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Hemadsorption Expressed by Cloned H Genes from Subacute Sclerosing Panencephalitis (SSPE) Viruses and Their Possible Progenitor Measles Viruses Isolated in Osaka, Japan
Author(s) -
Furukawa Kyoko,
Ayata Minoru,
Kimura Masatsugu,
Seto Toshiyuki,
Matsunaga Isamu,
Murata Ryosuke,
Yamano Tsunekazu,
Ogura Hisashi
Publication year - 2001
Publication title -
microbiology and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.664
H-Index - 70
eISSN - 1348-0421
pISSN - 0385-5600
DOI - 10.1111/j.1348-0421.2001.tb01275.x
Subject(s) - subacute sclerosing panencephalitis , virology , biology , measles virus , vero cell , morbillivirus , gene , virus , measles , genetics , vaccination
Most subacute sclerosing panencephalitis (SSPE) viruses, including our Osaka‐1, −2, and −3 strains isolated in Osaka, have shown negative hemadsorption (HAD) by African green monkey red blood cells. This property has been thought to be characteristic of SSPE virus as compared to the positive reaction of the standard Edmonston strain of measles virus (MV). However, this assumption has become quite obscure because MV mutates frequently at the genetic level during its multiplication and also because recent field strains isolated by lymphoblastoid cell lines have shown negative HAD. To investigate the above issue, the nucleotide sequences of the hemagglutinin (H) genes from SSPE virus Osaka‐1, −2, or −3 strains were compared to those of various MV field strains isolated in Osaka by Vero cells. The H gene sequences of three SSPE strains were relatively conserved without such biased hypermutation as had been observed in the matrix (M) gene of three SSPE strains. However, this analysis of the H gene sequence of the SSPE viruses enabled us to deduce possible progenitor MVs, which are in agreement with the deduction from the M gene analysis we reported previously. The HAD of Vero cells transfected with the cloned H cDNAs from the SSPE strains and their progenitors suggested that negative HAD of the SSPE viruses has been maintained as one of original properties of the progenitor MVs rather than having been acquired as an altered one during long‐term persistent infection in the brains of patients with SSPE.