Bocavirus

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Oliver Schildgen - One of the best experts on this subject based on the ideXlab platform.

  • Human Bocavirus Can Be Cultured in Differentiated Human Airway
    2020
    Co-Authors: Ronald Dijkman, Oliver Schildgen, Sylvie M Koekkoek, Richard Molenkamp, Lia Van Der Hoek
    Abstract:

    In 2005, a human Bocavirus was discovered in children with respiratory tract illnesses. Attempts to culture this virus on conventional cell lines has failed thus far. We investigated whether the virus can replicate on pseudostratified human airway epithelium. This cell culture system mimics the human airway environment and facilitates culturing of various respiratory agents. The cells were inoculated with human Bocavirus-positive nasopharyngeal washes from children, and virus replication was monitored by measuring apical release of the virus via real-time PCR. Furthermore, we identified different viral mRNAs in the infected cells. All mRNAs were transcribed from a single promoter but varied due to alternative splicing and alternative polyadenylation, similar to what has been described for bovine parvovirus and minute virus of canines, the other two members of the Bocavirus genus. Thus, transcription of human Bocavirus displays strong homology to the transcription of the other Bocaviruses. In conclusion, we report here for the first time that human Bocavirus can be propagated in an in vitro culture system and present a detailed map of the set of mRNAs that are produced by the virus.

  • the human Bocavirus is associated with some lung and colorectal cancers and persists in solid tumors
    PLOS ONE, 2013
    Co-Authors: Verena Schildgen, Monika Malecki, Ramonaliza Tillmann, Michael Brockmann, Oliver Schildgen
    Abstract:

    Human Bocavirus is the second autonomous human parvovirus with assumed pathogenic potential. Other parvoviruses are known to persist and even integrate into the host genome, eventually contributing to the multi-step development of cancer. Human Bocavirus also persists in an unknown percentage of clinically asymptomatic patients in addition to those with primary infection. The aim of the present study was to analyze the role of Human Bocavirus in lung and colorectal cancers. Therefore, formalin-fixed, paraffin-embedded, archived tumor samples were screened for Human Bocavirus DNA by PCR, Southern blotting, and sequencing. Positive tissues were further subjected to fluorescence in situ hybridization analysis to specifically detect human Bocavirus DNA in the infected cells. In total, 11 of the 60 (18.3%) lung and 9 of the 44 (20.5%) colorectal tumors tested positive for human Bocavirus DNA by PCR and were confirmed by sequencing and fluorescence in situ hybridization analysis. Thus, human Bocavirus DNA is present in the nuclei of infected cells, in either single or multiple copies, and appears to form concatemers. The occurrence of these human Bocavirus DNA structures supports the existence of the postulated σ- or rolling-hairpin replication mechanism. Moreover, the fluorescence in situ hybridization patterns inspired the hypothesis that human Bocavirus DNA either persists as cccDNA or is integrated into the host genome. This finding suggests that this virus may indirectly contribute to the development of some colorectal and lung cancers, as do other DNA viruses, such as the human hepatitis B virus, or may play an active role in cancer by interacting with the host genome.

  • severe human Bocavirus infection germany
    Emerging Infectious Diseases, 2011
    Co-Authors: Robert Walter Korner, Monika Malecki, Maria Soderlundvenermo, Silke Van Koningsbruggenrietschel, Rolf Kaiser, Oliver Schildgen
    Abstract:

    Human Bocavirus (HBoV), discovered in 2005, can cause respiratory disease or no symptoms at all. We confi rmed HBoV infection in an 8-month-old girl with hypoxia, respiratory distress, wheezing, cough, and fever. This case demonstrates that lower respiratory tract infection caused by HBoV can lead to severe and life-threatening disease.

  • Human Bocavirus: still more questions than answers
    Future Virology, 2011
    Co-Authors: Monika Malecki, Verena Schildgen, Oliver Schildgen
    Abstract:

    The human Bocavirus was first detected in 2005 and since then has been found in both respiratory secretions from patients with airway infections and in stool samples from patients with gastroenteritis. Meanwhile, four different genotypes have been identified that most likely derive from recombination events. Although the modified Koch’s postulates have not yet been fulfilled completely, owing to the lack of an animal model or a simple cell culture system, there is increasing evidence that the human Bocaviruses are serious participants in infectious diseases of the respiratory and the GI tracts. This article reviews the current status of the clinical features of human Bocaviruses and provides an overview of the latest findings concerning the biology, phylogeny, epidemiology and diagnostic tools related to human Bocaviruses. Furthermore, it discusses the potential pathogenicity of human Bocavirus, as well as its persistence and reactivation in hosts.

