Volume 9, Number 8—August 2003
Pseudomonas aeruginosa and the Oropharyngeal Ecosystem of Tube-Fed Patients
We evaluated whether elderly patients fed with nasogastric tubes (NGT) are predisposed to Pseudomonas aeruginosa colonization in the oropharynx. Fifty-three patients on NGT feeding and 50 orally fed controls with similar clinical characteristics were studied. The tongue dorsum was swabbed and cultured. P. aeruginosa was isolated in 18 (34%) of the NGT-fed group but in no controls (p<0.001). Other gram-negative bacteria were cultured from 34 (64%) of NGT-fed patients as compared with 4 (8%) of controls (p<0.001). Antibiotic susceptibility of the oropharyngeal P. aeruginosa isolates was compared with that of isolates from sputum cultures obtained from our hospital’s bacteriologic laboratory. The oropharyngeal isolates showed a higher rate of resistance; differences were significant for amikacin (p<0.03). Scanning electron microscope studies showed a biofilm containing P. aeruginosa organisms. The pulsed-field gel electrophoresis profile of these organisms was similar to that of P. aeruginosa isolates from the oropharynx. NGT-fed patients may serve as vectors of resistant P. aeruginosa strains.
The oral cavity has long been considered a potential reservoir for pathogenic microorganisms. It is the only normally accessible site in the body that has hard, nonshedding surfaces for microbial colonization. Those unique tissues allow the accumulation of extracellular products and the formation of biofilms that serve as culture media for bacteria and contribute to the development of antibiotic resistance (1). Within the mouth, distinct habitats provide different ecologic conditions including mucosal surfaces, cheeks, palate, periodontal region, tongue, and abiotic structures (teeth). Ecologic conditions within the mouth may vary and change the ecosystem, facilitating the growth of pathogenic organisms.
Patients on nasogastric tube (NGT) feeding are a growing segment of the frail elderly population. We have recently reported an increased rate of gram-negative bacteria in the nasopharynx of these patients, including a high proportion of Pseudomonas aeruginosa (2). P. aeruginosa has a predilection for wet sites and respiratory equipment and may create reservoirs that threaten hospitalized patients (3). The oropharynx of NGT-fed elderly patients may provide such an ecosystem and promote the colonization of P. aeruginosa. This colonization could be due to several factors such as the papillary structure of the dorsum of the tongue, the lack of mastication and swallowing (eliminating their mechanical cleansing effect), and the tube itself. P. aeruginosa, a well-known biofilm-producing microorganism (4,5), may be exploiting the NGT to create a thriving habitat.
The purpose of this study was to reconfirm the high incidence of P. aeruginosa isolations from the oropharynx of NGT-fed elderly patients, determine its antibiotic susceptibility, and explore the possibility of biofilm formation on the feeding tube. If these assumptions are true, the oropharynx of NGT-fed patients could constitute a potential reservoir for P. aeruginosa in long-term-care facilities.
This prospective cross-sectional comparative study was conducted in the four skilled nursing wards of a 158-bed geriatric hospital. Skilled nursing wards are licensed for providing care for nursing patients who also have an active disease requiring close medical supervision (e.g., NGT feeding, severe bed sores, advanced cancer, or hemodynamic instability). Eligible for the study were all patients who had been receiving NGT feeding for at least 2 weeks.
The control group comprised matched orally fed patients, with no swallowing disturbances, who resided in the same wards. The orally fed patients received a regular solid hospital diet with occasional supplements. Excluded from both groups were patients who had received any antibiotic treatment up to 2 weeks before the study, patients with advanced cancer, and patients who had received chemotherapy or radiotherapy to the neck. Informed consent was obtained from the patients or their proxies.
Cultures were obtained by applying sterile cotton swabs to the base of the tongue dorsum and rubbing the buccal mucosa. The sample was then placed in transport medium. Samples were taken in the morning, before breakfast and the daily oral cleansing procedure.
