Molecular Characterization of Chimeric Staphylococcus aureus Strains from Waterfowl

被引:1
作者
Monecke, Stefan [1 ,2 ,3 ]
Braun, Sascha D. [1 ,2 ]
Collatz, Maximillian [1 ,2 ]
Diezel, Celia [1 ,2 ]
Mueller, Elke [1 ,2 ]
Reinicke, Martin [1 ,2 ]
Rosel, Adriana Cabal [4 ]
Fessler, Andrea T. [5 ,6 ]
Hanke, Dennis [5 ,6 ]
Loncaric, Igor [7 ]
Schwarz, Stefan [5 ,6 ]
de Jaeckel, Sonia Cortez [8 ]
Ruppitsch, Werner [4 ]
Gavier-Widen, Dolores [9 ,10 ]
Hotzel, Helmut [11 ]
Ehricht, Ralf [1 ,2 ,12 ]
机构
[1] Leibniz Inst Photon Technol IPHT, Leibniz Ctr Photon Infect Res LPI, D-07745 Jena, Germany
[2] InfectoGnost Res Campus, D-07743 Jena, Germany
[3] Dresden Univ Hosp, Inst Med Microbiol & Virol, D-01307 Dresden, Germany
[4] Austrian Agcy Hlth & Food Safety, Inst Med Microbiol & Hyg, A-1220 Vienna, Austria
[5] Free Univ Berlin, Inst Microbiol & Epizoot, Ctr Infect, Med Sch Vet Med, D-14163 Berlin, Germany
[6] Free Univ Berlin, Vet Ctr Resistance Res TZR, Sch Vet Med, D-14163 Berlin, Germany
[7] Univ Vet Med, Inst Microbiol, A-1210 Vienna, Austria
[8] Poultry Clin & Lab Poppel, D-33129 Delbruck, Germany
[9] Natl Vet Inst SVA, Dept Pathol & Wildlife Dis, S-75189 Uppsala, Sweden
[10] Swedish Univ Agr Sci SLU, Dept Biomed Sci & Vet Publ Hlth, S-75007 Uppsala, Sweden
[11] Friedrich Loeffler Inst, Fed Res Inst Anim Hlth, Inst Bacterial Infect & Zoonoses, D-07743 Jena, Germany
[12] Friedrich Schiller Univ, Inst Phys Chem, D-07743 Jena, Germany
关键词
Staphylococcus aureus; clonal complex 133; clonal complex 522; clonal complex 692; next generation sequencing; bacteriophages; chimerism; horizontal gene transfer; pathogens in waterfowl; One Health; FOOD; DIVERSITY; MRSA;
D O I
10.3390/microorganisms12010096
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Staphylococcus aureus is a versatile pathogen that does not only occur in humans but also in various wild and domestic animals, including several avian species. When characterizing S. aureus isolates from waterfowl, isolates were identified as atypical CC133 by DNA microarray analysis. They differed from previously sequenced CC133 strains in the presence of the collagen adhesin gene cna; some also showed a different capsule type and a deviant spa type. Thus, they were subjected to whole-genome sequencing. This revealed multiple insertions of large regions of DNA from other S. aureus lineages into a CC133-derived backbone genome. Three distinct strains were identified based on the size and extent of these inserts. One strain comprised two small inserts of foreign DNA up- and downstream of oriC; one of about 7000 nt or 0.25% originated from CC692 and the other, at ca. 38,000 nt or 1.3% slightly larger one was of CC522 provenance. The second strain carried a larger CC692 insert (nearly 257,000 nt or 10% of the strain's genome), and its CC522-derived insert was also larger, at about 53,500 nt or 2% of the genome). The third strain carried an identical CC692-derived region (in which the same mutations were observed as in the second strain), but it had a considerably larger CC522-like insertion of about 167,000 nt or 5.9% of the genome. Both isolates of the first, and two out of four isolates of the second strain also harbored a hemolysin-beta-integrating prophage carrying "bird-specific" virulence factors, ornithine cyclodeaminase D0K6J8 and a putative protease D0K6J9. Furthermore, isolates had two different variants of SCC elements that lacked mecA/mecC genes. These findings highlight the role of horizontal gene transfer in the evolution of S. aureus facilitated by SCC elements, by phages, and by a yet undescribed mechanism for large-scale exchange of core genomic DNA.
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