  • detection of head to tail dna sequences of human Bocavirus in clinical samples
    PLOS ONE, 2011
    Co-Authors: Jessica Lusebrink, Verena Schildgen, Ramonaliza Tillmann, Felix Wittleben, Anne C Bohmer, Andreas Muller, Oliver Schildgen
    Abstract:

    Parvoviruses are single stranded DNA viruses that replicate in a so called “rolling-hairpin” mechanism, a variant of the rolling circle replication known for bacteriophages like ϕX174. The replication intermediates of parvoviruses thus are concatemers of head-to-head or tail-to-tail structure. Surprisingly, in case of the novel human Bocavirus, neither head-to-head nor tail-to-tail DNA sequences were detected in clinical isolates; in contrast head-to-tail DNA sequences were identified by PCR and sequencing. Thereby, the head-to-tail sequences were linked by a novel sequence of 54 bp of which 20 bp also occur as conserved structures of the palindromic ends of parvovirus MVC which in turn is a close relative to human Bocavirus.

Tobias Allander - One of the best experts on this subject based on the ideXlab platform.

  • life threatening respiratory tract disease with human Bocavirus 1 infection in a 4 year old child
    Journal of Clinical Microbiology, 2012
    Co-Authors: Niklas Edner, Paul Castillorodas, Lars Falk, Klaus Hedman, Maria Soderlundvenermo, Tobias Allander
    Abstract:

    The disease spectrum associated with human Bocavirus-1 infection remains to be fully defined. We report a case of Bocavirus-1-associated bronchiolitis, leading to severe respiratory failure and extracorporeal membrane oxygenation in a 4-year-old child, and suggest blood testing for human Bocavirus-1 in children with severe respiratory tract infection.

  • human Bocavirus the first 5 years
    Reviews in Medical Virology, 2012
    Co-Authors: Tuomas Jartti, Tobias Allander, Klaus Hedman, Olli Ruuskanen, Laura Jartti, Maria Soderlundvenermo
    Abstract:

    SUMMARY Four species of human Bocavirus (HBoV) have been recently discovered and classified in the Bocavirus genus (family Parvoviridae, subfamily Parvovirinae). Although detected both in respiratory and stool samples worldwide, HBoV1 is predominantly a respiratory pathogen, whereas HBoV2, HBoV3, and HBoV4 have been found mainly in stool. A variety of signs and symptoms have been described in patients with HBoV infection including rhinitis, pharyngitis, cough, dyspnea, wheezing, pneumonia, acute otitis media, fever, nausea, vomiting, and diarrhea. Many of these potential manifestations have not been systematically explored, and they have been questioned because of high HBoV co-infection rates in symptomatic subjects and high HBoV detection rates in asymptomatic subjects. However, evidence is mounting to show that HBoV1 is an important cause of lower respiratory tract illness. The best currently available diagnostic approaches are quantitative PCR and serology. This concise review summarizes the current clinical knowledge on HBoV species. Copyright © 2011 John Wiley & Sons, Ltd.

  • Human Bocavirus—the first 5 years
    Reviews in Medical Virology, 2011
    Co-Authors: Tuomas Jartti, Tobias Allander, Klaus Hedman, Olli Ruuskanen, Laura Jartti, Maria Söderlund-venermo
    Abstract:

    SUMMARY Four species of human Bocavirus (HBoV) have been recently discovered and classified in the Bocavirus genus (family Parvoviridae, subfamily Parvovirinae). Although detected both in respiratory and stool samples worldwide, HBoV1 is predominantly a respiratory pathogen, whereas HBoV2, HBoV3, and HBoV4 have been found mainly in stool. A variety of signs and symptoms have been described in patients with HBoV infection including rhinitis, pharyngitis, cough, dyspnea, wheezing, pneumonia, acute otitis media, fever, nausea, vomiting, and diarrhea. Many of these potential manifestations have not been systematically explored, and they have been questioned because of high HBoV co-infection rates in symptomatic subjects and high HBoV detection rates in asymptomatic subjects. However, evidence is mounting to show that HBoV1 is an important cause of lower respiratory tract illness. The best currently available diagnostic approaches are quantitative PCR and serology. This concise review summarizes the current clinical knowledge on HBoV species. Copyright © 2011 John Wiley & Sons, Ltd.

