PMID- 34858874 OWN - NLM STAT- MEDLINE DCOM- 20220127 LR - 20220127 IS - 2235-2988 (Electronic) IS - 2235-2988 (Linking) VI - 11 DP - 2021 TI - Molecular Epidemiological Survey of Staphylococcus lugdunensis Isolates With Variable Number of Repeats in the von Willebrand Factor-Binding Protein Gene. PG - 748640 LID - 10.3389/fcimb.2021.748640 [doi] LID - 748640 AB - The von Willebrand factor binding protein in Staphylococcus lugdunensis (vWbl) comprises four major regions: the signal peptide (S), the non-repetitive (A) region, the repeat (R) region, and the wall-associated (W) region. Previous studies have demonstrated that the R region contains 10 copies of repeating sequences; however, we reveal that the copy number of repeats in the vWbl gene varies among different S. lugdunensis isolates. In this study, an epidemiological surveillance was conducted to determine whether the copy number of repeats in vWbl in different isolates of S. lugdunensis correlates with their infectivity. The number of repeats was estimated in a total of 212 isolates, consisting of 162 isolates of oxacillin-sensitive S. lugdunensis (OSSL) and 50 isolates of oxacillin-resistant S. lugdunensis (ORSL). Our data showed that 72.5% (116/162) of OSSL isolates contained 9 (25, 15.4%), 12 (43, 26.5%), or 13 (48, 29.6%) repeats, and 90% (45/50) of ORSL isolates had 9 (32, 64%) or 13 (13, 26%) repeats. In addition, 89.6% (26 of 29) of the sequence type (ST)27 strain had 12 repeats, and 86.8% (13 of 15) of the ST4 strain had 14 repeats. Twenty-seven of the 28 isolates with nine repeats were of the staphylococcal cassette chromosome mec (SCCmec) V or V(t) type and belonged to ST3, and all isolates with 13 repeats were of SCCmec II type and belonged to ST6. All isolates with nine repeats had a stop codon at the 18(th) codon of the third repeat, suggesting that these isolates coded for nonfunctional vWbl. Further, western blot analysis confirmed that all strains translated vWbl, and only vWbl proteins coded by genes with nine repeats were exported outside the cell. These results suggest that number of vWbl repeats in S. lugdunensis have clonal specificities and may correlate with potential pathogenicity. CI - Copyright (c) 2021 Lin, Cheng, Chang and Lu. FAU - Lin, Lee-Chung AU - Lin LC AD - Department of Laboratory Medicine, Chang Gung Memorial Hospital, Taoyuan, Taiwan. FAU - Cheng, Chun-Wen AU - Cheng CW AD - Division of Infectious Diseases, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, Taiwan. FAU - Chang, Shih-Cheng AU - Chang SC AD - Department of Laboratory Medicine, Chang Gung Memorial Hospital, Taoyuan, Taiwan. AD - Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taoyuan, Taiwan. FAU - Lu, Jang-Jih AU - Lu JJ AD - Department of Laboratory Medicine, Chang Gung Memorial Hospital, Taoyuan, Taiwan. AD - Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taoyuan, Taiwan. AD - Department of Medicine, College of Medicine, Chang Gung University, Taoyuan, Taiwan. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20211111 PL - Switzerland TA - Front Cell Infect Microbiol JT - Frontiers in cellular and infection microbiology JID - 101585359 RN - 0 (Anti-Bacterial Agents) RN - 0 (Carrier Proteins) RN - 0 (von Willebrand Factor) SB - IM MH - Anti-Bacterial Agents MH - Carrier Proteins/genetics MH - Humans MH - *Methicillin-Resistant Staphylococcus aureus MH - Microbial Sensitivity Tests MH - *Staphylococcal Infections/epidemiology MH - *Staphylococcus lugdunensis/genetics MH - von Willebrand Factor PMC - PMC8632046 OTO - NOTNLM OT - MLST OT - S. lugdunensis OT - SCCmec OT - pathogenesis OT - von Willebrand factor binding protein COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2021/12/04 06:00 MHDA- 2022/01/28 06:00 PMCR- 2021/01/01 CRDT- 2021/12/03 07:07 PHST- 2021/07/28 00:00 [received] PHST- 2021/10/27 00:00 [accepted] PHST- 2021/12/03 07:07 [entrez] PHST- 2021/12/04 06:00 [pubmed] PHST- 2022/01/28 06:00 [medline] PHST- 2021/01/01 00:00 [pmc-release] AID - 10.3389/fcimb.2021.748640 [doi] PST - epublish SO - Front Cell Infect Microbiol. 2021 Nov 11;11:748640. doi: 10.3389/fcimb.2021.748640. eCollection 2021.