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1.
Epidemiol Infect ; 141(12): 2650-7, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23445723

ABSTRACT

The objective of this study was to assess the prevalence of Ureaplasma urealyticum and Mycoplasma hominis infections and to investigate associations between their presence in the lower female genital tract and lifestyle characteristics. The study was performed on a population of 3115 women, comparing the demographic and behavioural characteristics of 872 women with U. urealyticum infection and 142 women with M. hominis with uninfected women, using univariate and multiple logistic regression analysis. The prevalence of infection with U. urealyticum was 28% and M. hominis was 4.6%. In multivariate logistic regression analysis, intrauterine device, number of sexual partners and age (<35 years) were significantly associated with U. urealyticum while previous induced abortion, condom use and young age at first intercourse (<16 years) were associated with M. hominis infection. U. urealyticum infection presents the same demographic and behavioural characteristics of a sexually transmitted disease. The unprotective role of condom use suggests a non-sexual mode of transmission of M. hominis infection.


Subject(s)
Mycoplasma Infections/epidemiology , Mycoplasma hominis/isolation & purification , Reproductive Tract Infections/epidemiology , Ureaplasma Infections/epidemiology , Ureaplasma urealyticum/isolation & purification , Adolescent , Adult , Female , Humans , Middle Aged , Outpatients , Prevalence , Rome/epidemiology , Sexual Behavior , Young Adult
2.
Euro Surveill ; 17(25)2012 Jun 21.
Article in English | MEDLINE | ID: mdl-22748006

ABSTRACT

As reliable data on Chlamydia trachomatis infection in Italy are lacking and as there is no Italian screening policy, epidemiological analyses are needed to optimise effective strategies for surveillance of the infection in the country. We collected data from 6,969 sexually active women aged 15 to 55 years who underwent testing for endocervical C. trachomatis infection at the Cervico-Vaginal Pathology Unit in the Department of Gynaecology and Obstetrics of Sapienza University in Rome between 2000 and 2009. The mean prevalence of C. trachomatis endocervical infection during this period was 5.2%. Prevalence over time did not show a linear trend. Univariate analysis demonstrated a significant association of infection with multiple lifetime sexual partners, younger age (<40 years), never having been pregnant, smoking, use of oral contraceptives, and human papillomavirus and Trichomonas vaginalis infections. Multivariate stepwise logistic regression showed that T. vaginalis infection, age under 20 years and more than one lifetime sexual partner remained significantly associated with C. trachomatis infection in the final model. Prevalence of C. trachomatis in this study was high, even among women aged 25­39 years (5.1%): our data would suggest that a C. trachomatis screening policy in Italy is warranted, which could lead to a more extensive testing strategy.


Subject(s)
Chlamydia Infections/diagnosis , Chlamydia Infections/epidemiology , Chlamydia trachomatis/isolation & purification , Uterine Cervicitis/diagnosis , Adolescent , Adult , Age Distribution , Amplified Fragment Length Polymorphism Analysis , Chlamydia Infections/microbiology , Chlamydia trachomatis/genetics , DNA, Bacterial/analysis , DNA, Bacterial/genetics , Female , Hospitals, University , Humans , Italy/epidemiology , Logistic Models , Mass Screening/methods , Middle Aged , Population Surveillance , Prevalence , Risk Factors , Sexual Behavior , Socioeconomic Factors , Surveys and Questionnaires , Uterine Cervicitis/epidemiology , Uterine Cervicitis/microbiology , Young Adult
3.
Int J Immunopathol Pharmacol ; 24(2): 523-7, 2011.
Article in English | MEDLINE | ID: mdl-21658329

ABSTRACT

Keratosis pilaris (KP) is a follicular hyperkeratosis disorder which is frequently detected in the adult population (44%), mostly in female adolescents (80%). It is a genetic autodominant dermatosis with variable penetrance, but no specific gene association has been determined, even though association to the presence of chromosome 18p deletion has been reported in some cases. We report the case of a 51-year-old Caucasian woman affected by keratosis pilaris gradually progressing with age and with a story of multiple abortions. Standard karyotype and CGH array analyses did not reveal any genetic abnormality. Virological analyses detected the presence of HPV 36 DNA inside the dorsum biopsy, leading to hypothesize its involvement in the evolution of the lesion. Clinical history and patient examination led the diagnosis of an idiopathic case of Ulerythema ophryogenes. The analysis of more cases could be useful to verify the involvement of cutaneous HPV in the progression of the clinical manifestation of the KP variants.


