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. 2014 Oct;88(19):11411–11429. doi: 10.1128/JVI.00876-14

TABLE 3.

Summary of phenotypes with mutations in the SAM binding site in hMPV and VSV L proteins

Virus family Mutant Methylation Attenuation in cell culturea Attenuation in animal modelb Immunogenicityc
Paramyxoviridae rhMPV wild type WTd WT Virulent WT
rhMPV G1696A Defective in 2′-O Attenuated Highly attenuated WT
rhMPV G1700A Defective in 2′-O Attenuated Attenuated WT
rhMPV D1755A Defective in 2′-O Attenuated Highly attenuated WT
Rhabdoviridae rVSV wild type WT WT Virulent WT
rVSV G1670A Lacked G-N-7 but not 2′-O Attenuated Low virulence WT
rVSV G1674A Sensitive to SAM concn Not attenuated Virulent NDe
rVSV D1735A Diminished G-N-7 and 2′-O Attenuated ND ND
a

Attenuation was judged by plaque size, infectivity, and growth curve. Data for VSV are from reference 27.

b

For hMPV, attenuation was judged by viral replication and pathology in nasal turbinate and lung tissue in cotton rats; for VSV, attenuation was judged by clinical symptoms, body weight loss, viral replication, and pathology in lung and brain tissues in mice. Data for VSV are from reference 54.

c

Immunogenicity was judged by the antibody level and protection rate after challenge with virulent virus.

d

WT, wild-type level.

e

ND, not done.