key: cord-0914603-fk4rbps9
authors: Tsiftsoglou, Stefanos A.
title: SARS-CoV-2 associated Complement genetic variants possibly deregulate the activation of the Alternative pathway affecting the severity of infection()
date: 2021-03-26
journal: Mol Immunol
DOI: 10.1016/j.molimm.2021.03.021
sha: 2d09cf04f003ed93e6acdcb03b2748f3fc5f2aa8
doc_id: 914603
cord_uid: fk4rbps9

nan

Aspects of the pandemic COVID-19 pathology resemble clinical features traditionally associated with complementopathies. Some of these are associated with disease phenotypes characterised by the deregulated activation of the Alternative pathway resulting in complement C3 consumption and deprivation of the downstream activation processes.

Targeting complement activation in COVID-19 has been recently discussed, as a couple of studies have showed that the SARS-CoV-2 surface proteins N and S can activate the Lectin and Alternative pathways, respectively. The potential exploitation of the Alternative pathway via the amplification loop by SARS-CoV-2 can explain to a considerable extent the gradual diminishment of complement responses during the systemic establishment of the virus. This prompted me to explore further published advanced complement genotyping datasets from hospitalised COVID-19 patients in order to find clinical genetic evidence supporting this working hypothesis. My online database and literature searches identified 4 SNPs located within exons of the 3 complement genes C3, C4BPA and C5AR1 that encode for missense amino acid substitutions in the expressed proteins. In this correspondence I describe the potential biochemical implications that these genetic variants introduce in the regulation of complement and provide rational evidence proposing how the virus can exploit the activation of the Alternative pathway.

Keywords: SARS-CoV-2, Covid-19, Complement system, Alternative pathway, SNPs, Variants

Several studies attempting to dissect the molecular and cellular aspects of the SARS-CoV-2 virus pathophysiology have investigated the host immune responses and the roles of complement in viral sensing and the inflammation dynamics during infection (Yuki et al., 2020 )(Kaneko et al., 2020 (Wilk, 2020) (Yu et al., 2020 )(Java et al., 2020 . Aspects of the pandemic COVID-19 pathology resemble, from moderate to severe cases, clinical features traditionally associated with complementopathies (Marcos-Jiménez et al., 2021 )(Joseph et al., 2020 (Baines and Brodsky, 2017) . Some of these are associated with disease phenotypes characterised by the deregulated activation of the Alternative pathway resulting in complement C3 consumption and deprivation of the downstream activation processes (Fig. 1) J o u r n a l P r e -p r o o f (Łukawska et al., 2018) (Sim and Tsiftsoglou, 2004) (Roversi et al., 2011) . Therefore, there is a rationale for targeting complement in COVID-19 (Polycarpou et al., 2020) .

Targeting complement activation in COVID-19 has been recently discussed more extensively, as a couple of studies have showed that the SARS-CoV-2 surface proteins N (Wilk, 2020) and S (Yu et al., 2020) can activate the Lectin and Alternative pathways, respectively (Fig. 1) . The activation of the Alternative pathway by the spike glycoprotein S has been of particular interest as it promotes entry of the virus into cells and is a major antigenic target for B cell responses (Walls et al., 2020) . Furthermore, the potential A very recently published study aiming to associate genetic variation at the chromosome multigene cluster 3p21.31 and the ABO blood group with complement activation and COVID-19 severity, identified a variant (rs11385942) that predisposes to severe and is associated with enhanced complement activation, as manifested by circulating C5a and sC5-C9 and C5a only in the non-O blood group . Although, the particular variant is not directly mapped in any complement gene coding loci, it may be linked with enhanced complement activation indirectly at subsequent stages of the disease during systemic inflammation and tissue damage and/or organ failure (Bianco et al., 2021) .

The potential exploitation of the activation of the Alternative pathway via the by SARS-CoV-2 is an attractive working hypothesis that prompted me to explore further published advanced complement genotyping datasets from hospitalised COVID-19 patients in order to identify clinical genetic evidence supporting this notion (Ramlall et al., 2020) . In the Supplementary Table S2 of their study, Ramlall et al. had reported among all, 23 study-wide significant SNPs that lie within 60Kb of 12 complement genes in at least one of the reported analyses examined (Ramlall et al., 2020) . My online database search using the NCBI dbSNP database (Sherry et al., 2001) (https://www.ncbi.nlm.nih.gov/snp/) revealed that the majority of those SNPs, 19 (83%), are genomically located in introns or in upstream or downstream untranslated regions that may contain elements or harbour sites important for epigenetic regulation. The remaining 4 SNPs (17%), are located within exons of the 3 complement genes C3, C4BPA and C5AR1 and encode for missense amino acid substitutions in the expressed proteins (Table 1) . Given the nature of the protein-protein interactions among complement components and the influences that polymorphisms may contribute to the relevant protein complex structures, I investigated further in the NCBI ClinVar (Landrum et al., 2018) (https://www.ncbi.nlm.nih.gov/clinvar/) and PubMed J o u r n a l P r e -p r o o f (https://pubmed.ncbi.nlm.nih.gov/) databases for published evidence reporting altered properties of the polymorphic variants corresponding to the missense mutations of interest (Roversi et al., 2011) . In ClinVar I found some relevant clinical evidence only for the R102G and the P314L amino acid substitutions of C3, but none for the others (Table 1 ).