  • No efficacy of prednisolone in acute wheezing associated with human Bocavirus infection.
    Pediatric Infectious Disease Journal, 2011
    Co-Authors: Tuomas Jartti, Tobias Allander, Tytti Vuorinen, Klaus Hedman, Maria Söderlund-venermo, Olli Ruuskanen
    Abstract:

    The efficacy of prednisolone in acute wheezing associated with human Bocavirus infection was investigated in 232 hospitalized children (median age, 1.6 years). Clinical history, atopy status, and viral etiology were carefully studied. Outcomes included hospitalization time, duration of symptoms, and occurrence of relapses. No efficacy of prednisolone was found in children with serologically confirmed acute human Bocavirus infection.

  • human Bocavirus in children with acute lymphoblastic leukemia
    European Journal of Pediatrics, 2008
    Co-Authors: Minna Koskenvuo, Tobias Allander, Matti Waris, Merja Mottonen, Toivo T Salmi, Olli Ruuskanen
    Abstract:

    A new human parvovirus, human Bocavirus, has recently been identified in respiratory secretions, feces and serum. It is associated with lower and most likely also upper respiratory tract infections. Most commonly reported symptoms are cough, rhinorrhea, expiratory wheezing and fever, and the virus is preferentially detected in young children. We report three children with acute lymphoblastic leukemia who had acute febrile episodes with concomitant detection of human Bocavirus in their respiratory secretions. One of them had five consecutive febrile episodes during 6 months, all associated with the presence of human Bocavirus at varying viral loads, suggesting prolonged shedding or reactivation of the virus.

Zhao-jun Duan - One of the best experts on this subject based on the ideXlab platform.

  • Human Bocavirus Infection, People’s Republic of China
    Emerging Infectious Diseases, 2020
    Co-Authors: Xiaowang Qu, Can-ping Huang, Zhao-jun Duan, Zhengyu Qi, Fuwang Peng, Lishu Zheng
    Abstract:

    A newly identified parvovirus, human Bocavirus (HBoV), was found in 21 (8.3%) of 252 nasopharyngeal aspirates from hospitalized children with lower respiratory tract infection in Hunan Province, People’s Republic of China. Viral loads were 104 to 1010 copies/mL. Phylogenetic analysis of the VP1 gene showed a single genetic lineage of HBoV worldwide.

  • Identification and characterization of porcine Bocavirus episomes
    Chinese journal of virology, 2012
    Co-Authors: Wan-zhu Yang, Can-ping Huang, Zhao-jun Duan
    Abstract:

    To verify that the circular forms of Bocavirus genome exist in their host, Bocavirus episomes were detected in fecal samples of healthy piglets using a semi-nested PCR method. Two species of porcine Bocaviruses (PBoVG2-episome and PBoVG3-episome) were identified for the first time. The relevant terminal sequences of the noncoding region (405 and 511 nt, respectively) were also obtained. Sequence analyses and secondary structure prediction indicated that the PBoVG2-episome was more similar to that of human Bocavirus 3 (HBoV3) but the PBoVG3-episome was quite different from that of other members of the genus Bocavirus. Discovery of episomal forms of porcine Bocaviruses (PBoV) suggested that PBoV, like HBoV, used a different replication mechanism from other parvoviruses. The sequencing of episome Inverted Terminal Repeats (ITRs) also contributes to a possible alternative strategy for constructing infectious molecular clones of Bocavirus in a future study.

  • phylogenetic and recombination analysis of human Bocavirus 2
    BMC Infectious Diseases, 2011
    Co-Authors: Can-ping Huang, Zi-qian Xu, Weixia Cheng, Jinan Chen, Jiemei Yu, Huiying Li, Ming Zhang, Zhao-jun Duan
    Abstract:

    Human Bocavirus 2(HBoV2) and other human Bocavirus species (HBoV, HBoV3, and HBoV4) have been discovered recently. But the precise phylogenetic relationships among these viruses are not clear yet. We collected 632 diarrhea and 162 healthy children in Lanzhou, China. Using PCR, Human Bocavirus (HBoV), HBoV2, HBoV3 and HBoV4 were screened. The partial genes of NS, NP1 and VP, and two nearly complete sequences of HBoV2 were obtained. Phylogenetic analysis showed the different genes of HBoV2 strain were homogenous with different reference strains. HBoV3 may be a recombinant derived from HBoV and HBoV4. We also observed that the VP1 and VP2 region of HBoV3 is as similar to HBoV2 as to HBoV4. A single genetic lineage of HBoV2 is circulating in children with and without gastroenteritis in Lanzhou, China. Current evidence in this study was not enough to support recombination between HBoV2 strains, and HBoV3 may be a recombinant between HBoV and the common ancestor of HBoV2 and HBoV4.