Within 1 h of collection, specimens were spread on blood and MacConkey agar plates and were incubated at 35°C for 18 h. Five colonies of each morphotype were selected for identification. Gram-negative bacteria, including P. aeruginosa, were identified by using the BBL Crystal ID system (Becton Dickinson, Sparks, MD). Antimicrobial susceptibility testing was performed by the disc-diffusion technique, according to guidelines of the National Committee for Clinical Laboratory Standards (6), with OXOID test discs (OXOID, Basingstoke, Hampshire, England).
Routine oral hygiene for the tuboenteral patients was performed by cleansing the oral cavity before meals three times a day with lemon-glycerine wadding sticks impregnated with a solution of glycerine-citric acid, lemon flavoring, and sodium benzoate 0.1% (7). NGTs in use in our hospital are made from polyvinyl chloride (Duodenal Levin Tube–Maersk Medical, Lynge, Denmark).
For the biofilm study, samples of the oropharyngeal section of the NGT were fixed overnight with 2.5% glutaraldehyde in 0.1 M cacodylate buffer, pH 7.4, washed with the same buffer, dehydrated in increasing concentrations of ethanol, dried with a critical point drier, and coated with gold (Polaron-sem coating unit E5100, Thermo VG Scientific, Beverly, MA). The outer surface of the samples was examined by a Jeol-840A scanning electron microscope (JEOL USA, Peabody, MA). Biofilm studies were performed on four patients with a oropharyngeal culture that was positive for P. aeruginosa 2–4 weeks after the NGT was inserted.
From three NGT-fed patients with isolations of P. aeruginosa, samples were taken concomitantly from the oropharynx and the NGT surface for strain typing by pulsed-field gel electrophoresis (PFGE). DNA preparation and cleavage with 20 U of Spel endonuclease (New England Biolabs, Eldan, Rosh Ha’ain, Israel) were performed, as originally described (8). Electrophoresis was performed in a 1% agarose gel (BMA Products, Hann Woong Yoo, South Korea) prepared and run in 0.5 x Tris-borate-EDTA buffer on a CHEF-DR III apparatus (Bio-Rad Laboratories Ltd. Rishon Le Zion, Israel). The initial switch time was 0.5 s, the final switch time was 35 s, and the run time was 22 h at 6 V/cm with a temperature of 14°C. Gels were stained in ethidium bromide, de-stained in distilled water, and photographed with a Bio-Rad GelDoc 2000 camera. PFGE DNA patterns were compared and interpreted according to the criteria of Tenover et al. (9).
The antibiotic susceptibility of P. aeruginosa isolates from the oropharynx was compared to that of P. aeruginosa isolates obtained from sputum cultures and recorded in the laboratory logbook in the preceding year. Statistical processing was performed by using SPSS software (SPSS Inc., Chicago, IL). Chi-square test was used for comparative studies; p<0.05 was considered significant.
The study group consisted of 53 elderly long-term-care residents who had been receiving NGT feeding for an average of 14 ± 17 months. The control group consisted of 50 counterparts receiving oral feeding. No statistically significant differences in demographic and medical characteristics occurred between the study groups (Table).
Gram-negative bacteria, including P. aeruginosa, were cultured from the oropharynges of 34 (64%) of the 53 NGT-fed patients. P. aeruginosa was isolated in 18 (34%) patients of this group or in 60% of the patients colonized with gram-negative bacteria. In the control group, gram-negative bacteria were isolated in only 4 (8%) patients (p<0.001). P. aeruginosa was not isolated in any of the control group samples (p<0.001). Two patients from the NGT-fed group had a mixture of other gram-negative bacteria and P. aeruginosa. No association was found between predisposing factors such as age, gender, diabetes mellitus, chronic lung disease, presence of residual teeth, and isolation of P. aeruginosa.
