Chryseobacterium spp., a new opportunistic pathogen associated with cystic fibrosis?

被引:3
|
作者
Guiu, Alba [1 ,3 ]
Buendia, Buenaventura [1 ,3 ]
Llorca, Laura [1 ,3 ]
Gomez Punter, Rosa Maria [2 ,3 ]
Giron, Rosa [2 ,3 ]
机构
[1] Hosp Univ Princesa, Serv Microbiol, Madrid, Spain
[2] Hosp Univ Princesa, Unidad Fibrosis Quist, Serv Neumol, Madrid, Spain
[3] Hosp Princesa, Inst Invest, Madrid, Spain
来源
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA | 2014年 / 32卷 / 08期
关键词
Chryseobacterium spp; Infection; Cystic fibrosis; PSEUDOMONAS-AERUGINOSA; FLAVOBACTERIUM MENINGOSEPTICUM; INFECTION; COLONIZATION; INDOLOGENES; BACTERIA; FEV1;
D O I
10.1016/j.eimc.2013.08.003
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: There is an increase in the isolation of non-fermenting gramnegative bacilli in patients with cystic fibrosis (CF). The present study evaluates the frequency of isolates of Chryseobacterium spp., analyzing its characteristics, resistance patterns and clinical outcome of patients. Methods: It has been collected all respiratory isolates of Chryseobacterium spp. of patients attended in the CF unit of Hospital de la Princesa for three years (march 2009-march 2012). For phenotypic and genotypic identification and sensitivity study conventional methodology was used. For the assessment of the patients lung function was considered the forced expiratory volume in one second (FEV1) and the results were analyzed with SPSS. Results: There was an increase in the incidence of Chryseobacterium spp. with 17 isolates from 9 patients. Three patients had chronic colonization by this microorganism and one showed significant impairment of lung function. Seven patients showed also colonization with Staphylococcus aureus and 4 of them with Pseudomonas aeruginosa. Conclusion: Chtyseobacterium spp. should be considered as a new emerging opportunistic pathogen in patients with CF. It is essential the clinical and microbiological monitoring of this group of patients for detection of Cluyseobacterium spp. colonization and to prevent the chronic infection. In these circumstances it must assess its possible eradication, though its clinical impact is unknown. Cotrimoxazole being the best treatment option. (C) 2013 Elsevier Espana, S.L.U. and Sociedad Espanola de Enfermedades Infecciosas y Microbiologia Clinica. All rights reserved.
引用
收藏
页码:497 / 501
页数:5
相关论文
共 50 条
  • [1] Study of a Cohort of Patients With Cystic Fibrosis and Isolation of Scedosporium spp.
    Erro Iribarren, Marta
    Giron Moreno, Rosa Maria
    Diab Caceres, Layla
    Pastor Sanz, Maria Teresa
    Buendia Moreno, Buenaventura
    Alarcon Cavero, Teresa
    Granja Torrecillas, Silvia
    Zurita Cruz, Nelly Daniela
    Ancochea Bermudez, Julio
    ARCHIVOS DE BRONCONEUMOLOGIA, 2019, 55 (11): : 559 - 564
  • [2] Impact of airway Exophiala spp. on children with cystic fibrosis
    Mills, Rowena
    Rautemaa-Richardson, Riina
    Wilkinson, Stuart
    Patel, Latifa
    Maitra, Anirban
    Horsley, Alex
    JOURNAL OF CYSTIC FIBROSIS, 2021, 20 (04) : 702 - 707
  • [3] Achromobacter spp. prevalence and adaptation in cystic fibrosis lung infection
    Veschetti, Laura
    Boaretti, Marzia
    Saitta, Giulia Maria
    Mantovani, Rebeca Passarelli
    Lleo, Maria M.
    Sandri, Angela
    Malerba, Giovanni
    MICROBIOLOGICAL RESEARCH, 2022, 263
  • [4] Impact of Achromobacter spp. isolation on clinical outcomes in children with cystic fibrosis
    Sunman, Birce
    Emiralioglu, Nagehan
    Hazirolan, Gulsen
    Tural, Dilber Ademhan
    Ozsezen, Beste
    Buyuksahin, Halime Nayir
    Guzelkas, Ismail
    Yalcin, Ebru
    Dogru, Deniz
    Ozcelik, Ugur
    Kiper, Nural
    PEDIATRIC PULMONOLOGY, 2022, 57 (03) : 658 - 666
  • [5] Streptococcus pseudopneumoniae, an opportunistic pathogen in patients with cystic fibrosis
    Dupont, Chloe
    Michon, Anne-Laure
    Normandin, Marion
    Salom, Guillaume
    Latypov, Marie
    Chiron, Raphael
    Marchandin, Helene
    JOURNAL OF CYSTIC FIBROSIS, 2020, 19 (04) : E28 - E31
  • [6] Evidence of persistence of Prevotella spp. in the cystic fibrosis lung
    Gilpin, D. F.
    Nixon, K. A.
    Bull, M.
    McGrath, S. J.
    Sherrard, L.
    Rolain, J. M.
    Mahenthiralingam, E.
    Elborn, J. S.
    Tunney, M. M.
    JOURNAL OF MEDICAL MICROBIOLOGY, 2017, 66 (06) : 825 - 832
  • [7] A French multicentric study and review of pulmonary Nocardia spp. in cystic fibrosis patients
    Rodriguez-Nava, Veronica
    Durupt, Stephane
    Chyderiotis, Sandra
    Freydiere, Anne-Marie
    Karsenty, Judith
    de Montclos, Michele
    Reix, Philippe
    Durieu, Isabelle
    Nove-Josserand, Raphaele
    Chiron, Raphael
    Bremont, Francois
    Tetu, Laurent
    Murris, Marlene
    Terru, Dominique
    Godreuil, Sylvain
    Bergeron, Emmanuelle
    Freney, Jean
    Boiron, Patrick
    Vandenesch, Francois
    Marchandin, Helene
    Segonds, Christine
    Doleans-Jordheim, Anne
    MEDICAL MICROBIOLOGY AND IMMUNOLOGY, 2015, 204 (04) : 493 - 504
  • [8] Achromobacter spp. genetic adaptation in cystic fibrosis
    Gabrielaite, Migle
    Nielsen, Finn C.
    Johansen, Helle K.
    Marvig, Rasmus L.
    MICROBIAL GENOMICS, 2021, 7 (07):
  • [9] Stenotrophomonas maltophilia: to be or not to be a cystic fibrosis pathogen
    Hansen, Christine R.
    CURRENT OPINION IN PULMONARY MEDICINE, 2012, 18 (06) : 628 - 631
  • [10] Prevalence of hypermutator isolates of Achromobacter spp. from cystic fibrosis patients
    Ridderberg, Winnie
    Handberg, Kurt Jensen
    Norskov-Lauritsen, Niels
    INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2020, 310 (02)