183
Views
8
CrossRef citations to date
0
Altmetric
Original Research

Pseudomonas aeruginosa Type III Secretion System Virulotypes and Their Association with Clinical Features of Cystic Fibrosis Patients

ORCID Icon, ORCID Icon, ORCID Icon, ORCID Icon, , ORCID Icon, , & ORCID Icon show all
Pages 3771-3781 | Published online: 22 Oct 2020

References

  • Athanazio RA, da Silva Filho LVRF, Vergara AA, et al. Brazilian guidelines for the diagnosis and treatment of cystic fibrosis. J Bras Pneumol. 2017;43(3):219–245.28746534
  • Marson FAL, Hortencio TDR, Aguiar KCA, et al. Demographic, clinical, and laboratory parameters of cystic fibrosis during the last two decades: a comparative analysis. BMC Pulm Med. 2015;15(3). doi:10.1186/1471-2466-15-3.
  • Elborn JS. Cystic fibrosis. Lancet. 2016;388(10059):2519–2531. doi:10.1016/S0140-6736(16)00576-627140670
  • Silva Filho LVRFD, Ferreira FDA, Reis FJC, et al. Infecção por Pseudomonas aeruginosa em pacientes com fibrose cística: evidências científicas sobre o impacto clínico, diagnóstico e tratamento. J Bras Pneumol. 2013;39(4):495–512. doi:10.1590/S1806-3713201300040001524068273
  • Crull MR, Ramos KJ, Caldwell E, Mayer-Hamblett N, Aitken ML, Goss CH. Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time. BMC Pulm Med. 2016;16(1):1–7. doi:10.1186/s12890-016-0333-y26728359
  • Parkins MD, Somayaji R, Waters VJ. Epidemiology, biology, and impact of clonal Pseudomonas aeruginosa infections in cystic fibrosis. Clin Microbiol Rev. 2018;31(4).
  • Pournajaf A, Razavi S, Irajian G, et al. Integron types, antimicrobial resistance genes, virulence gene profile, alginate production and biofilm formation in Iranian cystic fibrosis Pseudomonas aeruginosa isolates. Infez Med. 2018;26(3):226–236.30246765
  • Vidya P, Smith L, Beaudoin T, et al. Chronic infection phenotypes of Pseudomonas aeruginosa are associated with failure of eradication in children with cystic fibrosis. Eur J Clin Microbiol Infect Dis. 2016;35(1):67–74. doi:10.1007/s10096-015-2509-426492874
  • Saiman L, Siegel JD, LiPuma JJ, et al. Infection prevention and control guideline for cystic fibrosis: 2013 update. Infect Control Hosp Epidemiol. 2014;35(S1):s1–s67. doi:10.1086/676882
  • Lee AC, Jones AL. Multi-resistant Pseudomonas aeruginosa ST235 in cystic fibrosis. Paediatr Respir Rev. 2018;27:18–20. doi:10.1016/j.prrv.2018.05.00929914746
  • Gellatly SL, Hancock RE. Pseudomonas aeruginosa: new insights into pathogenesis and host defenses. Pathog Dis. 2013;67(3):159–173. doi:10.1111/2049-632X.1203323620179
  • Harmer CJ, Triccas JA, Hu H, et al. Pseudomonas aeruginosa strains from the chronically infected cystic fibrosis lung display increased invasiveness of A549 epithelial cells over time. Microb Pathog. 2012;53(1):37–43. doi:10.1016/j.micpath.2012.03.01122516803
  • Sawa T, Shimizu M, Moriyama K, Wiener-Kronish JP. Association between Pseudomonas aeruginosa type III secretion, antibiotic resistance, and clinical outcome: a review. Crit Care. 2014;18(6):668. doi:10.1186/s13054-014-0668-925672496
  • Hu H, Harmer C, Anuj S, et al. Type 3 secretion system effector genotype and secretion phenotype of longitudinally collected Pseudomonas aeruginosa isolates from young children diagnosed with cystic fibrosis following newborn screening. Clin Microbiol Infect. 2013;19(3):266–272. doi:10.1111/j.1469-0691.2012.03770.x22329595
  • Bradbury RS, Roddam LF, Merritt A, Reid DW, Champion AC. Virulence gene distribution in clinical, nosocomial and environmental isolates of Pseudomonas aeruginosa. J Med Microbiol. 2010;59(8):881–890. doi:10.1099/jmm.0.018283-020430902
  • Feltman H, Schulert G, Khan S, Jain M, Peterson L, Hauser AR. Prevalence of type III secretion genes in clinical and environmental isolates of Pseudomonas aeruginosa. Microbiology. 2001;147(10):2659–2669. doi:10.1099/00221287-147-10-265911577145
  • Horna G, Amaro C, Palacios A, Guerra H, Ruiz J. High frequency of the exoU+/exoS+ genotype associated with multidrug-resistant “high-risk clones” of Pseudomonas aeruginosa clinical isolates from Peruvian hospitals. Sci Rep. 2019;9(1):1–13. doi:10.1038/s41598-019-47303-430626917
  • Morales-Espinosa R, Delgado G, Espinosa LF, et al. Fingerprint analysis and identification of strains ST309 as a potential high risk clone in a Pseudomonas aeruginosa population isolated from children with bacteremia in Mexico City. Front Microbiol. 2017;8:13. doi:10.3389/fmicb.2017.0031328167933
