Human herpesvirus 6 infection in febrile infants ninety days of age and younger

被引:12
作者
Byington, CL
Zerr, DM
Taggart, EW
Nguy, L
Hillyard, DR
Carroll, KC
Corey, L
机构
[1] Univ Utah, Dept Pediat, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USA
[3] Reg Unit Pathologists, Salt Lake City, UT 84112 USA
[4] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[5] Univ Washington, Dept Med, Seattle, WA 98195 USA
[6] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
关键词
human herpesvirus 6; fever; infant;
D O I
10.1097/00006454-200211000-00004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The importance of human herpesvirus 6 (HVV-6) as a pathogen in febrile infants less than or equal to90 days of age is unknown. Objective. To determine whether febrile infants 90 days of age and younger evaluated for sepsis have evidence of HHV-6 DNA in plasma or cerebrospinal fluid (CSF). Methods. Febrile infants :590 days of age were tested for HHV-6 DNA using a real time quantitative fluorescent probe polymerase chain reaction assay. Results. Eighty samples from 47 infants were tested for HHV-6 DNA, 5 of 47 infants (10.6%) had EMV-6 DNA in plasma. In 2 of the 5 infants with HHV-6 DNA in plasma, HHV-6 DNA was also detected in the CSF. Both infants with evidence of HHV-6 DNA in plasma and CSF had HHV-6 Variant A infection. The quantity of HHV-6 DNA detected ranged from 70 to 169 000 DNA copies/ml. One infant with HHV-6 variant B infection had concomitant Escherichia coli bacteremia and urinary tract infection. Conclusions. Approximately 10% of febrile infants less than or equal to90 days of age evaluated for sepsis had evidence of HHV-6 infection. HHV-6 Variant A and B infections were seen in these young infants. HHV-6 DNA was found in infants with and without another explanation for fever. Quantification of viral DNA may be important in determining the relevance of HHV-6 DNA in clinical specimens.
引用
收藏
页码:996 / 999
页数:4
相关论文
共 37 条
[1]   Congenital infections with human herpesvirus 6 [J].
Adams, O ;
Krempe, C ;
Kögler, G ;
Wernet, P ;
Scheid, A .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (02) :544-546
[2]   The utility of plasma polymerase chain reaction for human herpes virus-6 among pediatric bone marrow transplant recipients: results of a pilot study [J].
Allen, UD ;
Tellier, R ;
Doyle, J ;
Petric, M ;
Wasfy, S ;
Kumar, P ;
Calderwood, S ;
Freedman, M ;
Saunders, F .
BONE MARROW TRANSPLANTATION, 2001, 28 (05) :473-477
[3]   Sepsis evaluations in hospitalized infants with bronchiolitis [J].
Antonow, JA ;
Hansen, K ;
McKinstry, CA ;
Byington, CL .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1998, 17 (03) :231-236
[4]   Epidemiology of human herpesvirus 6 (HHV-6) infection in pregnant and nonpregnant women [J].
Baillargeon, J ;
Piper, J ;
Leach, CT .
JOURNAL OF CLINICAL VIROLOGY, 2000, 16 (03) :149-157
[5]   A polymerase chain reaction-based epidemiologic investigation of the incidence of nonpolio enteroviral infections in febrile and afebrile infants 90 days and younger [J].
Byington, CL ;
Taggart, EW ;
Carroll, KC ;
Hillyard, DR .
PEDIATRICS, 1999, 103 (03) :art. no.-e27
[6]  
Byington CL, 2002, PEDIATR RES, V51, p279A
[7]   NEUROINVASION AND PERSISTENCE OF HUMAN HERPESVIRUS-6 IN CHILDREN [J].
CASERTA, MT ;
HALL, CB ;
SCHNABEL, K ;
MCINTYRE, K ;
LONG, C ;
COSTANZO, M ;
DEWHURST, S ;
INSEL, R ;
EPSTEIN, LG .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (06) :1586-1589
[8]   Early diagnosis of primary human herpesvirus 6 infection in childhood: Serology, polymerase chain reaction, and virus load [J].
Chin, SS ;
Cheung, CY ;
Tse, CYC ;
Peiris, M .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (05) :1250-1256
[9]   Quantification of human herpesvirus 6 in immunocompetent persons and post-mortem tissues from AIDS patients by PCR [J].
Clark, DA ;
AitKhaled, M ;
Wheeler, AC ;
Kidd, IM ;
McLaughlin, JE ;
Johnson, MA ;
Griffiths, PD ;
Emery, VC .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :2271-2275
[10]  
DUNNE WM, 1992, LANCET, V340, P121