Subject(s)
Diagnostic Errors/prevention & control , Skin/pathology , Abnormalities, Multiple/diagnosis , Abnormalities, Multiple/genetics , Abnormalities, Multiple/pathology , Abnormalities, Multiple/virology , Abortion, Spontaneous/genetics , Base Sequence , Biopsy , Comparative Genomic Hybridization , DNA, Viral/analysis , Darier Disease , Eyebrows/abnormalities , Eyebrows/pathology , Eyebrows/virology , Female , Humans , Karyotyping , Keratosis/diagnosis , Keratosis/genetics , Keratosis/pathology , Keratosis/virology , Middle Aged , Molecular Sequence Data , Papillomaviridae/genetics , Predictive Value of Tests , Skin/virology , Stillbirth/genetics
4.
Int J Immunopathol Pharmacol ; 24(1): 217-23, 2011.
Article in English | MEDLINE | ID: mdl-21496405

ABSTRACT

The aim of this study is to monitor type I interferon (IFN) activation in the cervical mucosa of Human Papillomavirus (HPV)-infected and uninfected women attending a routine gynaecologic clinic. The expression of three IFN-induced genes (MxA coding for human Mixovirus resistance protein A, ISG15 Interferon Stimulated Gene coding for a 15 kDa ubiquitin-like protein and UBP43 coding for the ISG15 isopeptidase) was determined as the mRNA copy number in cervical cells, normalized to the mRNA ones of the beta-glucuronidase gene. Type-specific HPV-DNA load was concurrently determined in the HPV-positive samples. Out of 127 samples tested, 54 were sufficient for both DNA and RNA extraction. The type-specific HPV-DNA copy numbers in the 34 HPV-positive samples varied widely. No significant association was found between copy numbers of MxA, ISG15, UBP43 and HPV status or viral load. However, despite a marked inter-individual variability, ISG15 expression was significantly higher when low-risk HPV infections were compared with HPV-negative samples, while high-risk HPV infections had very low ISG15 levels. The lack of ISG15 activation in high-risk HPV-infected cervical cells could be due to the lack of p53-mediated induction or to HPV-directed specific inhibition of type I IFN pathways. This study approach might be of value in clarifying the role of type I IFN activation in determining the clearance or persistence of HPV infections.


Subject(s)
Cervix Uteri/immunology , Interferon Type I/physiology , Mucous Membrane/immunology , Papillomavirus Infections/immunology , Adolescent , Adult , Cervix Uteri/virology , Cytokines/genetics , DNA, Viral/analysis , Endopeptidases/genetics , Female , GTP-Binding Proteins/genetics , Gene Expression Regulation , Humans , Middle Aged , Mucous Membrane/virology , Myxovirus Resistance Proteins , Papillomaviridae/isolation & purification , Papillomavirus Infections/virology , RNA, Messenger/analysis , Ubiquitin Thiolesterase , Ubiquitins/genetics , Viral Load
5.
Int J Immunopathol Pharmacol ; 23(1): 369-72, 2010.
Article in English | MEDLINE | ID: mdl-20378026

ABSTRACT

Scrotal elephantiasis is very rare disease in industrialized countries, where it is mainly due to surgery, irradiation or malignancies. It can be defined as idiopathic only when the possible congenital, infectious and compressive causes are excluded. We report a case of massive scrotal lymphoedema in an adult Caucasian patient, in Italy. He presented an extremely voluminous scrotal mass measuring 50 x 47 x 13 cm (weight 18 kg), which extended below his knees, invalidating all his daily activities. The patient was hospitalized in order to undergo to surgical treatment. Although genetic causes were searched and the possible role of infectious agents and compressive factors was evaluated, no etiology was ascertained. Histopathologic examination showed non-specific chronic inflammation, confirming the diagnosis of idiopathic elephantiasis. One year after surgical treatment, the patient is healthy without recurrence signs.


