ABSTRACT
Oral poliovirus vaccine (OPV) developed by A. Sabin has been effectively used to control poliomyelitis in Brazil, and the last case with the isolation of a wild poliovirus strain occourred in March 1989. Although the vaccine controlled the circulation ...
Subject(s)
Humans , Facial Paralysis/genetics , Facial Paralysis/virology , Myelitis, Transverse/genetics , Myelitis, Transverse/virology , Poliomyelitis/prevention & control , Poliovirus Vaccine, Oral/adverse effects , Poliovirus/genetics , Polyradiculoneuropathy/genetics , Polyradiculoneuropathy/virology , Brazil , Polymerase Chain ReactionABSTRACT
Thirty eigth paralysis classified as Guillain-Barre syndrome (GBS) in Brazil were analysed. In all these cases Sabin-related poliovirus vaccine strains were isolated. In most of the cases the last vaccine dose was given months or years before the onset of GBS, suggesting a persistent infection or transmission of the Sabin-related strains to the patients...
Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Poliovirus/isolation & purification , Polyradiculoneuropathy/epidemiology , Poliovirus Vaccine, Oral/adverse effects , Polyradiculoneuropathy/complications , Time FactorsABSTRACT
This study reports a type 1 poliovirus strain isolated in Brazil from a case classified as vaccine-associated paralytic poliomyelitis (VAPP). After serotyping of the viral isolate with hyperimmune equine sera, PCR and molecular hybridization techniques characterized the strain as P1/Sabin-derived. The isolate was partially sequenced to identify mutations at nucleotides 480, 525 and 6203, which are important for reversion of the P1/Sabin strain to neurovirulence. In a recent study, a P1/ Sabin-derived strain isolated from the central nervous system of a VAPP case did not mutate at these positions, but maintained 480-G and 525-U (and 6203-C), suggesting that these mutations are not essential for the occurrence of disease (Georgescu et al., (1994), Journal of Virology, 68: 8089-8101). Although the Brazilian strain also maintained 480-G and 525-U (and 6203-C) and was isolated from the stool, the possibility that this isolate invaded the central nervous system after replicating in the gut, causing the paralysis, cannot be ruled out. This is the first report of a type I VAPP case in Brazil, although some cases caused by type 2 and type 3 strains have been described.
Subject(s)
Humans , Child, Preschool , Poliomyelitis/virology , Poliovirus Vaccine, Oral/adverse effects , Brazil , Mutation , Polymerase Chain Reaction , Poliovirus Vaccine, Oral/geneticsABSTRACT
Twenty strains of P2/Sabin-related polioviruses isolated in Brazil were analyzed; ten from persistent paralytic poliomyelitis cases, three from suspected polio cases with transient paralysis, and seven from healthy contacts. The serotypes of the viral isolates were identified by the neutralization test with hyperimmune equine sera. The relationship of the isolates to the P2/Sabin strain was demonstrated by molecular hydridization and polymerase chain reaction (PCR). Partial sequencing demonstrated mutations at nucleotide 481 in the 5' noncoding region and at amino acid 143 of the capsid protein VP1 in most of these isolates from accine-associated cases in Brazil. These data support previous studies on the importance of mutations at these attenuated determinants in the establishment of the disease. However, the existence of isolates without mutations at these positions suggests that they are not essential. The results also strengthen the possibility of the participation of a mutation at nucleotide 398 in the establishment of the disease, and suggest that a mutation at nucleotide 491 or 500 may also be involved in this process. The isolates from healthy contacts presented the same mutations as the isolates from vaccine-associated cases with they were in contact. This strengthens the observation that, although mutations in the genome of the P2/Sabin strain are important for the establishment of the disease, host factors are also involved
Subject(s)
Humans , Infant , Child, Preschool , Child , Mutation , Poliomyelitis/virology , Brazil , Feces/virology , Genome, Viral , Polymerase Chain Reaction , RNA, Viral , Sequence Analysis, RNAABSTRACT
Eight strains of P3/Sabin-related polioviruses were analyzed; four from persistent paralytic poliomyelitis cases classified as vaccine associated, one from a transient paralysis case classified as transverse myelitis, one from a transient paralysis case classified as Guillain-Barr'e syndrome, one from a transient facial paralysis case, and one from a healthy vaccine. The serotypes of the viral isolates were identified by the neutralization test with hyperimmune equine sera and the relationship of the isolates with the P3/Sabin strain was demonstrated by molecular hybridization of the viral RNA of the isolates with a P3/Sabin-specific probe. The P3/Sabin relationship was confirmed by PCR, using a pair of specific primers for P3/Sabin-related isolates. The available data indicate that a U C mutation at nucleotide 472 in the 5' noncoding region of the genome of the type 3 Sabin strain increases the neurovirulence of this strain and this mutation was observed in all type 3 isolates from vaccine-associated cases. These eight P3/Sabin-related isolates were partially sequenced in the 5" noncoding region and seven presented a U C mutation at nucleotide 472, except the isolate from a transient paralysis case classfied as transverse myelitis, that maintained a U at nucleotide 472. Although this virus maintaining U at nucleotide 472 may not be the etiological agent of the disease, the possibility that virus was the causative agent of the disease could not be ruled out