  • Finnan S, Morrissey JP, O’gara F, Boyd EF. Genome diversity of Pseudomonas aeruginosa isolates from cystic fibrosis patients and the hospital environment. J Clin Microbiol. 2004;42(12):5783–5792. doi:10.1128/JCM.42.12.5783-5792.200415583313
  • Peña C, Cabot G, Gómez-Zorrilla S, et al. Influence of virulence genotype and resistance profile in the mortality of Pseudomonas aeruginosa bloodstream infections. Clin Infect Dis. 2015;60(4):539–548. doi:10.1093/cid/ciu86625378459
  • El-Solh AA, Hattemer A, Hauser AR, Alhajhusain A, Vora H. Clinical outcomes of type III Pseudomonas aeruginosa bacteremia. Crit Care Med. 2012;40(4):1157–1163. doi:10.1097/CCM.0b013e318237790622080633
  • Jabalameli F, Mirsalehian A, Khoramian B, et al. Evaluation of biofilm production and characterization of genes encoding type III secretion system among Pseudomonas aeruginosa isolated from burn patients. Burns. 2012;38(8):1192–1197. doi:10.1016/j.burns.2012.07.03022995427
  • Shwachman H, Kulczycki LL. Long-term study of one hundred five patients with cystic fibrosis: studies made over a five-to fourteen-year period. AMA J Dis Child. 1958;96(1):6–15. doi:10.1001/archpedi.1958.0206006000800213544726
  • Pereira C. Sociedade Brasileira de Pneumologia e Tisiologia, Sociedade Brasileira de Pneumologia e Tisiologia. Diretrizes para testes de função pulmonar. J Pneumol. 2002;28(Suppl 3):S1–238.
  • Zhu H, Conibear TC, Bandara R, Aliwarga Y, Stapleton F, Willcox MD. Type III secretion system–associated toxins, proteases, serotypes, and antibiotic resistance of Pseudomonas aeruginosa isolates associated with keratitis. Curr Eye Res. 2006;31(4):297–306. doi:10.1080/0271368050053674616603462
  • Ayres M, Ayres Júnior M, Ayres DL, Santos AS. BioEstat 5.0. Aplicações Estatísticas Nas Áreas Das Ciências Bio-Médicas. Belém (PA): Instituto de Desenvolvimento Sustentável Mamirauá; 2008.
  • Juarez-Colunga E, Rosenfeld M, Zemanick ET, Wagner B. Application of multiple event analysis as an alternative approach to studying pulmonary exacerbations as an outcome measure. J Cyst Fibros. 2020;19(1):114–118. doi:10.1016/j.jcf.2018.12.00530642785
  • Luo RG, Miao XY, Luo LL, Mao B, Yu FY, Xu JF. Presence of pldA and exoU in mucoid Pseudomonas aeruginosa is associated with high risk of exacerbations in non–cystic fibrosis bronchiectasis patients. Clin Microbiol Infect. 2019;25(5):601–606. doi:10.1016/j.cmi.2018.07.00830036669
  • Lanotte P, Mereghetti L, Lejeune B, Massicot P, Quentin R. Pseudomonas aeruginosa and cystic fibrosis: correlation between exoenzyme production and patient’s clinical state. Pediatr Pulmonol. 2003;36(5):405–412. doi:10.1002/ppul.1038014520723
  • Mitov I, Strateva T, Markova B. Prevalence of virulence genes among bulgarian nosocomial and cystic fibrosis isolates of Pseudomonas aeruginosa. Braz J Microbiol. 2010;41(3):588–595. doi:10.1590/S1517-8382201000030000824031533
  • Khodayary R, Nikokar I, Mobayen MR, et al. High incidence of type III secretion system associated virulence factors (exoenzymes) in Pseudomonas aeruginosa isolated from Iranian burn patients. BMC Res Notes. 2019;12(1):1–6. doi:10.1186/s13104-019-4071-030602384
  • Engel J, Balachandran P. Role of Pseudomonas aeruginosa type III effectors in disease. Curr Opin Microbiol. 2009;12(1):61–66. doi:10.1016/j.mib.2008.12.00719168385
  • Lanotte P, Watt S, Mereghetti L, et al. Genetic features of Pseudomonas aeruginosa isolates from cystic fibrosis patients compared with those of isolates from other origins. J Med Microbiol. 2004;53(1):73–81. doi:10.1099/jmm.0.05324-014663109
  • Römling U, Fiedler B, Boßhammer J, et al. Epidemiology of chronic Pseudomonas aeruginosa infections in cystic fibrosis. J Infect Dis. 1994;170(6):1616–1621. doi:10.1093/infdis/170.6.16167996008
  • Parkins MD, Glezerson BA, Sibley CD, et al. Twenty-five-year outbreak of Pseudomonas aeruginosa infecting individuals with cystic fibrosis: identification of the prairie epidemic strain. J Clin Microbiol. 2014;52(4):1127–1135. doi:10.1128/JCM.03218-1324452167
  • Logan C, Habington A, Lennon G, et al. Genetic relatedness of Pseudomonas aeruginosa isolates among a paediatric cystic fibrosis patient cohort in Ireland. J Med Microbiol. 2012;61(1):64–70. doi:10.1099/jmm.0.035642-021921114
  • Hauser AR, Cobb E, Bodí M, et al. Type III protein secretion is associated with poor clinical outcomes in patients with ventilator-associated pneumonia caused by Pseudomonas aeruginosa. Crit Care Med. 2002;30(3):521–528. doi:10.1097/00003246-200203000-0000511990909