HIGH PREVALENCE OF ROTAVIRUS INFECTION AMONG NEONATES BORN AT HOSPITALS IN DELHI, INDIA - PREDISPOSITION OF NEWBORNS FOR INFECTION WITH UNUSUAL ROTAVIRUS

被引:52
作者
CICIRELLO, HG
DAS, BK
GUPTA, A
BHAN, MK
GENTSCH, JR
KUMAR, R
GLASS, RI
机构
[1] ALL INDIA INST MED SCI, DEPT PEDIAT, NEW DELHI, INDIA
[2] ALL INDIA INST MED SCI, DEPT MICROBIOL, NEW DELHI 110029, INDIA
[3] CTR DIS CONTROL & PREVENT, NATL CTR INFECT DIS, DIV VIRAL & RICKETTSIAL DIS, ATLANTA, GA USA
关键词
ROTAVIRUS; NEONATAL ROTAVIRUS; ROTAVIRUS VACCINE; EPIDEMIOLOGY;
D O I
10.1097/00006454-199408000-00008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although rotavirus is the most common cause of diarrhea in children older than 3 months of age, neonatal infections, which are asymptomatic, have rarely been surveyed and have been identified in only a few discrete nosocomial outbreaks. After such a nosocomial outbreak of rotavirus infection among newborns at a hospital in Delhi, we screened infants born at five other nurseries in the immediate area to assess the prevalence of neonatal infections and to determine whether the unique neonatal rotavirus strain, 116E, previously identified in Delhi, was present in other settings. Infection was documented in 43 to 78% of hospitalized infants between 4 and 6 days of life born at five of the six hospitals. Infection with strains related to 116E were the most common, but other unusual strains and no strains common in the community were detected. In addition a shift in genotype was observed among specimens collected from two of these hospitals during a 2-year period. Our observation that neonatal rotavirus infections are more common than recognized previously would encourage the administration of rotavirus vaccines during the newborn period and suggests that the low efficacy of vaccines observed during trials in developing countries may be caused by early natural exposure of infants before immunization. The extraordinary predisposition of neonates for unusual rotavirus strains not commonly found in the community should encourage others to screen neonates for this infection, characterize the strains more fully and attempt to understand at a molecular level the unique relationship between the infecting strain type and the age of the host.
引用
收藏
页码:720 / 724
页数:5
相关论文
共 42 条
[1]   CULTIVATION AND CHARACTERIZATION OF ROTAVIRUS STRAINS INFECTING NEWBORN BABIES IN MELBOURNE, AUSTRALIA, FROM 1975 TO 1979 [J].
ALBERT, MJ ;
UNICOMB, LE ;
BARNES, GL ;
BISHOP, RF .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (09) :1635-1640
[2]   ROTAVIRUS DIARRHEA IN BANGLADESHI CHILDREN - CORRELATION OF DISEASE SEVERITY WITH SEROTYPES [J].
BERN, C ;
UNICOMB, L ;
GENTSCH, JR ;
BANUL, N ;
YUNUS, M ;
SACK, RB ;
GLASS, RI .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (12) :3234-3238
[3]   PROTECTION CONFERRED BY NEONATAL ROTAVIRUS INFECTION AGAINST SUBSEQUENT ROTAVIRUS DIARRHEA [J].
BHAN, MK ;
LEW, JF ;
SAZAWAL, S ;
DAS, BK ;
GENTSCH, JR ;
GLASS, RI .
JOURNAL OF INFECTIOUS DISEASES, 1993, 168 (02) :282-287
[4]   CLINICAL IMMUNITY AFTER NEONATAL ROTAVIRUS INFECTION - A PROSPECTIVE LONGITUDINAL-STUDY IN YOUNG-CHILDREN [J].
BISHOP, RF ;
BARNES, GL ;
CIPRIANI, E ;
LUND, JS .
NEW ENGLAND JOURNAL OF MEDICINE, 1983, 309 (02) :72-76
[5]   ROTAVIRUS CARRIAGE, ASYMPTOMATIC INFECTION, AND DISEASE IN THE 1ST 2 YEARS OF LIFE .2. SEROLOGICAL RESPONSE [J].
CHAMPSAUR, H ;
HENRYAMAR, M ;
GOLDSZMIDT, D ;
PREVOT, J ;
BOURJOUANE, M ;
QUESTIAUX, E ;
BACH, C .
JOURNAL OF INFECTIOUS DISEASES, 1984, 149 (05) :675-682
[6]  
CHRYSTIE IL, 1975, LANCET, V2, P79
[7]  
CHRYSTIE IL, 1983, LANCET, V2, P1028
[8]  
COULSON BS, 1993, J CLIN MICROBIOL, V31, P1
[9]   CHARACTERIZATION OF THE G-SEROTYPE AND GENOGROUP OF NEW-DELHI NEWBORN ROTAVIRUS STRAIN-116E [J].
DAS, BK ;
GENTSCH, JR ;
HOSHINO, Y ;
ISHIDA, SI ;
NAKAGOMI, O ;
BHAN, MK ;
KUMAR, R ;
GLASS, RI .
VIROLOGY, 1993, 197 (01) :99-107
[10]   CHARACTERIZATION OF ROTAVIRUS STRAINS FROM NEWBORNS IN NEW-DELHI, INDIA [J].
DAS, BK ;
GENTSCH, JR ;
CICIRELLO, HG ;
WOODS, PA ;
GUPTA, A ;
RAMACHANDRAN, M ;
KUMAR, R ;
BHAN, MK ;
GLASS, RI .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (07) :1820-1822