23 results on '"Baldassarri L."'
Search Results
2. Analysis of uni and bi-parental markers in mixture samples: Lessons from the 22nd GHEP-ISFG Intercomparison Exercise
- Author
-
Toscanini, U., Gusmão, L., Álava Narváez, M.C., Álvarez, J.C., Baldassarri, L., Barbaro, A., Berardi, G., Betancor Hernández, E., Camargo, M., Carreras-Carbonell, J., Castro, J., Costa, S.C., Coufalova, P., Domínguez, V., Fagundes de Carvalho, E., Ferreira, S.T.G., Furfuro, S., García, O., Goios, A., González, R., de la Vega, A. González, Gorostiza, A., Hernández, A., Jiménez Moreno, S., Lareu, M.V., León Almagro, A., Marino, M., Martínez, G., Miozzo, M.C., Modesti, N.M., Onofri, V., Pagano, S., Pardo Arias, B., Pedrosa, S., Penacino, G.A., Pontes, M.L., Porto, M.J., Puente-Prieto, J., Pérez, R. Ramírez, Ribeiro, T., Rodríguez Cardozo, B., Rodríguez Lesmes, Y.M., Sala, A., Santiago, B., Saragoni, V.G., Serrano, A., Streitenberger, E.R., Torres Morales, M.A., Vannelli Rey, S.A., Velázquez Miranda, M., Whittle, M.R., Fernández, K., and Salas, A.
- Published
- 2016
- Full Text
- View/download PDF
3. Is peak height important for the statistical evaluation of the weight of evidence in DNA mixtures?
- Author
-
Caglià, A., Baldassarri, L., Boschi, I., Scarnicci, F., and Pascali, V.L.
- Published
- 2015
- Full Text
- View/download PDF
4. Paroxysmal arousals in Sleep-related Hypermotor Epilepsy (SHE) and Simple arousal movements in Disorders of Arousal (DoA): semiological and clinical features make a difference
- Author
-
Loddo, G., primary, Baldassarri, L., additional, Zenesini, C., additional, Licchetta, L., additional, Bisulli, F., additional, Cirignotta, F., additional, Mondini, S., additional, Tinuper, P., additional, and Provini, F., additional
- Published
- 2022
- Full Text
- View/download PDF
5. Highly predictive genetic markers distinguish drug-type from fiber-type cannabis sativa L
- Author
-
Cascini, F., Farcomeni, A., Migliorini, D., Baldassarri, L., Boschi, I., Martello, S., Amaducci, S., Lucini, L., Bernardi, J., Cascini F. (ORCID:0000-0001-6499-0734), Baldassarri L., Martello S., Amaducci S. (ORCID:0000-0002-6184-9257), Lucini L. (ORCID:0000-0002-5133-9464), Bernardi J., Cascini, F., Farcomeni, A., Migliorini, D., Baldassarri, L., Boschi, I., Martello, S., Amaducci, S., Lucini, L., Bernardi, J., Cascini F. (ORCID:0000-0001-6499-0734), Baldassarri L., Martello S., Amaducci S. (ORCID:0000-0002-6184-9257), Lucini L. (ORCID:0000-0002-5133-9464), and Bernardi J.
- Abstract
Genetic markers can be used in seeds and in plants to distinguish drug-type from fiber-type Cannabis Sativa L. varieties even at early stages, including pre-germination when cannabinoids are not accumulated yet. With this aim, this paper reports sequencing results for tetrahydrocannabinolic acid synthase (THCAS) and cannabidiolic acid synthase (CBDAS) genes from 21 C. sativa L. varieties. Taking into account that THCAS-and CBDAS-derived enzymes compete for the same substrate, the novelty of this work relies in the identification of markers based on both THCAS and CBDAS rather than THCAS alone. Notably, in our panel, we achieved an adequate degree of discrimination (AUC 100%) between drug-type and fiber-type cannabis samples. Our sequencing approach allowed identifying multiple genetic markers (single-nucleotide polymorphisms—SNPs—and a deletion/insertion) that effectively discriminate between the two subgroups of cannabis, namely fiber type vs. drug type. We identified four functional SNPs that are likely to induce decreased THCAS activity in the fiber-type cannabis plants. We also report the finding on a deletion in the CBDAS gene sequence that produces a truncated protein, possibly resulting in loss of function of the enzyme in the drug-type varieties. Chemical analyses for the actual concentration of cannabinoids confirmed the identification of drug-type rather than fiber-type genotypes. Genetic markers permit an early identification process for forensic applications while simplifying the procedures related to detection of therapeutic or industrial hemp.
- Published
- 2019
6. Analysis of a DNA mixture involving Romani reference populations
- Author
-
Dotto, F., Mortera, J., Baldassarri, Laura, Pascali, Vincenzo Lorenzo, Baldassarri L., Pascali V. (ORCID:0000-0001-6520-5224), Dotto, F., Mortera, J., Baldassarri, Laura, Pascali, Vincenzo Lorenzo, Baldassarri L., and Pascali V. (ORCID:0000-0001-6520-5224)
- Abstract
Here we present an Italian criminal case that shows how statistical methods can be used to extract information from a series of mixed DNA profiles. The case involves several different individuals and a set of different DNA traces. The case possibly involves persons of interest of a small population of Romani origin. First, a brief description of the case is provided. Secondly, we introduce some heuristic tools that can be used to evaluate the data and we also briefly outline the statistical model used for analysing DNA mixtures. Finally, we illustrate some of the findings on the case and discuss further directions of research. The results show how the use of different population database allele frequencies for analysing the DNA mixtures can lead to very different results, some seemingly inculpatory and some seemingly exculpatory. We also illustrate the results obtained from combining the evidence from different samples.
