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      An rRNA fragment in extracellular vesicles secreted by human airway epithelial cells increases the fluoroquinolone sensitivity of P. aeruginosa

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          Abstract

          Abstract

          Lung infections caused by antibiotic-resistant strains of Pseudomonas aeruginosa are difficult to eradicate in immunocompromised hosts such as those with cystic fibrosis. We previously demonstrated that extracellular vesicles (EVs) secreted by primary human airway epithelial cells (AECs) deliver microRNA let-7b-5p to P. aeruginosa to suppress biofilm formation and increase sensitivity to beta-lactam antibiotics. In this study, we show that EVs secreted by AECs transfer multiple distinct short RNA fragments to P. aeruginosa that are predicted to target the three subunits of the fluoroquinolone efflux pump MexHI-OpmD, thus increasing antibiotic sensitivity. Exposure of P. aeruginosa to EVs resulted in a significant reduction in the protein levels of MexH (−48%), MexI (−50%), and OpmD (−35%). Moreover, EVs reduced planktonic growth of P. aeruginosa in the presence of the fluoroquinolone antibiotic ciprofloxacin by 20%. A mexGHI-opmD deletion mutant of P. aeruginosa phenocopied this increased sensitivity to ciprofloxacin. Finally, we found that a fragment of an 18S ribosomal RNA (rRNA) external transcribed spacer that was transferred to P. aeruginosa by EVs reduced planktonic growth of P. aeruginosa in the presence of ciprofloxacin, reduced the minimum inhibitory concentration of P. aeruginosa for ciprofloxacin by over 50%, and significantly reduced protein levels of both MexH and OpmD. In conclusion, an rRNA fragment secreted by AECs in EVs that targets the fluoroquinolone efflux pump MexHI-OpmD downregulated these proteins and increased the ciprofloxacin sensitivity of P. aeruginosa. A combination of rRNA fragments and ciprofloxacin packaged in nanoparticles or EVs may benefit patients with ciprofloxacin-resistant P. aeruginosa infections.

          NEW & NOTEWORTHY Human RNA fragments transported in extracellular vesicles interfere with Pseudomonas aeruginosa drug efflux pumps. A combination of rRNA fragments and ciprofloxacin packaged in nanoparticles or EVs may benefit patients with antibiotic-resistant P. aeruginosa infections.

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          fastp: an ultra-fast all-in-one FASTQ preprocessor

          Abstract Motivation Quality control and preprocessing of FASTQ files are essential to providing clean data for downstream analysis. Traditionally, a different tool is used for each operation, such as quality control, adapter trimming and quality filtering. These tools are often insufficiently fast as most are developed using high-level programming languages (e.g. Python and Java) and provide limited multi-threading support. Reading and loading data multiple times also renders preprocessing slow and I/O inefficient. Results We developed fastp as an ultra-fast FASTQ preprocessor with useful quality control and data-filtering features. It can perform quality control, adapter trimming, quality filtering, per-read quality pruning and many other operations with a single scan of the FASTQ data. This tool is developed in C++ and has multi-threading support. Based on our evaluation, fastp is 2–5 times faster than other FASTQ preprocessing tools such as Trimmomatic or Cutadapt despite performing far more operations than similar tools. Availability and implementation The open-source code and corresponding instructions are available at https://github.com/OpenGene/fastp.
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            BLAST+: architecture and applications

            Background Sequence similarity searching is a very important bioinformatics task. While Basic Local Alignment Search Tool (BLAST) outperforms exact methods through its use of heuristics, the speed of the current BLAST software is suboptimal for very long queries or database sequences. There are also some shortcomings in the user-interface of the current command-line applications. Results We describe features and improvements of rewritten BLAST software and introduce new command-line applications. Long query sequences are broken into chunks for processing, in some cases leading to dramatically shorter run times. For long database sequences, it is possible to retrieve only the relevant parts of the sequence, reducing CPU time and memory usage for searches of short queries against databases of contigs or chromosomes. The program can now retrieve masking information for database sequences from the BLAST databases. A new modular software library can now access subject sequence data from arbitrary data sources. We introduce several new features, including strategy files that allow a user to save and reuse their favorite set of options. The strategy files can be uploaded to and downloaded from the NCBI BLAST web site. Conclusion The new BLAST command-line applications, compared to the current BLAST tools, demonstrate substantial speed improvements for long queries as well as chromosome length database sequences. We have also improved the user interface of the command-line applications.
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              The PRIDE database resources in 2022: a hub for mass spectrometry-based proteomics evidences