Antibiotic susceptibility studies of P. aeruginosa isolated from the oropharynx showed that the highest susceptibility rates were registered for tazobactam-piperacillin, with 89% of the isolates being susceptible, followed by ceftazidim (79%) and imipenem, (78%). The P. aeruginosa isolates from the oropharynx were less sensitive to most antibiotics than those cultured from sputum; for amikacin, this difference was significant (p<0.03).
The samples were taken from four patients with cultures positive for P. aeruginosa, who had NGTs inserted 2–4 weeks previously. A biofilm with a bacterial organism with a typical form for P. aeruginosa was clearly visualized on the outer surface of all four sections. The identity of the bacterium seen in the biofilm was confirmed by culture. Figure 3 shows the results of the PFGE studies on three patients; in each one, the same clone was isolated from both the oral cavity and the NGT.
NGT-fed elderly patients may constitute a human reservoir of P. aeruginosa. Determination of the antibiotic susceptibility of these P. aeruginosa isolates showed that they had a higher rate of resistance to most antibiotics than to P. aeruginosa isolates from sputum obtained from hospitalized patients with bronchopulmonary infections during the same period. This difference reached statistical significance for amikacin. Early studies had reported on the propensity of gram-negative bacteria to colonize elderly patients’ oropharynges (10–13). Our recently published study (2) and the present one are the only reports documenting the colonization of the oropharynx in NGT-fed patients by pathogenic florae.
Two factors may explain the high prevalence of P. aeruginosa in the NGT-fed patients. One is the lack of mechanical clearance of the mouth provided by chewing and swallowing, an important mechanism in preventing gram-negative bacteria from colonizing the oropharynx of the elderly (14). The other factor is P. aeruginosa’s known ability to adhere and form biofilm on plastic tubes, including those made of polyvinyl chloride (15,16). The biofilms formed on NGTs probably play a major role in the persistence of its colonization of the oropharynges of these patients and interfere with its eradication by antibiotics.
The clinical implications of such a reservoir are far reaching. An opportunistic organism such as P. aeruginosa in the oropharynx constitutes a threat to NGT-fed patients, who are at risk for aspiration pneumonia and systemic infections (17). Moreover, these elderly NGT-fed patients, most of whom reside in long-term-care facilities, are under “antibiotic pressure” because of frequent clinical infections and may constitute “reservoirs of resistance” (18). The existence of a biofilm in such a reservoir would facilitate antibiotic resistance (19). A similar effect was reported with polyvinyl chloride endotracheal tubes (20). The increased resistance rate of oropharyngeal P. aeruginosa isolates to relevant antibiotics in our study as compared with the isolates from sputum is in agreement with this observation.
The epidemiologic importance of a human reservoir of P. aeruginosa is not limited to the patient. NGT-fed patients are often transferred to general hospitals and may possibly serve as vectors of resistant organisms to other medical settings (emergency departments, surgical, orthopedic, urologic wards, and intensive care units).
One limitation of our study is that it was performed at a single facility. However, each of the four wards that participated is located in a pavilion separated by 50 m to 100 m from another. Moreover, the factors involved in the oropharyngeal ecosystem colonization by P. eruginosa discussed in this study exist everywhere. Similar studies from other long-term-care facilities could provide further evidence.
Dr. Leibovitz is specialist in internal medicine and geriatrics and director of a skilled nursing ward at Shmuel Harofe Hospital, Geriatric Medical Center, affiliated with the Sackler School of Medicine, Tel-Aviv University. His present subject of clinical research is the mucosal orifices of frail elderly patients.
We thank Mel Rosenberg for helpful professional advice and Yehuda Ben Shaul and Yacob Delarea for performing scanning electron microscopy.
- Donlan RM. Biofilms: Microbial life on surfaces. Emerg Infect Dis. 2002;8:881–90.
- Leibovitz A, Plotnikov G, Habot B, Rosenberg M, Segal R. Pathogenic colonization of the oral flora in frail elderly patients fed by naso-gastric tube or percutaneous entero-gastric tube. J Gerontol Biol Sci Med Sci. 2003;58A:52–5.
