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Comparative quantification of varicella-zoster virus in air, pharyngeal swabs, and vesicle content in patients with varicella, disseminated zoster, and localized herpes zoster

Published online by Cambridge University Press:  15 November 2024

Kei Yamamoto,
Maki Nagashima,
Motoko Ishida,
Masayuki Ota,
Yuichi Katanami,
Ryoko Adachi,
Ayako Shigeno,
Takeshi Tamaki and
Norio Ohmagari
Kei Yamamoto*
Affiliation:
Diseases Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan
Maki Nagashima
Affiliation:
Diseases Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan
Motoko Ishida
Affiliation:
Diseases Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan
Masayuki Ota
Affiliation:
Diseases Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan
Yuichi Katanami
Affiliation:
Diseases Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan
Ryoko Adachi
Affiliation:
Department of Pharmacy, National Center for Global Health and Medicine, Tokyo, Japan
Ayako Shigeno
Affiliation:
Department of Pharmacy, National Center for Global Health and Medicine, Tokyo, Japan
Takeshi Tamaki
Affiliation:
Department of Dermatology, National Center for Global Health and Medicine, Tokyo, Japan
Norio Ohmagari
Affiliation:
Diseases Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan
*
Corresponding author: Kei Yamamoto; Email: kyamamoto@hosp.ncgm.go.jp
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Abstract

We evaluated the viral load of varicella-zoster virus (VZV) in ambient air, vesicle, and pharyngeal swabs in VZV-infected patients. Of 46 cases, 6 had VZV detected in indoor air samples from patient rooms. Results suggest an association between viral load in the pharyngeal swab and indoor air.

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Concise Communication
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Infection Control & Hospital Epidemiology , Volume 46 , Issue 1 , January 2025, pp. 99 - 101
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Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

Introduction

Varicella-zoster virus (VZV) is known to spread by the airborne route, underscoring the importance of effective containment measures for primary varicella (VA) and immunosuppressed patients with disseminated or localized zoster. Reference Siegel, Rhinehart, Jackson and Chiarello1 Airborne precautions are not considered necessary for immunocompetent patients with localized herpes zoster (HZ), although nosocomial cases of secondary varicella without direct contact with HZ lesions have been reported. Reference Viner, Perella and Lopez2,Reference Cholongitas and Ilonidis3 VZV has been isolated from the air or air filters of hospital rooms of such patients, Reference Suzuki, Yoshikawa, Tomitaka, Suzuki, Matsunaga and Asano4–Reference Sawyer, Chamberlin, Wu, Aintablian and Wallace6 although there are no reports on VZV viral in room air with quantitative evaluation and comparison of VZV disease types. Therefore, we aimed to evaluate the concentration of VZV in hospital isolation rooms of patients with VZV infection.

Methods

This single-center, prospective, observational study was conducted from November 1, 2015, to July 31, 2018. Hospitalized patients admitted to a private room with VA, disseminated herpes zoster (DZ), or HZ, as suspected by dermatology, internal medicine, or infectious disease physicians, were included. The ambient air inside (“inside air”) and outside (“outside air”) of the patients’ rooms was collected. At least 1 pharyngeal and vesicular swab was collected for quantitative polymerase chain reaction (PCR) for VZV (Supplemental Material). Patients who had taken antivirals for VZV >5 days or in whom VZV was not detected from vesicles or pharyngeal swabs were excluded.

This study was approved by the Research Ethics Committee of the National Center for Global Health and Medicine (NCGM-G-001822-02).

We obtained written informed consent and clinical information from the clinical review (Supplemental Material). DZ was defined as a case of HZ with skin lesions on 3 or more adjacent or 2 nonadjacent dermatomes or a generalized rash due to VZV infection in a patient with a history of VA.

Statistical analysis

Characteristics of study patients were compared using the Mann–Whitney test for continuous variables and Fisher’s exact test for categorical variables. For multiple comparisons, P values were corrected using the Benjamini–Hochberg method. Statistical significance was set at P < .05. All analyses were performed using R software (version 4.3.0, R Development Core Team 2023).

Results

One hundred six patients had VZV infection, with 120 excluded mainly owing to lack of private room or having received antivirals for >5 days (Supplemental Figure S1). Forty-six patients were included (Table 1). All vesicular swab VZV PCR tests were positive, with no difference in median viral load among the 3 disease types (Table 1). Twenty-four cases (57.1%) had positive pharyngeal swabs, including 100% of VA patients (7/7) and 33.3% of those with HZ (6/18) (P = .016). The median pharyngeal viral load for VA was significantly higher than that for DZ or HZ (P = .047, P = .002, respectively). Although 2 DZ cases (4.0%) were VZV PCR-positive upon testing outside air samples, neither was in a negative pressure room; in 1 case, the virus was not detected in the inside air. Although the viral load in pharyngeal secretions tended to decrease over time from the appearance of skin lesions or starting antivirals, no clear trend was observed for vesicular content (Supplemental Figures S2 and S3).

Table 1.

Characteristics of study patients

Note. VZV, varicella zoster virus; WBC, white blood count; ANC, absolute neutrophil count; ALC, absolute lymphocyte count; PCR, polymerase chain reaction.

*1,*2,*3: significant difference (P < 0.05) by pairwise comparison adjusted by Benjamini–Hochberg procedure. The number reflects paired items.

†“log0” is a value that does not exist, but for convenience, less than 1 copy/test was replaced by “0.”