- Published
- 2020
7. Highly predictive genetic markers distinguish drug-type from fiber-type cannabis sativa L
- Author
-
Cascini, Fidelia, Farcomeni, A., Migliorini, D., Baldassarri, Laura, Boschi, I., Martello, Simona, Amaducci, Stefano, Lucini, Luigi, Bernardi, Jamila, Cascini F. (ORCID:0000-0001-6499-0734), Baldassarri L., Martello S., Amaducci S. (ORCID:0000-0002-6184-9257), Lucini L. (ORCID:0000-0002-5133-9464), Bernardi J., Cascini, Fidelia, Farcomeni, A., Migliorini, D., Baldassarri, Laura, Boschi, I., Martello, Simona, Amaducci, Stefano, Lucini, Luigi, Bernardi, Jamila, Cascini F. (ORCID:0000-0001-6499-0734), Baldassarri L., Martello S., Amaducci S. (ORCID:0000-0002-6184-9257), Lucini L. (ORCID:0000-0002-5133-9464), and Bernardi J.
- Abstract
Genetic markers can be used in seeds and in plants to distinguish drug-type from fiber-type Cannabis Sativa L. varieties even at early stages, including pre-germination when cannabinoids are not accumulated yet. With this aim, this paper reports sequencing results for tetrahydrocannabinolic acid synthase (THCAS) and cannabidiolic acid synthase (CBDAS) genes from 21 C. sativa L. varieties. Taking into account that THCAS- and CBDAS-derived enzymes compete for the same substrate, the novelty of this work relies in the identification of markers based on bothTHCASandCBDASrather than THCAS alone. Notably, in our panel, we achieved an adequate degree of discrimination (AUC 100%) between drug-type and fiber-type cannabis samples. Our sequencing approach allowed identifying multiple genetic markers (single-nucleotide polymorphisms—SNPs—and a deletion/insertion) that effectively discriminate between the two subgroups of cannabis, namely fiber type vs. drug type. We identified four functional SNPs that are likely to induce decreased THCAS activity in the fiber-type cannabis plants. We also report the finding on a deletion in the CBDAS gene sequence that produces a truncated protein, possibly resulting in loss of function of the enzyme in the drug-type varieties. Chemical analyses for the actual concentration of cannabinoids confirmed the identification of drug-type rather than fiber-type genotypes. Genetic markers permit an early identification process for forensic applications while simplifying the procedures related to detection of therapeutic or industrial hemp.
- Published
- 2019
8. Genomic analysis reveals the molecular basis for capsule loss in the group B Streptococcus population
- Author
-
Rosini, Roberto, Campisi, Edmondo, De Chiara, Matteo, Tettelin, Hervé, Rinaudo, Daniela, Toniolo, Chiara, Metruccio, Matteo, Guidotti, Silvia, Skov Sørensen, Uffe B., Kilian, Mogens, Ramirez, Mario, Janulczyk, Robert, Donati, Claudio, Grandi, Guido, Margarit, Immaculada, Melin, P., Decheva, A., Petrunov, B., Kriz, P., Berner, R., Hufnagel, M., Kunze, M., Creti, R., Baldassarri, L., Berardi, A., Orefici, G., Granger, J. R., De La Rosa Fraile, M., Afshar, B., Efstratiou, A., Maione, D., and Telford, J. L.
- Subjects
Bacterial capsule ,Genetics and Molecular Biology (all) ,Evoluzione del genoma ,lcsh:Medicine ,Evolutionary biology ,medicine.disease_cause ,Genome ,Biochemistry ,lcsh:Science ,Mastitis, Bovine ,Genetics ,0303 health sciences ,education.field_of_study ,Multidisciplinary ,Medicine (all) ,Genomics ,Stop codon ,3. Good health ,Complementation ,Female ,Genomica ,Research Article ,DNA, Bacterial ,Settore BIO/18 - GENETICA ,Population ,Biology ,Polymorphism, Single Nucleotide ,Microbiology ,Streptococcus agalactiae ,03 medical and health sciences ,Bacterial Proteins ,Streptococcal Infections ,medicine ,Animals ,Humans ,Agricultural and Biological Sciences (all) ,Biochemistry, Genetics and Molecular Biology (all) ,education ,Gene ,Bacterial Capsules ,030304 developmental biology ,Base Sequence ,Cattle ,Multilocus Sequence Typing ,Sequence Alignment ,Sequence Analysis, DNA ,030306 microbiology ,Point mutation ,lcsh:R ,lcsh:Q - Abstract
The human and bovine bacterial pathogen Streptococcus agalactiae (Group B Streptococcus, GBS) expresses a thick polysaccharide capsule that constitutes a major virulence factor and vaccine target. GBS can be classified into ten distinct serotypes differing in the chemical composition of their capsular polysaccharide. However, non-typeable strains that do not react with anti-capsular sera are frequently isolated from colonized and infected humans and cattle. To gain a comprehensive insight into the molecular basis for the loss of capsule expression in GBS, a collection of well-characterized non-typeable strains was investigated by genome sequencing. Genome based phylogenetic analysis extended to a wide population of sequenced strains confirmed the recently observed high clonality among GBS lineages mainly containing human strains, and revealed a much higher degree of diversity in the bovine population. Remarkably, non-typeable strains were equally distributed in all lineages. A number of distinct mutations in the cps operon were identified that were apparently responsible for inactivation of capsule synthesis. The most frequent genetic alterations were point mutations leading to stop codons in the cps genes, and the main target was found to be cpsE encoding the portal glycosyl trasferase of capsule biosynthesis. Complementation of strains carrying missense mutations in cpsE with a wild-type gene restored capsule expression allowing the identification of amino acid residues essential for enzyme activity.
