Item request has been placed!
×
Item request cannot be made.
×

Processing Request
Phenotypic and genotypic characterization of commensal staphylococci isolated from young volunteers in Alexandria, Egypt.
Item request has been placed!
×
Item request cannot be made.
×

Processing Request
- Additional Information
- Source:
Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
- Publication Information:
Original Publication: London : Nature Publishing Group, copyright 2011-
- Subject Terms:
- Abstract:
Nasally colonized staphylococci carry antibiotic resistance genes and may lead to serious opportunistic infections. We are investigating nasal carriage of Staphylococcus aureus and Staphylococci other than S. aureus (SOSA) among young volunteers in Egypt to determine their risk potential. Nasal swabs collected over 1 week in June 2019 from 196 volunteers were cultured for staphylococcus isolation. The participants were interviewed to assess sex, age, general health, hospitalization and personal hygiene habits. Identification was carried out using biochemical tests and VITEK 2 automated system. Disc diffusion and minimum inhibitory concentration tests were performed to determine antibiotic susceptibility. Screening for macrolide resistance genes (ermA, ermB, ermC, ermT and msrA) was performed using polymerase chain reaction. Thirty four S. aureus and 69 SOSA were obtained. Multi-drug resistance (MDR) was detected among most staphylococcal species, ranging from 30.77% among S. hominis to 50% among S. epidermidis. Phenotypic resistance to all tested antibiotics, except for linezolid, was observed. Susceptibility to rifampicin, vancomycin and teicoplanin was highest. ermB showed the highest prevalence among all species (79.41% and 94.2% among S. aureus and SOSA, respectively), and constitutive macrolide-lincosamide-streptogramin B (MLS B ) resistance was equally observed in S. aureus and SOSA (11.11% and 16.22%, respectively), whereas inducible MLS B resistance was more often found in S. aureus (77.78% and 43.24%, respectively). The species or resistance level of the carried isolates were not significantly associated with previous hospitalization or underlying diseases. Although over all colonization and carriage of resistance genes are within normal ranges, the increased carriage of MDR S. aureus is alarming. Also, the fact that many macrolide resitance genes were detected should be a warning sign, particularly in case of MLS B inducible phenotype. More in depth analysis using whole genome sequencing would give a better insight into the MDR staphylococci in the community in Egypt.
(© 2024. The Author(s).)
- References:
Antibiotics (Basel). 2014 Jun 20;3(2):233-43. (PMID: 27025746)
Afr Health Sci. 2011 Jun;11(2):176-81. (PMID: 21857847)
Egypt Heart J. 2020 Aug 13;72(1):49. (PMID: 32789717)
Nat Rev Dis Primers. 2018 May 31;4:18033. (PMID: 29849094)
Microb Ecol. 2017 Nov;74(4):1001-1008. (PMID: 28492988)
Microbiol Spectr. 2019 Mar;7(2):. (PMID: 31004422)
J Antimicrob Chemother. 2000 Dec;46(6):941-9. (PMID: 11102413)
Indian J Med Microbiol. 2010 Apr-Jun;28(2):124-6. (PMID: 20404457)
Antibiotics (Basel). 2021 Nov 17;10(11):. (PMID: 34827344)
J Antimicrob Chemother. 2010 Apr;65(4):601-4. (PMID: 20181573)
Clin Infect Dis. 2002 Feb 15;34(4):482-92. (PMID: 11797175)
Clin Microbiol Rev. 2014 Oct;27(4):870-926. (PMID: 25278577)
Virulence. 2021 Dec;12(1):547-569. (PMID: 33522395)
N Engl J Med. 2001 Jan 4;344(1):11-6. (PMID: 11136954)
PLoS One. 2016 Feb 03;11(2):e0148437. (PMID: 26840492)
Int J Bacteriol. 2016;2016:5751785. (PMID: 27433480)
Afr Health Sci. 2015 Sep;15(3):861-7. (PMID: 26957975)
Front Public Health. 2021 Jun 17;9:684456. (PMID: 34222184)
Microb Drug Resist. 2020 Aug;26(8):951-970. (PMID: 32043916)
Clin Microbiol Infect. 2019 Sep;25(9):1071-1080. (PMID: 30502487)
Lancet Infect Dis. 2002 Nov;2(11):677-85. (PMID: 12409048)
BMC Res Notes. 2017 Jun 2;10(1):187. (PMID: 28577365)
BMC Infect Dis. 2023 Apr 26;23(1):263. (PMID: 37101125)
Lancet. 2010 May 1;375(9725):1557-68. (PMID: 20206987)
Microb Drug Resist. 2017 Jan;23(1):8-17. (PMID: 27228193)
Infect Prev Pract. 2020 May 19;2(3):100059. (PMID: 34368710)
Lancet. 2022 Feb 12;399(10325):629-655. (PMID: 35065702)
Front Microbiol. 2018 Oct 08;9:2419. (PMID: 30349525)
J Clin Diagn Res. 2013 Feb;7(2):257-60. (PMID: 23543837)
Antimicrob Resist Infect Control. 2018 Feb 17;7:24. (PMID: 29468052)
Res Social Adm Pharm. 2014 Jan-Feb;10(1):168-84. (PMID: 23665078)
Eur J Clin Microbiol Infect Dis. 2021 Apr;40(4):815-823. (PMID: 33104900)
Expert Rev Anti Infect Ther. 2022 Feb;20(2):139-146. (PMID: 34152887)
Clin Microbiol Rev. 2015 Jul;28(3):603-61. (PMID: 26016486)
BMJ Open. 2018 Apr 20;8(4):e020391. (PMID: 29678979)
Clin Microbiol Rev. 2020 May 13;33(3):. (PMID: 32404435)
Clin Microbiol Infect. 2012 Mar;18(3):268-81. (PMID: 21793988)
Clin Microbiol Infect. 2007 Aug;13(8):777-81. (PMID: 17501977)
Front Microbiol. 2015 Apr 30;6:348. (PMID: 25983721)
J Clin Microbiol. 2006 Jan;44(1):229-31. (PMID: 16390977)
Antimicrob Agents Chemother. 2012 Jan;56(1):315-23. (PMID: 22064532)
Nat Rev Microbiol. 2017 Oct 12;15(11):675-687. (PMID: 29021598)
PLoS One. 2023 Jan 27;18(1):e0274248. (PMID: 36706112)
- Grant Information:
ZI665/3-1 Deutsche Forschungsgemeinschaft; ZI665/3-1 Deutsche Forschungsgemeinschaft
- Contributed Indexing:
Keywords: S. aureus; Antibiotic resistance; Community acquired infections; Egypt; Nasal colonization; SOSA
- Accession Number:
0 (Anti-Bacterial Agents)
- Publication Date:
Date Created: 20240627 Date Completed: 20240627 Latest Revision: 20240630
- Publication Date:
20250114
- Accession Number:
PMC11211488
- Accession Number:
10.1038/s41598-024-60924-8
- Accession Number:
38937465
No Comments.