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1.
Phytopathology ; 108(3): 362-373, 2018 Mar.
Article in English | MEDLINE | ID: mdl-29027886

ABSTRACT

Bois noir (BN) is the most widespread disease of the grapevine yellows complex in the Euro-Mediterranean area. BN is caused by 'Candidatus Phytoplasma solani' (BNp), transmitted from herbaceous plants to grapevine by polyphagous insect vectors. In this study, genetic diversity among BNp strains and their prevalence and possible association with grapevine symptom severity were investigated in a Sangiovese clone organic vineyard in the Chianti Classico area (Tuscany). Field surveys over 2 years revealed a range of symptom severity on grapevine and an increase of BN incidence. A TaqMan allelic discrimination assay detected only tufB type b among BNp strains, suggesting the prevalence of the bindweed-related ecology. Nucleotide sequence analyses of vmp1 and stamp genes identified 12 vmp1 and 16 stamp sequence variants, showing an overall positive selection for such genes. The prevalent genotype was Vm43/St10, reported for the first time in this study and closely related to strains identified only in the French Eastern Pyrenees. BNp strains identified in the examined vineyard and mostly grouped in separate bindweed-related phylogenetic clusters showed statistically significant differences in their distribution in grapevines exhibiting distinct symptom severity. These results suggest the possible occurrence of a range of virulence within BNp strain populations in the Chianti Classico area.


Subject(s)
Phytoplasma/classification , Plant Diseases/microbiology , Vitis/microbiology , DNA, Bacterial/genetics , DNA, Bacterial/metabolism , Italy , Molecular Typing , Phylogeny , Phytoplasma/genetics
2.
Arzneimittelforschung ; 44(12A): 1503-5, 1994 Dec.
Article in English | MEDLINE | ID: mdl-7857352

ABSTRACT

The aim of this study was to evaluate the activity of pidotimod ((R)-3-[(S)-(5-oxo-2-pyrrolidinyl)carbonyl]-thiazolidine-4-carboxylic acid, PGT/1A, CAS 121808-62-6) on 52 patients affected with chronic obstructive pulmonary disease (COPD). The study was carried out in a randomized, parallel, double-blind trial, followed by incomplete blocks design. Pidotimod 800 mg was administered orally twice a day for 30 days. The follow-up period was 5 weeks. Our results show that in patients with COPD pidotimod potentiates T-cell activity. The effects on T-cells appear after 15 days of treatment and last for 5 weeks after the end of therapy. Since other studies demonstrated that pidotimod displays an immunopotentiating activity also on macrophages and granulocytes, the drug is useful to increase the immune defense during infections. The drug has a good compliance and is well tolerated also during long-term treatment.


Subject(s)
Adjuvants, Immunologic/therapeutic use , Lung Diseases, Obstructive/drug therapy , Pyrrolidonecarboxylic Acid/analogs & derivatives , Thiazoles/therapeutic use , Adjuvants, Immunologic/adverse effects , Adult , Aged , Aged, 80 and over , Double-Blind Method , Female , Follow-Up Studies , Granulocytes/drug effects , Granulocytes/immunology , Humans , Lung Diseases, Obstructive/immunology , Lymphocyte Activation/drug effects , Lymphocytes/drug effects , Lymphocytes/immunology , Macrophages/drug effects , Macrophages/immunology , Male , Middle Aged , Pyrrolidonecarboxylic Acid/adverse effects , Pyrrolidonecarboxylic Acid/therapeutic use , Thiazoles/adverse effects , Thiazolidines
4.
Minerva Med ; 76(1-2): 43-52, 1985 Jan 14.
Article in Italian | MEDLINE | ID: mdl-3974918

ABSTRACT

After a thorough description of the physiological background, the problem of chest pain is examined with extensive documentation including pictures. It is suggested that meticulous clinical assessment is of even greater value than laboratory tests or instrumental explorations for the accurate diagnosis and appropriate treatment of the condition causing the pain. In other words laboratory and instrumental assessments should be based on and used to confirm an approximate diagnosis formed on clinical data.


Subject(s)
Pain/etiology , Thorax/physiopathology , Abdomen/physiopathology , Diagnosis, Differential , Heart Diseases/diagnosis , Heart Diseases/physiopathology , Humans , Lung Diseases/diagnosis , Lung Diseases/physiopathology , Pain/physiopathology , Spinal Diseases/diagnosis , Spinal Diseases/physiopathology , Thoracic Injuries/diagnosis , Thoracic Injuries/physiopathology , Thorax/innervation
5.
Minerva Med ; 72(25): 1599-603, 1981 Jun 23.
Article in Italian | MEDLINE | ID: mdl-7254608

ABSTRACT

Following a brief mention of the classification of Hammer-Rich disease within idiopathic diffuse pulmonary fibrosis, the main clinical, radiological and laboratory features of these disease are outlined in brief. A personal case, subsequently controlled neroptically and histologically, is then described. From comparison between reported data and findings in the personal case, it is concluded that it was a typical, rare case (less than 150 others have so far been reported in all world literature) of Hamman-Rich disease. Other diagnostic hypotheses can be rejected because they are less correspondent to the typical picture and for various other considerations.


Subject(s)
Pulmonary Fibrosis/pathology , Pulmonary Heart Disease/etiology , Cyanosis/etiology , Diagnosis, Differential , Dyspnea/etiology , Humans , Male , Middle Aged , Pulmonary Fibrosis/diagnosis , Tuberculosis, Pulmonary/diagnosis
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