Enterococcus montenegrensis sp. nov., isolated from artisanal Montenegrin dry sausage

Author:

Daza-Prieto Beatriz12ORCID,Raicevic Nadja3,Cabal Adriana2,Hyden Patrick2,Mösenbacher Tobias2,Ladstätter Johann2,Richter Susanne4,Stöger Anna2,Joao Cardoso Maria52,Chakeri Ali62,Hasenberger Petra2,Stadlbauer Silke2,Mach Robert L.1,Martinovic Aleksandra3ORCID,Ruppitsch Werner72

Affiliation:

1. Institute of Chemical, Environmental and Bioscience Engineering, Research Area of Biochemical Technology, Technical University Vienna, Vienna, Austria

2. Institute of Medical Microbiology and Hygiene, Austrian Agency for Health and Food Safety, Vienna, Austria

3. FoodHub - Centre of Excellence for Digitalisationof Microbial Food Safety Risk Assessment and Quality Parameters for Accurate Food Authenticity Certification, University of Donja Gorica, Podgorica, Montenegro

4. Institute of Veterinary Disease Control, Austrian Agency for Health and Food Safety, Mödling, Austria

5. ECDC Fellowship Programme, Public Health Microbiology path (EUPHEM), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden

6. Center for Public Health, Medical University Vienna, Vienna, Austria

7. Department of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria

Abstract

A novel, Gram-positive, facultative anaerobe, coccoid and non-motile bacterium, designated as CoE-012-22T was isolated from dried beef sausage (the original name in Montenegro is Govedji Kulen) manufactured in the municipality of Rozaje (Montenegro) in 2021. Cells of this strain were oxidase- and catalase-negative. Growth occurred at 4–50 °C, at pH 5.0–8.0 and with 0–6.5 % (w/v) NaCl in diverse growth media. MALDI-TOF analysis identified the strain as Enterococcus canintestini (log score 2). Phylogenetic analysis of the 16S rRNA gene and whole genome sequences assigned the strain to the genus Enterococcus . The closest relatives were E. canintestini DSM 21207T and E. dispar ATCC 51266T with 16S rRNA gene sequence pairwise similarities of 99.34 and 98.59 %, respectively. The average nucleotide identity (ANI) and digital DNA–DNA hybridization (dDDH) values between isolate CoE-012-22T and other enterococci species were below the thresholds for species delineation thresholds (95.0 % ANI; 70.0 % dDDH) with maximum identities of 84.13 % (ANIb), 86.43 % (ANIm) and 28.4 % (dDDH) to E. saigonensis JCM 31193T and 70.97 % (ANIb), 88.99 % (ANIm) and 32.4 % (dDDH) to E. malodoratus ATCC 43197T. Two unknown Enterococcus isolates, Enterococcus sp. MJM12 and Enterococcus SMC-9, showed identities of 99.87 and 99.94 % (16S rRNA), 98.57 and 98.65 % (ANIb), 98.93 and 99.02 % (ANIm), and 89.8 and 90.0 % (dDDH) to strain CoE-012-22T and can therefore be regarded as the same species. Based on the characterization results, strain CoE-012-22T was considered to represent a novel species, for which the name Enterococcus montenegrensis sp. nov. is proposed. The type strain is CoE-012-22T (=DSM 115843T=NCIMB 15468T).

Funder

Ministry of Science and Technological Development of Montenegro

European Public Health Microbiology Training Programme

Publisher

Microbiology Society

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