top phytoplasma (Accession no. KM212951, a ‘Ca. P. aurantifolia/citri’-related strain), identified in Guangdong, China (Cheng et al. 2019). To further confirm phytoplasma identity, an additional gene marker, secY gene was amplified by semi-nested PCR using group-specific primers SecYF1(II)/SecYR1(II) and SecYF2(II) /SecYR1(II) (Lee et al. 2010). The 1,263-bp amplicons were obtained from all symptomatic samples. Sequencing results revealed identical secY sequences across samples, and a representative sequence was deposited in GenBank (Accession no. PV567544). BLASTn analysis indicated 100% (1263/1263) identity with the secY gene of the phytoplasmas, including black gram witches’-broom phytoplasma in Myanmar (Accession no. AB703249), which is classified within the 16SrII-A subgroup (Win and Jung, 2012). Phytoplasma infections associated with buckwheat have been rarely reported, with only a single case documented in India, though the short 16S rRNA gene sequence limited subgroup classification (Bandakkanavar et al. 2023). Similar symptoms, such as phyllody, have also been observed in Ukraine, but the causal agent remains unconfirmed due to the absence of molecular diagnostics (Demchenko et al. 2016). Our study confirmed the first identification of a ‘Ca. P. aurantifolia/citri’-related strain (16SrII-A subgroup) in buckwheat in Taiwan. Phytoplasmas of the 16SrII-A subgroup have been widely documented across Taiwan, including in Taichung (Tseng et al. 2012). Given the rising popularity of buckwheat for its dietary benefits and its increasing incorporation into crop rotation systems, especially as a winter cover crop, the presence of phytoplasma presents potential concerns. Infected buckwheat plants may inadvertently serve as hosts or reservoirs for phytoplasmas and their insect vectors, indicating a need for ongoing monitoring, especially in areas where buckwheat is part of crop rotations.

ABSTRACT Huanglongbing (HLB) is a devastating citrus disease associated with the gram-negative, phloem-limited, and unculturable bacterium “ Candidatus Liberibacter asiaticus ( C Las),” which is transmitted by the Asian citrus psyllid Diaphorina citri . Despite extensive research, effective, long-term, and sustainable solutions for managing HLB remain elusive. Oxytetracycline (OTC) is currently used as an emergency measure, but there is an urgent need for alternative compounds to complement or replace OTC. In this study, we identified amicoumacins, a class of antimicrobial compounds produced by the bacterium Bacillus safensis CB729 isolated from the citrus microbiome, and demonstrated their ability to suppress C Las. Genome mining of B. safensis CB729, combined with metabolomic analysis and bioassay-guided fractionation, revealed the presence of amicoumacins and related derivatives in fractions inhibitory to Liberibacter crescens , a culturable surrogate for C Las. We tested commercially available synthetic amicoumacins A and B, along with a B. safensis -derived amicoumacin mixture, against L. crescens and C Las. We determined the MICs of amicoumacin A (1.25 µg/mL) and amicoumacin B (10 µg/mL) against L. crescens . Furthermore, amicoumacin B and the amicoumacin mixture significantly reduced C Las populations in ex vivo citrus hairy root assays. This study highlights the potential of amicoumacins as a promising group of natural products for the management of HLB, offering valuable insights for the development of novel and sustainable disease control strategies. IMPORTANCE For two decades, the citrus industry has been severely impacted by Huanglongbing (HLB), a devastating disease caused by “ Candidatus Liberibacter asiaticus ( C Las)” and transmitted by the Asian citrus psyllid ( Diaphorina citri ). Despite extensive research, effective, long-term, and sustainable solutions remain unavailable for growers. Currently, medically relevant antibiotics, such as oxytetracycline (OTC), are used as an emergency response to combat HLB in Florida, the most affected citrus-producing state in the U.S. This underscores the urgent need for alternative treatments that can be used in rotation or as replacements for OTC. Here, we present amicoumacins, a group of bioactive secondary metabolites with antibiotic properties. We identified amicoumacin B and its derivatives from the culture broth of a Bacillus safensis isolate, native to citrus, and demonstrated their ability to inhibit Liberibacter spp. and reduce C Las populations in citrus tissue. This study highlights how microbial discovery can lead to the identification of antimicrobial compounds with potential applications in plant disease management.

Infection of cranberry by the 16SrIII-Y group phytoplasma responsible for cranberry false blossom disease results in floral disfigurement, fruit abortion, and phyllody, ultimately sterilizing infected plants. The pathogen almost devastated the cranberry industry in the 1930s, until control measures involving resistant cultivars and insect vector management were implemented. Recent discoveries of the pathogen and its vector in Wisconsin have renewed interest in exploring the pathosystem to gain deeper insights into host-pathogen interactions. A qPCR assay was used to detect phytoplasma infection, both spatially and temporally, in both symptomatic and asymptomatic cranberry plants. Dissection of infected vines by tissue type allowed detection of the phytoplasma throughout the entirety of the plant, revealing the systemic nature of the infection in cranberry vines. Furthermore, sampling throughout the growing season demonstrated that phytoplasma detection is possible at multiple time points, suggesting that diagnosis may be feasible even in the absence of clear symptoms like flower abnormalities, thereby enhancing diagnostic capabilities. Additionally, the qPCR method proved effective in detecting the causal agent within the insect vector, the blunt-nosed leafhopper. Phytoplasma acquisition occurs during feeding, colonizes various organs of the insect, and ultimately infect salivary glands making transmission possible. While the rate of colonization of both the plant and insect hosts is unknown, these findings provide valuable insights in industry decision-making for control and detection, as well as expanding understanding of a returning threat.

