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1.
J Nutr ; 141(5): 957-63, 2011 May.
Article in English | MEDLINE | ID: mdl-21411606

ABSTRACT

Vitamin A supplementation is associated with divergent clinical norovirus (NoV) outcomes in Mexican children. Fecal cytokine concentrations following NoV genogroup infections among 127 Mexican children 5-15 mo old enrolled in a randomized, double-blind, placebo-controlled, vitamin A supplementation trial were determined to clarify the role the gut immune response plays in these associations. Stools collected from supplemented children [20,000 IU retinol (3.3 IU = 1 µg retinol) for children < 12 mo of age; 45,000 iu for children ≥ 12 mo] or children in the placebo group were screened for NoV genogroups I (GI) and II (GII). Monocyte chemoattractant protein-1 (MCP-1), TNFα, IL-5, IL-6, IL-8, IL-4, IFNγ, and IL-10 fecal concentrations were also determined. Differences in cytokine levels between the 2 groups following GI and GII infections were determined using ordered logistic regression models. MCP-1 and IL-8 levels were greater among GI- and GII-infected children, respectively, compared with uninfected children, whereas IL-5 levels were greater following both genogroup infections. MCP-1, IL-8, and IL-6 fecal levels were reduced among supplemented children with GII-associated diarrhea compared with the placebo group. Vitamin A-supplemented, GII-infected children had reduced MCP-1 and TNFα levels compared with GII-infected children in the placebo group (P-interaction = 0.02 and 0.03, respectively). Supplemented children with GI-associated diarrhea had higher TNFα and IL-4 levels compared with children in the placebo group with diarrhea (P-interaction = 0.02 and 0.02, respectively). The divergent effects of supplementation on NoV outcomes may result from the different effects vitamin A has on the genogroup-specific immune responses.


Subject(s)
Caliciviridae Infections/prevention & control , Chemokines/analysis , Cytokines/analysis , Host-Pathogen Interactions , Intestines/immunology , Norovirus/physiology , Vitamin A/therapeutic use , Adaptive Immunity , Caliciviridae Infections/immunology , Chemokines/immunology , Cytokines/immunology , Dietary Supplements , Double-Blind Method , Feces/chemistry , Feces/microbiology , Female , Gastroenteritis/immunology , Gastroenteritis/prevention & control , Humans , Immunity, Innate , Immunomodulation , Infant , Intestines/microbiology , Male , Mexico , Norovirus/classification , Norovirus/immunology , Norovirus/isolation & purification , Vitamin A Deficiency/immunology , Vitamin A Deficiency/prevention & control
2.
J Infect Dis ; 196(7): 978-85, 2007 Oct 01.
Article in English | MEDLINE | ID: mdl-17763317

ABSTRACT

BACKGROUND: The effect of vitamin A supplementation on viral gastrointestinal infections among young children living in developing countries remains unclear. METHODS: The effect of vitamin A supplementation on norovirus (NoV) infection among 127 Mexican children 5-15 months of age was studied in a randomized, placebo-controlled trial during June-August 1998. Stool samples collected every 2 weeks and after diarrheal episodes were screened for NoV and characterized at the genogroup level (GI and GII). RESULTS: Of the stool samples collected, 29.9% were positive for NoV, and NoV GI and NoV GII were found in 55.4% and 46.4% of the positive samples, respectively. Vitamin A supplementation reduced the prevalence of NoV GII infections (rate ratio [RR], 0.60 [95% confidence interval {CI}, 0.20-0.82]), increased the length of both NoV GI and GII shedding, and decreased the prevalence of NoV-associated diarrhea (RR, 0.51 [95% CI, 0.26-0.97]). CONCLUSIONS: These findings suggest that NoV is an important cause of pediatric diarrhea in this study population and that vitamin A supplementation has divergent effects on specific outcomes of NoV infection.


