|Year : 2017 | Volume
| Issue : 6 | Page : 527-531
The emergence of multidrug-resistant Pseudomonas aeruginosa in cystic fibrosis patients on inhaled antibiotics
Atqah AbdulWahab1, Khalid Zahraldin2, Mazen A Sid Ahmed3, Sulieman Abu Jarir4, Mohammed Muneer5, Shehab F Mohamed4, Jemal M Hamid6, Abubaker A. I. Hassan4, Emad Bashir Ibrahim7
1 Department of Pediatrics, Hamad Medical Corporation; Weill Cornell Medicine, Qatar
2 Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar
3 Department of Laboratory Medicine and Pathology, Microbiology Division, Hamad Medical Corporation, Doha, Qatar; The Life Science Centre - Biology, School of Science and Technology, Örebro University, Örebro, Sweden
4 Department of Internal Medicine, Hamad Medical Corporation, Doha, Qatar
5 Plastic Surgery, Hamad Medical Corporation, Doha, Qatar
6 Department of Laboratory Medicine and Pathology, Microbiology Division, Hamad Medical Corporation, Doha, Qatar
7 Weill Cornell Medicine; Department of Laboratory Medicine and Pathology, Microbiology Division, Hamad Medical Corporation, Doha, Qatar
|Date of Web Publication||1-Nov-2017|
Department of Pediatrics, Hamad Medical Corporation, Weill Cornell Medicine, Doha
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Introduction: Multidrug-resistant Pseudomonas aeruginosa (MDR-PA) is an important and growing issue in the care of patients with cystic fibrosis (CF), and a major cause of morbidity and mortality. Objective: The objective of the study was to describe the frequency of MDR-PA recovered from the lower respiratory samples of pediatric and adult CF patients, and its antibiotic resistance pattern to commonly used antimicrobial agents including β-lactams, aminoglycosides, and fluoroquinolones. Materials and Methods: The lower respiratory isolates of P. aeruginosa were obtained from inpatients and outpatients CF clinics from a tertiary care teaching hospital for the period from October 2014 to September 2015. The identification and antimicrobial susceptibility for all the isolates were performed by using the BD Phoenix™ and E-test in compliance with Clinical and Laboratory Standards Institute (CLSI) guidelines. Results: A total of 61 P. aeruginosa samples were isolated from thirty CF patients from twenty families. Twelve sputum samples were positive for MDR-PA (seven nonmucoid and five mucoid isolates) from five CF patients (five families) with moderate-to-very severe lung disease given MDR-PA frequency of 19.7%. The median age of the study group was 20 (range 10–30) years. Three CF patients were on chronic inhaled tobramycin and two on nebulized colistin. The antimicrobial patterns of isolates MDR-PA showed the highest rate of resistance toward each gentamycin, amikacin, and cefepime (100%), followed by 91.7% to ciprofloxacin, 75% to tobramycin, 58.3% to meropenem, and 50% to piperacillin-tazobactam. None of the isolates were resistant to colistin during the study period. Conclusion: The study results emphasize that the emergence of a significant problem in the clinical isolates of P. aeruginosa in CF patients that dictate appropriate attention to the antibiotic management after proper surveillance.
Keywords: Cystic fibrosis, inhaled antibiotics, multidrug-resistant Pseudomonas aeruginosa
|How to cite this article:|
AbdulWahab A, Zahraldin K, Sid Ahmed MA, Jarir SA, Muneer M, Mohamed SF, Hamid JM, Hassan AA, Ibrahim EB. The emergence of multidrug-resistant Pseudomonas aeruginosa in cystic fibrosis patients on inhaled antibiotics. Lung India 2017;34:527-31
|How to cite this URL:|
AbdulWahab A, Zahraldin K, Sid Ahmed MA, Jarir SA, Muneer M, Mohamed SF, Hamid JM, Hassan AA, Ibrahim EB. The emergence of multidrug-resistant Pseudomonas aeruginosa in cystic fibrosis patients on inhaled antibiotics. Lung India [serial online] 2017 [cited 2018 May 23];34:527-31. Available from: http://www.lungindia.com/text.asp?2017/34/6/527/217578
| Introduction|| |
About 70,000 people have cystic fibrosis (CF) worldwide, with prevalence varying by location and ethnic background.
