Investigation of hospital water systems contamination to bacterial agents of nosocomial infections
Zahra Shamsizadeh1, Mohammad Hassan Ehrampoush2, Mahnaz Nikaeen3, Ali Asghar Ebrahimi2, Farzaneh Baghal Asghari4
1 Student Research Committee; Environmental Science and Technology Research Center, Department of Environmental Health Engineering, School of Public Health, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
2 Environmental Science and Technology Research Center, Department of Environmental Health Engineering, School of Public Health, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
3 Department of Environmental Health Engineering, School of Health, Isfahan University of Medical Sciences, Isfahan, Iran
4 Department of Environmental Health Engineering, School of public health, Tehran University of Medical Sciences, Tehran, Iran
|Date of Submission||24-Dec-2019|
|Date of Acceptance||20-Jun-2020|
|Date of Web Publication||31-Jul-2020|
Department of Environmental Health Engineering, School of Health, Isfahan University of Medical Sciences, Isfahan
Source of Support: None, Conflict of Interest: None
Aim: Nosocomial infections have become increasingly a major health concern in many hospitals. Gram-negative bacteria (GNB), including Acinetobacter baumannii, Pseudomonas aeruginosa and Legionella have emerged among the most problematic microorganisms in hospital settings, which can cause a variety of nosocomial infections, especially in susceptible individuals. Biofilm formation allows these waterborne agents to persist in hospital water systems for extended periods. Since the transmission is the initial step in disease occurrence, effective prevention of nosocomial infections requires a better knowledge about waterborne bacteria. The aim of this study was to investigate the frequency of presence of GNB in hospital water systems by a rapid and reliable assay. Materials and Methods: A total of 33 water samples were collected from 11 hospitals of Isfahan University of Medical Sciences, Iran and analyzed for the presence of GNB by a polymerase chain reaction (PCR) assay with the application of specific primer sets. Results: From the 11 hospitals surveyed, 91% (10 of 11) were positive for at least one of the types of GNB. GNB were detected in 58% (19 of 33) of water samples. 45% (15 of 33) of samples were positive for legionella. A. baumannii and P. aeruginosa were detected in 18% (6 of 33) of water samples. The mean concentration of heterotrophic bacteria was 36 CFU/ml. Conclusion: Detection of GNB in hospital water systems with a relatively high frequency revealed that hospital water may act as an important route for transmission of nosocomial infections. The results emphasize the importance of rapid microbiological monitoring and the implementation of strict control measures in hospital water systems.
Keywords: Gram-negative bacteria, hospital, nosocomial infection, polymerase chain reaction, water
|How to cite this article:|
Shamsizadeh Z, Ehrampoush MH, Nikaeen M, Ebrahimi AA, Asghari FB. Investigation of hospital water systems contamination to bacterial agents of nosocomial infections. Int J Env Health Eng 2020;9:10
|How to cite this URL:|
Shamsizadeh Z, Ehrampoush MH, Nikaeen M, Ebrahimi AA, Asghari FB. Investigation of hospital water systems contamination to bacterial agents of nosocomial infections. Int J Env Health Eng [serial online] 2020 [cited 2023 Apr 2];9:10. Available from: https://www.ijehe.org/text.asp?2020/9/1/10/291244
| Introduction|| |
Nosocomial infections are among the most important health concerns, with a prevalence of 1.4 million cases worldwide. At the moment, the rate of these infections in developed and developing countries is estimated at about 11% and 25%, respectively. Gram-negative bacteria (GNB), including Acinetobacter baumannii, Pseudomonas aeruginosa, and Legionella, are among the most important causes of nosocomial infections. Pneumonia, urinary tract infections, and blood infection are the most prevalent infections caused by A. baumannii and P. aeruginosa, as well as legionellosis and Pontiac fever by Legionella. Immunocompromised patients are the most susceptible individual and at risk of developing these infections. The hospital water system could serve as a potential source for the dissemination of Gram-negative microorganisms, which are the cause of nosocomial infections. The biofilm formation in the water system promotes the growth of these bacteria in the hospital water systems and causes various infections through contaminated water.,
Exposure to waterborne microorganisms in the hospital environment can occur during bathing, breathing of bio-aerosols and contact with medical equipment contaminated with water containing these microorganisms., In several studies, the role of water has been proven as the source of A. baumannii infections. The prevalence of amikacin and ciprofloxacin-resistant A. baumannii in Tokai University Hospital emergency ward was due to the use of contaminated tap water for oral care. In the case of legionella, inhalation of contaminated bioaerosols is the principal route of exposure to the bacterium.
In recent years, due to the increasing number of immunocompromised patients, GNB infections are one of the biggest challenges facing hospitals, especially in developing countries. Therefore, it is necessary to reduce the exposure of patients to infectious agents by rapid monitoring of the source of these bacteria. The culture technique is a common method for the detection of GNB. However, this method is time-consuming and costly. In addition, the culture technique cannot detect bacteria in viable but nonculturable (VBNC) state. Therefore, the use of molecular techniques such as polymerase chain reaction (PCR) as a quick, sensitive, and reliable method for detecting GNB could be useful in the prevention and management of nosocomial infections.