              The PRoteomics IDEntifications (PRIDE) database ( https://www.ebi.ac.uk/pride/ ) is the world's largest data repository of mass spectrometry-based proteomics data. PRIDE is one of the founding members of the global ProteomeXchange (PX) consortium and an ELIXIR core data resource. In this manuscript, we summarize the developments in PRIDE resources and related tools since the previous update manuscript was published in Nucleic Acids Research in 2019. The number of submitted datasets to PRIDE Archive (the archival component of PRIDE) has reached on average around 500 datasets per month during 2021. In addition to continuous improvements in PRIDE Archive data pipelines and infrastructure, the PRIDE Spectra Archive has been developed to provide direct access to the submitted mass spectra using Universal Spectrum Identifiers. As a key point, the file format MAGE-TAB for proteomics has been developed to enable the improvement of sample metadata annotation. Additionally, the resource PRIDE Peptidome provides access to aggregated peptide/protein evidences across PRIDE Archive. Furthermore, we will describe how PRIDE has increased its efforts to reuse and disseminate high-quality proteomics data into other added-value resources such as UniProt, Ensembl and Expression Atlas.
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                Author and article information

                Journal
                Am J Physiol Lung Cell Mol Physiol
                Am J Physiol Lung Cell Mol Physiol
                AJPLUNG
                American Journal of Physiology - Lung Cellular and Molecular Physiology
                American Physiological Society (Rockville, MD )
                1040-0605
                1522-1504
                1 July 2023
                31 May 2023
                31 May 2023
                : 325
                : 1
                : L54-L65
                Affiliations
                [1] 1Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, United States
                [2] 2Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, United States
                [3] 3Mass Spectrometry Technology Access Center, McDonnell Genome Institute, Washington University School of Medicine , St. Louis, Missouri, United States
                Author notes
                Correspondence: K. Koeppen ( Koeppen.Katja@ 123456gmail.com ).
                Author information
                https://orcid.org/0000-0003-1094-0621
                https://orcid.org/0000-0003-0543-402X
                https://orcid.org/0000-0002-6366-2971
                Article
                L-00150-2022 L-00150-2022
                10.1152/ajplung.00150.2022
                10390050
                37256658
                92f94dc9-eaed-4f70-97d0-ed1e6773a5df
                Copyright © 2023 The Authors.

                Licensed under Creative Commons Attribution CC-BY 4.0. Published by the American Physiological Society.

                History
                : 5 May 2022
                : 10 April 2023
                : 28 May 2023
                Funding
                Funded by: Cystic Fibrosis Foundation (CFF) , doi 10.13039/100000897;
                Award ID: STANTO19G0
                Award Recipient : Bruce A. Stanton
                Funded by: Cystic Fibrosis Foundation (CFF) , doi 10.13039/100000897;
                Award ID: STANTO20P0
                Award Recipient : Bruce A. Stanton
                Funded by: Cystic Fibrosis Foundation (CFF) , doi 10.13039/100000897;
                Award ID: STANTO19R0
                Award Recipient : Bruce A. Stanton
                Funded by: Cystic Fibrosis Foundation (CFF) , doi 10.13039/100000897;
                Award ID: GREENE21G0
                Award Recipient : Deborah A. Hogan
                Funded by: HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) , doi 10.13039/100000050;
                Award ID: R01HL151385
                Award Recipient : Bruce A. Stanton
                Funded by: HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) , doi 10.13039/100000062;
                Award ID: P30-DK117469
                Award Recipient : Bruce A. Stanton
                Funded by: HHS | NIH | National Institute of General Medical Sciences (NIGMS) , doi 10.13039/100000057;
                Award ID: R01GM122846
                Award Recipient : Scott A. Gerber
                Categories
                Research Article
                Extracellular Vesicles in Lung Health, Disease, and Therapy
                Custom metadata
                True

                Anatomy & Physiology
                antibiotic resistance,ciprofloxacin,evs,host-pathogen interaction,pseudomonas
                Anatomy & Physiology
                antibiotic resistance, ciprofloxacin, evs, host-pathogen interaction, pseudomonas

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