- Pollack M. Pseudomomas aeruginosa. In: Mandell GL, Bennett JE, Dolin R, editors. Principles and practice of infectious disease. Edinburgh: Churchill Livingstone, Ltd; 2000.
- Sauer K, Camper AK, Ehrlich GD, Costerton JW, Davies DG. Pseudomonas aeruginosa displays multiple phenotypes during development as a biofilm. J Bacteriol. 2002;184:1140–54.
- Whiteley M, Bangera MG, Bumgarner RE, Parsek MR, Teitzel GM, Lory S, Gene expression in Pseudomonas aeruginosa biofilms. Nature. 2001;413:860–4.
- National Committee for Clinical Laboratory Standards. Performance standards for antimicrobial susceptibility testing. M100-S11. Wayne (PA): The Committee; 2001.
- Warner LA. Lemon-glycerine swabs should be used for routine oral care. Crit Care Nurse. 1986;6:82–3.
- D’Agata E, Venkataraman L, DeGirolami P, Samore M. Molecular epidemiology of ceftazidime-resistant gram-negative bacilli in a non-outbreak setting. J Clin Microbiol. 1997;35:2602–5.
- Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH, Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol. 1995;33:2233–9.
- Valenti WM, Trudell RG, Bentley DW. Factors predisposing to oropharyngeal colonization with gram-negative bacilli in the aged. N Engl J Med. 1978;298:1108–11.
- Irwin RS, Whitaker S, Pratter MR, Millard CE, Tarpey JT, Corwin RW. The transiency of oropharyngeal colonization with gram-negative bacilli in residents of a skilled nursing facility. Chest. 1982;81:31–5.
- Scannapieco FA, Stewart EM, Mylotte JM. Colonization of dental plaque by respiratory pathogens in medical intensive care patients. Crit Care Med. 1992;20:740–5.
- Terpenning MS, Taylor GW, Lopatin DE, Kerr CK, Domingues BL, Loesche WJ. Aspiration pneumonia: dental and oral risk factors in an older veteran population. J Am Geriatr Soc. 2001;49:557–63.
- Palmer LB. Albulak, Fields S, Filkin AM, Simon S, Smaldone GC. Oral clearance and pathogenic oropharyngeal colonization in the elderly. Am J Respir Crit Care Med. 2001;164:464–8.
- Martinez-Martinez L, Pascual A, Perea EJ. Effect of three plastic catheters on survival and growth of Pseudomonas aeruginosa. J Hosp Infect. 1990;16:311–8.
- Martinez-Martinez L, Pascual A, Perea EJ. Kinetics of adherence of mucoid and non-mucoid Pseudomonas aeruginosa to plastic catheters. J Med Microbiol. 1991;34:7–12.
- Limeback H. Implications of oral infections on systemic diseases in the institutionalized elderly with a special focus on pneumonia. Ann Periodontol. 1998;3:262–75.
- Strausbaugh LJ, Crossley KB, Nurse BA, Thrupp LD. Antimicrobial resistance in long term care facilities. Infect Control Hosp Epidemiol. 1996;17:129–40.
- Brooun A, Liu S, Lewis K. A dose-response study of antibiotic resistance in Pseudomonas aeruginosa biofilms. Antimicrob Agents Chemother. 2000;44:640–6.
- Gorman SP, McGovern JG, Woolfson AD, Adair CG, Jones DS. The concomitant development of poly (vinyl chloride) related biofilm and antimicrobial resistance in relation to ventilator-associated pneumonia. Biomaterials. 2001;22:2741–7.
Suggested citation for this article: Leibovitz A, Dan M, Zinger J, Carmeli Y, Habot B, and Segal R. Pseudomonas aeruginosa and the oropharyngeal ecosystem of tube-fed patients. Emerg Infect Dis [serial online] 2003 Aug [date cited]. Available from: URL: http://wwwnc.cdc.gov/eid/article/9/8/03-0054.htm
Comments to the Authors
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