| Literature DB >> 33321823 |
Khatuna Makalatia1,2, Elene Kakabadze1,2, Jeroen Wagemans3, Nino Grdzelishvili1,4, Nata Bakuradze1,2, Gulnara Natroshvili1, Nino Macharashvili5, Anahit Sedrakyan6, Karine Arakelova6, Zhanna Ktsoyan6, Magdalina Zakharyan6, Zaruhi Gevorgyan7, Armine Mnatsakanyan8, Farida Tishkova9, Cédric Lood3,10, Dieter Vandenheuvel11, Rob Lavigne3, Jean-Paul Pirnay12, Daniel De Vos12, Nina Chanishvili1, Maia Merabishvili1,12.
Abstract
Non-typhoidal Salmonella present a major threat to animal and human health as food-borne infectious agents. We characterized 91 bacterial isolates from Armenia and Georgia in detail, using a suite of assays including conventional microbiological methods, determining antimicrobial susceptibility profiles, matrix assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry, serotyping (using the White-Kauffmann-Le Minor scheme) and genotyping (repetitive element sequence-based PCR (rep-PCR)). No less than 61.5% of the isolates were shown to be multidrug-resistant. A new antimicrobial treatment strategy is urgently needed. Phage therapy, the therapeutic use of (bacterio-) phages, the bacterial viruses, to treat bacterial infections, is increasingly put forward as an additional tool for combatting antibiotic resistant infections. Therefore, we used this representative set of well-characterized Salmonella isolates to analyze the therapeutic potential of eleven single phages and selected phage cocktails from the bacteriophage collection of the Eliava Institute (Georgia). All isolates were shown to be susceptible to at least one of the tested phage clones or their combinations. In addition, genome sequencing of these phages revealed them as members of existing phage genera (Felixounavirus, Seunavirus, Viunavirus and Tequintavirus) and did not show genome-based counter indications towards their applicability against non-typhoidal Salmonella in a phage therapy or in an agro-food setting.Entities:
Keywords: Armenia; Georgia; Salmonella; antibiotic resistance; bacteriophages; clinical isolates; foodborne pathogens; genome sequencing; genotyping; phage therapy
Year: 2020 PMID: 33321823 PMCID: PMC7764154 DOI: 10.3390/v12121418
Source DB: PubMed Journal: Viruses ISSN: 1999-4915 Impact factor: 5.048