Risk assessment and quantitative measurement along with monitoring of Legionella in hospital water sources

被引:3
作者
Bavari, S. [1 ]
Mirkalantari, S. [1 ]
Jazi, F. Masjedian [1 ]
Darban-Sarokhalil, D. [1 ]
Marani, B. Golnari [2 ]
机构
[1] Iran Univ Med Sci, Sch Med, Microbiol Dept, Tehran, Iran
[2] Iran Univ Med Sci, Cellular & Mol Res Ctr, Tehran, Iran
关键词
HeLa cell; hospital water sources; invasion; Legionella; PCR; quantitative PCR; REAL-TIME PCR; LEGIONNAIRES-DISEASE; NOSOCOMIAL LEGIONELLOSIS; PNEUMOPHILA; IDENTIFICATION; CULTURE; SPP; CONTAMINATION; ASSAY; FLOW;
D O I
10.1016/j.nmni.2021.100948
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Legionella spp. as a causative agent of Legionnaires' disease (LD) and an opportunistic pathogen creates a public health problem. Isolation and quantification of this bacteria from clinic water sources are essential for hazard appraisal and sickness avoidance. This study aimed at risk assessment and quantitative measurement along with Legionella monitoring in educational hospital water sources in Tehran, Iran. A crosssectional study was carried out in 1 year. The conventional culture method was used in this study to isolate Legionella from water samples. The polymerase chain reaction (PCR) technique was used to confirm the identity of the isolates and ensure that they were all Legionella. Quantitative PCR (qPCR) was used to determine the count of bacteria, and HeLa cell culture was used to determine the invasion of isolates. A total of 100 water samples were collected and inoculated on GVPC (glycine, vancomycin, polymyxin, and cycloheximide) agar; 12 (12%) and 42 (42%) cases were culture and PCR positive, respectively. Percentage of Legionella presence in PCRpositive samples by the qPCR method in <103 GU/L, in about 103 and lower than 104 GU/L, and in 104 GU/L was 40.47 (17 cases), 4.76% (two cases), and 54.76% (23 cases), respectively. Invasion analysis revealed that five and four isolates had invaded HeLa cells more than twice and equally, respectively, and the others had a lower invasion than the reference strain. The findings revealed that the spread of LD in hospitals was linked to the water system. Given the importance of nosocomial infections in the medical community, establishing a hospital water monitoring system is the most effective way to control these infections, particularly Legionella infections.(c) 2021 The Authors. Published by Elsevier Ltd.
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页数:8
相关论文
共 39 条
[1]   Assessing risk of health care-acquired Legionnaires' disease from environmental sampling: The limits of using a strict percent positivity approach [J].
Allen, Joseph G. ;
Myatt, Theodore A. ;
MacIntosh, David L. ;
Ludwig, Jerry F. ;
Minegishi, Taeko ;
Stewart, James H. ;
Connors, Bryan F. ;
Grant, Michael P. ;
McCarthy, John F. .
AMERICAN JOURNAL OF INFECTION CONTROL, 2012, 40 (10) :917-921
[2]   Long-Term Survival of Legionella pneumophila in the Viable But Nonculturable State After Monochloramine Treatment [J].
Alleron, Laetitia ;
Merlet, Nicole ;
Lacombe, Christian ;
Frere, Jacques .
CURRENT MICROBIOLOGY, 2008, 57 (05) :497-502
[3]  
Anyfantakis Dimitrios, 2015, Maedica (Bucur), V10, P264
[4]   Detection of Legionella pneumophila using a real-time PCR hybridization assay [J].
Ballard, AL ;
Fry, NK ;
Chan, L ;
Surman, SB ;
Lee, JV ;
Harrison, TG ;
Towner, KJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (11) :4215-4218
[5]   Development and evaluation of a Taqman duplex real-time PCR quantification method for reliable enumeration of Legionella pneumophila in water samples [J].
Behets, Jonas ;
Dederck, Priscilla ;
Delaedt, Yasmine ;
Creemers, Bart ;
Ollevier, Frans .
JOURNAL OF MICROBIOLOGICAL METHODS, 2007, 68 (01) :137-144
[6]   An update on Legionella [J].
Carratala, Jordi ;
Garcia-Vidal, Carolina .
CURRENT OPINION IN INFECTIOUS DISEASES, 2010, 23 (02) :152-157
[7]   The Purified and Recombinant Legionella pneumophila Chaperonin Alters Mitochondrial Trafficking and Microfilament Organization [J].
Chong, Audrey ;
Lima, Celia A. ;
Allan, David S. ;
Nasrallah, Gheyath K. ;
Garduno, Rafael A. .
INFECTION AND IMMUNITY, 2009, 77 (11) :4724-4739
[8]   Real-time PCR to supplement gold-standard culture-based detection of Legionella in environmental samples [J].
Collins, S. ;
Jorgensen, F. ;
Willis, C. ;
Walker, J. .
JOURNAL OF APPLIED MICROBIOLOGY, 2015, 119 (04) :1158-1169
[9]  
De Roxas DMA., 2015, ACTA MED PHILIPPINA, V49
[10]   VIRULENCE ASSOCIATED INGESTION OF LEGIONELLA-PNEUMOPHILA BY HELA-CELLS [J].
DREYFUS, LA .
MICROBIAL PATHOGENESIS, 1987, 3 (01) :45-52