Streptococcus iniae SF1: complete genome sequence, proteomic profile, and immunoprotective antigens.

PLoS One

Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China; Collaborative Innovation Center of Deep Sea Biology, Zhejiang University, Hangzhou, China.

Published: May 2015

AI Article Synopsis

  • Streptococcus iniae is a serious pathogen in aquaculture with a wide range of fish hosts and potential to infect humans.
  • The complete genome of a pathogenic S. iniae strain, SF1, has been sequenced, revealing key information like its 2.14 million base pairs and numerous genes related to metabolism and immune defense.
  • Proteomic analysis identified 21 proteins secreted in response to host serum, with some showing promise as protective vaccines against S. iniae infection.

Article Abstract

Streptococcus iniae is a Gram-positive bacterium that is reckoned one of the most severe aquaculture pathogens. It has a broad host range among farmed marine and freshwater fish and can also cause zoonotic infection in humans. Here we report for the first time the complete genome sequence as well as the host factor-induced proteomic profile of a pathogenic S. iniae strain, SF1, a serotype I isolate from diseased fish. SF1 possesses a single chromosome of 2,149,844 base pairs, which contains 2,125 predicted protein coding sequences (CDS), 12 rRNA genes, and 45 tRNA genes. Among the protein-encoding CDS are genes involved in resource acquisition and utilization, signal sensing and transduction, carbohydrate metabolism, and defense against host immune response. Potential virulence genes include those encoding adhesins, autolysins, toxins, exoenzymes, and proteases. In addition, two putative prophages and a CRISPR-Cas system were found in the genome, the latter containing a CRISPR locus and four cas genes. Proteomic analysis detected 21 secreted proteins whose expressions were induced by host serum. Five of the serum-responsive proteins were subjected to immunoprotective analysis, which revealed that two of the proteins were highly protective against lethal S. iniae challenge when used as purified recombinant subunit vaccines. Taken together, these results provide an important molecular basis for future study of S. iniae in various aspects, in particular those related to pathogenesis and disease control.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951389PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0091324PLOS

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