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Unambiguous identification of JC polyomavirus strains transmitted from parents to children
H-Y Zheng1, T Kitamura, T Takasaka
1Department of Urology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan. teizhy-tky@umin.ac.jp
Insights
JC polyomavirus (JCV) is transmitted from parents to children during cohabitation. Genetic analysis of JCV DNA sequences in families confirmed parent-to-child transmission, revealing identical viral sequences in both generations.
Area of Science:
- Virology
- Human Genetics
- Infectious Diseases
Background:
- JC polyomavirus (JCV) causes progressive multifocal leukoencephalopathy.
- JCV is widespread in humans, infecting children asymptomatically and persisting in the kidneys.
- Parent-to-child transmission via cohabitation is a proposed route for JCV spread.
Purpose of the Study:
- To investigate and clarify the transmission patterns of JC polyomavirus.
- To analyze the genetic relatedness of JCV strains within family units.
Main Methods:
- Studied 5 families with probable JCV transmission between parents and children.
- Generated and sequenced multiple complete JCV DNA clones from urine samples.
- Compared JCV DNA sequences using phylogenetic analysis.
Main Results:
- Identical JCV DNA sequences were found between parents and children in 4 out of 5 families.
- Sequence variations, including substitutions, deletions, and duplications, were observed within families.
- Phylogenetic analysis confirmed that JCV sequence diversity originated within each family, not from multiple infections.
Conclusions:
- Findings support the hypothesis of parent-to-child transmission of JCV.
- Long-term cohabitation appears to be a significant factor in JCV transmission.
- JCV genetic diversity within families arises from transmission events during cohabitation.
Abstract:
JC polyomavirus (JCV), the etiological agent of progressive multifocal leukoencephalopathy, is ubiquitous in humans, infecting children asymptomatically, then persisting in renal tissue. It has been proposed that JCV is transmitted mainly from parents to children through long-term cohabitation. The objective of this study was to further elucidate the mode of JCV transmission. In 5 families, we selected parent/child pairs between whom JCV was probably transmitted (judged on the basis of the identity of a 610-bp JCV DNA sequence between the parent and child). We established 5 to 9 complete JCV DNA clones from the urine of each parent or child. The complete sequences of these clones were determined and compared in each family. Nucleotide substitutions were detected in 4 parents and 1 child, and sequence rearrangements (deletions or duplications) were found in 2 parents and 2 children. Phylogenetic comparison of the detected sequences indicated that the diversity of JCV DNA sequences was generated in each family (i.e. not caused by multiple infection). We found that in 4 of the 5 families, a sequence detected in the parent was completely identical to one in the child. These findings provided further support for the proposed mode of JCV transmission, i.e. parent-to-child transmission during cohabitation.
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