2018
DOI: 10.1007/s10142-018-0596-x
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Genomic and physiological analyses of an indigenous strain, Enterococcus faecium 17OM39

Abstract: The human gut microbiome plays a crucial role in human health and efforts need to be done for cultivation and characterisation of bacteria with potential health benefits. Here, we isolated a bacterium from a healthy Indian adult faeces and investigated its potential as probiotic. The cultured bacterial strain 17OM39 was identified as Enterococcus faecium by 16S rRNA gene sequencing. The strain 17OM39 exhibited tolerance to acidic pH, showed antimicrobial activity and displayed strong cell surface traits such a… Show more

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Cited by 27 publications
(32 citation statements)
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“…The NPNP group had two strains: NRRL B-2354 and 64/3 [25, 26]. The probiotic group had the marketed strain T110 [9] and strain 17OM39 isolated from healthy human gut [31]. …”
Section: Resultsmentioning
confidence: 99%
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“…The NPNP group had two strains: NRRL B-2354 and 64/3 [25, 26]. The probiotic group had the marketed strain T110 [9] and strain 17OM39 isolated from healthy human gut [31]. …”
Section: Resultsmentioning
confidence: 99%
“…The carbohydrate metabolism was abundant in probiotic group while later in the pathogenic group (Fig. 3), this can be been attributed to the properties of probiotic strains to utilize various carbohydrates [31], while the pathogenic group had higher abundance of replication and recombination genes known to be associated with a large number of mobile elements [1, 2]. Comparison of accessory genes between probiotic and pathogenic group helped in identifying two manganese-containing catalase gene, which provide resistance to hydrogen peroxide present in human GIT [4042].…”
Section: Discussionmentioning
confidence: 99%
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“…Three self-declared healthy volunteers were selected with consent prior to collection of the samples. We immediately transported the collected faecal samples to the lab at 4°C and processed for isolation of faecal bacteria within 6 h. Faecal samples (1g) were transferred to 9 ml of sterile saline (0.85% sodium chloride, Sigma) and mixed well (50). The serial dilutions were subsequently prepared in sterile saline, and appropriate dilutions of the samples plated on Nutrient Agar (HiMedia, Mumbai, India).…”
Section: Methodsmentioning
confidence: 99%
“…Plates were incubated at 37°C for 48 h under aerobic condition. Glycerol [20% (v/v)] stocks were prepared to preserve the isolated pure cultures and froze at −80°C (50).…”
Section: Methodsmentioning
confidence: 99%