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Human otic progenitor cell models of congenital hearing loss reveal potential pathophysiologic mechanisms of Zika virus and cytomegalovirus infections.
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- Author(s): Harding AT;Harding AT;Harding AT; Ocwieja K; Ocwieja K; Ocwieja K; Jeong M; Jeong M; Jeong M; Zhang Y; Zhang Y; Leger V; Leger V; Jhala N; Jhala N; Stankovic KM; Stankovic KM; Stankovic KM; Stankovic KM; Stankovic KM; Gehrke L; Gehrke L; Gehrke L
- Source:
MBio [mBio] 2024 Apr 10; Vol. 15 (4), pp. e0019924. Date of Electronic Publication: 2024 Mar 05.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: American Society for Microbiology Country of Publication: United States NLM ID: 101519231 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2150-7511 (Electronic) NLM ISO Abbreviation: mBio Subsets: MEDLINE
- Publication Information: Original Publication: Washington, D.C. : American Society for Microbiology
- Subject Terms:
- Abstract: Congenital hearing loss is a common chronic condition affecting children in both developed and developing nations. Viruses correlated with congenital hearing loss include human cytomegalovirus (HCMV) and Zika virus (ZIKV), which causes congenital Zika syndrome. The mechanisms by which HCMV and ZIKV infections cause hearing loss are poorly understood. It is challenging to study human inner ear cells because they are encased in bone and also scarce as autopsy samples. Recent advances in culturing human stem cell-derived otic progenitor cells (OPCs) have allowed us herein to describe successful in vitro infection of OPCs with HCMV and ZIKV, and also to propose potential mechanisms by which each viral infection could affect hearing. We find that ZIKV infection rapidly and significantly induces the expression of type I interferon and interferon-stimulated genes, while OPC viability declines, at least in part, from apoptosis. In contrast, HCMV infection did not appear to upregulate interferons or cause a reduction in cell viability, and instead disrupted expression of key genes and pathways associated with inner ear development and function, including Cochlin, nerve growth factor receptor, SRY-box transcription factor 11, and transforming growth factor-beta signaling. These findings suggest that ZIKV and HCMV infections cause congenital hearing loss through distinct pathways, that is, by inducing progenitor cell death in the case of ZIKV infection, and by disruption of critical developmental pathways in the case of HCMV infection.
Importance: Congenital virus infections inflict substantial morbidity and devastating disease in neonates worldwide, and hearing loss is a common outcome. It has been difficult to study viral infections of the human hearing apparatus because it is embedded in the temporal bone of the skull. Recent technological advances permit the differentiation of otic progenitor cells (OPCs) from human-induced pluripotent stem cells. This paper is important for demonstrating that inner ear virus infections can be modeled in vitro using OPCs. We infected OPCs with two viruses associated with congenital hearing loss: human cytomegalovirus (HCMV), a DNA virus, or Zika virus (ZIKV), an RNA virus. An important result is that the gene expression and cytokine production profiles of HCMV/ZIKV-infected OPCs are markedly dissimilar, suggesting that mechanisms of hearing loss are also distinct. The specific molecular regulatory pathways identified in this work could suggest important targets for therapeutics.
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Sci Transl Med. 2017 Sep 27;9(409):. (PMID: 28954927) - Grant Information: U19 AI131135 United States AI NIAID NIH HHS; P30 AI060354 United States AI NIAID NIH HHS; P30 CA014051 United States CA NCI NIH HHS
- Contributed Indexing: Keywords: Zika virus; hearing loss; human cytomegalovirus; inner ear; model system; organoid; virus infection
- Accession Number: 9008-11-1 (Interferons)
- Publication Date: Date Created: 20240305 Date Completed: 20240411 Latest Revision: 20240425
- Publication Date: 20240425
- Accession Number: PMC11005345
- Accession Number: 10.1128/mbio.00199-24
- Accession Number: 38440980
- Source:
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