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1.
Parasite Immunol ; 38(9): 535-47, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27454991

ABSTRACT

Cryptosporidium is a major cause of moderate-to-severe diarrhoea in humans worldwide, second only to rotavirus. Due to the wide host range and environmental persistence of this parasite, cryptosporidiosis can be zoonotic and associated with foodborne and waterborne outbreaks. Currently, 31 species are recognized as valid, and of these, Cryptosporidium hominis and Cryptosporidium parvum are responsible for the majority of infections in humans. The immune status of the host, both innate and adaptive immunity, has a major impact on the severity of the disease and its prognosis. Immunocompetent individuals typically experience self-limiting diarrhoea and transient gastroenteritis lasting up to 2 weeks and recover without treatment, suggesting an efficient host antiparasite immune response. Immunocompromised individuals can suffer from intractable diarrhoea, which can be fatal. Effective drug treatments and vaccines are not yet available. As a result of this, the close cooperation and interaction between veterinarians, health physicians, environmental managers and public health operators is essential to properly control this disease. This review focuses on a One Health approach to prophylaxis, including the importance of understanding transmission routes for zoonotic Cryptosporidium species, improved sanitation and better risk management, improved detection, diagnosis and treatment and the prospect of an effective anticryptosporidial vaccine.


Subject(s)
Cryptosporidiosis/prevention & control , Cryptosporidium , Adaptive Immunity , Animals , Cryptosporidiosis/parasitology , Cryptosporidium/physiology , Cryptosporidium parvum , Humans , Immunocompromised Host
2.
Bioelectromagnetics ; 29(4): 312-23, 2008 May.
Article in English | MEDLINE | ID: mdl-18175331

ABSTRACT

To analyze possible effects of microwaves on gene expression, mice were exposed to global system for mobile communication (GSM) 1800 MHz signal for 1 h at a whole body SAR of 1.1 W/kg. Gene expression was studied in the whole brain, where the average SAR was 0.2 W/kg, by expression microarrays containing over 22,600 probe sets. Comparison of data from sham and exposed animals showed no significant difference in gene expression modulation. However, when less stringent constraints were adopted to analyze microarray results, 75 genes were found to be modulated following exposure. Forty-two probes showed fold changes ranging from 1.5 to 2.8, whereas 33 were down-regulated from 0.67- to 0.29-fold changes, but these differences in gene expression were not confirmed by real-time PCR. Under these specific limited conditions, no consistent indication of gene expression modulation in whole mouse brain was found associated to GSM 1800 MHz exposure.


Subject(s)
Brain/metabolism , Brain/radiation effects , Microwaves , Nerve Tissue Proteins/metabolism , Transcription Factors/metabolism , Transcriptional Activation/physiology , Transcriptional Activation/radiation effects , Animals , Cell Phone , Dose-Response Relationship, Radiation , Female , Male , Mice , Mice, Inbred BALB C , Radiation Dosage
3.
Ann Ig ; 19(4): 303-14, 2007.
Article in Italian | MEDLINE | ID: mdl-17937323

ABSTRACT

Administration of prohibited substances to enhance athletic performance represents an emerging medical, social, ethical and legal issue. Traditional controls are based on direct detection of substances or their catabolites. However out-of-competition doping may not be easily revealed by standard analytical methods. Alternative indirect control strategies are based on the evaluation of mid- and long-term effects of doping in tissues. Drug-induced long-lasting changes of gene expression may be taken as effective indicators of doping exposure. To validate this approach, we used real-time PCR to monitor the expression pattern of selected genes in human haematopoietic cells exposed to nandrolone, insulin-like growth factor I (IGF-I) or growth hormone (GH). Some candidate genes were found significantly and consistently modulated by treatments. Nandrolone up-regulated AR, ESR2 and PGR in K562 cells, and SRD5A1, PPARA and JAK2 in Jurkat cells; IGF-I up-regulated EPOR and PGR in HL60 cells, and SRD5A1 in Jurkat; GH up-regulated SRD5A1 and GHR in K562. GATA1 expression was down-regulated in IGF-1-treated HL60, ESR2 was down-regulated in nandrolone-treated Jurkat, and AR and PGR were down-regulated in GH-treated Jurkat. This pilot study shows the potential of molecular biology-based strategies in anti-doping controls.


