“…The results obtained in this way are not always satisfactory, and the identification concerns the bacterial species, not the strain [31]. A more accurate answer to the question of whether the probiotic strain used has developed, survived, and dominated the natural microflora in the meat environment can be obtained by combined culture-dependent and culture-independent methods, i.e., genetic engineering methods, including, for example, DNA polymerase chain reactions (PCR) or sequencing of the 16S rRNA (ribosomal ribonucleic acid) gene characteristic of LAB bacteria [5,9,32]. In our study, a specific pair of primers for PCR reaction was used, designed to the V1 region of the 16S rRNA gene, which enables the differentiation of the Lacticaseibacillus rhamnosus species even from the closely related L. casei group [24].…”