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Role of Severe Acute Respiratory Syndrome Coronavirus Viroporins E, 3a, and 8a in Replication and Pathogenesis
Carlos Castaño-Rodriguez1, Jose M Honrubia1, Javier Gutiérrez-Álvarez1
1Department of Molecular and Cell Biology, Centro Nacional de Biotecnología (CNB-CSIC), Campus Universidad Autónoma de Madrid, Madrid, Spain.
Abstract:
Viroporins are viral proteins with ion channel (IC) activity that play an important role in several processes, including virus replication and pathogenesis. While many coronaviruses (CoVs) encode two viroporins, severe acute respiratory syndrome CoV (SARS-CoV) encodes three: proteins 3a, E, and 8a. Additionally, proteins 3a and E have a PDZ-binding motif (PBM), which can potentially bind over 400 cellular proteins which contain a PDZ domain, making them potentially important for the control of cell function. In the present work, a comparative study of the functional motifs included within the SARS-CoV viroporins was performed, mostly focusing on the roles of the IC and PBM of E and 3a proteins. Our results showed that the full-length E and 3a proteins were required for maximal SARS-CoV replication and virulence, whereas viroporin 8a had only a minor impact on these activities. A virus missing both the E and 3a proteins was not viable, whereas the presence of either protein with a functional PBM restored virus viability. E protein IC activity and the presence of its PBM were necessary for virulence in mice. In contrast, the presence or absence of the homologous motifs in protein 3a did not influence virus pathogenicity. Therefore, dominance of the IC and PBM of protein E over those of protein 3a was demonstrated in the induction of pathogenesis in mice.IMPORTANCE Collectively, these results demonstrate key roles for the ion channel and PBM domains in optimal virus replication and pathogenesis and suggest that the viral viroporins and PBMs are suitable targets for antiviral therapy and for mutation in attenuated SARS-CoV vaccines.
Insights
Severe acute respiratory syndrome coronavirus (SARS-CoV) E and 3a viroporins are crucial for virus replication and virulence. The E protein
Area of Science:
- Virology
- Molecular Biology
- Immunology
Background:
- Viroporins are viral proteins with ion channel (IC) activity essential for virus replication and pathogenesis.
- Coronaviruses (CoVs) encode multiple viroporins; SARS-CoV encodes three: 3a, E, and 8a.
- Proteins 3a and E possess PDZ-binding motifs (PBMs) that interact with cellular proteins, influencing host cell functions.
Purpose of the Study:
- To comparatively analyze the functional roles of ion channel (IC) and PDZ-binding motif (PBM) domains in SARS-CoV proteins 3a and E.
- To determine the impact of these viroporins and their motifs on SARS-CoV replication, virulence, and pathogenesis.
Main Methods:
- Comparative functional analysis of SARS-CoV viroporins (3a, E, 8a) and their motifs (IC, PBM).
- Assessment of virus replication and virulence in vitro and in vivo (mice).
- Generation of virus mutants lacking specific proteins or functional motifs.
Main Results:
- Full-length SARS-CoV E and 3a proteins are essential for maximal viral replication and virulence.
- A virus lacking both E and 3a proteins is non-viable; either protein with a functional PBM restores viability.
- E protein's IC activity and PBM are critical for mouse virulence, while 3a's motifs do not affect pathogenicity.
- The E protein's IC and PBM dominate over 3a's in inducing pathogenesis.
Conclusions:
- The ion channel and PBM domains of SARS-CoV viroporins play key roles in viral replication and pathogenesis.
- Viral viroporins and PBMs represent promising targets for antiviral therapies.
- Targeting these domains could lead to the development of attenuated SARS-CoV vaccines.
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