Phytoplasmas ('Candidatus Phytoplasma') are intracellular pleomorphic plant pathogens belonging to the class Mollicutes. They colonize both plant hosts and insect vectors in their life cycle. Apple proliferation (AP) is one of the most important phytoplasmoses present in Europe causing significant economic losses in apple production. The causal agent, ‘Ca. P. mali', was identified in apple and Cacopsylla picta samples using both real-time PCR and nested PCR based on the amplification of 16S rDNA. The objective of this study was to gain deeper insights into the epidemiology of apple proliferation in Croatia. Variability of genetic markers other than 16S rRNA was used for characterization of strains. Four molecular markers differing in level of conservation, aceF, pnp, imp and secY, were selected in line with previously typed fruit tree phytoplasmas. New genotypes were discerned for each genetic marker and 20 different sequence types were revealed in the Croatian isolates of ‘Ca. P. mali’. On the basis of this comprehensive analysis, the founder sequence type ST1 (A13-P10-S12-I21) can be proposed. This is the first extensive research and multigene typing performed on Croatian ‘Ca. P. mali’ isolates. Obtained results reveal considerable genetic diversity of epidemiological relevance limited to only two locations in north-western Croatia. Additionally, novel primers were constructed to amplify fragments larger than the entire coding region for all four genes in order to further expand phytoplasma multi locus sequence typing scheme.

A Gram-stain-negative, aerobic, non-motile and short rod-shaped bacterium, designated strain SCSIO 64248T, was isolated from the stony coral Fungia sp. collected from South China Sea. Phylogenetic analysis indicated that strain SCSIO 64248T belonged to the family Geminicoccaceae and showed the highest 16S rRNA gene similarities with the types of Marinimicrococcus flavescens (90.5%), Arboricoccus pini (90.2%) and Benzoalithermus flavus (89.8%). The whole genome of strain SCSIO 64248T was 4.9 Mbp with a 68.8mol% G+C content. It shared average amino acid identity (AAI) values of 52–56.2%, which is below the proposed AAI threshold at the genus level and when compared to the known species of Geminicoccaceae. Colonies of strain SCSIO 64248T are circular, pink and convex. It was able to grow in the range of 4–37 °C, at pH 6.0–10.0 and in the presence of up to 8.0% (w/v) NaCl concentration. The major cellular fatty acid (>9%) was summed feature 8, C19 : 0 cyclo ω8c and C16 : 0, and the sole respiratory quinone was Q-10. The polar lipids were phosphatidylglycerol, phosphatidylethanolamine, phosphatidylcholine and an unidentified phospholipid. Data of polyphasic characteristics revealed that strain SCSIO 64248T represented a novel species of a new genus within the family Geminicoccaceae, for which the name Marinivivus gen. nov. is proposed with the type strain of the type species Marinivivus vitaminiproducens SCSIO 64248T (=MCCC 1K08013T=KCTC 92503T).

Most micro-organisms remain unculturable under standard laboratory conditions, limiting our understanding of microbial diversity and ecological interactions. One major cause of this uncultivability is the loss of access to essential cross-fed metabolites when bacteria are removed from their natural communities. During a bioprospecting campaign targeting actinomycetes of an Apis mellifera beehive, we identified five isolates (DT32, DT45T, DT55, DT59 and DT194) that required co-cultivation for growth recovery, suggesting a dependence on microbial interactions in their native habitat. Whole-genome sequencing and phylogenetic analysis positioned these isolates within a distinct lineage of Micromonosporaceae, separate from the five officially recognized clades of the Micromonospora genus. A combination of microscopic, chemotaxonomic and physiological characterizations further supported their uniqueness. Notably, they exhibited high auxotrophy, being unable to use all carbon sources tested, likely due to genome reduction (4.6 Mbp) compared to other Micromonosporaceae. Pangenomic comparisons with their closest Micromonospora relatives revealed gene losses in key metabolic pathways, including the glyoxylate bypass and the Entner–Doudoroff pathway, which may explain their metabolic reliance. These findings reveal a highly specialized, ecologically adapted lineage with deep evolutionary divergence and further support microbial interdependence isolation strategies to explore the microbial dark matter. We propose Melissospora conviva as a novel genus and species within the Actinomycetota phylum, with isolate DT45T as the representative type species and type strain, which has been deposited in public collections under the accession numbers DSM 117791 and LMG 33580.