CF is caused by a mutation in the CF transmembrane conductance regulator (CFTR) gene, leading to altered chloride ion exchange and hyperviscous mucus in the affected organs.,
Pulmonary complications resulting from CF currently account for up to 85% of CF mortality. CF pulmonary disease begins early in life and is characterized by progressive airway obstruction, as measured by the expiratory volume over the first second of a forced exhalation (FEV1).
In the lung, the CFTR gene produces a protein whose basic function is regulation of ion transport on the surface of the airways that contributes to mucus hydration and periciliary transport, which are altered on mucosal surfaces in CF patients resulting in air defective mucociliary clearance with the production of viscous and sticky bronchial mucus airway obstruction. This provides a good environment for microbial growth, and as a consequence, CF patients suffer from recurrent infections of the respiratory tract and chronic inflammation, thus leads to tissue remodeling and finally to premature death caused by respiratory insufficiency. The respiratory tract of the CF patients is colonized by pathogenic microorganisms early in childhood, and in the vast majority of cases, chronic infections are established.,,
Pseudomonas aeruginosa is the main bacterial pathogen that infects the lungs of patients; with the prevalence of P. aeruginosa, infection increases with age and becomes the most frequently identified pathogen in adulthood. Initial pulmonary infections with P. aeruginosa in patients with CF are typically intermittent and caused by nonmucoid environmental strains that are susceptible to anti-P. aeruginosa antibiotics.,, Eventually, a single strain becomes established and develops a mucoid phenotype, which makes eradication from the airways difficult. The alginate-containing matrix of the mucoid strain is thought to allow the formation of protected microcolonies and provide increased resistance to opsonization, phagocytosis, and destruction by antibiotics. As a result, conversion to mucoid phenotype is associated with a significant increase in morbidity and mortality and demonstrated a greater loss of lung function in comparison to CF patients with intermittent or no colonization.,,, Eradication strategies have emerged over the past several years that target nonmucoid strains and can delay the development of chronic infection.,,, Patients with CF are at very high risk of developing infections with multidrug-resistant (MDR) pathogens, particularly P. aeruginosa, owing to the frequent and often prolonged courses of oral, intravenous, and aerosolized antibiotics that are used to treat the chronic lung disease of CF.
The objectives of this study described the frequency of MDR P. aeruginosa (MDR-PA) recovered from the lower respiratory samples of CF patients, and its antibiotic resistance pattern to the commonly used antimicrobial agents.
| Materials and Methods|| |
Patients and sampling
Respiratory specimens such as sputa, deep pharyngeal swab, or bronchoalveolar lavages were collected from CF patients during visits to the CF clinic and as part of inpatient care from October 2014 to September 2015 at Hamad Medical Corporation, in the state of Qatar. The diagnosis of CF was based on one or more clinical features consistent with CF, positive family history of CF in siblings and close relatives, pathologically elevated sweat chloride (>60 mmol/L) on two separate occasions, in addition to the presence of two disease-causing mutations in the CFTR gene. Screening for CFTR mutations was performed initially by mutation detection enhancement heteroduplex analyses and currently coding DNA Sanger sequences method.
Routine culture for P. aeruginosa was performed on blood agar and MacConkey agar. The media were incubated for 18–24 h at 37°C and P. aeruginosa was identified by biochemical tests.
