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      Biological aspects of phage therapy versus antibiotics against Salmonella enterica serovar Typhimurium infection of chickens

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          Abstract

          Phage therapy is a promising alternative treatment of bacterial infections in human and animals. Nevertheless, despite the appearance of many bacterial strains resistant to antibiotics, these drugs still remain important therapeutics used in human and veterinary medicine. Although experimental phage therapy of infections caused by Salmonella enterica was described previously by many groups, those studies focused solely on effects caused by bacteriophages. Here, we compared the use of phage therapy (employing a cocktail composed of two previously isolated and characterized bacteriophages, vB_SenM-2 and vB_Sen-TO17) and antibiotics (enrofloxacin and colistin) in chickens infected experimentally with S. enterica serovar Typhimurium. We found that the efficacies of both types of therapies (i.e. the use of antibiotics and phage cocktail) were high and very similar to one another when the treatment was applied shortly (one day) after the infection. Under these conditions, S. Typhimurium was quickly eliminated from the gastrointestinal tract (GIT), to the amount not detectable by the used methods. However, later treatment (2 or 4 days after detection of S. Typhimurium in chicken feces) with the phage cocktail was significantly less effective. Bacteriophages remained in the GIT for up to 2-3 weeks, and then were absent in feces and cloaca swabs. Interestingly, both phages could be found in various organs of chickens though with a relatively low abundance. No development of resistance of S. Typhimurium to phages or antibiotics was detected during the experiment. Importantly, although antibiotics significantly changed the GIT microbiome of chickens in a long-term manner, analogous changes caused by phages were transient, and the microbiome normalized a few weeks after the treatment. In conclusion, phage therapy against S. Typhimurium infection in chickens appeared as effective as antibiotic therapy (with either enrofloxacin or colistin), and less invasive than the use the antibiotics as fewer changes in the microbiome were observed.

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          Most cited references41

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          QIIME allows analysis of high-throughput community sequencing data.

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            Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies

            16S ribosomal RNA gene (rDNA) amplicon analysis remains the standard approach for the cultivation-independent investigation of microbial diversity. The accuracy of these analyses depends strongly on the choice of primers. The overall coverage and phylum spectrum of 175 primers and 512 primer pairs were evaluated in silico with respect to the SILVA 16S/18S rDNA non-redundant reference dataset (SSURef 108 NR). Based on this evaluation a selection of ‘best available’ primer pairs for Bacteria and Archaea for three amplicon size classes (100–400, 400–1000, ≥1000 bp) is provided. The most promising bacterial primer pair (S-D-Bact-0341-b-S-17/S-D-Bact-0785-a-A-21), with an amplicon size of 464 bp, was experimentally evaluated by comparing the taxonomic distribution of the 16S rDNA amplicons with 16S rDNA fragments from directly sequenced metagenomes. The results of this study may be used as a guideline for selecting primer pairs with the best overall coverage and phylum spectrum for specific applications, therefore reducing the bias in PCR-based microbial diversity studies.
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              Greengenes, a Chimera-Checked 16S rRNA Gene Database and Workbench Compatible with ARB

              A 16S rRNA gene database ( http://greengenes.lbl.gov ) addresses limitations of public repositories by providing chimera screening, standard alignment, and taxonomic classification using multiple published taxonomies. It was found that there is incongruent taxonomic nomenclature among curators even at the phylum level. Putative chimeras were identified in 3% of environmental sequences and in 0.2% of records derived from isolates. Environmental sequences were classified into 100 phylum-level lineages in the Archaea and Bacteria .
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                Author and article information

                Contributors
                Journal
                Front Cell Infect Microbiol
                Front Cell Infect Microbiol
                Front. Cell. Infect. Microbiol.
                Frontiers in Cellular and Infection Microbiology
                Frontiers Media S.A.
                2235-2988
                04 August 2022
                2022
                : 12
                : 941867
                Affiliations
                [1] 1 Laboratory of Phage Therapy, Institute of Biochemistry and Biophysics, Polish Academy of Sciences , Gdansk, Poland
                [2] 2 Department of Medical Microbiology, Faculty of Medicine, Medical University of Gdansk , Gdansk, Poland
                [3] 3 Department of Molecular Biology, Faculty of Biology, University of Gdansk , Gdansk, Poland
                [4] 4 Department of Cell Biology and Immunology, Intercollegiate Faculty of Biotechnology of University of Gdansk and Medical University of Gdansk , Gdansk, Poland
                [5] 5 Institute of Physical Culture, Kazimierz Wielki University , Bydgoszcz, Poland
                [6] 6 Department of Microbiology, Faculty of Biology, University of Gdansk , Gdansk, Poland
                [7] 7 Department of Animal and Human Physiology, Faculty of Biology, University of Gdansk , Gdansk, Poland
                Author notes

                Edited by: Anthony Buckley, University of Leeds, United Kingdom

                Reviewed by: Janice Spencer, Glasgow Caledonian University, United Kingdom; Marie Titecat, Centre Hospitalier Regional et Universitaire de Lille, France

                *Correspondence: Alicja Węgrzyn, alicja.wegrzyn@ 123456ug.edu.pl

                This article was submitted to Clinical Microbiology, a section of the journal Frontiers in Cellular and Infection Microbiology

                Article
                10.3389/fcimb.2022.941867
                9385949
                35992162
                37c2cb1e-e3b1-4b57-ae2a-cc0e4934d372
                Copyright © 2022 Kosznik-Kwaśnicka, Podlacha, Grabowski, Stasiłojć, Nowak-Zaleska, Ciemińska, Cyske, Dydecka, Gaffke, Mantej, Myślińska, Necel, Pierzynowska, Piotrowska, Radzanowska-Alenowicz, Rintz, Sitko, Topka-Bielecka, Węgrzyn and Węgrzyn

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 11 May 2022
                : 11 July 2022
                Page count
                Figures: 10, Tables: 2, Equations: 1, References: 41, Pages: 16, Words: 7862
                Funding
                Funded by: Narodowe Centrum Nauki , doi 10.13039/501100004281;
                Award ID: 2017/27/B/NZ9/00393
                Categories
                Cellular and Infection Microbiology
                Original Research

                Infectious disease & Microbiology
                phage therapy, salmonella enterica infection,antibiotics,chicken,microbiome

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