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1.
J Infect Dis ; 164(4): 673-8, 1991 Oct.
Article in English | MEDLINE | ID: mdl-1894931

ABSTRACT

The relative importance of astrovirus and adenoviruses as etiologic agents of diarrhea among children in day care was examined. Stool specimens from this prospective study were screened for both astrovirus and adenovirus hexon with two new indirect double-antibody assays and for enteric adenoviruses with an EIA specific for serotypes 40 and 41. Astrovirus was detected in a significantly greater percentage of children with diarrhea (4%, 21/524) than of those without (less than 1%, 1/138) (P less than .05); however, no difference between such such children with adenovirus infections was found (8%, 43/565, and 8%, 10/129, respectively). Overall, 30% (13/43) of all adenovirus hexon-positive specimens were enteric serotypes, and by extrapolation, enteric adenoviruses were identified in an equal percentage of children (2%) with and without diarrhea. This study documents the presence of astrovirus and enteric adenoviruses among children in day care in the United States, associates astrovirus with diarrhea in this setting, and suggests that viral agents may be the most common enteric pathogens among children with diarrhea in day care.


Subject(s)
Adenovirus Infections, Human/microbiology , Adenoviruses, Human/isolation & purification , Capsid Proteins , Child Day Care Centers , Diarrhea/microbiology , Mamastrovirus/isolation & purification , Virus Diseases/microbiology , Adenovirus Infections, Human/epidemiology , Capsid/analysis , Child, Preschool , Diarrhea/epidemiology , Enzyme-Linked Immunosorbent Assay , Feces/microbiology , Humans , Immunoenzyme Techniques , Infant , Infant, Newborn , Longitudinal Studies , Prospective Studies , Virus Diseases/epidemiology
2.
Biologicals ; 18(4): 271-80, 1990 Oct.
Article in English | MEDLINE | ID: mdl-2126734

ABSTRACT

The objective of this study was to apply the pertinent findings from gamma inactivation of virus infectivity to the production of high quality diagnostic reagents. A Gammacell 220 (Atomic Energy of Canada, Ltd., Ottawa, Canada) was used to subject 38 viruses grown in either susceptible tissue cultures or embryonated chicken eggs to various doses of gamma radiation from a cobalt-60 source. The radiation required to reduce viral infectivity was 0.42 to 3.7 megarads (Mrad). The effect of gamma treatment on the antigenic reactivity of reagents for the complement fixation (CF), hemagglutination (HA) and neuraminadase assays was determined. Influenza antigens inactivated with 1.7 Mrad displayed comparable potency, sensitivity, specificity and stability to those inactivated by standard procedures with beta-propiolactone (BPL). Significant inactivation of influenza N1 and B neuraminidase occurred with greater than 2.4 Mrad radiation at temperatures above 4 degrees C. All 38 viruses were inactivated, and CF or HA antigens were prepared successfully. Antigenic potency remained stable with all antigens for 3 years and with 83% after 5 years storage. Influenza HA antigens evaluated after 9 years of storage demonstrated 86% stability. Gamma radiation is safer than chemical inactivation procedures and is reliable and effective replacement for BPL in preparing diagnostic reagents.


Subject(s)
Biological Products/radiation effects , Indicators and Reagents/radiation effects , Virus Diseases/diagnosis , Animals , Antigens, Viral/radiation effects , Biological Products/antagonists & inhibitors , Chick Embryo , Drug Stability , Gamma Rays , Humans , Virus Cultivation , Viruses/radiation effects
3.
J Clin Microbiol ; 24(4): 527-31, 1986 Oct.
Article in English | MEDLINE | ID: mdl-3021808

ABSTRACT

Suspensions of herpes simplex virus types 1 and 2, cytomegalovirus, and parainfluenzavirus type 2 were inactivated within 24 h when treated at 37 degrees C with 1 mg (5.05 mM) of copper-catalyzed sodium ascorbate per ml. The infectivity titer of respiratory syncytial virus was reduced substantially after 24 h but required 48 h for inactivation. Under these conditions, inactivation of these viruses was also successfully achieved with 5.68 mM catalyzed ascorbic acid. Copper (Cu2+), when added with the ascorbate solution at 5 micrograms/ml (0.022 mM), exhibited a catalytic effect on the inactivation of these viruses. The rate of inactivation was affected by the incubation temperature, time of exposure, and the virus concentration. Ascorbate concentrations as high as 10 mg/ml (50.5 mM) demonstrated only a minimum increase in effect on viral inactivation. The loss of infectivity did not alter either the hemagglutination or complement fixation qualities of the antigens.


Subject(s)
Ascorbic Acid/pharmacology , Cytomegalovirus/drug effects , Parainfluenza Virus 2, Human/drug effects , Respiratory Syncytial Viruses/drug effects , Respirovirus/drug effects , Simplexvirus/drug effects , Animals , Complement Fixation Tests , Cytomegalovirus/pathogenicity , Cytopathogenic Effect, Viral , Fibroblasts , Hemagglutination Inhibition Tests , Hemagglutination Tests , Humans , Hydrogen-Ion Concentration , Parainfluenza Virus 2, Human/pathogenicity , Respiratory Syncytial Viruses/pathogenicity , Simplexvirus/pathogenicity , Temperature , Vero Cells
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