Abstract

COVID-19 is challenging healthcare preparedness, world economies, and livelihoods. The infection and death rates associated with this pandemic are strikingly variable in different countries. To elucidate this discrepancy, we analyzed 2431 early spread SARS-CoV-2 sequences from GISAID. We estimated continental-wise admixture proportions, assessed haplotype block estimation, and tested for the presence or absence of strains' recombination. Herein, we identified 1010 unique missense mutations and seven different SARS-CoV-2 clusters. In samples from Asia, a small haplotype block was identified, whereas samples from Europe and North America harbored large and different haplotype blocks with nonsynonymous variants. Variant frequency and linkage disequilibrium varied among continents, especially in North America. Recombination between different strains was only observed in North American and European sequences. In addition, we structurally modelled the two most common mutations, Spike_D614G and Nsp12_P314L, which suggested that these linked mutations may enhance viral entry and replication, respectively. Overall, we propose that genomic recombination between different strains may contribute to SARS-CoV-2 virulence and COVID-19 severity and may present additional challenges for current treatment regimens and countermeasures. Furthermore, our study provides a possible explanation for the substantial second wave of COVID-19 presented with higher infection and death rates in many countries.

Highlights

  • The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) outbreaks have grievously impacted the world in a short span of time

  • European (NSS test, P-value of 0.001) and North American (NSS and Pairwise Homoplasy Index (Phi), P-value of 0.007, 0.042 respectively) show evidence for the presence of recombination events, while African, Oceanic, South American, and Asian datasets show no recombination in early spread of SARS-CoV-2 in respective continents

  • The recombination events in European population were further confirmed with significant P-values by MaxChi2, Chimera, and 3Seq tools, while possible recombination events in North American populations were confirmed by MaxChi2 and 3Seq tools

Read more

Summary

Introduction

The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) outbreaks have grievously impacted the world in a short span of time. Coinfection with different SARS-CoV-2 strains increases the severity of COVID-19. We were the first to report the major role of D614G (23403A>G) mutation located at the S1-S2 proximal junction This mutation generates conformational changes in the protein structure rendering the furin cleavage site (664-RRAR-667) more flexible and enhancing viral entry [9]. Studies on understanding the genetic diversity and evolution of SARS-CoV-2 are emerging [11]. We extended our previous studies [9,14] by analyzing the population genetics aspects within genome sequences of SARS-CoV-2 to understand the contiguous spread of SARS-CoV-2, its rapid evolution, and the differential severity of COVID-19 among different continents. We modelled two major mutations and their possible effects on the stability of the encoded protein and thereby on SARS-CoV-2 virulence

Methods
Results
Discussion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call