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. 2015:1221:1-10.
doi: 10.1007/978-1-4939-1571-2_1.

Classification and evolution of human rhinoviruses

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Classification and evolution of human rhinoviruses

Ann C Palmenberg et al. Methods Mol Biol. 2015.

Abstract

The historical classification of human rhinoviruses (RV) by serotyping has been replaced by a logical system of comparative sequencing. Given that strains must diverge within their capsid sequenced by a reasonable degree (>12-13 % pairwise base identities) before becoming immunologically distinct, the new nomenclature system makes allowances for the addition of new, future types, without compromising historical designations. Currently, three species, the RV-A, RV-B, and RV-C, are recognized. Of these, the RV-C, discovered in 2006, are the most unusual in terms of capsid structure, receptor use, and association with severe disease in children.

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Figures

Figure 1
Figure 1
Genome map of a typical RV shows the protein names and their involvement is capsid formation or replication processes.
Figure 2
Figure 2
Circle phylogram of relationships for currently recognized genotypes (8) of RV-A, RV-B and RV-C. The tree was calculated with neighbor-joining methods from aligned, VP1 RNA sequences, and rooted with data from four enteroviruses (EV) of the EV-A, EV-B and EV-C species, similar to ref (10). The Major (“M”, ICAM-1) and minor (“m”, LDLR) receptor groups are indicated if determined experimentally. The RV-C receptor is unknown. Bootstrap values (percent of 200 replicates) are indicated at key nodes.
Figure 3
Figure 3
Recombinant origins for many RV-A&B were uncovered by full genome sequencing (10). Parents (solid boxes) or progeny (2-color boxes) are founders of many extant clades. This illustration is reproduced, with minor variation, from “Field’s Virology” (2013), Ch 18, “Rhinoviruses”, Wolters Kluwer, publishers.

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