Distribution of serotypes and antibiotic resistance of invasive Pseudomonas aeruginosa in a multi-country collection.

Journal Article (Journal Article)

BACKGROUND: Pseudomonas aeruginosa is an opportunistic pathogen that causes a wide range of acute and chronic infections and is frequently associated with healthcare-associated infections. Because of its ability to rapidly acquire resistance to antibiotics, P. aeruginosa infections are difficult to treat. Alternative strategies, such as a vaccine, are needed to prevent infections. We collected a total of 413 P. aeruginosa isolates from the blood and cerebrospinal fluid of patients from 10 countries located on 4 continents during 2005-2017 and characterized these isolates to inform vaccine development efforts. We determined the diversity and distribution of O antigen and flagellin types and antibiotic susceptibility of the invasive P. aeruginosa. We used an antibody-based agglutination assay and PCR for O antigen typing and PCR for flagellin typing. We determined antibiotic susceptibility using the Kirby-Bauer disk diffusion method. RESULTS: Of the 413 isolates, 314 (95%) were typed by an antibody-based agglutination assay or PCR (n = 99). Among the 20 serotypes of P. aeruginosa, the most common serotypes were O1, O2, O3, O4, O5, O6, O8, O9, O10 and O11; a vaccine that targets these 10 serotypes would confer protection against more than 80% of invasive P. aeruginosa infections. The most common flagellin type among 386 isolates was FlaB (41%). Resistance to aztreonam (56%) was most common, followed by levofloxacin (42%). We also found that 22% of strains were non-susceptible to meropenem and piperacillin-tazobactam. Ninety-nine (27%) of our collected isolates were resistant to multiple antibiotics. Isolates with FlaA2 flagellin were more commonly multidrug resistant (p = 0.04). CONCLUSIONS: Vaccines targeting common O antigens and two flagellin antigens, FlaB and FlaA2, would offer an excellent strategy to prevent P. aeruginosa invasive infections.

Full Text

Duke Authors

Cited Authors

  • Nasrin, S; Hegerle, N; Sen, S; Nkeze, J; Sen, S; Permala-Booth, J; Choi, M; Sinclair, J; Tapia, MD; Johnson, JK; Sow, SO; Thaden, JT; Fowler, VG; Krogfelt, KA; Brauner, A; Protonotariou, E; Christaki, E; Shindo, Y; Kwa, AL; Shakoor, S; Singh-Moodley, A; Perovic, O; Jacobs, J; Lunguya, O; Simon, R; Cross, AS; Tennant, SM

Published Date

  • January 6, 2022

Published In

Volume / Issue

  • 22 / 1

Start / End Page

  • 13 -

PubMed ID

  • 34991476

Pubmed Central ID

  • PMC8732956

Electronic International Standard Serial Number (EISSN)

  • 1471-2180

Digital Object Identifier (DOI)

  • 10.1186/s12866-021-02427-4

Language

  • eng

Conference Location

  • England