  • human Bocavirus infection in children hospitalized with acute gastroenteritis in china
    Journal of Clinical Virology, 2008
    Co-Authors: Jiemei Yu, Zi-qian Xu, Weixia Cheng, Huiying Li, Dandi Li, Qing Zhang, Suhua Yang, Zhaoyin Fang, Zhao-jun Duan
    Abstract:

    Abstract Background Human Bocavirus (HBoV) was first identified in children with acute respiratory-tract infections, but recent studies have revealed that HBoV is also frequently detected in fecal specimens from children with gastroenteritis. Objectives To investigate the prevalence of HBoV in children hospitalized with gastroenteritis in different areas of China. Study design Employing ELISA, RT-PCR or PCR, we evaluated 1216 fecal samples for common diarrheal agents from children aged less than 5-year-old hospitalized with acute gastroenteritis. MEGA software was used to construct phylogenetic trees of the VP1/VP2 partial sequences of the HBoV genome. Results There were 67 HBoV-positive specimens, 52 (77.6%) were co-infected with rotavirus, norovirus, astrovirus, or enteric adenovirus. Statistical analysis of the clinical data indicated that children infected with both rotavirus and Bocavirus did not have more severe clinical symptoms than children infected with rotavirus. The phylogenetic analysis of the VP1/VP2 partial sequences of the HBoV genome revealed a single genetic lineage. Conclusions Despite its high infection rate, there was no statistically significant a causual relationship between HBoV and gastroenteritis in children.

  • human Bocavirus infection people s republic of china
    Emerging Infectious Diseases, 2007
    Co-Authors: Xiaowang Qu, Can-ping Huang, Zhao-jun Duan, Zhengyu Qi, Fuwang Peng, Lishu Zheng
    Abstract:

    A newly identified parvovirus, human Bocavirus (HBoV), was found in 21 (8.3%) of 252 nasopharyngeal aspirates from hospitalized children with lower respiratory tract infection in Hunan Province, People’s Republic of China. Viral loads were 104 to 1010 copies/mL. Phylogenetic analysis of the VP1 gene showed a single genetic lineage of HBoV worldwide.

Weixia Cheng - One of the best experts on this subject based on the ideXlab platform.

  • phylogenetic and recombination analysis of human Bocavirus 2
    BMC Infectious Diseases, 2011
    Co-Authors: Can-ping Huang, Zi-qian Xu, Weixia Cheng, Jinan Chen, Jiemei Yu, Huiying Li, Ming Zhang, Zhao-jun Duan
    Abstract:

    Human Bocavirus 2(HBoV2) and other human Bocavirus species (HBoV, HBoV3, and HBoV4) have been discovered recently. But the precise phylogenetic relationships among these viruses are not clear yet. We collected 632 diarrhea and 162 healthy children in Lanzhou, China. Using PCR, Human Bocavirus (HBoV), HBoV2, HBoV3 and HBoV4 were screened. The partial genes of NS, NP1 and VP, and two nearly complete sequences of HBoV2 were obtained. Phylogenetic analysis showed the different genes of HBoV2 strain were homogenous with different reference strains. HBoV3 may be a recombinant derived from HBoV and HBoV4. We also observed that the VP1 and VP2 region of HBoV3 is as similar to HBoV2 as to HBoV4. A single genetic lineage of HBoV2 is circulating in children with and without gastroenteritis in Lanzhou, China. Current evidence in this study was not enough to support recombination between HBoV2 strains, and HBoV3 may be a recombinant between HBoV and the common ancestor of HBoV2 and HBoV4.

  • human Bocavirus infection in children hospitalized with acute gastroenteritis in china
    Journal of Clinical Virology, 2008
    Co-Authors: Jiemei Yu, Zi-qian Xu, Weixia Cheng, Huiying Li, Dandi Li, Qing Zhang, Suhua Yang, Zhaoyin Fang, Zhao-jun Duan
    Abstract:

    Abstract Background Human Bocavirus (HBoV) was first identified in children with acute respiratory-tract infections, but recent studies have revealed that HBoV is also frequently detected in fecal specimens from children with gastroenteritis. Objectives To investigate the prevalence of HBoV in children hospitalized with gastroenteritis in different areas of China. Study design Employing ELISA, RT-PCR or PCR, we evaluated 1216 fecal samples for common diarrheal agents from children aged less than 5-year-old hospitalized with acute gastroenteritis. MEGA software was used to construct phylogenetic trees of the VP1/VP2 partial sequences of the HBoV genome. Results There were 67 HBoV-positive specimens, 52 (77.6%) were co-infected with rotavirus, norovirus, astrovirus, or enteric adenovirus. Statistical analysis of the clinical data indicated that children infected with both rotavirus and Bocavirus did not have more severe clinical symptoms than children infected with rotavirus. The phylogenetic analysis of the VP1/VP2 partial sequences of the HBoV genome revealed a single genetic lineage. Conclusions Despite its high infection rate, there was no statistically significant a causual relationship between HBoV and gastroenteritis in children.