- Published
- 2015
- Full Text
- View/download PDF
9. Mutations upstream of fabI in triclosan resistant Staphylococcus aureus strains are associated with elevated fabI gene expression
- Author
-
Grandgirard, D., Furi, L., Ciusa, M.L., Baldassarri, L., Knight, D.R., Morrissey, I., Largiadèr, C.R., Leib, S.L., Oggioni, M.R., Grandgirard, D., Furi, L., Ciusa, M.L., Baldassarri, L., Knight, D.R., Morrissey, I., Largiadèr, C.R., Leib, S.L., and Oggioni, M.R.
- Abstract
Background The enoyl-acyl carrier protein (ACP) reductase enzyme (FabI) is the target for a series of antimicrobial agents including novel compounds in clinical trial and the biocide triclosan. Mutations in fabI and heterodiploidy for fabI have been shown to confer resistance in S. aureus strains in a previous study. Here we further determined the fabI upstream sequence of a selection of these strains and the gene expression levels in strains with promoter region mutations. Results Mutations in the fabI promoter were found in 18% of triclosan resistant clinical isolates, regardless the previously identified molecular mechanism conferring resistance. Although not significant, a higher rate of promoter mutations were found in strains without previously described mechanisms of resistance. Some of the mutations identified in the clinical isolates were also detected in a series of laboratory mutants. Microarray analysis of selected laboratory mutants with fabI promoter region mutations, grown in the absence of triclosan, revealed increased fabI expression in three out of four tested strains. In two of these strains, only few genes other than fabI were upregulated. Consistently with these data, whole genome sequencing of in vitro selected mutants identified only few mutations except the upstream and coding regions of fabI, with the promoter mutation as the most probable cause of fabI overexpression. Importantly the gene expression profiling of clinical isolates containing similar mutations in the fabI promoter also showed, when compared to unrelated non-mutated isolates, a significant up-regulation of fabI. Conclusions In conclusion, we have demonstrated the presence of C34T, T109G, and A101C mutations in the fabI promoter region of strains with fabI up-regulation, both in clinical isolates and/or laboratory mutants. These data provide further observations linking mutations upstream fabI with up-regulated expression of the fabI gene.
- Published
- 2015
10. Seizures with paroxysmal arousals in sleep-related hypermotor epilepsy (SHE): Dissecting epilepsy from NREM parasomnias
- Author
-
Francesca Bisulli, Paolo Tinuper, Laura Licchetta, Corrado Zenesini, Federica Provini, Susanna Mondini, Fabio Cirignotta, Giuseppe Loddo, Lorenzo Baldassarri, Loddo G., Baldassarri L., Zenesini C., Licchetta L., Bisulli F., Cirignotta F., Mondini S., Tinuper P., and Provini F.
- Subjects
0301 basic medicine ,Adult ,Male ,medicine.medical_specialty ,Parasomnias ,motor pattern ,sleepwalking ,Adolescent ,Polysomnography ,Video Recording ,Epilepsy, Partial, Motor ,Audiology ,Non-rapid eye movement sleep ,Arousal ,03 medical and health sciences ,Epilepsy ,Young Adult ,0302 clinical medicine ,disorders of arousal ,Seizures ,Medicine ,Humans ,Hyperkinetic seizures ,Child ,business.industry ,Eye movement ,focal seizure ,Semiology ,Middle Aged ,video-polysomnography ,medicine.disease ,030104 developmental biology ,Neurology ,Sleepwalking ,Child, Preschool ,Ambulatory ,Female ,Neurology (clinical) ,Sleep Stages ,business ,030217 neurology & neurosurgery - Abstract
Objective: Sleep-related hypermotor epilepsy (SHE) is a focal epilepsy characterized by seizures occurring mostly during sleep, ranging from brief seizures with paroxysmal arousals (SPAs) to hyperkinetic seizures and ambulatory behaviors. SPAs are brief and stereotypic seizures representing the beginning of a major seizure. Distinguishing SPAs from disorders of arousal (DOAs) and their briefest episodes called simple arousal movements (SAMs) is difficult. We performed a characterization of SPAs and SAMs to identify video-polysomnographic (VPSG) features that can contribute to the diagnosis of SHE or DOA. Methods: Fifteen SHE, 30 DOA adult patients, and 15 healthy subjects underwent full-night VPSG. Two neurologist experts in sleep disorders and epilepsy classified all the sleep-related movements and episodes recorded. For each SPAs and SAMs, sleep stage at onset, duration, limb involvement, progression, and semiology have been identified. Results: A total of 121 SPAs were recorded, emerging mostly during stage 1-2 non–rapid eye movement (NREM) sleep (median duration: 5seconds). At the beginning, the SPAs motor pattern was hyperkinetic in 78 cases (64%), involving more than three non-contiguous or all body parts. The standard was a constant progression of movements during SPAs without any motor arrests. In DOA patients a total of 140 SAMs were recorded (median duration: 12seconds) mostly emerging during stage 3 NREM sleep. In SAMs, we did not observe any tonic/dystonic or hypermotor patterns or stereotypy; motor arrest was present over the course of about half of the episodes. In comparison with both DOA and healthy subjects, SHE patients showed a higher number of sleep-related movements per night and a reduction of sleep efficiency. Significance: SPAs and SAMs present different semiological and clinical features. Their recognition could be useful to drive the diagnosis when major episodes are not recorded during VPSG in patients with a clear clinical history of SHE or DOA.
