Identification of Three Clf-Sdr Subfamily Proteins in Staphylococcus warneri, and Comparative Genomics Analysis of a Locus Encoding CWA Proteins in Staphylococcus Species
Coagulase-negative Staphylococcus warneri is an opportunistic pathogen that is capable of causing several infections, especially in patients with indwelling medical devices. Here, we determined the complete genome sequence of a clinical S. warneri strain isolated from the blood culture of a 1-year-o...
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Veröffentlicht in: | Frontiers in microbiology 2021-07, Vol.12, p.691087-691087 |
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Zusammenfassung: | Coagulase-negative
Staphylococcus warneri
is an opportunistic pathogen that is capable of causing several infections, especially in patients with indwelling medical devices. Here, we determined the complete genome sequence of a clinical
S. warneri
strain isolated from the blood culture of a 1-year-old nursling patient with acute upper respiratory infection. Genome-wide phylogenetic analysis confirmed the phylogenetic relationships between
S. warneri
and other
Staphylococcus
species. Using comparative genomics, we identified three cell wall-anchored (CWA) proteins at the same locus (
sdr
), named SdrJ, SdrK, and SdrL, on the chromosome sequences of different
S. warneri
strains. Structural predictions showed that SdrJ/K/L have structural features characteristic of Sdr proteins but exceptionally contained an unusual N-terminal repeat region. However, the C-terminal repetitive (R) region of SdrJ contains a significantly larger proportion of alanine (142/338, 42.01%) than the previously reported SdrI (37.00%). Investigation of the genetic organization revealed that the
sdrJ/K/L
genes were always followed by one or two glycosyltransferase genes,
gtfA
and
gtfB
and were present in an ∼56 kb region bordered by a pair of 8 bp identical direct repeats, named Sw-Sdr. This region was further found to be located on a 160-kb region subtended by a pair of 160-bp direct repeats along with other virulence genes and resistance genes. Sw-Sdr contained a putative integrase that was probably a remnant of a functional integrase. Evidence suggests that Sw-Sdr is improbably an efficient pathogenicity island. A large-scale investigation of
Staphylococcus
genomes showed that
sdr
loci were a potential hotspot of insertion sequences (ISs), which could lead to intraspecific diversity at these loci. Our work expanded the repository of
Staphylococcus
Sdr proteins, and for the first time, we established the connection between
sdr
loci and phylogenetic relationships and compared the
sdr
loci in different
Staphylococcus
species, which provided large insights into the genetic environment of CWA genes in
Staphylococcus
. |
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ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2021.691087 |