Abstract:Plasma from patients with dengue-like symptoms was collected in 2013 to 2016 from the Brazilian states of Tocantins and Amapa. 781 samples testing negative for IgM against Dengue, Zika, and Chikungunya viruses and for flaviviruses, alphaviruses and enteroviruses RNA using RT-PCRs were analyzed using viral metagenomics. Viral particles-associated nucleic acids were enriched, randomly amplified, and deep sequenced in 102 mini-pools generating over 2 billion reads. Sequence data was analyzed for the presence of k… Show more
“…However, while the phylogenetic placement of the DAC sequences within a clade that is dominated by avian viruses within a genus that includes many vertebrate viruses, some of which even proven to be pathogenic [ 47 , 48 ], clearly points towards ducks as DAC hosts, such a clear conclusion cannot be made for DAAD. Densoviruses are frequently identified during metagenomic investigations of samples collected from vertebrates [ 43 , 44 , 49 ], including human plasma and cerebrospinal fluid [ 50 , 51 ], and some of the densoviruses genetically close to DAAD were also vertebrate-associated as they were detected in fecal specimens of birds, monkeys, and bats [ 43 , 44 ]. However, dipteran and lepidopteran viruses were also included in the same clade as DAAD and no proof exists that densoviruses can replicate in vertebrate hosts.…”
Parvoviruses are small single-stranded DNA viruses that can infect both vertebrates and invertebrates. We report here the full characterization of novel viruses we identified in ducks, including two viral species within the subfamily Hamaparvovirinae (duck-associated chapparvovirus, DAC) and a novel species within the subfamily Densovirinae (duck-associated ambidensovirus, DAAD). Overall, 5.7% and 21.1% of the 123 screened ducks (American black ducks, mallards, northern pintail) were positive for DAC and DAAD, respectively, and both viruses were more frequently detected in autumn than in winter. Genome organization and predicted transcription profiles of DAC and DAAD were similar to viruses of the genera Chaphamaparvovirus and Protoambidensovirus, respectively. Their association to these genera was also demonstrated by subfamily-wide phylogenetic and distance analyses of non-structural protein NS1 sequences. While DACs were included in a highly supported clade of avian viruses, no definitive conclusions could be drawn about the host type of DAAD because it was phylogenetically close to viruses found in vertebrates and invertebrates and analyses of codon usage bias and nucleotide frequencies of viruses within the family Parvoviridae showed no clear host-based viral segregation. This study highlights the high parvoviral diversity in the avian reservoir with many avian-associated parvoviruses likely yet to be discovered.
“…However, while the phylogenetic placement of the DAC sequences within a clade that is dominated by avian viruses within a genus that includes many vertebrate viruses, some of which even proven to be pathogenic [ 47 , 48 ], clearly points towards ducks as DAC hosts, such a clear conclusion cannot be made for DAAD. Densoviruses are frequently identified during metagenomic investigations of samples collected from vertebrates [ 43 , 44 , 49 ], including human plasma and cerebrospinal fluid [ 50 , 51 ], and some of the densoviruses genetically close to DAAD were also vertebrate-associated as they were detected in fecal specimens of birds, monkeys, and bats [ 43 , 44 ]. However, dipteran and lepidopteran viruses were also included in the same clade as DAAD and no proof exists that densoviruses can replicate in vertebrate hosts.…”
Parvoviruses are small single-stranded DNA viruses that can infect both vertebrates and invertebrates. We report here the full characterization of novel viruses we identified in ducks, including two viral species within the subfamily Hamaparvovirinae (duck-associated chapparvovirus, DAC) and a novel species within the subfamily Densovirinae (duck-associated ambidensovirus, DAAD). Overall, 5.7% and 21.1% of the 123 screened ducks (American black ducks, mallards, northern pintail) were positive for DAC and DAAD, respectively, and both viruses were more frequently detected in autumn than in winter. Genome organization and predicted transcription profiles of DAC and DAAD were similar to viruses of the genera Chaphamaparvovirus and Protoambidensovirus, respectively. Their association to these genera was also demonstrated by subfamily-wide phylogenetic and distance analyses of non-structural protein NS1 sequences. While DACs were included in a highly supported clade of avian viruses, no definitive conclusions could be drawn about the host type of DAAD because it was phylogenetically close to viruses found in vertebrates and invertebrates and analyses of codon usage bias and nucleotide frequencies of viruses within the family Parvoviridae showed no clear host-based viral segregation. This study highlights the high parvoviral diversity in the avian reservoir with many avian-associated parvoviruses likely yet to be discovered.
