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. 2025 May;97(5):e70380.
doi: 10.1002/jmv.70380.

Parvovirus B19 Rebound

Affiliations

Parvovirus B19 Rebound

Stefania Ranno et al. J Med Virol. 2025 May.

Abstract

Human parvovirus B19 (B19V) is responsible for a wide clinical spectrum ranging from asymptomatic infection, through mild disease, up to life-threatening one. Outbreaks are registered every 3-4 years, and a recent international alert for a new outbreak has been released. The experience of B19 virus circulation in a 600-bed tertiary care pediatric hospital in Rome from 2018 to 2024 is reported here. This retrospective study involved a total of 9695 blood samples (about 8500 patients), 11 amniotic fluids (11 pregnant women), and 10 827 sera (about 9500 patients), processed in the Virology Unit of Bambino Gesù Children's Hospital in Rome for B19V direct and indirect detection. In our population, the annual positivity rate for B19V DNA ranged from 0.8% in 2023 to 9.8% in 2018 and 32.8% in 2024; the same trend resulted from the analysis of the immunoglobulins M and G anti-B19V. Focusing on the last year, 314 patients resulted positive for B19V DNA detection: 204/314 (65%) had a primary infection, 150/204 (73.5%) were hospitalized, and 17/150 (11.3%) needed Intensive Care Unit (ICU) for cardiovascular, central nervous, and gastrointestinal pathologies. Two patients died from myocarditis. Among patients with the most severe clinical picture, over half had no concurring disease, and one patient died. Four amniotic fluids were positive for pregnant women who came to our observation. B19V typing of a subset of samples revealed the presence of only subtype 1A and a low intragenotypic diversity between strains from severe and mild disease. In conclusion, in 2024, a significant increase in B19V circulation was observed with profound effects on clinical outcome and consequent hospitalisation, either in patients with comorbidities or those without. This widespread circulation of the virus also had an impact on infections in pregnancy, with the known severe consequences for unborn children.

Keywords: B19 virus; epidemiology; immunoglobulin; infection; parvovirus.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
B19V DNA trend 20182024. The vertical axes indicate the number of samples analyzed and the percentage of positive samples detected over the period. The gray bar represents a negative result, and the red bar represents a positive one. The red line indicates the B19V DNA positivity rate.
Figure 2
Figure 2
Anti‐B19V Igs trend 2018–2024. The vertical axes indicate the number of samples analyzed and the percentage of positive IgG (blue line) and IgM (violet line) samples detected throughout the period. The gray bar represents the number of samples investigated.
Figure 3
Figure 3
B19V DNA trend in 2024. The vertical axes indicate the number of patients investigated and the percentage of positive patients detected in 2024. The gray bar represents a negative result, and the red bar represents a positive one. The red line indicates the B19V DNA positivity rate.
Figure 4
Figure 4
IgM (A) and IgG (B) anti‐B19V trend January–December 2024. The vertical axes indicate the number of patients investigated and the percentage of positive patients detected during the year 2024. The gray bar represents a negative result, and the red bar represents a positive one. Violet and blue lines indicate IgM and IgG anti‐B19V positivity rate, respectively.
Figure 5
Figure 5
Estimated maximum likelihood phylogeny of the Parvovirus B19 sequences (n = 2328) and samples sequenced in this study (n = 50). Bootstrap values higher than 90 are shown on branches. Information regarding the samples is reported: genotype, country of isolation (in lime samples sequenced in this study), disease severity, age, and department.

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