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Report of HKU-1 coronavirus nosocomial cluster in a city hospital in Japan during the coronavirus disease 2019 (COVID-19) pandemic

Published online by Cambridge University Press:  17 January 2023

Aoi Yogo*
Affiliation:
Department of Infectious Disease, Kyoto City Hospital, Kyoto, Japan
Shougen Sumiyoshi
Affiliation:
Department of Infectious Disease, Kyoto City Hospital, Kyoto, Japan
Kazuaki Aoki
Affiliation:
Department of Infectious Disease, Kyoto City Hospital, Kyoto, Japan
Hirofumi Motobayashi
Affiliation:
Department of Infectious Disease, Kyoto City Hospital, Kyoto, Japan
Kentaro Tochitani
Affiliation:
Department of Infectious Disease, Kyoto City Hospital, Kyoto, Japan
Shungo Yamamoto
Affiliation:
Department of Transformative Infection Control Development Studies, Osaka University Graduate School of Medicine, Suita, Osaka, Japan Division of Fostering Required Medical Human Resources, Center for Infectious Disease Education and Research (CiDER), Osaka University, Suita, Osaka, Japan
Tsunehiro Shimizu
Affiliation:
Department of Infectious Disease, Kyoto City Hospital, Kyoto, Japan
*
Author for correspondence: Aoi Yogo, Department of Infectious Disease, Kyoto City Hospital, 1-2 Higashi Takada-cho, Mibu, Nagagyo-ku, Kyoto 6048845, Japan. E-mail: ygai0430@gmail.com

Abstract

Type
Research Brief
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2023. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

Human coronaviruses (HCoVs) cause respiratory tract infections. HCoV-229E, OC43, NL63, and HKU1 are common human coronavirus, and severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome coronavirus (MERS-CoV), and SARS-CoV-2 are highly pathogenic. 1 Common human coronaviruses are globally transmitted via inhalation of respiratory droplets with a 2- to 4-day incubation period, presumably accounting for 10%–15% of cases of common cold, especially in winter. Reference Wat2 HCoV-HKU1 causes mild, and self-limiting upper-respiratory diseases like common colds, bronchiolitis, and pneumonia, with symptoms such as rhinorrhea, fever, cough, and wheezing. 1 More severe respiratory infections can occur in children or adults with underlying diseases and in the elderly. Reference Pyrc, Berkhout and van der Hoek3

We identified the only report of a common human coronavirus outbreak with nosocomial transmission during the COVID-19 pandemic. Reference Moulin, Kampouri and Glampedakis4 Our HCoV-HKU1 outbreak occurred among healthcare workers (HCWs) in a single general ward at Kyoto City Hospital in Japan in January 2022, in a small, poorly ventilated break room where people were unmasked.

On January 19, 2022, the ward had 52 HCWs, and we identified 7 HCWs with respiratory symptoms, such as fever, rhinorrhea, and sore throats; no inpatients or other HCWs exhibited symptoms (Table 1). All 7 HCWs were confirmed to be SARS-CoV-2 negative via polymerase chain reaction (PCR) tests by nasopharyngeal swab samples (NPS; GeneXpert Xpress CoV-2 plus, Cepheid, Sunnyvale, CA). On January 20, 2022, we performed multiple respiratory panels using nasopharyngeal swab samples (BioFire FilmArray, bioMèrieux, Marcy-l'Étoile, France), a PCR-based multiplexed nucleic acid test for common respiratory microorganisms. Of the 7 HCWs, 6 tested positive for HCoV-HKU1.

All 7 HCWs had been assigned to the same general ward and had been wearing surgical masks while caring for patients. We identified a shared break room as a potential transmission route; 6 of the HCWs had used this room unmasked for a few days before their symptom onset. It was difficult to sufficiently distance from others in the small and poorly ventilated room. We could not identify the accurate transmission route among HCWs, and we did not investigate inpatients and other HCWs on the ward because they had no respiratory symptoms and were less likely to be transmission sources. All respiratory symptoms in the HCoV-HKU1–postive HCWs improved, and they returned to work within a week after their symptom onset. An investigation revealed that a nurse on the same ward had returned from vacation a few days prior to the symptom onset in the 7 HCWs and had worked with rhinorrhea. Because her symptoms had resolved at that point, we did not test her for HCoV-HKU1, but we speculated that she was the index case.

Discussion

HKU1 coronaviruses cause common colds in healthcare populations, but they can have more critical impacts on children, elderly persons, and those with underlying diseases. Reference van Elden, van Loon and van Alphen5 A case series on community-acquired pneumonia at multiple hospitals in Hong Kong showed that 8 of 10 patients confirmed with HCoV-HKU1 had underlying diseases, and 2 of them died. Reference Woo, Lau and Tsoi6 Our HCWs had no underlying diseases, and no patients on this ward were symptomatic. However, common human coronavirus spreading at a hospital could be critical for elderly patients with underlying diseases. More careful nosocomial infection control is required, even for milder common respiratory viruses.

Currently, we are still advised to wear masks, to keep our distance from others (2 m or 6 feet) to avoid close contact, to avoid poorly ventilated spaces and crowds, and to wash our hands often. Universal masking is required for all patients, visitors, and personals in healthcare settings to reduce transmission of SARS-CoV-2 from unsuspected virus carriers. Reference Klompas, Morris, Sinclair, Pearson and Shenoy7 Furthermore, the US Center for Disease Control and Prevention (CDC) recommends wearing a well-fitting mask indoors in public spaces, regardless of vaccination status or individual risk, because surgical masks can prevent transmission of human coronavirus—as well as influenza—from individuals with acute respiratory symptoms. 8,Reference Leung, Chu and Shiu9 Our assessment of the reported hospital outbreak shows that transmission occurred when the symptomatic HCWs were unmasked. The BNT162b2 vaccine has been reported to induce antibodies against the spike protein of human seasonal β coronavirus (HKU1 and OC43), and all 7 HCWs, including the 6 confirmed positive by PCR, had received the BNT162b2 vaccine at least twice. However, this vaccination did not prevent their HKU1 infections. Reference Angyal, Longet and Moore10 Universal masking is therefore extremely important for infection control at medical institutions as new SARS-CoV-2 variants that decrease the efficacy of the COVID-19 vaccine continue to emerge.

