TY - JOUR
T1 - Characterization of salmonella isolates from various geographical regions of the caucasus and their susceptibility to bacteriophages
AU - Makalatia, Khatuna
AU - Kakabadze, Elene
AU - Wagemans, Jeroen
AU - Grdzelishvili, Nino
AU - Bakuradze, Nata
AU - Natroshvili, Gulnara
AU - Macharashvili, Nino
AU - Sedrakyan, Anahit
AU - Arakelova, Karine
AU - Ktsoyan, Zhanna
AU - Zakharyan, Magdalina
AU - Gevorgyan, Zaruhi
AU - Mnatsakanyan, Armine
AU - Tishkova, Farida
AU - Lood, Cédric
AU - Vandenheuvel, Dieter
AU - Lavigne, Rob
AU - Pirnay, Jean Paul
AU - De Vos, Daniel
AU - Chanishvili, Nina
AU - Merabishvili, Maia
N1 - Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/12
Y1 - 2020/12
N2 - 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.
AB - 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.
KW - Antibiotic resistance
KW - Armenia
KW - Bacteriophages
KW - Clinical isolates
KW - Foodborne pathogens
KW - Genome sequencing
KW - Genotyping
KW - Georgia
KW - Phage therapy
KW - Salmonella
UR - http://www.scopus.com/inward/record.url?scp=85098534591&partnerID=8YFLogxK
U2 - 10.3390/v12121418
DO - 10.3390/v12121418
M3 - Article
C2 - 33321823
AN - SCOPUS:85098534591
SN - 1999-4915
VL - 12
JO - Viruses
JF - Viruses
IS - 12
M1 - 1418
ER -