- Published
- 2020
11. Analysis of a DNA mixture involving Romani reference populations
- Author
-
Francesco Dotto, Julia Mortera, Vincenzo Lorenzo Pascali, Laura Baldassarri, Dotto, Francesco, Mortera, Julia, Baldassarri, Laura, Pascali, Vincenzo, Dotto, F., Mortera, J., Baldassarri, L., and Pascali, V.
- Subjects
Male ,0301 basic medicine ,Computer science ,Population ,Settore BIO/08 - ANTROPOLOGIA ,Criminal case ,computer.software_genre ,Pathology and Forensic Medicine ,Set (abstract data type) ,03 medical and health sciences ,0302 clinical medicine ,Gene Frequency ,Dna, Mixture, Populations ,Databases, Genetic ,Ethnicity ,Mixture ,Genetics ,Humans ,A-DNA ,030216 legal & forensic medicine ,education ,Likelihood Functions ,education.field_of_study ,Models, Statistical ,Heuristic ,business.industry ,Populations ,Statistical model ,Dna ,DNA Fingerprinting ,Genetics, Population ,030104 developmental biology ,Italy ,DNA profiling ,Artificial intelligence ,business ,computer ,Natural language processing - Abstract
Here we present an Italian criminal case that shows how statistical methods can be used to extract information from a series of mixed DNA profiles. The case involves several different individuals and a set of different DNA traces. The case possibly involves persons of interest of a small population of Romani origin. First, a brief description of the case is provided. Secondly, we introduce some heuristic tools that can be used to evaluate the data and we also briefly outline the statistical model used for analysing DNA mixtures. Finally, we illustrate some of the findings on the case and discuss further directions of research. The results show how the use of different population database allele frequencies for analysing the DNA mixtures can lead to very different results, some seemingly inculpatory and some seemingly exculpatory. We also illustrate the results obtained from combining the evidence from different samples.
- Published
- 2019
12. Mutations upstream of fabI in triclosan resistant Staphylococcus aureus strains are associated with elevated fabI gene expression
- Author
-
Ian Morrissey, Maria Laura Ciusa, Marco R. Oggioni, Stephen L. Leib, Leonardo Furi, Daniel R. Knight, Carlo R. Largiadèr, Lucilla Baldassarri, Denis Grandgirard, Grandgirard D, Furi L, Ciusa ML, Baldassarri L, Knight DR, Morrissey I, Largiadèr CR, Leib SL, and Oggioni MR
- Subjects
Staphylococcus aureus ,Genotype ,Biocide ,Mutant ,Molecular Sequence Data ,Resistance ,Down-Regulation ,610 Medicine & health ,Biology ,Microarray ,medicine.disease_cause ,Microbiology ,Bacterial Proteins ,Gene expression ,Drug Resistance, Bacterial ,medicine ,Genetics ,Cross-resistance ,Promoter Regions, Genetic ,Gene ,Mutation ,Promoter mutation ,drug resistance ,Base Sequence ,Promoter ,fabI ,Enoyl-(Acyl-Carrier-Protein) Reductase (NADH) ,Triclosan ,Up-Regulation ,Gene expression profiling ,Anti-Infective Agents, Local ,570 Life sciences ,biology ,Biotechnology ,Research Article - Abstract
Background The enoyl-acyl carrier protein (ACP) reductase enzyme (FabI) is the target for a series of antimicrobial agents including novel compounds in clinical trial and the biocide triclosan. Mutations in fabI and heterodiploidy for fabI have been shown to confer resistance in S. aureus strains in a previous study. Here we further determined the fabI upstream sequence of a selection of these strains and the gene expression levels in strains with promoter region mutations. Results Mutations in the fabI promoter were found in 18% of triclosan resistant clinical isolates, regardless the previously identified molecular mechanism conferring resistance. Although not significant, a higher rate of promoter mutations were found in strains without previously described mechanisms of resistance. Some of the mutations identified in the clinical isolates were also detected in a series of laboratory mutants. Microarray analysis of selected laboratory mutants with fabI promoter region mutations, grown in the absence of triclosan, revealed increased fabI expression in three out of four tested strains. In two of these strains, only few genes other than fabI were upregulated. Consistently with these data, whole genome sequencing of in vitro selected mutants identified only few mutations except the upstream and coding regions of fabI, with the promoter mutation as the most probable cause of fabI overexpression. Importantly the gene expression profiling of clinical isolates containing similar mutations in the fabI promoter also showed, when compared to unrelated non-mutated isolates, a significant up-regulation of fabI. Conclusions In conclusion, we have demonstrated the presence of C34T, T109G, and A101C mutations in the fabI promoter region of strains with fabI up-regulation, both in clinical isolates and/or laboratory mutants. These data provide further observations linking mutations upstream fabI with up-regulated expression of the fabI gene. Electronic supplementary material The online version of this article (doi:10.1186/s12864-015-1544-y) contains supplementary material, which is available to authorized users.