Our study had several limitations. We drew conclusions about the index case in a clinical situation without access to laboratory evidence. Therefore, we could not clearly determine the incubation time since exposure to the index case and onset of symptoms in our 7 secondarily infected HCWs. This investigation was made more difficult by the fact that HCW activities outside the hospital ward were not known to us. Ideally, epidemiologic information should be collected in real time and supplemented by laboratory findings.

In conclusion,

we report a nosocomial HCoV-HKU1 outbreak among HCWs on a general ward. The first important implication of this outbreak is the possibility of common respiratory viruses circulating at hospitals, which might pose a severe risk for the elderly or those with underlying respiratory diseases. Another point our report emphasizes is the higher transmission risk when unmasked, which could be a pitfall during mealtimes and breaks. We should screen HCWs with respiratory symptoms.

Fig. 1. COVID-19, coronavirus disease 19; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; HCoV-HKU1, human coronavirus-HKU1. *A person vaccinated with 2-dose vaccine had completed the primary series of COVID-19 vaccine >14 days before illness onset. A person with a 3-dose vaccine had completed the booster vaccine after primary series of COVID-19 vaccine. Note. Respiratory multiple PCR tests included adenovirus, SARS-CoV2, human coronavirus (229E, HKU1, NL63, OC43), human metapneumovirus, influenza virus A/B, parainfluenza virus, respiratory syncytial virus, human rhinovirus (type 1A)/enterovirus (D68), Bordetella parapertussis, Bordetella pertussis, Chlamydophila pneumonia, and Mycoplasma pneumonia.

Acknowledgments

The Ethics Committee of Kyoto City Hospital approved this study. Because the study design was observational and data were collected anonymously, the institutional review board waived the need for patient consent. We thank all infectious control team members; Ritsuko Kanazawa, Aoi Murakami, Tatsunori Murata, Noriko Matsubara, and microbiology and clinical laboratory staff at Kyoto City Hospital.

Financial support

No financial support was provided relevant to this article.

Conflicts of interest

All authors report no conflicts of interest relevant to this article.

References

Common human coronavirus. US Centers for Disease Control and Prevention website. https://www.cdc.gov/coronavirus/general-information.html. Accessed February 13, 2020.Google Scholar
Wat, Dennis. The common cold: a review of the literature. Eur J Intern Med 2004;15:7988.CrossRefGoogle ScholarPubMed
Pyrc, K, Berkhout, B, van der Hoek, L. The novel human coronaviruses NL63 and HKU1. J Viro 2007;81:30513057.CrossRefGoogle ScholarPubMed
Moulin, E, Kampouri, E, Glampedakis, E, et al. Outbreaks of seasonal OC43 coronavirus with nosocomial transmission during COVID-19 pandemic setting: when a coronavirus hides another. Antimicrob Resist Infect Control 2021;10 suppl 1.Google Scholar
van Elden, LJ, van Loon, AM, van Alphen, F, et al. Frequent detection of human coronaviruses in clinical specimens from patients with respiratory tract infection by use of a novel real-time reverse-transcriptase polymerase chain reaction. J Infect Dis 2004;189:652657.CrossRefGoogle ScholarPubMed
Woo, PC, Lau, SK, Tsoi, HW, et al. Clinical and molecular epidemiological features of coronavirus HKU1–associated community-acquired pneumonia. J Infect Dis 2005;192:18981907.Google ScholarPubMed
Klompas, M, Morris, CA, Sinclair, J, Pearson, M, Shenoy, ES. Universal masking in hospitals in the COVID-19 era. N Engl J Med 2020;382:e63.Google ScholarPubMed
COVID-19: how to protect yourself and others. US Centers for Disease Control and Prevention website. https://www.cdc.gov/coronavirus/2019-ncov/prevent-getting-sick/prevention.html. Accessed February 25, 2022.Google Scholar
Leung, NHL, Chu, DKW, Shiu, EYC, et al. Respiratory virus shedding in exhaled breath and efficacy of face masks. Nat Med 2020;26:676680.CrossRefGoogle ScholarPubMed
Angyal, A, Longet, S, Moore, SC, et al. T-cell and antibody responses to first BNT162b2 vaccine dose in previously infected and SARS-CoV-2-naive UK healthcare workers: a multicentre prospective cohort study. Lancet Microbe 2022;3:e21e31.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1. COVID-19, coronavirus disease 19; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; HCoV-HKU1, human coronavirus-HKU1. *A person vaccinated with 2-dose vaccine had completed the primary series of COVID-19 vaccine >14 days before illness onset. A person with a 3-dose vaccine had completed the booster vaccine after primary series of COVID-19 vaccine. Note. Respiratory multiple PCR tests included adenovirus, SARS-CoV2, human coronavirus (229E, HKU1, NL63, OC43), human metapneumovirus, influenza virus A/B, parainfluenza virus, respiratory syncytial virus, human rhinovirus (type 1A)/enterovirus (D68), Bordetella parapertussis, Bordetella pertussis, Chlamydophila pneumonia, and Mycoplasma pneumonia.