Literature DB >> 30740494

Draft genome sequence data of Lactobacillus paracasei strain DTA83 isolated from infant stools.

Wilson José Fernandes Lemos Junior1, André Fioravante Guerra2, Vinícius da Silva Duarte3, Laura Treu4,5, Armin Tarrah3, Stefano Campanaro5, Rosa Helena Luchese6, Alessio Giacomini3,7, Viviana Corich3,7.   

Abstract

Here the draft genome sequence of Lactobacillus paracasei strain DTA83, isolated from stools of healthy infants in Rio de Janeiro (Brazil), is reported. The 2.8-Mb genome possesses 2825 protein-coding sequences distributed on 330 SEED subsystems. This strain belongs to a set of potentially probiotic Lactobacillus spp. strains used to study genetic factors related to antibiotic resistance after stress conditions, such as simulated gastrointestinal conditions. The complete genome data have been deposited in GenBank under the accession number QRBH00000000, https://www.ncbi.nlm.nih.gov/nuccore/QRBH00000000.

Entities:  

Year:  2019        PMID: 30740494      PMCID: PMC6356017          DOI: 10.1016/j.dib.2019.01.041

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specification table Value of the data The compete genome of Lb. paracasei DTA83, isolated from infant stools, allows to study in depth the genetic information of this strain in view of its potential use as probiotic strain. The sequence data will be useful for comparative studies towards environmental strains or others of intestinal origin. The availability of genome sequence can allow the discovery of other technological or health related potentially relevant characteristics of this strain.

Data

Lactobacillus paracasei is a lactic acid bacterium (LAB) with interesting technological potentialities, mostly related to its capability to acidify the substrate, since it is known that a pH decrease affects bacterial [1], [2] and also yeast [3], [4] population composition and dynamics. Assembly of the shotgun reads generated 70 scaffolds, which were ordered and oriented with CONTIguator [5], using strain Lb. paracasei ATCC 334 as reference, giving a total genome size of 2.8 Mb, with a GC content of 46.4%. The average nucleotide identity (ANI) of 98.56% with Lb. paracasei ATCC 334, confirms that strain DTA83 belongs to the Lb. paracasei species [6]. The Rapid Annotations using Subsystems Technology (RAST) server [7] was used for gene prediction and annotation. The number of predicted protein-coding sequences (CDSs) in DTA83 was 2825, distributed on 330 SEED subsystems. Moreover, 59 structural RNAs were found. In total, 31 genes are related to the “resistance to antibiotics and toxic compounds” subsystem. Among these, it must be highlighted the presence of four genes associated to fluoroquinolones resistance, a feature not identified in the reference strain Lb. paracasei ATCC 334. PHASTER [8] analysis returned three prophage regions (1 intact, 1 incomplete and 1 questionable). Additionally, one confirmed two “questionable” clusters of regularly interspaced short palindromic repeats (CRISPRs) are present in this strain, as predicted by CRISPRFinder [9]. Data is available at https://www.ncbi.nlm.nih.gov/nuccore/ QRBH00000000.

Experimental design, materials and methods

The strain used in this work was isolated from the faeces of healthy infants aged between 7 to 21 days, assisted by the Human Milk Bank (HMB) and the Neonatal Intensive Care Unit (NICU) of the Neonatal Fernandes Figueira Institute of Oswaldo Cruz Foundation (FIOCRUZ), located in Rio de Janeiro, Brazil [10]. Approximately 1 g of stools was collected, serially diluted in Wilkins-Chalgren broth (Oxoid, Basingstoke, United Kingdom) and plated on LAMVAB agar [11]. Plates were incubated at 37 °C for 48 h under partial anaerobic conditions and characteristic colonies were selected and subjected to biochemical and genotypic tests. For DNA extraction, DTA83 was grown for 24 h at 37 °C on de Man Rogosa Sharp (MRS) broth. Afterwards, cells were harvested (5000 rpm for 5 min at 4 °C) and high-quality genomic DNA was extracted using the PowerFood™ Microbial DNA isolation kit (MoBio Laboratories Inc., Carlsbad, CA, USA) according to the manufacturer instructions. DNA quantification was performed using both NanoDrop (ThermoFisher Scientific, Waltham, MA, USA) and Qubit (ThermoFisher Scientific). Genome sequencing was carried out with an Illumina MiSeq sequencer and Nextera XT libraries at the Ramaciotti Centre (Sydney, Australia). The average number of paired-end reads (2 × 250 bp) for the strain was 3,034,380. The completed genome data was deposited in NCBI GenBank under the accession number QRBH00000000, https://www.ncbi.nlm.nih.gov/nuccore/ QRBH00000000.
Subject areaBiology
More specific subject areaMicrobiology, Genomics
Type of dataGenomic sequence, gene prediction of Lactobacillus paracasei
How data was acquiredShotgun whole-genome DNA sequencing using MiSeq platform (Illumina) at the Ramaciotti Centre, Sydney, Australia
Data formatRaw draft genome assembly and gene prediction
Experimental factorsDNA was extracted from Lactobacillus paracasei DTA83
Experimental featuresIsolation of Lb. paracasei DTA83, whole genome shotgun sequencing followed by assembly and annotation
Data source locationThe strain Lb. paracasei DTA83 was isolated from stools of infants between 7 and 21 days old at Fernandes Figueira Institute of FIOCRUZ, Rio de Janeiro, Brazil.
Data accessibilityThe Whole Genome Shotgun project of Lb. paracasei DTA83 has been deposited in DDBJ/ENA/GenBank under the accession no. QRBH00000000.
https://www.ncbi.nlm.nih.gov/nuccore/QRBH00000000
Related research articleA.F. Guerra, W.J.F. Lemos Junior, G.O. dos Santos, C. Andrighetto, A. Gianomini, V. Corich, R.H. Luchese, A.F. Guerra, W.J.F. Lemos Junior, G.O. dos Santos, C. Andrighetto, A. Gianomini, V. Corich, R.H. Luchese, Lactobacillus paracasei probiotic properties and survivability under stress-induced by processing and storage of ice cream bar or ice-lolly, Ciência Rural. 48 (2018). doi:10.1590/0103-8478cr20170601. [10]
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