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Stuehler et al. Microbiome Res Rep. 2025;4:19                 Microbiome Research
               DOI: 10.20517/mrr.2024.84
                                                                                               Reports




               Original Article                                                              Open Access



               Transcriptomic characterization of Wolbachia
               endosymbiont from Leuronota fagarae (Hemiptera:

               Psylloidae)


               Douglas S. Stuehler Jr. 1,2  , Wayne B. Hunter 2  , Jawwad A. Qureshi 3  , Liliana M. Cano 4
               1
                Oak Ridge Institute for Science and Education ORISE, Department of Energy and the United States Department of Agriculture
               DOE/USDA, Agricultural Research Station ARS, Fort Pierce, FL 34945, USA.
               2
                United States Department of Agriculture USDA, Agricultural Research Station ARS, U.S. Horticultural Research Laboratory, Fort
               Pierce, FL 34945, USA.
               3
                Department of Entomology and Nematology, Southwest Florida Research and Education Center SWFREC, Institute of Food and
               Agricultural Sciences IFAS, University of Florida, Immokalee, FL 34142, USA.
               4
                Department of Plant Pathology, Indian River Research and Education Center IRREC, Institute of Food and Agricultural Sciences
               IFAS, University of Florida, Fort Pierce, FL 34945, USA.
               Correspondence to: Dr. Liliana M. Cano, Department of Plant Pathology, Indian River Research and Education Center IRREC,
               Institute of Food and Agricultural Sciences IFAS, University of Florida, 2199 South Rock Road, Fort Pierce, FL 34945, USA. E-mail:
               Lmcano@ufl.edu

               How to cite this article: Stuehler DS Jr., Hunter WB, Qureshi JA, Cano LM. Transcriptomic characterization of Wolbachia
               endosymbiont from Leuronota fagarae (Hemiptera: Psylloidae). Microbiome Res Rep. 2025;4:19. https://dx.doi.org/10.20517/mrr.
               2024.84

               Received: 25 Nov 2024  First Decision: 14 Jan 2025  Revised: 11 Mar 2025  Accepted: 27 Mar 2025   Published: 3 Apr 2025

               Academic Editors: Douwe van Sinderen, Emma Allen-Vercoe   Copy Editor: Pei-Yun Wang   Production Editor: Pei-Yun Wang

               Abstract
               Aim: Wolbachia species are among the most abundant intracellular endosymbionts of insects worldwide. The
               extensive distribution of Gram-negative Wolbachia among insects highlights their evolutionary success and close
               relationship with many insect host species. This study aimed to characterize a novel Wolbachia strain from the
               Wild Lime Psyllid, Leuronota fagarae (L. fagarae), to understand its evolutionary relationship with Wolbachia from
               psyllid pests like Diaphorina citri, the vector of Huanglongbing (HLB).

               Methods: Wild-caught L. fagarae colonies from Florida, USA, were maintained on Zanthoxylum fagara. RNA was
               extracted from the salivary glands, heads, and whole bodies of male and female adult L. fagarae. Four cDNA
               libraries were sequenced using short read technology and de novo transcriptome assembly was performed.
               Multilocus sequence typing (MLST) of nine conserved loci and wsp gene analysis classified the strain’s phylogeny,
               while sequence mapping and functional annotation provided insight into host-microbe interactions.





                           © The Author(s) 2025. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing,
                           adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as
               long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and
               indicate if changes were made.

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