In terms of protein structure, the R80 amino acid residue is close to the N-terminal end of the C3 beta chain and located in the MG1 domain near the TED domain of the C3 protein (Janssen et al., 2006) . The three positively charged amino acids R72, R80 and K82 of the MG1 domain, along with the four negative amino acids D1007, E1008, E1010, E1013 of the TED domain, form the internal thioester bond that is critical for the reactivity of C3 with nucleophilic groups (Law and Dodds, 1997) . The rs2230199 introduced R102G (R80G) polymorphism was first reported in 1967 and has been described in the literature to distinguish the C3S (Slow, R80) and the C3F (Fast, G80) variants (Wieme and Demeulenaere, 1967) (Alper and Propp, 1968 ) (Botto et al., 1990) . The C3F variant, containing neutral glycine instead of the positively charged arginine has potentially reduced properties with regards to the stability of its thioester and its capacity to react with potential complement activator surfaces. It also exhibits a weaker ability to bind to complement factor H (FH) which is the major circulating cofactor for the complement factor I (FI) mediated downregulation of the C3bBb AP convertase Tsiftsoglou, 2004)(Janssen et al., 2006 ) (Torreira et al., 2009) (Roversi et al., 2011) . The common C3S/F comprises approximately 98% of all C3 phenotypes (Łukawska et al., 2018) . The frequency of F allele varies among different populations, and it is the highest in Caucasian (18%) and the lowest in Asian (1%) (Bazyar et al., 2012) . Carriers of C3F allele have been reported to be at higher risk for the development of age-related macular degeneration (AMD) (Yates et al., 2007) and various types of glomerulonephritis namely membranoproliferative glomerulonephritis type II (MPGN II) that is presently known as dense deposit disease (DDD) (Abrera-Abeleda et al., 2011), IgA nephropathy (IgAN) (Rambausek et al., 1987) and systemic vasculitis (SV) (Persson et al., 2013) .

The second C3 point mutation corresponding to rs1047286 in the exon 9 of the beta chain, the P314L (P292L) has also been historically characterised as HAV4-1+/- (Table 1) (Koch and Behrendt, 1986) (Botto et al., 1990) . The P292 (HAV 4-1-) residue is located in the MG3 domain of C3 that contains the major binding site for the activated complement factor B (Bb). Published structural studies have showed that the polymorphic variant HAV4-1+ (L292) exhibits stronger ability to bind to Bb (Torreira et al., 2009 ) (Forneris et al., 2010 . This practically suggests that the HAV4-1+ (L292) gain-of-function variant may form a hyperactive C3bBb AP convertase that may be also more resilient to inactivation by complement factor I (FI) in the presence of a cofactor such as complement factor H (FH) or C4BP (Blom et al., 2003) . It has been estimated that 98% of C3S allele carriers is HAV4-1-J o u r n a l P r e -p r o o f and only 2% is HAV4-1+; in contrast, 90% carriers of the C3F allele is HAV4-1+ and 10% is HAV4-1- (Botto et al., 1990) . For both C3 SNPs discussed above, the hypothetical impaired downregulation of any formed C3bBb AP convertase, can practically result in lower generation of iC3b, C3dg and C3d which are major opsonins of the complement system ( Fig.   1 ) (Carroll, 2004) . Impaired opsonisation during infection can contribute to poor immune synergies of complement with the various professional immune surveillance cell populations that include phagocytes, neutrophils and B cells (Carroll, 2004) . Thus, impaired downregulation of any C3bBb AP convertase formed during the Alternative pathway of complement activation, can enable the virus to exploit the alternative activation pathway amplification loop introducing C3 consumption (Fig. 1) . Based on the findings above, in theory, individuals carrying combinations of C3 alleles harbouring the C3F and/or the HAV4-1+ polymorphisms must be considerably more susceptible to SARS-CoV-2 infection based on the structural interactions of C3 with various antigen surfaces and the Bb, FH, FI and C4BP complement components.

The R240 (R192) residue that corresponds to the rs45574833 SNP is located in the 4 th N-terminal CCP (Sushi) domain of the C4BP alpha chain (C4BP) ( Table 1 ). C4BP can act as a cofactor for the inactivation of C3b (Blom et al., 2003) and C4b (Blom et al., 1999) by complement FI (Sim and Tsiftsoglou, 2004) . Refined mutagenesis studies in C4BP had mapped the C3b binding sites to CCP1-4 (Blom et al., 2003) and the C4b binding sites to CCP1-3 (Blom et al., 1999) . Given the ionic nature of these interactions and the position of R240, the R240H or R240P substitution may reduce the downregulation of the C3bBb AP convertase by FI in the presence of C4BP, especially in cases where the interaction of C3 with FH is weakened as discussed earlier for the R80G polymorphism. The inactivation of C4b by FI should not be directly affected (Blom et al., 1999) . Overall, in theory the allelic coexistence of the missense mutations encoding for the C3 R80, P292 and C4BP R192 polymorphisms, can create synergistic thresholds of enhanced susceptibility in the deregulation of the activation Alternative pathway by SARS-CoV-2.

Last, but not least is the rs4467185 SNP that encodes for a missense mutation at the extracellular 2 nd N-terminal end residue of the C5aR1 receptor. C5a is regarded as the most potent complement anaphylatoxin with a wide effect of pleiotropic effects (Java et al., 2020) (Carroll, 2004) . Mutagenesis studies had showed that the N-terminus accounts for at least 45% of the total energy required for the binding of C5a. When the region 2-30 containing aspartic acids was deleted, the C5a binding avidity diminished by 45,000-fold (DeMartino et al., 1994) . Overall, I consider these findings important, because at the protein level they may provide a hypothetical, but rational, frame proposing the exploitation of the activation of the Alternative pathway by SARS-CoV-2. In the context of the COVID-19 molecular pathology, this can gradually lead to complement deregulation, poor opsonisation, weakening of the immune clearance mechanisms and sustained inflammation resulting in various host tissue damage responses in severe cases of infection.

SAT conceived the study, searched the relevant databases and literature and wrote the manuscript.

None J o u r n a l P r e -p r o o f 

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