- Published
- 2015
- Full Text
- View/download PDF
13. Gender differences in borderline personality disorder: a narrative review.
- Author
-
Bozzatello P, Blua C, Brandellero D, Baldassarri L, Brasso C, Rocca P, and Bellino S
- Abstract
Borderline personality disorder (BPD) is a severe and complex mental disorder that traditionally has been found to be more frequent in the female gender in clinical samples. More recently, epidemiological studies have provided conflicting data about the prevalence of borderline disorder in the two genders in community samples. In order to explain this heterogeneity, some authors hypothesized the presence of a bias in the diagnostic criteria thresholds (more prevalent in one gender than another), in the population sampling (community versus clinical), in the instruments of evaluation (clinician versus self-report measures), and in the diagnostic construct of BPD. Beyond the question of the different prevalence of the disorder between genders, the debate remains open as to how personality and clinical characteristics, and attitude toward treatments express themselves in the two genders. This narrative review is aimed to provide an updated overview of the differences among genders in BPD in terms of diagnosis, temperamental and clinical characteristics, comorbidities, findings of neuroimaging, and treatment attitudes. Studies that specifically investigated the gender differences in BPD patients are rather limited. Most of the investigations did not consider gender as a variable or were characterized by a significant imbalance between the two genders (more commonly in favor the female gender). The main results indicated that men were more likely to endorse the criteria "intense and inappropriate anger" and "impulsivity," whereas women endorsed the criteria "chronic feelings of emptiness," "affective instability," and "suicidality/self-harm behaviors." These findings reflect differences in temperament and symptoms of the two genders. Other relevant differences concern pattern of comorbidity, specific neurobiological mechanisms and attitude to treatments. Main limitations were that only one database was searched, time of publications was limited, non-English manuscripts were excluded, and the quality of each paper was not commented., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision., (Copyright © 2024 Bozzatello, Blua, Brandellero, Baldassarri, Brasso, Rocca and Bellino.)
- Published
- 2024
- Full Text
- View/download PDF
14. Significant variations of dangerous exposures during COVID-19 pandemic in Italy: a possible association with the containment measures implemented to reduce the virus transmission.
- Author
-
Giordano F, Petrolini VM, Spagnolo D, Fidente RM, Lanciotti L, Baldassarri L, Moretti FL, Brambilla E, Lonati D, Schicchi A, Locatelli CA, and Draisci R
- Subjects
- Child, Communicable Disease Control, Humans, Italy epidemiology, Pandemics prevention & control, Poison Control Centers, SARS-CoV-2, COVID-19 prevention & control
- Abstract
Background: In response to the COVID-19 health emergency, mass media widely spread guidelines to stop the virus transmission, leading to an excessive and unaware use of detergents and disinfectants. In Italy and in other countries this tendency caused a significant increase of exposures to these products in 2020. Evaluating data collected by the Italian Pavia Poison Centre (PPC), this study intends to examine the relationship between the COVID-19 lockdown and the variations of exposures to specific product categories possibly associated to the containment measures implemented. Simultaneously, this work shows the effectiveness of the European Product Categorisation System (EuPCS) in surveillance activities of dangerous chemicals., Methods: Exposure cases managed by the PPC during March-May 2020 (lockdown) and during the same months of 2017-2018-2019 were compared. Differences in categorical variables were tested with the Chi-square test. The level of significance was set at Alpha = .05. The study included all EuPCS groups but specifically focused on cleaners, detergents, biocides and cosmetics., Results: During the lockdown, calls from private citizens showed a highly significant increase (+ 11.5%, p < .001) and occupational exposures decreased (- 11.7%, p = .011). Among Cleaners, exposures to Bleaches slightly increased while Drain cleaning products went through a significant reduction (- 13.9%, p = .035). A highly significant increase of exposures to Disinfectants was observed (+ 7.7%, p = .007), particularly to those for surfaces (+ 6.8%, p = .039). Regarding Cosmetics, both handwashing soaps and gel products significantly increased (respectively: + 25.0, p = .016 and + 9.7%, p = .028). Among children 1-5 years, the statistical significance is reached with exposures to Dishwashing detergents (+ 13.1%, p = .032), handwashing soaps (+ 28.6%, p = .014) and handwashing gel products (+ 16.8%, p = .010). Contrarily, Liquid Laundry Detergent Capsules decreased in a highly significant manner (- 25%; p = .001). The general severity of exposures showed a highly significant decrease (Moderate: - 10.1%, p = .0002)., Conclusions: This study investigated the relationship between the COVID-19 lockdown and the variations of exposures to some product categories related to the containment measures. The results obtained support any action to be taken by Competent Authorities to implement measures for a safer use of cleaners/disinfectants. This paper shows the benefit in applying the EuPCS to categorize products according to their intended use, though an extension of this system to products not covered by CLP Regulation may be a further advantage., (© 2022. The Author(s).)
- Published
- 2022
- Full Text
- View/download PDF
15. The Role of Trauma in Early Onset Borderline Personality Disorder: A Biopsychosocial Perspective.
- Author
-
Bozzatello P, Rocca P, Baldassarri L, Bosia M, and Bellino S
- Abstract
The role of childhood trauma in the development of borderline personality disorder (BPD) in young age has long been studied. The most accurate theoretical models are multifactorial, taking into account a range of factors, including early trauma, to explain evolutionary pathways of BPD. We reviewed studies published on PubMed in the last 20 years to evaluate whether different types of childhood trauma, like sexual and physical abuse and neglect, increase the risk and shape the clinical picture of BPD. BPD as a sequela of childhood traumas often occurs with multiple comorbidities (e.g. mood, anxiety, obsessive-compulsive, eating, dissociative, addictive, psychotic, and somatoform disorders). In such cases it tends to have a prolonged course, to be severe, and treatment-refractory. In comparison with subjects who suffer from other personality disorders, patients with BPD experience childhood abuse more frequently. Adverse childhood experiences affect different biological systems (HPA axis, neurotransmission mechanisms, endogenous opioid systems, gray matter volume, white matter connectivity), with changes persisting into adulthood. A growing body of evidence is emerging about interaction between genes (e.g. FKBP5 polymorphisms and CRHR2 variants) and environment (physical and sexual abuse, emotional neglect)., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Bozzatello, Rocca, Baldassarri, Bosia and Bellino.)