Subject(s)
Elephantiasis/surgery , Scrotum/pathology , Adult , Elephantiasis/diagnosis , Elephantiasis/pathology , Humans , Male , Vascular Endothelial Growth Factor Receptor-3/genetics
6.
J Appl Microbiol ; 106(5): 1608-17, 2009 May.
Article in English | MEDLINE | ID: mdl-19226391

ABSTRACT

AIMS: The aim of the work was to evaluate the circulation of the viruses and to determine a correlation between faecal indicators and viruses. METHODS AND RESULTS: Raw wastewater and effluent samples were collected from three wastewater treatment plants, during three sampling periods, and analysed, using cultural and molecular methods, to determine bacteria and virus presence. The results show a removal of bacterial indicators, but a limited reduction of the phages. The viral analysis displays the circulation of cultivable enteroviruses and differences in the seasonal-geographical distribution. Hepatitis A virus was found with only two genotypes: IA-IB. Rotavirus was present in 11.11%, 24.14%, 2.78% of the samples in the 1st, 2nd and 3rd sampling periods; Astrovirus in 33.33%, 6.9%, 25%; Adenovirus in 7.41%, 3.45%, 2.78%; Norovirus in 7.41%, 10.34%, 5.56% respectively. Adenovirus was never identified in plants B and C as Rotavirus in plant C. CONCLUSIONS: The presence of faecal indicators was not predictive of the enteric virus presence, whereas a different circulation of Enteroviruses was found in the wastewater treatment plants. SIGNIFICANCE AND IMPACT OF THE STUDY: The study shows the importance and the usefulness of molecular methods to evaluate the virus circulation and the genetic variability of Enteroviruses.


Subject(s)
Enterovirus/isolation & purification , Gastrointestinal Diseases/virology , Hepatitis A virus/isolation & purification , Waste Disposal, Fluid/methods , Water Microbiology , Coliphages/isolation & purification , Enterobacteriaceae/isolation & purification , Enterovirus/classification , Enterovirus/genetics , Feces/microbiology , Feces/virology , Genome, Viral , Hepatitis A virus/classification , Hepatitis A virus/genetics , Phylogeny , RNA Phages/isolation & purification , RNA, Viral/isolation & purification
7.
Int J Immunopathol Pharmacol ; 21(1): 145-52, 2008.
Article in English | MEDLINE | ID: mdl-18336740

ABSTRACT

Actinic keratoses (AK) are common, premalignant lesions cause mainly by UV DNA damage. Progression into squamous cell carcinoma may be influenced by other several factors such as chronic chemical exposure or viral infection. A carcinogenic role of Human Papillomaviruses (HPV) in early steps of skin tumour development was recently hypothesized; moreover the presence of HPV DNA seems to be higher in cancer precursor lesions. The aim of this work is to identify the presence of HPV DNA in biopsies from Actinic Keratoses (AK) and from normal skin samples collected from dermatological healthy subjects in Italy, in order to evaluate the severity and the clinical evolution of the HPV positive lesions. The DNA test revealed 37% HPV positivity in AK patients versus 0% in the control group; many different genotypes and variants were identified by direct sequencing of PCR product. The HPV positive AK were usually clinically indistinguishable from the HPV negative. All AK lesions were removed by laser treatment, but AK lesions recurred in all HPV positive patients after a period of 45-60 days whereas the same disappeared in the HPV negative ones. These data permit to hypothesize that the presence of HPV DNA could be an aggravating factor for AK lesion severity and recurrence.


Subject(s)
Keratosis/virology , Papillomaviridae/isolation & purification , Skin/virology , Adult , Aged , DNA, Viral/analysis , Female , Humans , Male , Middle Aged , Recurrence
8.
Clin Microbiol Infect ; 13(1): 94-7, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17184295

ABSTRACT

Human papillomavirus (HPV) genotypes and HPV DNA load were analysed in cervical smears from 76 human immunodeficiency virus (HIV)-positive and 54 HIV-negative women. The prevalence of genotypes was similar for all women, with the exception of HPV62, which was over-represented in HIV-positive samples. HIV-positive women showed a higher prevalence of multiple genotypes that correlated neither with CD4(+) T-cell counts nor with cervical dysplasia. No significant differences were observed in terms of total or single-type HPV DNA load. The HPV DNA load in both HIV-positive and HIV-negative women was significantly higher in squamous intra-epithelial lesions than in negative Pap smears.


