Abstract
Streptococcus agalactiae (Lancefield group B; GBS) is one of the major pathogens in fish production, especially in Nile tilapia (Oreochromis niloticus). The genomic characteristics of GBS isolated from fish must be more explored. Thus, we present here the genome of GBS S25, isolated from Nile tilapia from Brazil.
GENOME ANNOUNCEMENT
Streptococcus agalactiae (group B Streptococcus, GBS) is a major pathogen to human, bovine, and many fish species (1, 2). Previous studies have shown, through molecular biology methods (1, 3–5) and genomic approaches (6–8), that GBS has a significant genetic diversity. However, few studies have been performed to characterize fish strains isolated from different outbreaks in recent years from distinct geographic regions.
S. agalactiae SA25 was isolated from a moribund fish with increased abdominal cavity due to excess fluid from a fish farm of Parana state, Brazil, in July 2015. The genome sequencing of S. agalactiae SA25 was performed using the Illumina MiSeq platform (Illumina Inc., San Diego, CA, USA) using a 300-bp paired-end library, which generated 2,291,552 reads. After sequencing, those reads were subjected to trimming and filtering using the CLC Genomics Workbench software (version 8.0.2), in which reads with an average Phred quality of less than 30 and with one or more ambiguities were removed. Finally, reads with a size less than 50 bp, as well as the last 10 nucleotides of the 3′ end of each read, were removed.
After the trimming, 2,003,478 reads were used in the assembly, which generated a genome coverage corresponding to ~360-fold, based on the reference genome size of 1,820,886 bp for S. agalactiae strain SA20-06 (NC_019048) (9). The genome of SA25 was assembled using CLC Genomics Workbench software. A total of 35 contigs were generated, with an N50 of 109,762 bp and largest and smallest contig sizes of 340,795 bp and 511 bp, respectively. These contigs were ordered using CONTIGuator software (10) against many genomes of the same species. The genome of S. agalactiae strain SA20-06 was picked as a reference due to better synteny and number of contigs mapped. The gaps were removed with recursive rounds of short reads mapped against the scaffold (11). The annotation step was performed using the NCBI Prokaryotic Genome Annotation Pipeline.
Finally, the complete genome of S. agalactiae strain SA25 (with no gaps) was completed with a total size of 1,838,989 nucleotides and with 1,880 putative open reading frames, 35.52% G+C content, seven rRNA operons, 76 tRNA genes, and 140 pseudogenes. The S25 genome harbors the main virulence factors described for the species. SA25 belongs to serotype Ib, and the genetic profile resulting from multilocus sequence typing of this strain is related to host adaptability for heterothermic hosts (clonal complex 552 and sequence type 552). Interestingly, this strain has shown little virulence in experimental infection assays in Nile tilapia, with an LD50 value greater than 105 CFU/fish (unpublished data).
New studies of S. agalactiae strains isolated from fish are underway with the objective to find genomic differences that may justify the distinct profile of virulence and antibiotic resistance observed in the our laboratory routine.
Nucleotide sequence accession numbers.
The Streptococcus agalactiae SA25 genome sequence and annotation data have been deposited at DDBJ/EMBL/GenBank under the accession number CP015976. The version described in this paper is the first version, CP015976.1.
ACKNOWLEDGMENTS
This work was supported by Fundação Araucária and the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES).
Footnotes
Citation Mainardi RM, Lima Júnior EA, Ribeiro Júnior JC, Beloti V, Carmo AO, Kalapothakis E, Gonçalves DD, Padua SB, Pereira UP, 2016. Complete genome sequence of Streptococcus agalactiae strain S25 isolated from peritoneal liquid of Nile tilapia. Genome Announc 4(4):e00784-16. doi:10.1128/genomeA.00784-16.
