Non-clinical enterococci are relatively poorly studied by means of acquired antibiotic resistance to tetracycline and by the distribution, functionality and role of their CRISPR systems.
Background: In our study, 72 enterococcal strains, isolated from various non-clinical origins, were investigated for their phenotypic and
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Non-clinical enterococci are relatively poorly studied by means of acquired antibiotic resistance to tetracycline and by the distribution, functionality and role of their CRISPR systems.
Background: In our study, 72 enterococcal strains, isolated from various non-clinical origins, were investigated for their phenotypic and genotypic (
tet(M),
tet(O),
tet(S),
tet(L),
tet(K),
tet(T) and
tet(W)) tetracycline resistance.
Methods: The genetic determinants for HGT (MGEs (
Int-Tn and
prgW), inducible pheromones (
cpd,
cop and
cff), aggregation substances (
agg,
asa1,
prgB and
asa373) and CRISPR–Cas systems were characterized by PCR and whole-genome sequencing.
Results: Four
tet genes (
tetM,
tetO,
tetS and
tetT) were detected in 39% (n = 28) of our enterococcal population, with
tetM (31%) being dominant. The gene location was linked to the Tn6009 transposon. All strains that contained
tet genes also had genes for HGT. No
tet genes were found in
E. casseliflavus and
E. gilvus. In our study, 79% of all
tet-positive strains correlated with non-functional CRISPR systems. The strain
E. faecalis BM15 was the only one containing a combination of a functional CRISPR system (
cas1,
cas2,
csn2 and
csn1/
cas9) and
tet genes. The CRISPR subtype repeats II-A, III-B, IV-A2 and VI-B1 were identified among
E. faecalis strains (CM4-II-A, III-B and VI-B1; BM5-IV-A2, II-A and III-B; BM12 and BM15-II-A). The subtype II-A was the most present. These repeats enclosed a great number of spacers (1–10 spacers) with lengths of 31 to 36 bp. One CRISPR locus was identified in plasmid (p.Firmicutes1 in strain
E. faecalis BM5). We described the presence of CRISPR loci in the species
E. pseudoavium,
E. pallens and
E. devriesei and their lack in
E. gilvus,
E. malodoratus and
E. mundtii.
Conclusions: Our findings generally describe the acquisition of foreign DNA as a consequence of CRISPR inactivation, and self-targeting spacers as the main cause.
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