Subject(s)
HIV Infections/complications , HIV , Neoplasms, Squamous Cell/complications , Neoplasms, Squamous Cell/virology , Papillomaviridae/genetics , Papillomavirus Infections/complications , Papillomavirus Infections/virology , Uterine Cervical Dysplasia/complications , Uterine Cervical Dysplasia/virology , Adult , DNA, Viral/genetics , Female , Genetic Markers/genetics , Humans , Middle Aged , Papillomaviridae/classification , Polymerase Chain Reaction , Species Specificity
9.
Int J Immunopathol Pharmacol ; 19(1): 209-15, 2006.
Article in English | MEDLINE | ID: mdl-16569359

ABSTRACT

Our study is aimed at evaluating the presence of p53 and Ki67 expression by immunohistochemistry in a series of 11 paraffin-embedded penile carcinomas. We also investigated the presence of Human Papillomavirus (HPV) DNA in these tumours and performed an accurate typing by DNA sequencing on positive samples. Immunohistochemistry (IHC) was performed with the anti-p53 and Ki67 mouse monoclonal antibodies. DNA extracted from small sections of each specimen was submitted to amplification with HPV specific general primers; PCR products of the proper length were purified and sequenced. IHC demonstrated nuclear accumulation of mutated p53 and Ki 67 expression in 10/11 tumour samples (90.9%). The prevalence of HPV DNA was 72.7%; the most prevalent type was HPV16. Sequencing analysis revealed the presence of HPV53 (12.5%), HPV18 (25%) and HPV16 (62.5%). Out of the p53 or Ki67 positive carcinomas the percentage of HPV positives was 80% and 70% respectively. Our results indicate that penile carcinoma is frequently associated to high risk HPV and with diffuse p53 and Ki67 expression.


Subject(s)
DNA, Viral/biosynthesis , Ki-67 Antigen/biosynthesis , Papillomaviridae/metabolism , Penile Neoplasms/metabolism , Tumor Suppressor Protein p53/biosynthesis , DNA, Viral/analysis , DNA, Viral/genetics , Genotype , Humans , Immunohistochemistry , Ki-67 Antigen/analysis , Lymph Node Excision , Male , Papillomaviridae/genetics , Paraffin Embedding , Penile Neoplasms/chemistry , Penile Neoplasms/surgery , Reverse Transcriptase Polymerase Chain Reaction , Tumor Suppressor Protein p53/analysis
10.
Int J Immunopathol Pharmacol ; 18(2): 309-16, 2005.
Article in English | MEDLINE | ID: mdl-15888253

ABSTRACT

Hemorrhagic cystitis (HC) is a well-known complication after allogeneic bone marrow transplant (BMT) and can be related to adenovirus or human polyomavirus BK (BKV) infections. In this study a group of 20 patients after allogeneic BMT has been examined. BMT urine samples were analysed for the presence of Adenovirus and BKV DNAby means of polymerase chain reaction (PCR). 5/20 BMT patients developed HC after BMT. The presence of BKV DNA in urine samples was evident in 3/15 patients without HC and in 5/5 patients with HC. In 2/5 HC-patients the BKV DNA was not found after therapy with Cidofovir and Ribavirin. The search for adenovirus DNA in all samples was negative. The analysis of BKV non-coding control region (NCCR) isolated from urine samples revealed a structure very similar to the archetype in all samples. The RFLP (Restriction Fragment Length Polymorphism assay) showed the presence of BKV subtypes I and IV, with the prevalence of subtype I (4/5). This study supports the hypothesis that HC is mainly related to BKV rather than to adenovirus infection in BMT patients. Moreover, since BKV subtype I was predominant, it is reasonable to hypothesize that a specific BKV subtype could be associated with the development of HC.


Subject(s)
BK Virus/isolation & purification , Bone Marrow Transplantation , Cystitis/virology , DNA, Viral/analysis , Hemorrhage/virology , Polyomavirus Infections/virology , Adenoviridae/genetics , Adenoviridae/isolation & purification , Adenoviridae Infections/urine , Adenoviridae Infections/virology , Adult , BK Virus/genetics , Base Sequence , Cystitis/urine , DNA, Viral/urine , Female , Hemorrhage/urine , Humans , Locus Control Region/genetics , Male , Middle Aged , Molecular Sequence Data , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Polyomavirus Infections/urine , Sequence Alignment , Transplantation, Homologous , Urine/virology
11.
J Cell Physiol ; 204(3): 913-8, 2005 Sep.
Article in English | MEDLINE | ID: mdl-15828018