Drug susceptibility testing
Antibiotic susceptibility testing for all P. aeruginosa isolates was performed using BD Phoenix automated system and E-test (previously known as Epsilometer test) methods. BD Phoenix ™ Automated Microbiology System in compliance with Clinical and Laboratory Standards Institute. The identification and antimicrobial susceptibility analysis were performed, as described previously.,
The range of antimicrobial agents was routinely evaluated in two or more of the following groups: Aminoglycosides (tobramycin, gentamicin, and amikacin), fluoroquinolones.(ciprofloxacin), and beta-lactams (ceftazidime, meropenem, piperacillin, ticarcillin-clavulanate, and aztreonam). This method is internationally accepted, simple, and allows ease of use when screening a large number of isolates. This allowed the production of a large antibiogram including multiple classes of antibiotic. The United States CF Foundation consensus guidelines definition of MDR was defined as resistance to all agents tested in two or more of the following antibiotic categories: aminoglycosides, β-lactam antibiotics, and/or the fluoroquinolone, ciprofloxacin, according to the CF Foundation Microbiology and Infectious Disease Consensus Conference.
| Results|| |
A total of 61 P. aeruginosa samples were isolated from thirty CF patients from twenty families. The mean age of the study group was 20.56 ± 8.95 years, 11 males and 19 females. Twenty CF patients (66.7%) were above 18 years old. Twenty-five (83.3%) CF patients from 15 families were with homozygous CFTR I234V mutation, and the other five have other types of CFTR mutations (including three CF patients with homozygous delta F508 mutation, 1CF patient with homozygous Y569D mutation, and unidentified CFTR mutation in one CF patient).
P. aeruginosa isolates from all siblings (two families with four CF siblings, two families with three CF siblings, and 13 families contributed one sibling each). The remaining three families were two families with two CF siblings where P. aeruginosa isolates in one CF sibling and one family with three CF siblings where P. aeruginosa isolates in one CF sibling.
P. aeruginosa in lower respiratory samples of thirty CF patients showed the highest sensitivity to piperacillin/tazobactam (90.2%) followed by meropenem (88.5%), ciprofloxacin (77%), cefepime (70.5%), amikacin (67.2%), and gentamicin (59%). All the isolates were susceptible to colistin during the study period [Figure 1]. Twelve sputum samples were positive for MDR-PA (seven nonmucoid and five mucoid isolates) from five CF patients of five families with moderate-to-very severe lung disease given MDR-PA frequency of 19.7%. This includes one family with four CF siblings harbor P. aeruginosa; only one sibling had MDR-PA and one family with two CF siblings, only one had MDR-PA. The rest of three families were with one CF sibling in each. The demographic characteristic of CF patients with MDR-PA is shown in [Table 1].
|Figure 1: The antimicrobial susceptibility of Pseudomonas aeruginosa from lowe respiratory samples of thirty cystic fibrosis patients. COL: Colomycin, PIP-TAZO: Piperacillin-tazobactam, MERO: Meropenem, CIP: Ciprofloxacin, CEF: Cefepime, AMK: Amikacin, GENT: Gentamicin|
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|Table 1: Baseline demographic characteristics of cystic fibrosis patients with multidrug-resistant Pseudomonas aeruginosa|
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The antimicrobial susceptibility pattern of MDR-PA isolates showed the highest rate of resistance (100%) toward each gentamycin, amikacin, and cefepime, followed by 91.7% to ciprofloxacin, 75% to tobramycin, 58.3% to meropenem, and 50% to piperacillin-tazobactam [Figure 2].