The present study was undertaken to investigate the presence of GNB in hospital water systems using a PCR based method. Furthermore, the relationship of heterotrophic plate count (HPC) with the contamination of hospital water systems with GNB was investigated.
| Materials and Methods|| |
A total of 33 water samples were collected in sterilized 500-ml glass bottles, from 11 hospitals of Isfahan University of Medical Sciences, Iran. In each hospital, water samples were obtained from different locations, including taps and showers, and were transferred to the laboratory. The amount of residual free chlorine (METERRC) was measured at the time of sample collection. HPC bacteria were determined by culture on R2A agar and incubation at 35°C for 48 h.
Detection of Gram-negative bacteria
To detection of GNB, water samples were concentrated using membrane filters (0.22 μm, 47 mm diameter; Millipore). Membrane filters were washed in sterile phosphate buffer and shaken for 30 min. Finally, the suspensions were centrifuged, and the resulting sediment was used for DNA extraction. The DNA extraction was performed by several cycles of freezing-thawing and then DNA purified by a Promega DNA Extraction Kit (Promega Wizard® Genomic DNA Purification Kit Madison, WI) according to the manufacturer's instructions. The purified DNA was finally resolved in distilled water and used for PCR assay.
For the detection of P. aeruginosa and legionella, a nested PCR method was used to increase the sensitivity. In the first PCR step, a portion of the 16s-rRNA gene was amplified using general primers Eubac 27F and 1492R [Table 1]. The use of general primers also makes it possible to identify the problem of DNA extraction or the presence of PCR inhibitors in the extracted sample. In the second PCR step, the specific primer sets of P. aeruginosa and Legionella were used [Table 1]. For the detection of A. baumannii, the OXA-51 primer set was used [Table 1].
PCR amplification was conducted in a final volume of 25 μL, as described by Nikaeen et al. The PCR cycling conditions were as follows: initial denaturation at 94°C for 5 min, followed by 35 cycles of 45 s at 94°C, primer annealing at varied temperatures (according to the selected primers) for 45 s, primer extension at 72°C for 45 s, and final extension at 72°C for 10 min. PCR products were analyzed by agarose gel electrophoresis using 1.5% agarose gel. Gels were viewed on an ultraviolet transilluminator (UV Tech, France).
| Results|| |
In the present study, a total of 33 water samples were taken from different tap water outlets from 11 hospitals and examined for the presence of A. baumannii. Legionella and P. aeruginosa.
Among the studied bacteria, legionella was the most frequently (15/33) detected Gram-negative microorganism in hospital water. Furthermore, the frequency of A. baumannii (6/33) and P. aeruginosa (6/33) was in the next rate [Table 2]. [Figure 1] shows the agarose gel electrophoresis of PCR products.
|Table 2: Detection frequency of gram-negative bacteria in hospital water samples|
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|Figure 1: Agarose gel electrophoresis of polymerase chain reaction products: (a) Acinetobacter baumannii (b) Legionella. (c) Pseudomonas aeruginosa. M, DNA Marker (100 bp); 1–4, polymerase chain reaction products; 5, negative control 6, positive control|
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We found that the percentage of hospital systems that contaminated with Legionella was 82% (9/11) and in the case of A. baumannii and P. aeruginosa 36% (4/11). Furthermore, results of the PCR, revealed that 10 out of 11 hospital systems were contaminated to at least one of the GNB, and so GNB were detected in 91% of hospitals [Figure 2].
|Figure 2: Percentage of positive water samples which contained detected gram-negative bacteria|
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The mean concentration of heterotrophic bacteria was 36 CFU/ml and ranged from 4 to 100 CFU/ml. We found that the mean concentration of HPC was no different in GNB-positive samples and in GNB-negative samples. In other words, our study showed no relationship between the presence of GNB and the concentration of HPC bacteria. The mean chlorine residue concentration was 0.06 mg/l and in the range of 0–0.21 mg/l, and therefore, we could not find a relationship between the chlorine residue concentration and the presence of GNB or HPC concentration.
| Discussion|| |
Colonization of the hospital water systems with GNB can lead to nosocomial infections. The results of this study indicate the presence of GNB in hospital water [Table 2]. Several studies have confirmed the detection of GNB, including Acinetobacter, Legionella, Pseudomonas, and Enterobacteriaceae in hospital water.,,, However, because of the GNB susceptibility to environmental conditions, they may be found in VBNC form and so on, could not be detected with cultural-based methods. In fact, VBNC bacteria are alive and virulent but are not able to divide the cell and grow on the culture medium, but the PCR method can detect these microorganisms. Therefore, it is expected that the high prevalence of GNB in this study is due to the identification of VBNC bacteria by PCR. Shamsizadeh et al. have been reported the detection of A. baumannii in only one hospital water sample out of 42 samples that they analyzed using the culture method. In the present study, the PCR method was used as a qualitative method for identifying GNB, so it is suggesting to take into account quantitative methods such as real-time PCR to determine the number of bacteria in the hospital environment. However, there are disagreements over the importance of using quantitative methods in the detection of GNB because there is no acceptable level for the presence of GNB bacteria including Legionella in hospital environments. Centers for Disease Control and Prevention (CDC) emphasis on the importance of using a quick and accurate monitoring method for the detection of microorganisms in hospital water to reduce the potential exposure of patients to these bacteria.