ABSTRACT

JC virus (JCV) causes progressive multifocal leukoencephalopathy (PML), characterized by multiple areas of demyelination and attendant loss of brain function. PML is often associated with immunodepression and it is significantly frequent in AIDS patients. The viral genome is divided into early and late genes, between which lies a non-coding control region (NCCR) that regulates JCV replication and presents a great genetic variability. The NCCR of JCV archetype (CY strain) is divided into six regions: A-F containing binding sites for cell factors involved in viral transcription. Deletions and enhancements of these binding sites characterize JCV variants, which could promote viral gene expression and could be more suitable for the onset or development of PML. Therefore, we evaluated by means of polymerase chain reaction (PCR) the presence of JCV genome in cerebrospinal fluid (CSF) of HIV positive and negative subjects both with PML and after sequencing, we analyzed the viral variants found focusing on Sp1 binding sites (box B and D) and up-TAR sequence (box C). It is known that Sp1 activates JCV early promoter and can contribute in maintaining methylation-free CpG islands in active genes, while up-TAR sequence is important for HIV-1 Tat stimulation of JCV late promoter. Our results showed that in HIV-positive subjects all NCCR structures presented enhancements of up-TAR element, whereas in HIV-negative subjects both Sp1 binding sites were always retained. Therefore, we can support the synergism HIV-1/JCV in CNS and we can hypothesize that both Sp1 binding sites could be important to complete JCV replication cycle in absence of HIV-coinfection.


Subject(s)
Gene Products, tat/metabolism , Leukoencephalopathy, Progressive Multifocal/metabolism , Leukoencephalopathy, Progressive Multifocal/pathology , Sp1 Transcription Factor/metabolism , Adult , Aged , Base Sequence , Binding Sites , Consensus Sequence/genetics , Disease Progression , HIV Seronegativity , HIV Seropositivity/cerebrospinal fluid , HIV Seropositivity/complications , HIV Seropositivity/metabolism , HIV Seropositivity/virology , Humans , JC Virus/genetics , JC Virus/isolation & purification , Leukoencephalopathy, Progressive Multifocal/complications , Leukoencephalopathy, Progressive Multifocal/virology , Middle Aged , Molecular Sequence Data , Sequence Alignment , tat Gene Products, Human Immunodeficiency Virus
12.
J Cell Physiol ; 204(2): 402-6, 2005 Aug.
Article in English | MEDLINE | ID: mdl-15690396

ABSTRACT

In human cancer, a role has been suggested for the human polyomavirus BK, primarily associated with tubulointerstitial nephritis and ureteric stenosis in renal transplant recipients, and with hemorrhagic cystitis in bone marrow transplant (BMT) recipients. After the initial infection, primarily unapparent and without clinical signs, the virus disseminates and establishes a persistent infection in the urinary tract and lymphocytes. There is correlative evidence regarding potential role of polyomavirus BK in cancer. In fact, the BK virus (BKV) DNA (complete genome and/or subgenomic fragments containing the early region) is able to transform embryonic fibroblasts and cells cultured from kidney and brain of hamster, mouse, rat, rabbit, and monkey. Nevertheless, transformation of human cells by BKV is inefficient and often abortive. Evidence supporting a possible role for BKV in human cancer has accumulated slowly in recent years, after the advent of polymerase chain reaction (PCR). BKV is known to commonly establish persistent infections in people and to be excreted in the urine by individuals who are asymptomatic, complicating the evaluation of its potential role in development of human cancer. Therefore, there is no certain proof that human polyomavirus BK directly causes the cancer in humans or acts as a cofactor in the pathogenesis of some types of human cancer.


Subject(s)
BK Virus , Neoplasms/virology , Polyomavirus Infections/complications , Animals , Antigens, Viral, Tumor/metabolism , BK Virus/genetics , BK Virus/immunology , Cell Transformation, Neoplastic , Cell Transformation, Viral , Genome, Viral , Humans , Polyomavirus Infections/physiopathology
13.
Clin Microbiol Infect ; 11(1): 47-51, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15649303

ABSTRACT

Human papilloma virus type 5 (HPV-5) has been associated closely with psoriatic skin in Polish patients, while findings from other countries have indicated a more limited prevalence. The results of the present study, in which a type-specific nested PCR was used, indicated that scales of plaque-type psoriatic skin from 54 Italian patients had a high prevalence (74.1%) of HPV-5 DNA in lesional areas, and a reduced prevalence (33.3%) in non-lesional skin (33.3%), compared to 0% of 20 healthy subjects and 3.6% in the lesional areas of 28 patients with various other dermatological diseases. Individuals negative for HPV-5 DNA had a less severe disease. No correlation was found between the presence of HPV DNA and a patient's age or sex. The data demonstrated a statistically significant association between psoriasis and HPV-5, although results in other geographical areas suggest variable virus spread or ethnic variation in virus colonisation.