- Published
- 2021
- Full Text
- View/download PDF
16. Seizures with paroxysmal arousals in sleep-related hypermotor epilepsy (SHE): Dissecting epilepsy from NREM parasomnias.
- Author
-
Loddo G, Baldassarri L, Zenesini C, Licchetta L, Bisulli F, Cirignotta F, Mondini S, Tinuper P, and Provini F
- Subjects
- Adolescent, Adult, Child, Child, Preschool, Epilepsy, Partial, Motor diagnosis, Epilepsy, Partial, Motor epidemiology, Female, Humans, Male, Middle Aged, Parasomnias diagnosis, Parasomnias epidemiology, Polysomnography methods, Seizures diagnosis, Seizures epidemiology, Video Recording methods, Young Adult, Arousal physiology, Epilepsy, Partial, Motor physiopathology, Parasomnias physiopathology, Seizures physiopathology, Sleep Stages physiology
- Abstract
Objective: Sleep-related hypermotor epilepsy (SHE) is a focal epilepsy characterized by seizures occurring mostly during sleep, ranging from brief seizures with paroxysmal arousals (SPAs) to hyperkinetic seizures and ambulatory behaviors. SPAs are brief and stereotypic seizures representing the beginning of a major seizure. Distinguishing SPAs from disorders of arousal (DOAs) and their briefest episodes called simple arousal movements (SAMs) is difficult. We performed a characterization of SPAs and SAMs to identify video-polysomnographic (VPSG) features that can contribute to the diagnosis of SHE or DOA., Methods: Fifteen SHE, 30 DOA adult patients, and 15 healthy subjects underwent full-night VPSG. Two neurologist experts in sleep disorders and epilepsy classified all the sleep-related movements and episodes recorded. For each SPAs and SAMs, sleep stage at onset, duration, limb involvement, progression, and semiology have been identified., Results: A total of 121 SPAs were recorded, emerging mostly during stage 1-2 non-rapid eye movement (NREM) sleep (median duration: 5 seconds). At the beginning, the SPAs motor pattern was hyperkinetic in 78 cases (64%), involving more than three non-contiguous or all body parts. The standard was a constant progression of movements during SPAs without any motor arrests. In DOA patients a total of 140 SAMs were recorded (median duration: 12 seconds) mostly emerging during stage 3 NREM sleep. In SAMs, we did not observe any tonic/dystonic or hypermotor patterns or stereotypy; motor arrest was present over the course of about half of the episodes. In comparison with both DOA and healthy subjects, SHE patients showed a higher number of sleep-related movements per night and a reduction of sleep efficiency., Significance: SPAs and SAMs present different semiological and clinical features. Their recognition could be useful to drive the diagnosis when major episodes are not recorded during VPSG in patients with a clear clinical history of SHE or DOA., (© 2020 International League Against Epilepsy.)
- Published
- 2020
- Full Text
- View/download PDF
17. Analysis of a DNA mixture involving Romani reference populations.
- Author
-
Dotto F, Mortera J, Baldassarri L, and Pascali V
- Subjects
- Databases, Genetic, Gene Frequency, Humans, Italy, Likelihood Functions, Male, Models, Statistical, DNA genetics, DNA Fingerprinting, Ethnicity genetics, Genetics, Population
- Abstract
Here we present an Italian criminal case that shows how statistical methods can be used to extract information from a series of mixed DNA profiles. The case involves several different individuals and a set of different DNA traces. The case possibly involves persons of interest of a small population of Romani origin. First, a brief description of the case is provided. Secondly, we introduce some heuristic tools that can be used to evaluate the data and we also briefly outline the statistical model used for analysing DNA mixtures. Finally, we illustrate some of the findings on the case and discuss further directions of research. The results show how the use of different population database allele frequencies for analysing the DNA mixtures can lead to very different results, some seemingly inculpatory and some seemingly exculpatory. We also illustrate the results obtained from combining the evidence from different samples., (Copyright © 2019 Elsevier B.V. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
18. Highly Predictive Genetic Markers Distinguish Drug-Type from Fiber-Type Cannabis sativa L.
- Author
-
Cascini F, Farcomeni A, Migliorini D, Baldassarri L, Boschi I, Martello S, Amaducci S, Lucini L, and Bernardi J
- Abstract
Genetic markers can be used in seeds and in plants to distinguish drug-type from fiber-type Cannabis Sativa L. varieties even at early stages, including pre-germination when cannabinoids are not accumulated yet. With this aim, this paper reports sequencing results for tetrahydrocannabinolic acid synthase ( THCAS ) and cannabidiolic acid synthase ( CBDAS ) genes from 21 C. sativa L. varieties. Taking into account that THCAS - and CBDAS -derived enzymes compete for the same substrate, the novelty of this work relies in the identification of markers based on both THCAS and CBDAS rather than THCAS alone. Notably, in our panel, we achieved an adequate degree of discrimination (AUC 100%) between drug-type and fiber-type cannabis samples. Our sequencing approach allowed identifying multiple genetic markers (single-nucleotide polymorphisms-SNPs-and a deletion/insertion) that effectively discriminate between the two subgroups of cannabis, namely fiber type vs. drug type. We identified four functional SNPs that are likely to induce decreased THCAS activity in the fiber-type cannabis plants. We also report the finding on a deletion in the CBDAS gene sequence that produces a truncated protein, possibly resulting in loss of function of the enzyme in the drug-type varieties. Chemical analyses for the actual concentration of cannabinoids confirmed the identification of drug-type rather than fiber-type genotypes. Genetic markers permit an early identification process for forensic applications while simplifying the procedures related to detection of therapeutic or industrial hemp.
