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Featured researches published by F. Gagliardi.


BMC Microbiology | 2011

Duodenal and faecal microbiota of celiac children: molecular, phenotype and metabolome characterization

Raffaella Di Cagno; Maria De Angelis; Ilaria De Pasquale; Maurice Ndagijimana; Pamela Vernocchi; Patrizia Ricciuti; F. Gagliardi; Luca Laghi; Carmine Crecchio; Maria Elisabetta Guerzoni; Marco Gobbetti; Ruggiero Francavilla

BackgroundEpidemiology of celiac disease (CD) is increasing. CD mainly presents in early childhood with small intestinal villous atrophy and signs of malabsorption. Compared to healthy individuals, CD patients seemed to be characterized by higher numbers of Gram-negative bacteria and lower numbers Gram-positive bacteria.ResultsThis study aimed at investigating the microbiota and metabolome of 19 celiac disease children under gluten-free diet (treated celiac disease, T-CD) and 15 non-celiac children (HC). PCR-denaturing gradient gel electrophoresis (DGGE) analyses by universal and group-specific primers were carried out in duodenal biopsies and faecal samples. Based on the number of PCR-DGGE bands, the diversity of Eubacteria was the higher in duodenal biopsies of T-CD than HC children. Bifidobacteria were only found in faecal samples. With a few exceptions, PCR-DGGE profiles of faecal samples for Lactobacillus and Bifidobacteria differed between T-CD and HC. As shown by culture-dependent methods, the levels of Lactobacillus, Enterococcus and Bifidobacteria were confirmed to be significantly higher (P = 0.028; P = 0.019; and P = 0.023, respectively) in fecal samples of HC than in T-CD children. On the contrary, cell counts (CFU/ml) of presumptive Bacteroides, Staphylococcus, Salmonella, Shighella and Klebsiella were significantly higher (P = 0.014) in T-CD compared to HC children. Enterococcus faecium and Lactobacillus plantarum were the species most diffusely identified. This latter species was also found in all duodenal biopsies of T-CD and HC children. Other bacterial species were identified only in T-CD or HC faecal samples. As shown by Randomly Amplified Polymorphic DNA-PCR analysis, the percentage of strains identified as lactobacilli significantly (P = 0.011) differed between T-CD (ca. 26.5%) and HC (ca. 34.6%) groups. The metabolome of T-CD and HC children was studied using faecal and urine samples which were analyzed by gas-chromatography mass spectrometry-solid-phase microextraction and 1H-Nuclear Magnetic Resonance. As shown by Canonical Discriminant Analysis of Principal Coordinates, the levels of volatile organic compounds and free amino acids in faecal and/or urine samples were markedly affected by CD.ConclusionAs shown by the parallel microbiology and metabolome approach, the gluten-free diet lasting at least two years did not completely restore the microbiota and, consequently, the metabolome of CD children. Some molecules (e.g., ethyl-acetate and octyl-acetate, some short chain fatty acids and free amino acids, and glutamine) seems to be metabolic signatures of CD.


Applied and Environmental Microbiology | 2009

Different Fecal Microbiotas and Volatile Organic Compounds in Treated and Untreated Children with Celiac Disease

Raffaella Di Cagno; Carlo Giuseppe Rizzello; F. Gagliardi; Patrizia Ricciuti; Maurice Ndagijimana; Ruggiero Francavilla; M. Elisabetta Guerzoni; Carmine Crecchio; Marco Gobbetti; Maria De Angelis