Subject(s)
DNA, Viral/analysis , Papillomaviridae/isolation & purification , Psoriasis/virology , Skin/pathology , Skin/virology , Adult , DNA, Viral/isolation & purification , Female , Humans , Male , Middle Aged , Papillomaviridae/genetics , Papillomavirus Infections/pathology , Papillomavirus Infections/virology , Prevalence , Psoriasis/pathology , Severity of Illness Index
14.
Int J Immunopathol Pharmacol ; 18(4): 799-804, 2005.
Article in English | MEDLINE | ID: mdl-16388730

ABSTRACT

Interstitial cystitis (IC) is a syndrome consisting of severe refractory bladder symptoms of unknown etiology. The disease tends to affect Caucasian women with a mean age of 40 years, with 25% of patients under the age of 30. Few population based epidemiological studies of IC have been performed. We analyzed a case of interstitial cystitis in a 42-year-old non-smoker woman. In two biopsy samples the presence of viral DNA of human polyomavirus BK (BKV), human herpes virus type 1 and type 2 (HHV- 1 and HHV-2), adenovirus, human papillomavirus (HPV) and bacterial DNA (Chlamydia trachomatis and Mycoplasma genitalium) were evaluated by means of polymerase chain reaction (PCR). Both samples resulted positive only for BKV and HPV DNA. HPV genotyping revealed the presence of HPV-66 that is associated with a high risk of cancer development. Thus the finding of a viral co-infection could support the hypothesis of the multi-factorial origin of this pathology.


Subject(s)
Cystitis, Interstitial/microbiology , Cystitis, Interstitial/virology , Adenoviridae/chemistry , Adult , BK Virus/chemistry , BK Virus/genetics , Chlamydia trachomatis/chemistry , Chlamydia trachomatis/genetics , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Viral/analysis , DNA, Viral/genetics , Female , Genotype , Herpesvirus 1, Human/chemistry , Herpesvirus 1, Human/genetics , Herpesvirus 2, Human/chemistry , Herpesvirus 2, Human/genetics , Humans , Mycoplasma genitalium/chemistry , Mycoplasma genitalium/genetics , Papillomaviridae/chemistry , Papillomaviridae/genetics , Reverse Transcriptase Polymerase Chain Reaction
15.
Int J Immunopathol Pharmacol ; 17(1): 65-70, 2004.
Article in English | MEDLINE | ID: mdl-15000868

ABSTRACT

Human papillomaviruses (HPVs) have been proposed to be the most important etiological factors for cervical cancer although different agents may act in conjunction. Herpes simplex virus type 2 (HSV-2) infection is considered as a possible cofactor to malignant transformation. To examine the influence of HSV-2 infection on the HPV genes expression, CaSki cells bearing 60 to 600 copies of HPV-16 DNA per cell were used as a model system. Twenty hours post HSV-2 infection the mRNA transcripts for HPV-16 early (E1, E2 and E6) and late (L1) genes were analysed by RT-PCR assay. Results indicated that the level of transcription of E1, E2 and E6 genes was up to 3-fold enhanced in HSV-2 infected CaSki cells suggesting that HSV-2 infection could increase the risk of cervical cancer by overexpression of both HPV regulatory and oncogenic genes.


Subject(s)
Herpesvirus 2, Human/immunology , Oncogene Proteins, Viral/biosynthesis , Uterine Cervical Neoplasms/metabolism , Cell Line, Tumor , DNA-Binding Proteins/biosynthesis , DNA-Binding Proteins/genetics , Female , Herpesvirus 2, Human/genetics , Humans , Oncogene Proteins, Viral/genetics , Repressor Proteins/biosynthesis , Repressor Proteins/genetics , Uterine Cervical Neoplasms/genetics
16.
New Microbiol ; 27(1): 65-9, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14964407

ABSTRACT

The association of Human Papillomaviruses (HPV) DNA with female genital lesions has been widely documented whereas little has been reported about male genital pathologies. The aim of this work was to investigate the presence of HPV DNA and the genotype involved in male dysplastic genital lesions. All samples were analysed by polymerase chain reaction (PCR) to amplify HPV E1 and L1 genes. The PCR products were subjected to restriction fragment length polymorphism (RFLP) to determine the HPV genotype. We analysed 209 male genital biopsies from different lesions: mostly from acuminate condylomata and from Buschke-Lowenstein tumours, Bowen papulosis, leukoplakia of the glans, scrotal lymphangioma, penile horn and penile/perianal verrucous carcinoma. Our results revealed the constant presence of viral DNA in genital condylomata, mainly associated with low risk HPV; the presence of the same genotypes was also detected in some of the examined rare pathologies.


