Coronavirus pathogenesis and the emerging pathogen severe acute respiratory syndrome coronavirus

Abstract

Coronaviruses are a family of enveloped, single-stranded, positive-strand RNA viruses classified within the Nidovirales order. This coronavirus family consists of pathogens of many animal species and of humans, including the recently isolated severe acute respiratory syndrome coronavirus (SARS-CoV). This review is divided into two main parts; the first concerns the animal coronaviruses and their pathogenesis, with an emphasis on the functions of individual viral genes, and the second discusses the newly described human emerging pathogen, SARS-CoV. The coronavirus part covers (i) a description of a group of coronaviruses and the diseases they cause, including the prototype coronavirus, murine hepatitis virus, which is one of the recognized animal models for multiple sclerosis, as well as viruses of veterinary importance that infect the pig, chicken, and cat and a summary of the human viruses; (ii) a short summary of the replication cycle of coronaviruses in cell culture; (iii) the development and application of reverse genetics systems; and (iv) the roles of individual coronavirus proteins in replication and pathogenesis. The SARS-CoV part covers the pathogenesis of SARS, the developing animal models for infection, and the progress in vaccine development and antiviral therapies. The data gathered on the animal coronaviruses continue to be helpful in understanding SARS-CoV.

Figures

FIG. 1.

Coronavirus virion. (A) Electron micrograph of MHV particles. (B) Schematic of virion. Viral particles contain an internal helical RNA-protein nucleocapsid surrounded by an envelope containing viral glycoproteins. Nucleocapsid (N) protein is a phosphoprotein that is complexed with genome RNA to form the nucleocapsid. Spike glycoprotein (S) forms the large glycosylated peplomers that are characteristic of coronaviruses. M, the transmembrane protein, is highly hydrophobic and spans the membrane three times. E, a membrane-spanning protein, is a minor component of the membrane. Some group II viruses express another glycoprotein, hemagglutinin-esterase (HE), which forms smaller spikes on virions.

FIG. 2.

MHV genome organization and replicase proteins. The genome consists of seven genes. The first 22 kb contains the replicase gene, which is organized into two overlapping open reading frames, ORFs 1a and 1b. These ORFs are translated into the ∼400-kDa pp1a and the ∼800-kDa pp1ab replicase polyproteins. ORF 1b is translated via a translational frameshift encoded at the end of ORF 1a. The protein domains of the replicase polyprotein are indicated by nonstructural protein numbers (nsp1 to 16) and by confirmed or predicted functions: PLP1 and PLP2, papain-like proteases; X, domain encoding predicted adenosine diphosphate-ribose 1"-phosphatase activity (ADRP); 3CLpro, 3C-like protease; RdRp, putative RNA-dependent RNA polymerase; Hel, helicase; ExoN, putative exonuclease; XendoU, putative poly(U)-specific endoribonuclease; 2′-O-MT, methyltransferase. Genes 2 to 7 are translated from subgenomic mRNA species (not shown). Relative locations of coding regions for the structural proteins HE, S, E, M, N, and I are shown, as are the coding region for the group-specific ORF 2a (encoding a predicted cyclic phosphodiesterase), 4, and 5a proteins.

FIG. 3.

Model of coronavirus replication. After receptor interaction and fusion of viral and plasma membranes, virus-specific RNA and proteins are synthesized, probably entirely in the cytoplasm. Expression of coronaviruses starts with translation of two polyproteins, pp1a and pp1ab, which undergo cotranslational proteolytic processing into the proteins that form the replicase complex. This complex is used to transcribe a 3′-coterminal set of nested subgenomic mRNAs, as well as genomic RNA, that have a common 5′ “leader” sequence derived from the 5′ end of the genome. Proteins are translated from the 5′ end of each mRNA. New virions are assembled by budding into intracellular membranes and released through vesicles by the cell secretory mechanisms. RER, rough endoplasmic reticulum; ER/GIC, endoplasmic reticulum/Golgi intermediate compartment.

FIG. 4.

Schematic of coronavirus spike proteins. Shown are spike proteins representative of those of all group I to III coronaviruses and of SARS-CoV. The coronavirus spike protein is synthesized as a precursor, cotranslationally glycosylated, and, in some cases, cleaved in the approximate middle into S1 and S2 subunits at a site with dibasic amino acids (BBXBB). S1 forms the external domain containing the receptor binding domain (RBD) at its 5′ end, followed by, in the case of MHV, a hypervariable domain (HVR). A short signal sequence in cleaved from the 5′ end of the mature protein. S2 is the transmembrane subunit containing two heptad repeats (HR1 and HR2) and the transmembrane (TM) domain.

FIG. 5.

The molecular determinants of MHV pathogenesis. Chimeric A59/JHM recombinant viruses were selected by targeted recombination. These viruses were used to infect mice, and the abilities to infect the CNS and induce encephalitis and to infect the liver and cause hepatitis were assessed. The pathogenic phenotypes of the viruses are shown schematically and are discussed in the text.