ABSTRACT This study aimed at investigating the fecal microbiotas of children with celiac disease (CD) before (U-CD) and after (T-CD) they were fed a gluten-free diet and of healthy children (HC). Brothers or sisters of T-CD were enrolled as HC. Each group consisted of seven children. PCR-denaturing gradient gel electrophoresis (DGGE) analysis with V3 universal primers revealed a unique profile for each fecal sample. PCR-DGGE analysis with group- or genus-specific 16S rRNA gene primers showed that the Lactobacillus community of U-CD changed significantly, while the diversity of the Lactobacillus community of T-CD was quite comparable to that of HC. Compared to HC, the ratio of cultivable lactic acid bacteria and Bifidobacterium to Bacteroides and enterobacteria was lower in T-CD and even lower in U-CD. The percentages of strains identified as lactobacilli differed as follows: HC (ca. 38%) > T-CD (ca. 17%) > U-CD (ca. 10%). Lactobacillus brevis, Lactobacillus rossiae, and Lactobacillus pentosus were identified only in fecal samples from T-CD and HC. Lactobacillus fermentum, Lactobacillus delbrueckii subsp. bulgaricus, and Lactobacillus gasseri were identified only in several fecal samples from HC. Compared to HC, the composition of Bifidobacterium species of T-CD varied, and it varied even more for U-CD. Forty-seven volatile organic compounds (VOCs) belonging to different chemical classes were identified using gas-chromatography mass spectrometry-solid-phase microextraction analysis. The median concentrations varied markedly for HC, T-CD, and U-CD. Overall, the r2 values for VOC data for brothers and sisters were equal to or lower than those for unrelated HC and T-CD. This study shows the effect of CD pathology on the fecal microbiotas of children.


Archive | 2010

Functional Abdominal Pain GG in Children With Lactobacillus A Randomized Controlled Trial of

Lucia Peccarisi; Flavia Indrio; Luciano Cavallo; F. Gagliardi; Elena Lionetti; Stefania Castellaneta; Lorenzo Polimeno; Ruggiero Francavilla; Vito Leonardo Miniello; Anna Maria Magistà


Digestive and Liver Disease | 2008

PA.171 GRANULOCYTAPHERESIS (ADACOLUMN®) TREATMENT IN PATIENTS WITH ULCERATIVE COLITIS IN ACTIVE PHASE

Mariabeatrice Principi; A. Castellaneta; N. De Tullio; F. Gagliardi; A. Ricco; L. Cazzato; A. Pisani; A. Dileo; D. Dimonte; Antonio Francavilla


Digestive and Liver Disease | 2008

Plasmacytoid dendritic cell and interferon alfa (IFN-α) production in children with celiac disease

Ruggiero Francavilla; F. Gagliardi; A. De Canio; A. Castellaneta; F. Indio; L. Polimeno


Digestive and Liver Disease | 2007

T-cell stimulatory activity of liver and spleen dendritic cell during a murine model of hepatocarcinogenesis

A. Castellaneta; Leo Di; N. De Tullio; F. Gagliardi; A. Amoruso; Antonio Francavilla


Digestive and Liver Disease | 2007

Expression of estrogen receptor isoforms in liver dendritic cells

A. Castellaneta; N. De Tullio; F. Gagliardi; M. Margiotta; Sabina Tanzi; L. Demarinis; A. Di Leo; Antonio Francavilla


Digestive and Liver Disease | 2006

Characterisation of peripheral blood and resident intestinal dendritic cells in children with coeliac disease

A. Castellaneta; F. Gagliardi; Daniela Intini; Nicola De Tullio; Annacinzia Amoroso; Alfredo Di Leo; Luciano Cavallo; Antonio Francavilla; Ruggiero Francavilla


Digestive and Liver Disease | 2006

Estrogen receptor expression in liver dendritic cells in respect to their different subpopulations and their maturation state1

A. Castellaneta; N. De Tullio; F. Gagliardi; Ruggiero Francavilla; A. Di Leo; Antonio Francavilla


Digestive and Liver Disease | 2006

Impairment of T-cell stimulatory activity of liver and spleen dendritic cell in a murine model of hepatocarcinogenesis

A. Castellaneta; F. Gagliardi; N. De Tullio; A. Amoruso; A. Di Leo; Antonio Francavilla

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Elena Lionetti

Marche Polytechnic University

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