Subject(s)
Condylomata Acuminata/virology , Genital Neoplasms, Male/virology , Papillomaviridae/classification , Papillomaviridae/isolation & purification , Papillomavirus Infections/virology , Adult , Biopsy , Carcinoma, Verrucous/virology , Condylomata Acuminata/diagnosis , DNA, Viral/analysis , Genital Neoplasms, Male/diagnosis , Genotype , Humans , Male , Middle Aged , Papillomaviridae/genetics , Penile Neoplasms/virology , Polymerase Chain Reaction
17.
J Neurovirol ; 9(6): 603-11, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14602573

ABSTRACT

The JC virus (JCV) is generally considered the etiological agent of progressive multifocal leukoencephalopathy (PML), a demyelinating brain illness, often associated with immunosuppression and significantly frequent in acquired immunodeficiency syndrome (AIDS) patients. The primary infection by JCV is usually asymptomatic and the virus can remain in a latent status in the kidney. As a consequence of immunological alterations of the host, the virus can show a genetic variability in the noncoding control region (NCCR) due to deletions, duplications, and insertions as compared with the archetype. The NCCR of the archetype strain can be divided into six regions, named boxes A to F. In this study, the authors evaluated the presence of the JCV genome in different biological samples, such as urine, peripheral blood mononuclear cells (PBMCs) and cerebral spinal fluid (CSF) by means of polymerase chain reaction (PCR). After sequencing of the PCR fragments, the NCCR structure of isolated JCV strains was analyzed in order to verify the presence of different viral variants. An analysis of the homology and of the multiple alignment of the obtained sequences in comparison with the archetype strain has been carried out. The results indicated the presence of different rearrangements among the analyzed samples. Whereas in the urine, the NCCR structure always appeared very similar to that of the archetype, in the PBMCs and CSF, the NCCR sequences showed specific and characteristic rearrangements as compared to the archetype. These different rearrangements could be correlated with the emerging of an NCCR organization more suitable for the development of PML.


Subject(s)
Gene Rearrangement , JC Virus/genetics , Leukoencephalopathy, Progressive Multifocal/virology , Locus Control Region/genetics , AIDS-Related Opportunistic Infections/urine , AIDS-Related Opportunistic Infections/virology , Adult , Aged , Base Sequence , Gene Deletion , Gene Duplication , HIV Seropositivity/urine , HIV Seropositivity/virology , Humans , JC Virus/isolation & purification , Middle Aged , Molecular Sequence Data , Polymerase Chain Reaction , Sequence Alignment , Sequence Homology, Nucleic Acid
18.
New Microbiol ; 26(4): 329-37, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14596343

ABSTRACT

Some evidence suggests that intrauterine infection plays a major role in the pathogenesis of early pregnancy loss, but the implication and prevalence of microrganisms in the aetiology of spontaneous abortion during the first trimester of pregnancy has not yet been well established. In this study, we analysed the tissues relative to the product of conception from abortions during the first trimester (51 spontaneous abortions and 56 voluntary pregnancy interruptions) in women attending the Gynecological Sciences Perinatology and Puericulture Department of "Policlinico Umberto I". Specimens were investigated by cultural methods for the presence of yeasts, gram positive, gram negative bacteria, and genital mycoplasma. By molecular diagnostic procedures, DNA sequences of Chlamydia trachomatis, herpes simplex viruses, adenovirus, human papillomaviruses and human polyomaviruses BK and JC were searched. None of these agents could be found in voluntary pregnancy interruption samples, with the exception of 3.6% of specimens positive for adenovirus, whereas spontaneous abortion tissues were positive for at least one microrganism by 31.5%. Data analysis showed the occurrence of both monomicrobial and polymicrobial infections.


