Contreras J F, Menchaca G E, Padilla-Noriega L, Tamez R S, Greenberg H B, López S, Arias C F
Departamento de Microbiología e Inmunología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, Mexico.
Clin Diagn Lab Immunol. 1995 Jul;2(4):506-8. doi: 10.1128/cdli.2.4.506-508.1995.
We have used serotype-specific VP4 and VP7 neutralizing monoclonal antibodies (Nt-MAbs), as well as subgroup (SG)-specific MAbs, to characterize by enzyme immunoassay rotavirus strains isolated from diarrheic infants in the city of Monterrey, Mexico, from July 1993 to March 1994. Of a total of 465 children studied, 140 were rotavirus positive, including 3 patients infected with non-group A rotaviruses. The SG and VP7 (G) serotype specificities could be determined for 118 (84%) of the 140 rotavirus-positive stool specimens; 4 rotavirus strains were serotype G1 and SGII; 1 strain was serotype G2 and SGI+II; 112 strains were serotype G3 and SGII; 1 strain was serotype G3 and SGI; and none of the strains was serotype G4. Fifty-eight specimens, representing the 13 different group A rotavirus electropherotypes detected, were chosen for VP4 (P) serotyping. Of these, 48 (83%) strains reacted with the P1A serotype-specific Nt-MAb 1A10. None of the strains reacted with the serotype P2-specific Nt-MAbs tested. Not all viruses that reacted with Nt-MAb 1A10 were recognized by Nt-MAbs 2A3 and 2G1, which also recognize P1A strains, indicating heterogeneity of neutralization epitopes among serotype P1A human rotaviruses. This heterogeneity could be relevant for the specificity of the VP4-mediated neutralizing antibody immune response and indicates the need for antigenic characterization, in addition to genomic typing, of the VP4 proteins of circulating human rotavirus field strains.
我们使用血清型特异性的VP4和VP7中和单克隆抗体(Nt-MAbs)以及亚组(SG)特异性单克隆抗体,通过酶免疫测定法对1993年7月至1994年3月从墨西哥蒙特雷市腹泻婴儿中分离出的轮状病毒株进行特征分析。在总共研究的465名儿童中,140名轮状病毒呈阳性,其中3名患者感染了非A组轮状病毒。对于140份轮状病毒阳性粪便标本中的118份(84%),可以确定其SG和VP7(G)血清型特异性;4株轮状病毒株为G1血清型和SGII亚组;1株为G2血清型和SGI+II亚组;112株为G3血清型和SGII亚组;1株为G3血清型和SGI亚组;没有一株为G4血清型。选择了代表检测到的13种不同A组轮状病毒电泳型的58份标本进行VP4(P)血清分型。其中,48株(83%)与P1A血清型特异性Nt-MAb 1A10发生反应。所检测的菌株均未与P2血清型特异性Nt-MAbs发生反应。并非所有与Nt-MAb 1A10反应的病毒都能被同样识别P1A菌株的Nt-MAbs 2A3和2G1识别,这表明P1A血清型人轮状病毒中中和表位存在异质性。这种异质性可能与VP4介导的中和抗体免疫反应的特异性相关,并表明除了对循环中的人轮状病毒野毒株的VP4蛋白进行基因分型外,还需要进行抗原特征分析。