A PCR test of the inside air was positive for 6 patients (range, 0.7–3.1 log10 copies/test) (Table 1). Although the small number of VZV cases with VZV detected in inside air did not result in significant differences, VA had the highest positivity rate, followed by DZ and HZ. There were no significant differences in underlying disease or immunosuppressant use between those with and without VZV detected in the inside air. Those with VZV detected in the inside air were more likely to have not received antivirals at sampling, to have been on antivirals for fewer days, or to have lower white blood cell counts (Supplementary Table S1a). When VA was excluded, although no significant difference was observed owing to the sample size, a similar trend was observed (Supplemental Table S1b). VZV DNA was detected in room air in 5 (20.8%) of the 24 pharyngeal PCR-positive cases and none (0%) of 18 pharyngeal PCR-negative cases. VZV was detected in 2 (4.3%) of 46 samples of air outside the patient room (Table 1). A receiver operating characteristic curve was used to examine pharyngeal swab viral load to identify positive VZV PCR of indoor air, revealing an area under the curve (AUC) of 0.89 (95% CI 0.78–0.99, Figure 1).

Figure 1.

ROC curve demonstrating the varicella-zoster viral load of pharyngeal secretions used to detect the varicella-zoster virus in the air inside the room. AUC 0.89 (95% CI 0.78–0.99). Youden’s index showed a cutoff value of 2.9 log10 copies/test with a sensitivity of 0.78 and a specificity of 1.00. ROC, receiver operating characteristic.

No hospital-acquired symptomatic VA occurred during the study.

Discussion

In this study, VZV viral nucleic acids were detected in the air inside the room of 13% of patients with VZV infection, with VA having the highest positive percentage (43%), followed by DZ (11%) and HZ (5%). Although only 4.3% of patients were placed in negative pressure rooms, 95% of the PCR results for air outside the rooms were negative. VZV was detected in pharyngeal swabs in 31.6%–100% of cases. This was similar to the previously reported detection rate in VA (60%–100%) Reference Sawyer, Wu and Chamberlin7,Reference Leung, Harpaz and Baughman8 and HZ (5%–100%), depending on the phase of the disease. Reference Suzuki, Yoshikawa, Tomitaka, Suzuki, Matsunaga and Asano4,Reference Mehta, Tyring and Gilden9,Reference Yamakawa, Hamada and Takeda10

VZV infection transmission is airborne and via contact, with airborne transmission involving viral shedding from the respiratory tract. This study supports this, showing a high pharyngeal PCR positivity rate in patients with VA, who are assumed to be the most infectious. However, in patients with HZ without a high pharyngeal PCR positivity rate, some cases of secondary varicella without direct contact with HZ lesions have been reported. Reference Viner, Perella and Lopez2,Reference Cholongitas and Ilonidis3 VZV has been isolated from air samples collected by cellulose filters or air purifier filters in patients with VA, DZ, and HZ in the rooms. Reference Suzuki, Yoshikawa, Tomitaka, Suzuki, Matsunaga and Asano4–Reference Sawyer, Chamberlin, Wu, Aintablian and Wallace6 Because the positivity rate of VZV in air filters was decreased by covering the vesicles with a hydrocolloid dressing, VZV from vesicles was thought to contribute to airborne transmission. Reference Suzuki, Yoshikawa, Tomitaka, Matsunaga and Asano5 In this study, although the viral load of the vesicular content did not significantly correlate with that of the air in the room, the condition of the vesicles was not constant; for example, some were dried, some were numerous, and some were few. The volume of the swab samples was unstable. Therefore, it may be less meaningful to quantify the amount of VZV within vesicles to assess the risk of airborne transmission.

Although VZV was also detected in the air inside the patient rooms, the positivity rate was lower than that of previous studies. Reference Suzuki, Yoshikawa, Tomitaka, Suzuki, Matsunaga and Asano4,Reference Sawyer, Chamberlin, Wu, Aintablian and Wallace6 In a previous study, VZV was detected by swabbing air purifier filters after 24 hours of use. Reference Suzuki, Yoshikawa, Tomitaka, Suzuki, Matsunaga and Asano4 It is difficult to compare the quantitative differences among the 3 disease types of VZV in air using this method. Sawyer et al collected air samples at various suction rates and times but did not describe the amount of air collected. Reference Sawyer, Chamberlin, Wu, Aintablian and Wallace6 Therefore, it was difficult to compare the detection rates of viruses in the air for each disease in this report. Another limitation was that the appropriate amount of air to be collected for assessing infectivity remains unknown. Further studies are needed to ascertain the appropriate amount of air and confirm that differences in disease types are related to differences in the number of viral particles in the air. In addition to PCR, it is also desirable to examine the relationship with infectiousness using viral culture. The small sample of patients with VA was also a limitation.

This study suggests VZV detection in indoor air was associated with VZV disease type and viral load in pharyngeal swabs.

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/ice.2024.188.

Acknowledgments

We would like to express our deep appreciation to Mr. Fukano and Ms. Takeuchi of the Department of Academic-Industrial Partnerships Promotion, Center for Clinical Sciences, National Center, for their advice in conducting real-time PCR and to all the medical staff who treated the patients.

Financial support

This work was supported by grants from the National Center for Global Health and Medicine (27-6001).

Competing interests

K.Y. reports that he has received research grants from Fujirebio Inc., Canon Medical Systems Corp., Sanyo Chemical Industries Ltd., CarbGeM Inc., Sysmex Corp., and Toyobo Co. Ltd. outside the submitted work. The remaining authors report no conflicts of interest relevant to this article.

References

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Figure 0

Table 1.Characteristics of study patients

Figure 1

Figure 1.ROC curve demonstrating the varicella-zoster viral load of pharyngeal secretions used to detect the varicella-zoster virus in the air inside the room. AUC 0.89 (95% CI 0.78–0.99). Youden’s index showed a cutoff value of 2.9 log10 copies/test with a sensitivity of 0.78 and a specificity of 1.00. ROC, receiver operating characteristic.

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