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1.
J Cell Physiol ; 234(10): 17905-17911, 2019 08.
Article in English | MEDLINE | ID: mdl-30883747

ABSTRACT

Recently, there are controversial opinions on the presence of Mycoplasmas/Ureaplasmas as colonizers or pathogens, and on the use of a targeted therapy. This study aimed to characterize Mycoplasmas/Ureaplasmas infections in reproductive age women, including the acquisition of sexually transmitted (ST) pathogens and poor birth outcomes. A total of 646 healthy Italian women fulfilled the inclusion criteria including 521 infertile women, 65 pregnant women, and 60 fertile women with identified risk factors and symptomatic for vaginitis/cervicitis. Multiplex and quantitative molecular techniques and direct automatic DNA sequencing were performed to assess the genome structure of Mycoplasma/Ureaplasma species and ST infected pathogens. Ureaplasma parvum serovar 3 represented the predominant colonizer of the urogenital tract of this series and the unique species significantly associated with ST pathogens coinfection (p < 0.01). U. parvum load >104 bacteria/ml, suggestive of active infection, has been measured only in asymptomatic high-risk human papillomavirus infected women (24.3%) and in 40% of women with idiopathic infertility. To note, 16% of the follicular fluid from these idiopathic women resulted infected with U. parvum. In conclusion, the present study focused the attention on U. parvum serovar 3 as emerging microorganism in sexually active women that may have the benefit of targeted therapy.


Subject(s)
Infertility, Female/microbiology , Infertility, Female/virology , Papillomavirus Infections/microbiology , Ureaplasma/pathogenicity , Adult , Female , Humans , Mycoplasma/genetics , Mycoplasma/pathogenicity , Mycoplasma Infections/microbiology , Mycoplasma Infections/virology , Retrospective Studies , Serogroup , Ureaplasma/genetics , Ureaplasma Infections/microbiology , Ureaplasma Infections/virology , Young Adult
2.
J Med Microbiol ; 67(11): 1645-1654, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30299238

ABSTRACT

PURPOSE: Cervical cancer is the most frequently diagnosed female cancer in The Gambia, representing approximately 30 % of cases. In 2014, the quadrivalent human papilloma virus (HPV) vaccine was introduced, which offers protection against HPV genotypes 6, 11, 16 and 18. To evaluate the potential effectiveness of this vaccine, genotype distribution and risk factor analysis were assessed. METHODOLOGY: Endocervical samples (n=232) were collected from women aged 20-49 years residing in urban Gambia. A questionnaire was administered to capture socio-demographic and cervical cancer risk factors. HPV detection and genotyping was performed by PCR amplification of the L1 major capsid gene and analysis of sequenced PCR products.Results/Key findings. The prevalence of HPV was 12 % (28/232), and the high-risk (HR) genotype HPV 52 (5/28) was the most prevalent genotype. HR-HPV sequences had high identity (≥90 %) to isolates which originated from America, Europe and Asia but not from Africa. Half (14/28) of participants were co-infected with Ureaplasma urealyticum/parvum, which increases the risk of progression to cervical cancer. Female genital mutilation and the use of hormone contraception for >5 years were identified as potential risk factors for HPV infection. Ethnicity-associated differences were also noted; participants of the Fula ethnic group had a higher prevalence of HR-HPV infection (31.3 %) compared to the Mandinka (18.8 %) and Wollof (12.5 %) groups. CONCLUSION: These data may have a significant public health impact as the HPV quadrivalent vaccine may be of limited value if the circulating non-HPV 16/18 HR-genotypes are responsible for cytological abnormalities of the cervix.


Subject(s)
Genotype , Papillomaviridae/genetics , Papillomavirus Infections/epidemiology , Uterine Cervical Dysplasia/virology , Uterine Cervical Neoplasms/virology , Adult , Capsid Proteins/genetics , Coinfection/epidemiology , Coinfection/microbiology , Coinfection/virology , Contraception/adverse effects , Factor Analysis, Statistical , Female , Gambia/epidemiology , Genitalia, Female/injuries , Humans , Middle Aged , Oncogene Proteins, Viral/genetics , Papillomaviridae/classification , Papillomaviridae/isolation & purification , Papillomavirus Infections/microbiology , Papillomavirus Infections/virology , Papillomavirus Vaccines/administration & dosage , Papillomavirus Vaccines/adverse effects , Polymerase Chain Reaction , Prevalence , Risk Factors , Surveys and Questionnaires , Urban Population , Ureaplasma Infections/epidemiology , Ureaplasma Infections/microbiology , Ureaplasma Infections/virology , Ureaplasma urealyticum/isolation & purification , Uterine Cervical Neoplasms/epidemiology , Vaccine Potency , Young Adult , Uterine Cervical Dysplasia/epidemiology
3.
J Infect Chemother ; 17(4): 487-92, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21213011

