The intergenic small non-coding RNA ittA is required for optimal infectivity and tissue tropism in Borrelia burgdorferi

• Published in: PLoS pathogens Vol. 16; no. 5; p. e1008423
• Main Authors: Medina-Pérez, Diana N, Wager, Beau, Troy, Erin, Gao, Lihui, Norris, Steven J, Lin, Tao, Hu, Linden, Hyde, Jenny A, Lybecker, Meghan, Skare, Jon T
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01.05.2020; Public Library of Science (PLoS)
• Subjects: Attenuation; Biology and Life Sciences; Borrelia burgdorferi; Deactivation; Funding; Gene expression; Gene regulation; Genetic aspects; Immunology; Inactivation; Infections; Infectivity; Laboratories; Lyme disease; Mammals; Medicine; Medicine and Health Sciences; Methods; Molecular biology; Mutants; Non-coding RNA; Pathogenesis; Pathology; Post-transcription; Proteins; Proteomics; Research and Analysis Methods; Ribonucleic acid; RNA; RNA sequencing; Skin; Supervision; Tissue analysis; Tissues; Tropism; Virulence; United States; United States > US; Colorado; Texas; Massachusetts
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1008423

Post-transcriptional regulation via small regulatory RNAs (sRNAs) has been implicated in diverse regulatory processes in bacteria, including virulence. One class of sRNAs, termed trans-acting sRNAs, can affect the stability and/or the translational efficiency of regulated transcripts. In this study, we utilized a collaborative approach that employed data from infection with the Borrelia burgdorferi Tn library, coupled with Tn-seq, together with borrelial sRNA and total RNA transcriptomes, to identify an intergenic trans-acting sRNA, which we designate here as ittA for infectivity-associated and tissue-tropic sRNA locus A. The genetic inactivation of ittA resulted in a significant attenuation in infectivity, with decreased spirochetal load in ear, heart, skin and joint tissues. In addition, the ittA mutant did not disseminate to peripheral skin sites or heart tissue, suggesting a role for ittA in regulating a tissue-tropic response. RNA-Seq analysis determined that 19 transcripts were differentially expressed in the ittA mutant relative to its genetic parent, including vraA, bba66, ospD and oms28 (bba74). Subsequent proteomic analyses also showed a significant decrease of OspD and Oms28 (BBA74) proteins. To our knowledge this is the first documented intergenic sRNA that alters the infectivity potential of B. burgdorferi.