2021
DOI: 10.1128/mra.00698-21
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Draft Genome Sequences of Four Different Strains Belonging to Leptospira interrogans Serovar Pomona Isolated from Mammals in the Island of Sardinia, Italy

Abstract: Leptospirosis is a zoonotic disease of global importance caused by a pathogenic group of bacteria belonging to the genus Leptospira . Here, we report four draft genome sequences of Leptospira interrogans serovar Pomona isolated on Sardinia (Italy) from four different species of mammals (i.e., dolphin, wild boar, cow, and fox).

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Cited by 4 publications
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“…Reads were mapped against the reference genome NC_005336.1 (this genome is the only one branded as reference genome for ORFV in NCBI Virus portal) using an end-to-end read alignment (basic command line: bowtie2 [options]* -x <bt2-idx> {−1 <m1> −2 <m2> | -U <r> | --interleaved <i> | --sra-acc <acc> | b <bam>} -S [<sam>]). A de novo assembly was also performed to use an approach as complete as possible, using the software SPAdes v3.15.3 (Center for Algorithmic Biotechnology, St Petersburg, Russia) [ 27 ] (command line: --outdir out --cpus 6 --ram 30 --R1 fastq_r1.fastqsanger --R2 fastq_r2.fastqsanger --trim --namefmt contig%05d --depth 100 --nocorr --minlen 0 --mincov 2 --assembler spades) by following Scarpa et al [ 28 ] and Piredda et al [ 29 ]. Scaffolds were subsequently oriented with the reference genome NC_005336.1 by using Unipro UGENE v.35 (Unipro Center for Information Technologies, Novosibirsk, Russia) [ 30 ].…”
Section: Methodsmentioning
confidence: 99%
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“…Reads were mapped against the reference genome NC_005336.1 (this genome is the only one branded as reference genome for ORFV in NCBI Virus portal) using an end-to-end read alignment (basic command line: bowtie2 [options]* -x <bt2-idx> {−1 <m1> −2 <m2> | -U <r> | --interleaved <i> | --sra-acc <acc> | b <bam>} -S [<sam>]). A de novo assembly was also performed to use an approach as complete as possible, using the software SPAdes v3.15.3 (Center for Algorithmic Biotechnology, St Petersburg, Russia) [ 27 ] (command line: --outdir out --cpus 6 --ram 30 --R1 fastq_r1.fastqsanger --R2 fastq_r2.fastqsanger --trim --namefmt contig%05d --depth 100 --nocorr --minlen 0 --mincov 2 --assembler spades) by following Scarpa et al [ 28 ] and Piredda et al [ 29 ]. Scaffolds were subsequently oriented with the reference genome NC_005336.1 by using Unipro UGENE v.35 (Unipro Center for Information Technologies, Novosibirsk, Russia) [ 30 ].…”
Section: Methodsmentioning
confidence: 99%
“…Seven whole genome sequences were obtained for ORFV in the present study. The whole dataset ( n = 26) was aligned using the Clustal Omega package [ 31 ] (available at ; accessed on 15 April 2022) after editing by means of Unipro UGENE v.35 [ 29 ], and subsequently deposited in GenBank (see Table 2 for accession numbers).…”
Section: Methodsmentioning
confidence: 99%
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“…Recent studies in which pathogenic and intermediate strains of Leptospira have been isolated from clinical samples indicated that the disease is wide-spread among wildlife and domestic mammals on the island [16][17][18]. Whole-genome sequencing obtained from pathogenic Leptospira strains isolated from the two urine samples and all kidney samples had 100% identity with the deposited sequences in NCBI GenBank under BioProject accession number PRJNA731636 [36]. Furthermore, when the nucleotide sequence from environment strains isolated was compared with the other published genome sequences of Leptospira, we found a nucleotide similarity of 98.08% with the genomospecies L. vanthielii (NZ_RQHF00000000.1).…”
Section: Discussionmentioning
confidence: 99%
“…Samples have been sequenced through the WGS technique on the MiSeq platform by BMR Genomics in Padua, Italy, generating paired end reads 2 × 300 (Illumina, San Diego, California, Stati Uniti). The resulting FASTQ files were checked for quality using the tool fastQC from the FASTX-Toolkit v0.7 [35]; assembly with reference and de novo were performed with Bowtie 2 v2.4.2 (Johns Hopkins University, Baltimore, MD, USA) [36,37] and SPAdes v3.15.3 (Center for Algorithmic Biotechnology, St. Petersburg, Russia) [38] following Scarpa et al [39] and Piredda et al [40]. Scaffolds were aligned with the reference genome NC_005336.1 using Unipro UGENE v.35 (Unipro Center for Information Technologies, Novosibirsk, Russia) [41].…”
Section: Viral Dna Extraction Sequencing and Genome Assemblymentioning
confidence: 99%