ABSTRACT

To analyze the risk factors for HPV infection in the urethra, we examined the prevalence of various microorganisms, for example Neisseria gonorrhoeae, Chlamydia trachomatis, Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma urealyticum, Ureaplasma parvum, Gardnerella vaginalis, and human papillomavirus (HPV) in Japanese male patients with urethritis, and investigated their sexual backgrounds. Rubbed samples obtained from the distal urethra and questionnaires regarding sexual activity and demographic information were collected from 176 participants. N. gonorrhoeae, C. trachomatis, M. genitalium, M. hominis, U. urealyticum, U. parvum, G. vaginalis, and HPV were detected in 19, 26, 18, 12, 12, 8.5, 14, and 20%, respectively, of all cases in this study. Multivariate logistic regression analysis indicated that more than 4 sexual partners within the last year and presence of N. gonorrhoeae and/or C. trachomatis and/or M. genitalium infections were independent risk factors for urethral HPV infection, with odds ratios of 3.85 (95% CI 1.49-9.94) and 2.41 (95% CI 1.03-5.61), respectively. It is likely that urethral HPV detection is associated with current sexual activity and the presence of N. gonorrhoeae, C. trachomatis, and/or M. genitalium infections.


Subject(s)
Gram-Negative Bacterial Infections/epidemiology , Gram-Negative Bacterial Infections/microbiology , Papillomavirus Infections/epidemiology , Papillomavirus Infections/microbiology , Urethritis/epidemiology , Urethritis/microbiology , Adolescent , Adult , Aged , Chi-Square Distribution , Chlamydia trachomatis/isolation & purification , Gardnerella vaginalis/isolation & purification , Gram-Negative Bacterial Infections/virology , Humans , Japan/epidemiology , Male , Middle Aged , Multivariate Analysis , Mycoplasma Infections/epidemiology , Mycoplasma Infections/microbiology , Mycoplasma Infections/virology , Mycoplasma genitalium/isolation & purification , Mycoplasma hominis/isolation & purification , Neisseria gonorrhoeae/isolation & purification , Papillomaviridae/isolation & purification , Papillomavirus Infections/virology , Prevalence , Risk Factors , Surveys and Questionnaires , Ureaplasma/isolation & purification , Ureaplasma Infections/epidemiology , Ureaplasma Infections/microbiology , Ureaplasma Infections/virology , Urethritis/virology
4.
Br Med Bull ; 61: 247-62, 2002.
Article in English | MEDLINE | ID: mdl-11997310

ABSTRACT

Most children presenting with pneumonia in the industrialised world will have a viral or 'atypical' organism. The clinical features of these 'atypical' pneumonias may be indistinguishable from bacterial pneumonia. New diagnostic techniques such as the polymerase chain reaction may help in diagnosis and choice of treatment, where appropriate. The pathological and clinical features of infection with each agent are discussed, together with their sequelae.


Subject(s)
Pneumonia, Viral/diagnosis , Adenoviridae Infections/diagnosis , Adenoviridae Infections/drug therapy , Adenoviridae Infections/virology , Anti-Bacterial Agents/therapeutic use , Child , Child, Preschool , Humans , Infant , Influenza, Human/diagnosis , Influenza, Human/drug therapy , Influenza, Human/virology , Macrolides , Pneumonia, Mycoplasma/diagnosis , Pneumonia, Mycoplasma/drug therapy , Pneumonia, Mycoplasma/virology , Pneumonia, Viral/drug therapy , Pneumonia, Viral/virology , Ureaplasma Infections/diagnosis , Ureaplasma Infections/drug therapy , Ureaplasma Infections/virology
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