Publications

4870

Abstract Background Spirochetes are the most abundant bacterial group in the hindgut of termites. The largest species, with cell lengths of up to 100 µm, have been provisionally classified in the family “ Pillotinaceae ” based exclusively on morphological traits. However, in the absence of cultured representatives, their phylogenetic position and metabolism remain entirely unknown. Results We investigated phylogeny and metabolic capacities of “pillotinaceous” spirochetes using single-cell techniques, electron microscopy, and fluorescence in situ hybridization. All sequences of large spirochetes obtained from various termites fell into four distinct, well-supported clusters within the family Breznakiellaceae . Based on ultrastructural features, three of the clusters were assigned to the genera Pillotina , Hollandina , and the newly established genus Hollandinoides; a fourth cluster was tentatively assigned to the genus Clevelandina . Functional analysis of the single-cell genomes of Pillotina corrugata sp. nov., Hollandina grandis sp. nov., and Hollandinoides gharagozlouae gen. nov. sp. nov., combined with comparative genomics of other uncultured relatives, demonstrated differences in the capacity to degrade cellulose, hemicelluloses, and dextrins. While members of the genus Pillotina have a fermentative metabolism, members of the other genera encode a Wood–Ljungdahl pathway and, in the case of Hollandina , a group-III nitrogenase, suggesting roles in reductive acetogenesis and nitrogen fixation. Conclusions Our results provide the first molecular data on pillotinaceous spirochetes. We show that the three genera covered in our study belong to the family Breznakiellaceae , which harbors the majority of termite-gut spirochetes. Comparative genome analysis indicated that the large spirochetes in termite guts have distinct roles in symbiotic digestion.

<p>Huanglongbing (HLB), caused by <em>Candidatus </em>Liberibacter asiaticus (CLas), continues to challenge citrus production in Saudi Arabia. Although HLB is widespread, there is still limited understanding of how temperature, season, host species, and the type of tissue sampled influence the reliability of CLas detection. In this regard, 123 CLas-positive samples sourced from major citrus-growing areas were analyzed. These samples included data from 4 major citrus species and 4 tissue types. Additionally, cycle threshold<strong> </strong>(Ct) values obtained through quantitative PCR for each sample were used to examine how climate and CLas interact in bacterial detection. As lower Ct values indicate higher bacterial abundance, an analysis of covariance (ANCOVA) was conducted to assess the influence of season, tissue type, citrus species, and average seasonal temperature on Ct values. The results demonstrated significant differences among tissue types, with petiole and midrib tissues exhibiting consistently lower Ct values. Additionally, lower Ct values were observed in spring and autumn, and higher Ct values in warmer summers and colder winters, based on average temperatures. Among the citrus species, only <em>Citrus limon</em> illustrated a prominent increase in CLas levels as temperatures increased. CLas levels in <em>C. limon</em> showed only minor fluctuations with temperature. Taken together, these results indicated that temperature gradients strongly shape CLas population levels in Saudi Arabia and influence the reliability of pathogen detection. Considering climatic context, along with tissue type and season can substantially improve sampling strategies and enhance the effectiveness of HLB monitoring programs in arid and semi-arid citrus production systems.</p>

Abstract Candidatus Liberibacter asiaticus ( C Las), the causal agent of Huanglongbing, is transmitted by the Asian citrus psyllid ( Diaphorina citri ) in a persistent, propagative manner. Reproducible transmission studies require not only controlled inoculation assays but also standardized propagation of citrus host plants, maintenance of D. citri colonies, and reliable pathogen detection. This study presents a comprehensive set of coordinated protocols that collectively support controlled C Las transmission experimentation. The workflow includes propagation of Citrus macrophylla for colony and assay use; generation and maintenance of C Las‐infected citrus and D. citri colonies; synchronization of D. citri populations to enable C Las acquisition; and a controlled single‐ D. citri transmission assay with defined inoculation access periods, and a Dellaporta‐based nucleic acid extraction method compatible with citrus and psyllid tissues. Quantitative PCR detection is integrated throughout to verify infection status, determine C Las titer, and monitor C Las movement and systemic colonization in citrus over time. By combining standardized plant production, vector infection systems, transmission assays, and molecular diagnostics, these coordinated methods provide a unified framework for testing hypotheses about vector competence, pathogen–vector interactions, microbial co‐infections, host susceptibility, and environmental effects on transmission. Together, the procedures enable consistent and comparable assessment of C Las acquisition, dissemination, and transmission outcomes under controlled laboratory conditions. © 2026 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1 : Controlled laboratory method for assessing Candidatus Liberibacter asiaticus transmission by Diaphorina citri Support Protocol 1 : Generation of Candidatus Liberibacter asiaticus‐infected Citrus macrophylla and Diaphorina citri Basic Protocol 2 : Dellaporta total nucleic acid extraction Basic Protocol 3 : Citrus macrophylla propagation