|Figure 2: The antimicrobial pattern of MDR-PA isolates from lower respiratory samples of five cystic fibrosis patients. AMK: Amikacin, GENT: Gentamicin, CEF: Cefepime, CIP: Ciprofloxacin, TOB: Tobramycin, MERO: Meropenem, PIP-TAZO: Piperacillin-tazobactam|
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| Discussion|| |
Antibiotic resistance is a hallmark of chronically colonizing pathogens generally and particularly, in those associated with CF infections. The problem of antibiotic resistance in P. aeruginosa CF is on the increase.,
Several studies worldwide have reported of MDR-PA in patients with CF. There an increased prevalence of patients with an MDR-PA infection has been reported at Texas Children's Hospital in Houston, Texas. The Epidemiologic Study of CF assessed data from 110 United States and Canadian CF centers and found that approximately one-third of patients aged 18 years or over with a percentage forced expiratory volume in 1 s predicted to be <40% harbored MDR strains. In the Arabian Gulf region, Saudi Arabia has the largest CF population in the Arabian Gulf region, and in the state of Qatar, CF is common in a large kindred Arab tribe, consisting of some families who share a common ancestry and culture.
P. aeruginosa was the most common bacteria isolated from the first culture samples in 44% of CF patients in Saudi Arabia, and the prevalence of P. aeruginosa in lower respiratory cultures of CF patients from our institute was 60.9%. In the present study, we reported small frequency (19.7%) of MDR-PA among CF patients with moderate-to-very severe airflow obstruction. There is no report in the Arabian Gulf region of MDR-PA in CF patients.
P. aeruginosa has the capability of adapting to the environmental conditions, developing resistance to antibiotics, and producing a variety of virulence factors. It has been reported multiple antibiotic-resistant P. aeruginosa is more likely to be a marker of more severe disease and more intensive therapy and is less likely to be contributing independently to more rapid lung function decline, suggesting that this may be an important potential pathogen across all stages of airflow limitation.
P. aeruginosa is masterful at developing resistance by either spontaneous mutations or the acquisition of plasmids (extrachromosomal DNA) harboring resistance genes. Two such mechanisms, efflux pumps and beta-lactamases, are among the most common mechanisms of resistance detected in P. aeruginosa isolate from patients with CF. Another less conventional mechanism of resistance noted in P. aeruginosa strains infecting patients with CF is the biofilm mode of growth. The emergence of hypermutable P. aeruginosa strain that may contribute to increased resistance of P. aeruginosa to antibiotics and become more frequent in later stages or chronic infection. Mutations in mutS, mutL, and uvrD genes encoding proofreading proteins which normally correct errors during DNA replication give rise to these hypermutable strains. It is important to note that the increase in hypermutable P. aeruginosa isolates later in CF patients suggest that genetic and phenotypic diversification plays an essential role in the adaptation of P. aeruginosa to the hostile and diverse CF lung environment and plays a role in survivalin vivo by selecting for less virulent phenotypes.
We reported previously that clustering of P. aeruginosa isolate from CF patient with advanced lung disease and MDR P. aeruginosa isolates in different pulsed-field gel electrophoresis clusters suggests that the colonizing strain may occasionally be changed.
There is now evidence that P. aeruginosa survives in cough aerosols up to 4 m and for as long as 45 min, suggesting cough bioaerosols as a possible transmission pathway, may be possible to certain specific P. aeruginosa. In the present study, we found MDR P. aeruginosa isolates only in one sibling in the families having more than one sibling with CF suggesting that certain intrinsic mechanism of resistance and possible certain strain MDR P. aeruginosa with less transmissible.
| Conclusion|| |
Hygiene regulations in CF clinics should prevent a further spread of resistant bacterial strains, as antibacterial treatment options are limited in CF patients. Finally, adequately powered studies should be performed to determine the clinical utility of synergy studies in patients with CF infected with MDR pathogens.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
O'Sullivan BP, Flume P. The clinical approach to lung disease in patients with cystic fibrosis. Semin Respir Crit Care Med 2009;30:505-13.
Ratjen F. Recent advances in cystic fibrosis. Paediatr Respir Rev 2008;9:144-8.
Flume PA, O'Sullivan BP, Robinson KA, Goss CH, Mogayzel PJ Jr., Willey-Courand DB, et al.
Cystic fibrosis pulmonary guidelines: Chronic medications for maintenance of lung health. Am J Respir Crit Care Med 2007;176:957-69.