- Published
- 2019
- Full Text
- View/download PDF
19. Adhesion and biofilm formation by Staphylococcus aureus clinical isolates under conditions relevant to the host: relationship with macrolide resistance and clonal lineages.
- Author
-
Di Bonaventura G, Pompilio A, Monaco M, Pimentel de Araujo F, Baldassarri L, Pantosti A, and Gherardi G
- Subjects
- A549 Cells, Adolescent, Adult, Aged, Aged, 80 and over, Anti-Bacterial Agents pharmacology, Bacterial Adhesion drug effects, Bacterial Adhesion genetics, Bacterial Proteins genetics, Clindamycin pharmacology, Drug Resistance, Bacterial genetics, Electrophoresis, Gel, Pulsed-Field, Erythromycin pharmacology, Female, Genotype, Humans, Ketolides pharmacology, Male, Methicillin-Resistant Staphylococcus aureus classification, Methicillin-Resistant Staphylococcus aureus drug effects, Methicillin-Resistant Staphylococcus aureus genetics, Methicillin-Resistant Staphylococcus aureus physiology, Middle Aged, Multilocus Sequence Typing, Penicillin-Binding Proteins genetics, Phenotype, Staphylococcal Infections epidemiology, Staphylococcus aureus classification, Staphylococcus aureus genetics, Young Adult, Bacterial Adhesion physiology, Biofilms growth & development, Macrolides pharmacology, Staphylococcal Infections microbiology, Staphylococcus aureus drug effects, Staphylococcus aureus physiology
- Abstract
Purpose: Staphylococcus aureus isolates, collected from various clinical samples, were analysed to evaluate the contribution of the genetic background of both erythromycin-resistant (ERSA) and -susceptible (ESSA) S. aureus strains to biofilm formation., Methods: A total of 66 ESSA and 43 ERSA clinical isolates were studied for adhesiveness and biofilm formation under different atmospheres. All isolates were evaluated for phenotypic and genotypic macrolide resistance, and for clonal relatedness by pulsed-field gel electrophoresis (PFGE), and by spa typing on representative isolates., Results: A high genetic heterogeneity was encountered, although 10 major PFGE types accounted for 86 % with a few small spatially and temporally related clusters. Overall, biofilm formation under anoxia was significantly lower than under oxic and micro-aerophilic atmospheres. Biofilm formation by ESSA was significantly higher compared to ERSA under oxic and micro-aerophilic conditions. Adhesiveness to plastic was significantly higher among respiratory tract infection isolates under micro-aerophilic conditions, while surgical site infection isolates formed significantly higher biomass of biofilm under oxic and micro-aerophilic atmospheres compared to anoxia. Pulsotype 2 and 4 strains formed significantly higher biofilm biomass than pulsotype 1, with strains belonging to CC8 forming significantly more compared to those belonging to CC5, under both oxic and micro-aerophilic atmospheres., Conclusions: S. aureus biofilm formation appears to be more efficient in ESSA than ERSA, associated with specific S. aureus lineages, mainly CC8 and CC15, and affected by atmosphere. Further studies investigating the relationship between antibiotic resistance and biofilm formation could prove useful in the development of new strategies for the management of S. aureus infections.
- Published
- 2019
- Full Text
- View/download PDF
20. Neonatal Group B Streptococcus Infections: Prevention Strategies, Clinical and Microbiologic Characteristics in 7 Years of Surveillance.
- Author
-
Creti R, Imperi M, Berardi A, Pataracchia M, Recchia S, Alfarone G, and Baldassarri L
- Subjects
- Anti-Bacterial Agents pharmacology, Clindamycin pharmacology, Cross-Sectional Studies, Drug Resistance, Bacterial, Erythromycin pharmacology, Humans, Infant, Newborn, Molecular Epidemiology, Risk Factors, Serogroup, Streptococcal Infections diagnosis, Streptococcal Infections microbiology, Streptococcus agalactiae drug effects, Streptococcal Infections epidemiology, Streptococcal Infections prevention & control, Streptococcus agalactiae genetics
- Abstract
Background: The characteristics of group B streptococcus (GBS) neonatal disease in a period of 7 years are reported., Methods: The estimation of the neonatal GBS disease risk and prevention strategies adopted at delivery in absence of national guidelines was evaluated by the analysis of 3501 questionnaires. Notification of 194 neonatal GBS infections was recorded. In addition, 115 strains from neonatal early-onset disease (EOD) and late-onset disease, respectively, plus 320 strains from pregnant women were analyzed by molecular typing methods and for antibiotic resistance., Results: Preterm deliveries, precipitous labor and GBS negatively screened mothers were the prominent causes for an inadequate or lack of intrapartum antibiotic prophylaxis and EOD occurrence. The superimposable serotype distribution of GBS strains from EOD and from antenatal screening confirmed the vertical transmission from mother to neonate as the cause of disease. On the contrary, late-onset disease was almost exclusively caused by the internationally diffused clonal complex 17. Erythromycin resistance was detected in 17% of strains. Resistance to clindamycin was 15.3 %., Conclusions: The administration of intrapartum antibiotic prophylaxis to negatively GBS screened women in presence of risk factors was a deviation from the recommendations issued by the Centers for Disease Control and Prevention, and it should deserve further consideration. Routine surveillance and molecular typing of circulating clones are essential for the effective management of the neonatal GBS disease.
- Published
- 2017
- Full Text
- View/download PDF
21. The Protective Value of Maternal Group B Streptococcus Antibodies: Quantitative and Functional Analysis of Naturally Acquired Responses to Capsular Polysaccharides and Pilus Proteins in European Maternal Sera.