REFERENCES
- 1.Pereira UP, Mian GF, Oliveira IC, Benchetrit LC, Costa GM, Figueiredo HC. 2010. Genotyping of Streptococcus agalactiae strains isolated from fish, human and cattle and their virulence potential in Nile tilapia. Vet Microbiol 140:186–192. doi: 10.1016/j.vetmic.2009.07.025. [DOI] [PubMed] [Google Scholar]
- 2.Evans JJ, Bohnsack JF, Klesius PH, Whiting AA, Garcia JC, Shoemaker CA, Takahashi S. 2008. Phylogenetic relationships among Streptococcus agalactiae isolated from piscine, dolphin, bovine and human sources: a dolphin and piscine lineage associated with a fish epidemic in Kuwait is also associated with human neonatal infections in Japan. J Med Microbiol 57:1369–1376. doi: 10.1099/jmm.0.47815-0. [DOI] [PubMed] [Google Scholar]
- 3.Corrêa AB, Oliveira IC, Pinto Tde C, Mattos MC, Benchetrit LC. 2009. Pulsed-field gel electrophoresis, virulence determinants and antimicrobial susceptibility profiles of type Ia group B streptococci isolated from humans in Brazil. Mem Inst Oswaldo Cruz 104:599–603. doi: 10.1590/S0074-02762009000400011. [DOI] [PubMed] [Google Scholar]
- 4.Oliveira ICM, De Mattos MC, Pinto Ta, Ferreira-Carvalho BT, Benchetrit LC, Whiting AA, Bohnsack JF, Figueiredo a MS. 2006. Genetic relatedness between group B streptococci originating from bovine mastitis and a human group B streptococcus type V cluster displaying an identical pulsed-field gel electrophoresis pattern. Clin Microbiol Infect 12:887–893. doi: 10.1111/j.1469-0691.2006.01508.x. [DOI] [PubMed] [Google Scholar]
- 5.Godoy DT, Carvalho-Castro GA, Leal CA, Pereira UP, Leite RC, Figueiredo HC. 2013. Genetic diversity and new genotyping scheme for fish pathogenic Streptococcus agalactiae. Lett Appl Microbiol 57:476–483. doi: 10.1111/lam.12138. [DOI] [PubMed] [Google Scholar]
- 6.Rosinski-Chupin I, Sauvage E, Mairey B, Mangenot S, Ma L, Da Cunha V, Rusniok C, Bouchier C, Barbe V, Glaser P. 2013. Reductive evolution in Streptococcus agalactiae and the emergence of a host adapted lineage. BMC Genomics 14:252. doi: 10.1186/1471-2164-14-252. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Liu G, Zhang W, Lu C. 2013. Comparative genomics analysis of Streptococcus agalactiae reveals that isolates from cultured tilapia in China are closely related to the human strain A909. BMC Genomics 14:775. doi: 10.1186/1471-2164-14-775. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Pereira UP, Soares SC, Blom J, Leal CA, Ramos RT, Guimarães LC, Oliveira LC, Almeida SS, Hassan SS, Santos AR, Miyoshi A, Silva A, Tauch A, Barh D, Azevedo V, Figueiredo HC. 2013. In silico prediction of conserved vaccine targets in Streptococcus agalactiae strains isolated from fish, cattle, and human samples. Genet Mol Res 12:2902–2912. doi: 10.4238/2013.August.12.6. [DOI] [PubMed] [Google Scholar]
- 9.Pereira Ude P, Rodrigues Dos Santos A, Hassan SS, Aburjaile FF, Soares Sde C, Ramos RT, Carneiro AR, Guimarães LC, Silva de Almeida S, Diniz CA, Barbosa MS, Gomes de Sá P, Ali A, Bakhtiar SM, Dorella FA, Zerlotini A, Araújo FM, Leite LR, Oliveira G, Miyoshi A. 2013. Complete genome sequence of Streptococcus agalactiae strain SA20-06, a fish pathogen associated to meningoencephalitis outbreaks. Stand Genomic Sci 8:188–197. doi: 10.4056/sigs.3687314. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Galardini M, Biondi EG, Bazzicalupo M, Mengoni A. 2011. CONTIGuator: a bacterial genomes finishing tool for structural insights on draft genomes. Source Code Biol Med 6:11. doi: 10.1186/1751-0473-6-11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Tsai IJ, Otto TD, Berriman M. 2010. Improving draft assemblies by iterative mapping and assembly of short reads to eliminate gaps. Genome Biol 11:R41. doi: 10.1186/gb-2010-11-4-r41. [DOI] [PMC free article] [PubMed] [Google Scholar]