Que C, Cullinan P, Geddes D. Improving rate of decline of FEV1 in young adults with cystic fibrosis. Thorax 2006;61:155-7.
Kreda SM, Davis CW, Rose MC. CFTR, mucins, and mucus obstruction in cystic fibrosis. Cold Spring Harb Perspect Med 2012;2:a009589.
Griesenbach U, Alton EW. Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction. F1000Prime Rep 2015;7:64.
Lobo J, Rojas-Balcazar JM, Noone PG. Recent advances in cystic fibrosis. Clin Chest Med 2012;33:307-28.
Foweraker J. Recent advances in the microbiology of respiratory tract infection in cystic fibrosis. Br Med Bull 2009;89:93-110.
Accurso FJ. Update in cystic fibrosis 2007. Am J Respir Crit Care Med 2008;177:1058-61.
Cystic Fibrosis Foundation. Patient Registry. 2012 Annual Data Report.
Bethesda, MD: Cystic Fibrosis Foundation; 2013.
Burns JL, Gibson RL, McNamara S, Yim D, Emerson J, Rosenfeld M, et al.
Longitudinal assessment of Pseudomonas aeruginosa
in young children with cystic fibrosis. J Infect Dis 2001;183:444-52.
Kidd TJ, Ramsay KA, Vidmar S, Carlin JB, Bell SC, Wainwright CE, et al. Pseudomonas aeruginosa
genotypes acquired by children with cystic fibrosis by age 5-years. J Cyst Fibros 2015;14:361-9.
Mogayzel PJ Jr., Naureckas ET, Robinson KA, Brady C, Guill M, Lahiri T, et al.
Cystic Fibrosis Foundation pulmonary guideline. Pharmacologic approaches to prevention and eradication of initial Pseudomonas aeruginosa
infection. Ann Am Thorac Soc 2014;11:1640-50.
Hauser AR, Jain M, Bar-Meir M, McColley SA. Clinical significance of microbial infection and adaptation in cystic fibrosis. Clin Microbiol Rev 2011;24:29-70.
Kosorok MR, Zeng L, West SE, Rock MJ, Splaingard ML, Laxova A, et al.
Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa
acquisition. Pediatr Pulmonol 2001;32:277-87.
Li Z, Kosorok MR, Farrell PM, Laxova A, West SE, Green CG, et al.
Longitudinal development of mucoid Pseudomonas aeruginosa
infection and lung disease progression in children with cystic fibrosis. JAMA 2005;293:581-8.
Hogardt M, Heesemann J. Adaptation of Pseudomonas aeruginosa
during persistence in the cystic fibrosis lung. Int J Med Microbiol 2010;300:557-62.
Pritt B, O'Brien L, Winn W. Mucoid Pseudomonas
in cystic fibrosis. Am J Clin Pathol 2007;128:32-4.
Tiddens HA, De Boeck K, Clancy JP, Fayon M, Arets HG, Bresnik M, et al.
Open label study of inhaled aztreonam for Pseudomonas
eradication in children with cystic fibrosis: The ALPINE study. J Cyst Fibros 2015;14:111-9.
Mayer-Hamblett N, Rosenfeld M, Treggiari MM, Konstan MW, Retsch-Bogart G, Morgan W, et al.
Standard care versus protocol based therapy for new onset Pseudomonas aeruginosa
in cystic fibrosis. Pediatr Pulmonol 2013;48:943-53.
Treggiari MM, Retsch-Bogart G, Mayer-Hamblett N, Khan U, Kulich M, Kronmal R, et al.
Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa
infection in children with cystic fibrosis. Arch Pediatr Adolesc Med 2011;165:847-56.
Ratjen F, Munck A, Kho P, Angyalosi G; ELITE Study Group. Treatment of early Pseudomonas aeruginosa
infection in patients with cystic fibrosis: The ELITE trial. Thorax 2010;65:286-91.