- Author
-
Fabbrini M, Rigat F, Rinaudo CD, Passalaqua I, Khacheh S, Creti R, Baldassarri L, Carboni F, Anderloni G, Rosini R, Maione D, Grandi G, Telford JL, and Margarit I
- Subjects
- Europe epidemiology, Female, Humans, Immunoglobulin G blood, Pregnancy, Prospective Studies, Streptococcal Infections epidemiology, Antibodies, Bacterial blood, Fimbriae, Bacterial immunology, Immunity, Maternally-Acquired, Polysaccharides, Bacterial immunology, Streptococcal Infections immunology, Streptococcus agalactiae immunology
- Abstract
Background: Group B Streptococcus (GBS) is a major cause of neonatal sepsis and meningitis. A vaccine targeting pregnant women could protect infants through placentally transferred antibodies. The association between GBS maternal antibody concentrations and the risk of neonatal infection has been investigated in US and African populations. Here we studied naturally acquired immunoglobulin G (IgG) responses to GBS capsular polysaccharides (CPS) and pilus proteins in European pregnant women., Methods: Maternal sera were prospectively collected in 8 EU countries from 473 GBS non-colonized and 984 colonized pregnant women who delivered healthy neonates and from 153 mothers of infants with GBS disease. GBS strains from these colonized women and infected infants were obtained in parallel and their capsular and pilus types were identified by serological and molecular methods. Maternal serum concentrations of IgG anti- Ia, -Ib, -III and -V polysaccharides and anti-BP-1, -AP1-2a and -BP-2b pilus proteins were determined by enzyme-linked immunosorbent assay. Antibody functional activity was quantified by Opsonophagocytic Killing Assay., Results: Antibody levels against CPS and pilus proteins were significantly higher in GBS colonized women delivering healthy babies than in mothers of neonates with GBS disease or non-colonized women. Moreover, maternal anti-capsular IgG concentrations showed a significant correlation with functional titers measured by Opsonophagocytic Killing Assay., Conclusions: Maternal anti-capsular IgG concentrations above 1 µg/mL mediated GBS killing in vitro and were predicted to respectively reduce by 81% (95% confidence interval, 40%-100%) and 78% (45%-100%) the risk of GBS Ia and III early-onset disease in Europe., (© The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail journals.permissions@oup.com.)
- Published
- 2016
- Full Text
- View/download PDF
22. A new genotyping scheme based on MLVA for inter-laboratory surveillance of Streptococcus pyogenes.
- Author
-
Imperi M, Pittiglio V, D'Avenio G, Gherardi G, Ciammaruconi A, Lista F, Pourcel C, Baldassarri L, and Creti R
- Subjects
- Electrophoresis, Gel, Pulsed-Field, Humans, Minisatellite Repeats, Streptococcal Infections microbiology, Streptococcus pyogenes classification, Bacterial Proteins genetics, Genotyping Techniques economics, Multilocus Sequence Typing methods, Streptococcus pyogenes genetics
- Abstract
A newly developed MLVA seven-loci scheme for Streptococcus pyogenes is described. The method can be successfully applied by using both agarose gel with visual inspections of bands and Lab on Chip technology. The potential of the present MLVA has been tested on a collection of 100 clinical GAS strains representing the most common emm types found in high-income countries plus 18 published gap-free genomes, in comparison to PFGE and MLST. The MLVA analysis defined 30 MLVA types with ten out of the considered 15 emm types exhibiting multiple and specific MLVA types. In only one occasion the same MLVA profile was shared between isolates belonging to two different emm types. A robust congruency between the methods was observed, with MLVA discriminating within clonal complexes as defined by PFGE or MLST. This new MLVA scheme can be adopted as a quick, low-cost and reliable typing method to track the short-term diffusion of GAS clones in inter-laboratory-based surveillance., (Copyright © 2016 Elsevier B.V. All rights reserved.)
- Published
- 2016
- Full Text
- View/download PDF
23. Presence of Epsilon HCH Together with Four Other HCH Isomers in Drinking Water, Groundwater and Soil in a Former Lindane Production Site.
- Author
-
Fuscoletti V, Achene L, Gismondi F, Lamarra D, Lucentini L, Spina S, Veschetti E, and Turrio-Baldassarri L
- Subjects
- Animals, Cattle, Food Contamination, Geography, Isomerism, Italy, Milk chemistry, Rivers, Soil chemistry, Water Pollutants, Chemical analysis, Chemical Industry, Drinking Water analysis, Environmental Monitoring methods, Groundwater analysis, Hexachlorocyclohexane analysis, Industrial Waste analysis, Soil Pollutants analysis
- Abstract
In the frame of a long-standing action of remediation of industrial soil and prevention of water pollution, a monitoring of the drinking water of the Italian town of Colleferro was performed by the ISS. The town has 22,000 inhabitants and is adjacent to a big industrial site where HCH was produced. Industrial wastes were buried in the site, eventually contaminating superficial aquifers, while a canal serving the industrial plant spread the contamination into the Sacco river and thence to the agricultural soil and to cow milk. The contamination of superficial aquifers engendered fears of pollution of the deep aquifers whence the town draws its drinking water. The results of the monitoring indicate that there is no risk for the population from consumption of the water. In one of the wells the ε-HCH was the main isomer reaching a concentration of 66 ng/L: so far the presence of this isomer in water was never reported. The paper also summarily reports the main features of soil and superficial groundwater pollution in the area and briefly describes the main actions taken by the authorities.
- Published
- 2015
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.