“…Parvoviruses are associated with disease in a variety of host species, ranging from canines [ 47 ] to livestock [ 48 , 49 , 50 , 51 ], rodents [ 36 ], and humans [ 52 ]. Reptile parvoviruses were identified in several snake species (snake adeno-associated virus) [ 11 , 53 , 54 , 55 , 56 , 57 ] and some lizard species including bearded dragons [ 11 , 12 ].…”
Viral pathogens are being increasingly described in association with mass morbidity and mortality events in reptiles. However, our knowledge of reptile viruses remains limited. Herein, we describe the meta-transcriptomic investigation of a mass morbidity and mortality event in a colony of central bearded dragons (Pogona vitticeps) in 2014. Severe, extensive proliferation of the respiratory epithelium was consistently found in affected dragons. Similar proliferative lung lesions were identified in bearded dragons from the same colony in 2020 in association with increased intermittent mortality. Total RNA sequencing identified two divergent DNA viruses: a reptile-infecting circovirus, denoted bearded dragon circovirus (BDCV), and the first exogeneous reptilian chaphamaparvovirus—bearded dragon chaphamaparvovirus (BDchPV). Phylogenetic analysis revealed that BDCV was most closely related to bat-associated circoviruses, exhibiting 70% amino acid sequence identity in the Replicase (Rep) protein. In contrast, in the nonstructural (NS) protein, the newly discovered BDchPV showed approximately 31%–35% identity to parvoviruses obtained from tilapia fish and crocodiles in China. Subsequent specific PCR assays revealed BDCV and BDchPV in both diseased and apparently normal captive reptiles, although only BDCV was found in those animals with proliferative pulmonary lesions and respiratory disease. This study expands our understanding of viral diversity in captive reptiles.
“…In Brazil, B19V is the most frequent cause of rash/fever infections in cases where serum testing is negative for arboviruses and rubella, and several studies have shown an increase in PB19 rash/fever cases in a spatiotemporal manner compared to arboviruses and rubella [ 243 , 244 ]. Parvovirus B19 has been detected in 17% of cases when assaying the plasma of Brazilian patients with dengue fever-like symptoms, while samples were negative for arbovirus and were originally misdiagnosed (falsely positive for DENV) [ 245 , 246 , 247 , 248 , 249 ], A similar trend has also been reported for ZIKV [ 52 , 250 , 251 ].…”
Section: Human Latent Virus (Hlv) Selection With Common Interests In Czsmentioning
The emergence of the Zika virus (ZIKV) mirrors its evolutionary nature and, thus, its ability to grow in diversity or complexity (i.e., related to genome, host response, environment changes, tropism, and pathogenicity), leading to it recently joining the circle of closed congenital pathogens. The causal relation of ZIKV to microcephaly is still a much-debated issue. The identification of outbreak foci being in certain endemic urban areas characterized by a high-density population emphasizes that mixed infections might spearhead the recent appearance of a wide range of diseases that were initially attributed to ZIKV. Globally, such coinfections may have both positive and negative effects on viral replication, tropism, host response, and the viral genome. In other words, the possibility of coinfection may necessitate revisiting what is considered to be known regarding the pathogenesis and epidemiology of ZIKV diseases. ZIKV viral coinfections are already being reported with other arboviruses (e.g., chikungunya virus (CHIKV) and dengue virus (DENV)) as well as congenital pathogens (e.g., human immunodeficiency virus (HIV) and cytomegalovirus (HCMV)). However, descriptions of human latent viruses and their impacts on ZIKV disease outcomes in hosts are currently lacking. This review proposes to select some interesting human latent viruses (i.e., herpes simplex virus 2 (HSV-2), Epstein–Barr virus (EBV), human herpesvirus 6 (HHV-6), human parvovirus B19 (B19V), and human papillomavirus (HPV)), whose virological features and co-exposition with ZIKV may provide evidence of the syndemism process, shedding some light on the emergence of the ZIKV-induced global congenital syndrome in South America.
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