Subject(s)
Anabolic Agents/pharmacology , Doping in Sports , Genetic Markers/drug effects , Hematopoietic Stem Cells/metabolism , Human Growth Hormone/pharmacology , Insulin-Like Growth Factor I/pharmacology , Nandrolone/pharmacology , Substance Abuse Detection/methods , Anabolic Agents/administration & dosage , Cells, Cultured , Down-Regulation/drug effects , Drug Therapy, Combination , HL-60 Cells , Hematopoietic Stem Cells/drug effects , Human Growth Hormone/administration & dosage , Humans , Insulin-Like Growth Factor I/administration & dosage , Italy , Jurkat Cells , K562 Cells , Nandrolone/administration & dosage , Pilot Projects , Polymerase Chain Reaction/methods , Prospective Studies , Reproducibility of Results , Substance Abuse Detection/statistics & numerical data , Up-Regulation/drug effects
4.
J Prev Med Hyg ; 47(3): 100-4, 2006 Sep.
Article in English | MEDLINE | ID: mdl-17217186

ABSTRACT

Sequence-based approaches to prokaryotic systematics and typing represent a modern and promising strategy in epidemiology and environmental microbiology. GenEnv, a database-driven system for bacterial typing, was developed in order to provide user friendly tools for supporting biomolecular analysis of bacteria. The family Vibrionaceae represents a heterogeneous taxon of aquatic microrganisms, harbouring a plethora of genomes currently analyzed by different molecular techniques. Under the query "Vibrio", GenEnv retrieved 256 organisms, included in a total number of 19 families. Overall, 548 sequences, comprising 16S rRNA (n=402), rpoB (n=1), gyrB (n=145) were available. In addition, GenEnv system allowed primer design, homology analysis and restriction maps, for immediate applications to the study of Vibrionaceae.


Subject(s)
Biodiversity , Computational Biology/methods , Databases, Genetic , Vibrio/genetics , Bacterial Typing Techniques , Epidemiologic Methods , Genes, Bacterial , RNA, Ribosomal, 16S , Vibrio/pathogenicity , Water Microbiology
5.
Biotechnol Annu Rev ; 11: 335-54, 2005.
Article in English | MEDLINE | ID: mdl-16216782

ABSTRACT

Species identification represents a critical issue in food chain safety and quality control. Several procedures are available to detect animal proteins in cattle feed or to trace transgenic foods. The most effective approach is based on the use of DNA as a marker. Amplification of DNA provides rapid, sensitive and specific protocols. Several target genes can be used, but new insights come from the mitochondrial genome, which is naturally amplified in each cell and shows a remarkable resistance to degradation. These are key points when analysing complex matrices such as foods, animal feedstuff or environmental samples. Traceability is important to prevent BSE or to monitor novel foods, such as genetically modified organisms. Amplification is commonly performed, but it requires expertise and a molecular biology laboratory to perform restriction analysis, electrophoresis or gel staining for the visualisation of results. Hereby, we consider a strategy based on multiple nested amplification and reverse hybridisation assay that virtually requires only a thermocycler and a water bath. The protocol is rapid and simple and can simultaneously detect different species in a DNA sample. This promising approach allows microarray developments, opening up to further perspectives. An international application has been published under the patent cooperation treaty. Presently, a ban on feeding ruminants on cattle-derived proteins is in force in Europe and USA. The identification of metazoan traces in a sample is not only a mere preventive measure for BSE, but represents a possible screening system for monitoring biotechnology products and procedures, as well as a quality control strategy to assure consumer's rights.


Subject(s)
DNA, Mitochondrial/analysis , Food Analysis/methods , Public Health/methods , Animals , Cattle , Chickens , Consumer Product Safety/standards , DNA, Mitochondrial/genetics , Humans , Public Health/standards , Quality Control , Sheep , Swine
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