Abstract
We report a case of Legionella pneumonia in a dishwasher of a restaurant in Rome, Italy, just after the end of the lockdown that was in place to control the SARS-CoV-2 epidemic. The case highlights the importance of strict monitoring of water and air systems immediately before reopening business or public sector buildings, and the need to consider Legionella infections among the differential diagnosis of respiratory infections after lockdown due to the ongoing COVID-19 pandemic.
Keywords: acute respiratory distress syndrome; SARS-CoV-2; Legionella pneumonia, COVID-19 epidemic
In response to the coronavirus disease (COVID-19) epidemic in Italy, the Italian Government, on 9 March 2020, imposed a national quarantine [1] and mandated the temporary closure of non-essential shops and businesses, as well as a ban on recreational events. The quarantine lasted at least until 4 May, after which some restrictions were gradually eased, with certain business activities resuming from 18 May onwards. While these non-pharmaceutical measures helped to contain the spread of COVID-19 [2], buildings unoccupied or under-used during the prolonged lockdown pose a risk, through stagnating water in devices or piping systems, of providing conditions where harmful bacteria, including Legionella, can proliferate [3]. Here, we describe a case of Legionella pneumonia in a restaurant dishwasher, who occurred in conjunction with the end of the lockdown period in Italy, alerting to this potential issue.
Case presentation
A man aged in his 40s with no comorbidities was admitted to the emergency department (ED) on 3 June 2020 for fever (≥ 38.0°C), dry cough and headache since 28 May. The patient is employed in Rome as a dishwasher in a restaurant that had been closed until 25 May. He worked in the restaurant from 25 to 29 May 2020. Symptoms appeared 3 days after returning to work.
Combined respiratory, droplet and contact isolation measures were prescribed. Two consecutive nasopharyngeal swabs for the detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, were negative 24 hours apart.
In the ED, a chest computed tomography (CT) scan revealed unilateral single consolidation with air bronchograms in the lower right lobe with an arterial oxygen partial pressure (PaO2)/fractional inspired oxygen (FiO2) ratio of 376. Blood tests showed hyponatraemia (125 mEq/L, normal range: 135–145 mEq/L); mild leukocytosis (white blood cell count: 12,700/mm3, normal range: 4,000–10,000/mm3; neutrophil cell count: 8,920/mm3, normal range: 1,800–7,500/mm3), and elevated C-reactive protein (9.21 mg/dL, normal range: < 1 mg/dL). On 4 June, Legionella urinary antigen, serotype 1 was positive and intravenous levofloxacin (750 mg once daily) was started.
On 5 June, the patient was referred to the Lazzaro Spallanzani National Institute for Infectious Diseases in Rome, Italy.
Nasopharyngeal swab and serology for SARS-CoV-2 were both negative. In addition to the urine antigen test, we performed a culture and a PCR for Legionella detection, on sputum. Both the culture and PCR were negative. The patient was discharged in good clinical condition after a 14-day course of levofloxacin.
Environmental investigation
The Legionella pneumonia notification led to the alert of the epidemiological surveillance services at regional and district level. An epidemiological investigation plan was set up and multiple environmental samples were taken at the workplace. In the restaurant and in the kitchen where the case worked, there are no air conditioning systems. The staff toilets (shower, sink faucets, sink water and cold water, and hot and cold water bidets) and kitchen taps were sampled and all resulted negative for Legionella.
Discussion
Legionella bacteria are aerobic, Gram-negative, intracellular pathogens, with serotype 1 being the most commonly reported cause of human infections worldwide. Legionella infections can present as a mild, self-limiting influenza-like illness called Pontiac fever. Alternatively, they can be an important cause of community-acquired and nosocomial pneumonia, with the pneumonic form of infection known as Legionnaire's disease [4]. Symptoms typically arise 2 to 10 days after exposure to the pathogen [4].
The case of Legionella pneumonia described in this report became symptomatic 3 days after starting work as a dishwasher. Legionella bacteria are typically transmitted via inhalation aerosols from contaminated water or soil [4]. Reported sources of infection are diverse and include showers, pools, hot tubs, aquariums, fountains, birthing pools, drinking water systems, air conditioning systems and cooling towers, and other water collection systems [4]. The environmental contamination by Legionella of water systems can be difficult to eradicate as the organism may continue to survive in dead branches of complex plumbing structures.
Given the plethora of water sources to which a person may be exposed during the incubation period [5], determining the source of waterborne Legionella infection can be very challenging. In outbreak situations, the source of Legionella is commonly sought in order to attempt to stop these; however, for sporadic or isolated cases the finding of the origin of the causative pathogen is rarely pursued [5]. Few data are available on Legionnaires’ disease incidence linked to occupational setting. A review article on occupational Legionnaires’ disease identified 47 reports about 805 workers with nine fatal cases over a period of 66 years (1949–2015; on average, 12.2 cases/year) [6].
Legionnaires’ disease is possibly more common in late summer and early autumn [4]. The case reported here however occurred in spring during the COVID-19 epidemic in Rome. In the catchment area of the Rome 1 health district (ASL Rome 1), 62 Legionnaires’ disease cases were notified in the first semester of 2019 compared with 16 cases in the first semester of 2020, corresponding to a 74% overall case reduction. Whether this might be related or not, to the quarantine imposed in Italy at the beginning of March 2020 is unclear.