Subject(s)
Abortion, Spontaneous/microbiology , Abortion, Spontaneous/virology , Adenovirus Infections, Human/diagnosis , Ureaplasma Infections/diagnosis , Ureaplasma urealyticum , Abortion, Spontaneous/epidemiology , Adult , BK Virus , Female , Humans , Incidence , Mycoplasma Infections/diagnosis , Mycoplasma fermentans , Polyomavirus Infections/diagnosis , Pregnancy , Pregnancy Trimester, First , Tumor Virus Infections/diagnosis
19.
Int J Immunopathol Pharmacol ; 16(3): 269-76, 2003.
Article in English | MEDLINE | ID: mdl-14611731

ABSTRACT

The distribution of DNA of BK and JC human polyomaviruses (BKV and JCV) was investigated in samples from autopsies of different organs in 2 groups of patients: Human Immunodeficiency Virus -1 (HIV) positive and negative. Samples from various organs were analysed by a nested polymerase chain reaction (PCR) for the non-coding control and for the VP1 regions of both viruses. The results obtained showed that BKV DNA was present in both males and females with a higher prevalence in HIV-positive subject samples (spleen: 33%; kidney: 44%; brain: 22%, uterine cervix:100%; prostatic urethra: 50%). In prostatic urethra samples of HIV-positive subjects, the JCV DNA was revealed in a low percentage (33%), while it was not found at all in uterine cervix samples of both groups. The varying presence of BK and JC viral DNA in the different organs seems to reflect the different pathogenetic attitude of these viruses. JCV was mainly present in the brain (55%), confirming its typical neurotropism and its etiological role in neurological disorders found in immunodeficient patients. BKV, on the other hand, was mainly present in the kidney (44%) and in genital organs (uterine cervix: 100%; prostatic urethra: 50%) with the latter finding favouring the hypothesis of a possible sexual transmission of BKV. Furthermore, our results confirm the crucial role of the immune system in the persistence of human polyomaviruses in the host.


Subject(s)
BK Virus/genetics , HIV Seronegativity/genetics , HIV Seropositivity/genetics , HIV-1/genetics , JC Virus/genetics , Sequence Analysis, DNA , Adult , Aged , BK Virus/chemistry , BK Virus/isolation & purification , Brain Chemistry/genetics , Cervix Uteri/chemistry , Cervix Uteri/virology , Female , HIV Seropositivity/mortality , HIV Seropositivity/pathology , HIV Seropositivity/virology , HIV-1/chemistry , HIV-1/isolation & purification , Humans , JC Virus/chemistry , JC Virus/isolation & purification , Kidney/chemistry , Kidney/virology , Male , Middle Aged , Organ Specificity/genetics , Sequence Analysis, DNA/methods , Spleen/chemistry , Spleen/virology
20.
Int J Immunopathol Pharmacol ; 16(3): 283-8, 2003.
Article in English | MEDLINE | ID: mdl-14611733

ABSTRACT

Bladder cancer is the second most commonly occurring genitourinary cancer in adults. The interaction of different carcinogenic and cocarcinogenic agents are responsible for bladder urothelial carcinoma: alcohol and smoking habits, Schistosoma haematobium infection, exposition to chemicals, analgesic and antineoplastic drugs prolonged use. Recently also viral infections have been associated to this pathology. In this study the correlation between viral infections and bladder carcinoma has been evaluated. A group of 32 patients affected by primary bladder neoplasia has been analysed. A control group of 20 autoptic samples of healthy bladder was analysed. The DNA of the following viruses has been searched by polymerase chain reaction (PCR): Adenovirus, Herpes simplex virus type 1 (HSV-1), Herpes simplex virus type 2 (HSV-2), Human Papillomaviruses (HPV), Polyomaviruses (BKV and JCV). In the examined population the association bladder carcinoma-HPV, found by others, has not been confirmed. The high percentage of human polyomaviruses present in the samples is a statistically significant data (p=0.0087) and allows to presume that BKV and JCV may play a role in the aetiology of bladder tumor. In particular the polyomavirus BK, which is found in significative percentage both in single infection (p=0.0036) and in co-infections with other viral species (p=0.035), may be an important co-factor in the pathogenesis of bladder carcinoma.


Subject(s)
Papillomavirus Infections/virology , Polyomavirus Infections/virology , Tumor Virus Infections/virology , Urinary Bladder Neoplasms/virology , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Papillomaviridae/genetics , Papillomavirus Infections/genetics , Papillomavirus Infections/pathology , Polyomavirus/genetics , Polyomavirus Infections/genetics , Polyomavirus Infections/pathology , Tumor Virus Infections/genetics , Tumor Virus Infections/pathology , Urinary Bladder Neoplasms/genetics , Urinary Bladder Neoplasms/pathology
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