Zi-qian Xu - One of the best experts on this subject based on the ideXlab platform.

  • Novel Human Bocavirus in Children with Acute Respiratory
    2020
    Co-Authors: Jing-rong Song, Ni-guang Xiao, Wei-xia Chen, Zi-qian Xu, Yang Zhao
    Abstract:

    Human Bocavirus (HBoV) and HBoV2, two human Bocavirus species, were found in 18 and 10 of 235 nasopharyngeal aspirates, respectively, from children hospitalized with acute respiratory tract infection. Our results suggest that, like HBoV, HBoV2 is distributed worldwide and may be associated with respiratory and enteric diseases.

  • phylogenetic and recombination analysis of human Bocavirus 2
    BMC Infectious Diseases, 2011
    Co-Authors: Can-ping Huang, Zi-qian Xu, Weixia Cheng, Jinan Chen, Jiemei Yu, Huiying Li, Ming Zhang, Zhao-jun Duan
    Abstract:

    Human Bocavirus 2(HBoV2) and other human Bocavirus species (HBoV, HBoV3, and HBoV4) have been discovered recently. But the precise phylogenetic relationships among these viruses are not clear yet. We collected 632 diarrhea and 162 healthy children in Lanzhou, China. Using PCR, Human Bocavirus (HBoV), HBoV2, HBoV3 and HBoV4 were screened. The partial genes of NS, NP1 and VP, and two nearly complete sequences of HBoV2 were obtained. Phylogenetic analysis showed the different genes of HBoV2 strain were homogenous with different reference strains. HBoV3 may be a recombinant derived from HBoV and HBoV4. We also observed that the VP1 and VP2 region of HBoV3 is as similar to HBoV2 as to HBoV4. A single genetic lineage of HBoV2 is circulating in children with and without gastroenteritis in Lanzhou, China. Current evidence in this study was not enough to support recombination between HBoV2 strains, and HBoV3 may be a recombinant between HBoV and the common ancestor of HBoV2 and HBoV4.

  • Novel human Bocavirus in children with acute respiratory tract infection.
    Emerging Infectious Diseases, 2010
    Co-Authors: Jing-rong Song, Ni-guang Xiao, Wei-xia Chen, Zi-qian Xu, Yang Zhao
    Abstract:

    Human Bocavirus (HBoV) and HBoV2, two human Bocavirus species, were found in 18 and 10 of 235 nasopharyngeal aspirates, respectively, from children hospitalized with acute respiratory tract infection. Our results suggest that, like HBoV, HBoV2 is distributed worldwide and may be associated with respiratory and enteric diseases.

  • human Bocavirus infection in children hospitalized with acute gastroenteritis in china
    Journal of Clinical Virology, 2008
    Co-Authors: Jiemei Yu, Zi-qian Xu, Weixia Cheng, Huiying Li, Dandi Li, Qing Zhang, Suhua Yang, Zhaoyin Fang, Zhao-jun Duan
    Abstract:

    Abstract Background Human Bocavirus (HBoV) was first identified in children with acute respiratory-tract infections, but recent studies have revealed that HBoV is also frequently detected in fecal specimens from children with gastroenteritis. Objectives To investigate the prevalence of HBoV in children hospitalized with gastroenteritis in different areas of China. Study design Employing ELISA, RT-PCR or PCR, we evaluated 1216 fecal samples for common diarrheal agents from children aged less than 5-year-old hospitalized with acute gastroenteritis. MEGA software was used to construct phylogenetic trees of the VP1/VP2 partial sequences of the HBoV genome. Results There were 67 HBoV-positive specimens, 52 (77.6%) were co-infected with rotavirus, norovirus, astrovirus, or enteric adenovirus. Statistical analysis of the clinical data indicated that children infected with both rotavirus and Bocavirus did not have more severe clinical symptoms than children infected with rotavirus. The phylogenetic analysis of the VP1/VP2 partial sequences of the HBoV genome revealed a single genetic lineage. Conclusions Despite its high infection rate, there was no statistically significant a causual relationship between HBoV and gastroenteritis in children.