The presence of Legionella in hospital water is recognized as the main reason for Hospital-acquired legionellosis. Several studies have been reported the detection of Legionella in hospital water., Napoli et al. detected Legionella in 79.1% (102/109) of the health care facilities water samples in Italy. In the present study, 82% of hospitals and 45% of water samples were contaminated with Legionella [Figure 2]. Although the Legionella pneumophila (Lpn) does not form robust biofilms, the ability of this bacterium to join pre-established biofilms by other bacteria such as Mycobacterium chelonae, Acinetobacter lwoffii, Pseudomonas putida leads to stability of Legionella in biofilm. In contrast, P. aeruginosa and Pseudomonas fluoresces biofilms have an antagonistic effect on Legionella survive due to the production of antibiotic-like inhibitors.
P. aeruginosa and A. baumannii were detected in 18% of the water samples [Figure 2]. Furthermore, 36% of the investigated hospitals were contaminated with P. aeruginosa and A. baumannii [Table 2]. Several studies have reported the presence of P. aeruginosa in water., Rogues et al. detected P. aeruginosa in 11.4% of 484 tap water samples taken from patient rooms. One study in a hospital in Birmingham between 2013 and 2017 also showed that 1%–14% of water samples obtained from the hematology ward were contaminated with P. aeruginosa. In another study by Varin et al., P. aeruginosa was detected in 46.4% of samples (121 out of 261 samples).
Legionella, P. aeruginosa, and A. baumannii can also be detectable in hospital air. It is important to consider that GNB presence is probable in aerosols formed from contaminated water and so on airborne transmission. The study of Montagna et al. on the hospitals in Italy showed that air and water samples in hospitals (3/10) were Lpn positive. Molecular investigation showed that Lpn strains, which were detected in the air and water samples, had the same allelic profile.
A. baumannii was also found in 18% of samples. Although Acinetobacter has been identified as the relatively low virulence bacterium, it is now recognized as an important opportunistic pathogen that causes hospital infections, especially in immunocompromised patients, and in patients admitted to the intensive care units. Several studies have shown the role of water as a source of A. baumannii infection., Horii et al. Suggested that the shower bath could act as one of the factors causing Acinetobacter related hospital infections. The study of Volkow et al. also showed that A. baumannii isolates from showerhead water, intravenous catheter, and blood cultures of bloodstream-infected patients were related to the same strain.
Several factors affect the survival of GNB in the hospital environment. Pipe size and network design, water systems with low flow, temperature, the concentration of residual chlorine, nutrient level, and hydraulic of water system could affect the biofilm formation and consequently presence and survival of GNB in the hospital water systems.,
Therefore, the variation of these factors in different hospital water systems may, in part, lead to the different detection rates of GNB in various studies. The mean concentration of heterotrophic bacteria was 36 CFU/ml in a range of 4–100 CFU/ml. However, our study showed no relationship between the HPC and the presence of GNB.
Our results revealed that 91% of the hospital's water system was contaminated at least one type of GNB. Biofilm formation in the water supply system allows these bacteria to survive in the hospital environment for a long time., The low concentration of residual chlorine in the hospital's water system could be a reason for the growth of GNB. Although the detection rate of GNB varies in different studies, in accordance with our results, other studies have also shown that the hospital water system is often a proper haven for GNB and therefore requires enhanced monitoring and contaminant control techniques. An effective method for controlling hospital water contamination to inactivate etiological agents of hospital infection is point-of-use disinfection by ultraviolet radiation.
| Conclusion|| |
Our results showed that hospital water can act as a potential route for the transmission of GNB. A key factor in the prevention of hospital infections is the rapid identification of the contamination source to use effective control strategies for the proper management of nosocomial infection agents in hospital environments. The method used in this study to identify GNB is a sensitive and reliable method that provides rapid monitoring of GNB in the hospital water system.
This work was supported by the Shahid sadoughi University of Medical Sciences, Student Research Committee (grant number 5930). The authors would like to appreciate the all those who have assisted in conducting this study at Isfahan University of Medical Sciences.
Financial support and sponsorship
Shahid sadoughi University of Medical Sciences, Yazd, Iran.
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2]
[Table 1], [Table 2]