Abdul Wahab A, Al Thani G, Dawod ST, Kambouris M, Al Hamed M. Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V). J Trop Pediatr 2001;47:110-2.
Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing; Twenty-Fifth Informational Supplement. CLSI document M100-S25. Wayne, PA: Clinical and Laboratory Standards Institute; 2015.
Sid Ahmed MA, Bansal D, Acharya A, Elmi AA, Hamid JM, Sid Ahmed AM, et al.
Antimicrobial susceptibility and molecular epidemiology of extended-spectrum beta-lactamase-producing Enterobacteriaceae from intensive care units at Hamad Medical Corporation, Qatar. Antimicrob Resist Infect Control 2016;5:4.
Khanbabaee G, Akbarizadeh M, Sayyari A, Ashayeri-Panah M, Abdollahgorji F, Sheibani K, et al.
Asurvey on pulmonary pathogens and their antibiotic susceptibility among cystic fibrosis patients. Braz J Infect Dis 2012;16:122-8.
National Nosocomial Infections Surveillance System. National Nosocomial Infections Surveillance (NNIS) System Report, data summary from January 1992 through June 2004, issued October 2004. Am J Infect Control 2004;32:470-85.
Cystic Fibrosis Foundation. Patient Registry: Annual Data Report 2010. Bethesda, MD: Cystic Fibrosis Foundation; 2011.
Lechtzin N, John M, Irizarry R, Merlo C, Diette GB, Boyle MP. Outcomes of adults with cystic fibrosis infected with antibiotic-resistant Pseudomonas aeruginosa
. Respiration 2006;73:27-33.
Banjar H, Angyalosi G. The road for survival improvement of cystic fibrosis in Arab countries. Int J Pediatr Adolesc 2015;2:47-58.
Banjar H. Morbidity and mortality data of cystic fibrosis patients. Saudi Med J 2003;24:730-5.
Abdul Wahab A, Abushahin A. Pseudomonas aeruginosa
in cystic fibrosis patients with CFTR I1234V in a large kindred family. Qatar Med J 2010;19:28-31.
Ren CL, Konstan MW, Yegin A, Rasouliyan L, Trzaskoma B, Morgan WJ, et al.
Multiple antibiotic-resistant Pseudomonas aeruginosa
and lung function decline in patients with cystic fibrosis. J Cyst Fibros 2012;11:293-9.
Livermore DM. Multiple mechanisms of antimicrobial resistance in Pseudomonas aeruginosa
: Our worst nightmare? Clin Infect Dis 2002;34:634-40.
Singh PK, Schaefer AL, Parsek MR, Moninger TO, Welsh MJ, Greenberg EP. Quorum-sensing signals indicate that cystic fibrosis lungs are infected with bacterial biofilms. Nature 2000;407:762-4.
Oliver A, Cantón R, Campo P, Baquero F, Blázquez J. High frequency of hypermutable Pseudomonas aeruginosa
in cystic fibrosis lung infection. Science 2000;288:1251-4.
Hogardt M, Hoboth C, Schmoldt S, Henke C, Bader L, Heesemann J. Stage-specific adaptation of hypermutable Pseudomonas aeruginosa
isolates during chronic pulmonary infection in patients with cystic fibrosis. J Infect Dis 2007;195:70-80.
AbdulWahab A, Taj-Aldeen SJ, Ibrahim E, Abdulla SH, Muhammed R, Ahmed I, et al.
Genetic relatedness and host specificity of Pseudomonas aeruginosa
isolates from cystic fibrosis and non-cystic fibrosis patients. Infect Drug Resist 2014;7:309-16.
Knibbs LD, Johnson GR, Kidd TJ, Cheney J, Grimwood K, Kattenbelt JA, et al.
Viability of Pseudomonas aeruginosa
in cough aerosols generated by persons with cystic fibrosis. Thorax 2014;69:740-5.
[Figure 1], [Figure 2]