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Biology subjects

CHEN, H.-C.

Publications and source records attributed to CHEN, H.-C..

3 recordsLinked to original sources

Identification of potential SARS-CoV-2 genetic markers resulting from host domestication.

We developed a k-mer-based pipeline, namely the Pathogen Origin Recognition Tool using Enriched K-mers (PORT-EK) to identify genomic regions enriched in the respective hosts after the comparison of metagenomes of isolates between two host species. Using it we identified thousands of k-mers enriched in US white-tailed deer and betacoronaviruses in bat reservoirs while comparing them with human isolates. We demonstrated different coverage landscapes of k-mers enriched in deer and bats and unraveled 148 mutations in enriched k-mers yielded from the comparison of viral metagenomes between bat and human isolates. We observed that the third position within a genetic codon is prone to mutations, resulting in a high frequency of synonymous mutations of amino acids harboring the same physicochemical properties as unaltered amino acids. Finally, we classified and predicted the likelihood of host species based on the enriched k-mer counts. Altogether, PORT-EK showcased its feasibility for identifying enriched viral genomic regions, illuminating the different intrinsic tropisms of coronavirus after host domestication. TeaserA measure of enriched viral genomic correlates resulting from host domestication as a potential predictor of zoonotic risk.

systems biology↗

Distinguishable topological properties of functional genome networks in HIV-1 reservoirs

HIV-1 reservoirs display heterogeneous nature, lodging both intact and defective proviruses. Recent evidence has shed light on their difference, particularly in the context of immune-mediated selection. To deepen our understanding of such heterogeneous HIV-1 reservoirs and their functional implications, we pioneered the integration of basic concepts of graph theory to characterize the composition of HIV-1 reservoirs. Our analysis revealed noticeable topological properties in networks, featuring immunologic signatures enriched by genes harboring intact and defective proviruses, when comparing antiretroviral therapy (ART)-treated HIV-1-infected individuals and elite controllers. The key variable, the rich factor, played a pivotal role in classifying distinct topological properties in networks. The host gene expression strengthened the accuracy of classification between elite controllers and ART-treated patients. Overall, our work provides a prime example of leveraging genomic approaches alongside mathematical tools to unravel the complexities of HIV-1 reservoirs.

genomics↗

The dynamic linkage between intact provirus integration sites and the host functional genome property alongside HIV-1 infections associated with antiretroviral therapy

The HIV-1 latent reservoir harboring replication-competent proviruses, is the major barrier in the quest for a HIV-1 infection cure. HIV-1 infection at all stages of disease progression is associated with immune activation and dysfunctional production of proinflammatory soluble factors (cytokines and chemokines) and it is expected that during HIV-1 infection different immune components and immune cells, in turn, participate in immune responses, subsequently activating downstream biological pathways. However, whether HIV-1 infections activate only specific pathways or result in the global activation of functional pathways is presently not fully understood. Therefore, in this work, I used genes targeted by intact proviruses from published datasets to seek enriched immunologic signatures and host biological pathways alongside HIV-1 infections. I observed that different compositions of immune cell types and proinflammatory soluble factors appeared alongside HIV-1 infections associated with antiretroviral therapy based on the over-representation analysis. Moreover, KEGG pathways relevant to "cancer specific type", "immune system", "infectious disease viral" and "signal transduction" were frequently enriched in HIV-1-infected individuals subjected to antiretroviral therapy.

microbiology↗