Subject(s)
Caliciviridae Infections , Gastroenteritis , Norovirus/drug effects , Vitamin A , Caliciviridae Infections/drug therapy , Caliciviridae Infections/epidemiology , Caliciviridae Infections/physiopathology , Feces/virology , Female , Gastroenteritis/drug therapy , Gastroenteritis/epidemiology , Gastroenteritis/physiopathology , Gastroenteritis/virology , Humans , Infant , Male , Mexico/epidemiology , Norovirus/classification , Norovirus/isolation & purification , Prevalence , Treatment Outcome , Vitamin A/administration & dosage , Vitamin A/therapeutic use , Vitamins/administration & dosage , Vitamins/therapeutic use
3.
J Clin Microbiol ; 44(8): 2997-3000, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16891526

ABSTRACT

Sixty-three children in periurban Mexico City were examined for the occurrence of asymptomatic norovirus (NoV) infection from June to August 1998. NoV was detected in 48 of 161 stool specimens (29.8%), with 31 children (49.2%) having at least one positive stool. Asymptomatic NoV infection occurred commonly during summertime in a Mexican pediatric population.


Subject(s)
Caliciviridae Infections/physiopathology , Caliciviridae Infections/virology , Feces/virology , Norovirus/isolation & purification , Humans , Infant , Infant, Newborn , Mexico , Molecular Sequence Data , Norovirus/genetics , Phylogeny , RNA, Viral/analysis , RNA, Viral/genetics , Reverse Transcriptase Polymerase Chain Reaction , Sequence Analysis, DNA , Sequence Homology , Urban Population
4.
J Clin Microbiol ; 43(12): 6126-9, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16333110

ABSTRACT

Stool specimens from 124 international travelers with acute diarrhea were tested for the presence of enteropathogens. Noroviruses (NoVs) were the second most commonly identified enteric pathogen in diarrheal stool samples (21/124, 17%), exceeded only by enterotoxigenic Escherichia coli (50/106, 47%). This study indicates that NoV is an underappreciated cause of traveler's diarrhea.


Subject(s)
Caliciviridae Infections/virology , Diarrhea/etiology , Diarrhea/virology , Norovirus/isolation & purification , Students , Travel , Adolescent , Adult , Aged , Caliciviridae Infections/etiology , Feces/virology , Female , Humans , Male , Mexico , Middle Aged , Norovirus/genetics , Phylogeny , United States
5.
J Infect Dis ; 189(7): 1168-75, 2004 Apr 01.
Article in English | MEDLINE | ID: mdl-15031784

ABSTRACT

Twenty-one cases of acute flaccid paralysis (AFP) were reported on the island of Hispaniola in 2000. Laboratory analysis confirmed the presence of circulating vaccine-derived poliovirus (cVDPV) type 1 in stool samples obtained from patients. As a complement to the active search for cases of AFP, environmental sampling was conducted during November and December 2000, to test for cVDPV in sewage, streams, canals, and public latrines. Fifty-five environmental samples were obtained and analyzed for the presence of polioviruses by use of cell culture followed by neutralization and reverse-transcription polymerase chain reaction. Of the 23 positive samples, 10 tested positive for poliovirus type 1, 7 tested positive for poliovirus type 2, 5 tested positive for poliovirus type 3, and 1 tested positive for both poliovirus type 2 and type 3. By sequence analysis of the complete viral capsid gene 1 (VP1), a 2.1%-3.7% genetic sequence difference between 7 type 1 strains and Sabin type 1 vaccine strain was found. Phylogenetic analysis showed that these viruses are highly related to cVDPV isolated from clinical cases and form distinct subclusters related to geographic region. Our findings demonstrate a useful role for environmental surveillance of neurovirulent polioviruses in the overall polio eradication program.


Subject(s)
Disease Outbreaks , Poliomyelitis/virology , Poliovirus Vaccines/analysis , Poliovirus/isolation & purification , Sewage/virology , Water Microbiology , Animals , Dominican Republic/epidemiology , Female , Haiti/epidemiology , Humans , Male , Mice , Mice, Transgenic , Neutralization Tests , Poliomyelitis/epidemiology , Poliovirus/genetics , Poliovirus Vaccines/adverse effects , Poliovirus Vaccines/genetics , Poliovirus Vaccines/isolation & purification , Prevalence , RNA, Viral/chemistry , RNA, Viral/genetics , Reverse Transcriptase Polymerase Chain Reaction , Viral Nonstructural Proteins/chemistry , Viral Nonstructural Proteins/genetics
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