Due to the lockdown, the restaurant, where the case worked, had been previously closed. Potential health risks exist in buildings that have been shut down or operating with reduced occupancy during the COVID–19 pandemic [7]. Indeed, this may allow Legionella growth in water pipes and equipment using, or dispersing, water, such as evaporative air-conditioning systems or spa pools/tubs, if they are not managed adequately. In this scenario, the implementation of a suitable flushing regime, or other measures, such as draining the system – especially if weekly flushing cannot be maintained, are needed in order to reduce the risk of bacterial infection. In the context of the still ongoing COVID-19 pandemic, a risk reduction strategy for Legionella exposure and infection may avoid further overcrowding of already congested EDs.
In January 2020, SARS-CoV-2 infection was identified as the cause of COVID-19 pneumonia [8]. The occurrence in COVID-19 of non-specific symptoms such as fever, cough and dyspnoea implies the need for an accurate differential diagnosis of other causes of community-acquired pneumonia, such as Legionella. Legionella pneumonia can moreover lead to a series of radiological findings, including ground-glass opacities or a tree-in-bud appearance in CT, that are compatible with COVID-19 [9].
To conclude, although it was difficult to identify the source of infection for the case reported in this study, the importance of monitoring water and air conditioning systems is evident. Reopening of structures related to the work environment has to be conducted with consideration of the full safety of both workers and end-users, and the likely risks of Legionella growth have to be evaluated in advance, with decontamination of the water systems. Finally, ED clinicians need to consider Legionella pneumonia among other differential diagnoses after the end of the lockdown due to the COVID-19 pandemic.
Acknowledgements
This paper has been funded by Line 1, Ricerca Corrente of the Italian Ministry of Health, on emerging and re-emerging infections and by Progetto COVID 2020 12371675 both funded by Italian Ministry of Health.
Conflict of interest: None declared.
Authors’ contributions: MA, GML and PC were involved in patients’ management, PC, MG and LL performed the epidemiological investigations, ABT, PC, MG and LL carried out the study conception and design, drafting of manuscript, VA performed laboratory testing, DRE worked on the epidemiological investigation, ABT, DA, MA, GML and BN revised the manuscript critically, NE approved and revised the final manuscript. All authors reviewed and approved the final draft.
References
- 1.Presidenza del Consiglio dei Ministri (DPCM). Misure urgenti in materia di contenimento e gestione dell'emergenza epidemiologica da COVID-19. [Urgent measures to contain COVID-19 and to deal with the emergency caused by the COVID-19 epidemiological situation]. 9 March 2020. Italian. [Accessed 7 Jul 2020]. Available from: http://www.governo.it/it/articolo/firmato-il-dpcm-9-marzo-2020/14276#
- 2. Vicentini C, Bordino V, Gardois P, Zotti CM. Early assessment of the impact of mitigation measures on the COVID-19 outbreak in Italy. Public Health. 2020;185:99-101. 10.1016/j.puhe.2020.06.028 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Ricci ML, Rota MC, Scaturro M, Veschetti E, Lucentini L, Bonadonna L, et al. Guida per la prevenzione della contaminazione da Legionella negli impianti idrici di strutture turistico recettive, e altri edifici ad uso civile e industriale non utilizzati durante la pandemia COVID-19. [Guide for the prevention of Legionella contamination in the water systems of tourist accommodation facilities and other buildings for civil and industrial use, not used during the COVID-19 pandemic]. Rapporto ISS COVID-19 n. 21/2020. Rome: Istituto Superiore di Sanità. 3 May 2020. Italian. [Accessed 7 Jul 2020]. Available from: https://www.iss.it/documents/20126/0/Rapporto+ISS+COVID-19+21_2020.pdf/15088523-3e22-55e1-d28d-f37d9aafd186?t=1588953957255
- 4. Burillo A, Pedro-Botet ML, Bouza E. Microbiology and Epidemiology of Legionnaire’s Disease. Infect Dis Clin North Am. 2017;31(1):7-27. 10.1016/j.idc.2016.10.002 [DOI] [PubMed] [Google Scholar]
- 5. Orkis LT, Harrison LH, Mertz KJ, Brooks MM, Bibby KJ, Stout JEI. Environmental sources of community-acquired legionnaires’ disease: A review. Int J Hyg Environ Health. 2018;221(5):764-74. 10.1016/j.ijheh.2018.04.013 [DOI] [PubMed] [Google Scholar]
- 6. Principe L, Tomao P, Visca P. Legionellosis in the occupational setting. Environ Res. 2017;152:485-95. 10.1016/j.envres.2016.09.018 [DOI] [PubMed] [Google Scholar]
- 7.ESCMID Study Group for Legionella Infections. ESGLI Guidance for managing Legionella in building water systems during the COVID-19 pandemic. ESCMID. [Accessed 7 Jul 2020]. Available from: https://www.escmid.org/fileadmin/src/media/PDFs/3Research_Projects/ESGLI/ESGLI_Guidance_for_managing_Legionella_in_building_water_systems_during_the_COVID-19_pandemic_______________20200603_v_0300.pdf
- 8. Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395(10223):497-506. 10.1016/S0140-6736(20)30183-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Kim KW, Goo JM, Lee HJ, Lee HY, Park CM, Lee CH, et al. Chest computed tomographic findings and clinical features of legionella pneumonia. J Comput Assist Tomogr. 2007;31(6):950-5. 10.1097/RCT.0b013e31804b211d [DOI] [PubMed] [Google Scholar]