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1.
JAMA Netw Open ; 4(9): e2125308, 2021 09 01.
Article in English | MEDLINE | ID: mdl-34524433

ABSTRACT

Importance: Preterm birth remains a leading cause of perinatal mortality and lifelong morbidity worldwide. The cause of most preterm births is unknown, although several infectious processes have been implicated. Objective: To assess whether human papillomavirus (HPV) infection, a frequent infection among women of childbearing age, is associated with preterm birth. Design, Setting, and Participants: The prospective HERITAGE cohort study was conducted at 3 academic hospitals in Montreal, Québec, Canada, among 899 pregnant women recruited between November 8, 2010, and October 16, 2016. Follow-up was completed on June 15, 2017. Statistical analysis was conducted from February 6, 2020, to January 21, 2021. Exposures: Vaginal HPV DNA detection in the first and third trimesters of pregnancy and placental HPV infection. Main Outcomes and Measures: The main outcome was preterm birth (defined as a live birth or stillbirth between 20 weeks and 0 days and 36 weeks and 6 days of gestation). The association between HPV DNA detection and preterm birth was measured using logistic regression. Odds ratios (ORs) and 95% CIs were adjusted by inverse probability of treatment weights of the propensity score. Results: The study included 899 women (mean [SD] age, 31.3 [4.6] years [range, 19-47 years]) with singleton pregnancies. A total of 378 women (42.0%) had HPV DNA detected in vaginal samples collected during the first trimester, and it was detected in 91 of 819 placentas (11.1%) at delivery. Fifty-five participants experienced preterm birth (38 spontaneous and 17 medically indicated). Persistent vaginal HPV-16/18 detection was significantly associated with all preterm births (adjusted OR [aOR], 3.72; 95% CI, 1.47-9.39) and spontaneous preterm births (aOR, 3.32; 95% CI, 1.13-9.80), as was placental HPV infection (all preterm births: aOR, 2.53; 95% CI, 1.06-6.03; spontaneous preterm births: aOR, 2.92; 95% CI, 1.09-7.81). Results were similar when restricting the analysis to participants without a history of cervical intraepithelial neoplasia treatment. Conclusions and Relevance: The study's results suggest that persistent HPV-16/18 infection is associated with an increased risk of preterm birth, independent of cervical treatment. Future studies should investigate the association of HPV vaccination and vaccination programs with the risk of preterm birth.


Subject(s)
Papillomavirus Infections/complications , Pregnancy Complications, Infectious/virology , Premature Birth/virology , Vaginal Diseases/virology , DNA, Viral/analysis , Female , Human papillomavirus 16/isolation & purification , Human papillomavirus 18/isolation & purification , Humans , Infant, Newborn , Placenta/virology , Pregnancy , Prospective Studies , Quebec
2.
Cell Host Microbe ; 29(4): 579-593.e5, 2021 04 14.
Article in English | MEDLINE | ID: mdl-33857419

ABSTRACT

How helminths influence the pathogenesis of sexually transmitted viral infections is not comprehensively understood. Here, we show that an acute helminth infection (Nippostrongylus brasiliensis [Nb]) induced a type 2 immune profile in the female genital tract (FGT). This leads to heightened epithelial ulceration and pathology in subsequent herpes simplex virus (HSV)-2 infection. This was IL-5-dependent but IL-4 receptor alpha (Il4ra) independent, associated with increased FGT eosinophils, raised vaginal IL-33, and enhanced epithelial necrosis. Vaginal eosinophil accumulation was promoted by IL-33 induction following targeted vaginal epithelium damage from a papain challenge. Inhibition of IL-33 protected against Nb-exacerbated HSV-2 pathology. Eosinophil depletion reduced IL-33 release and HSV-2 ulceration in Nb-infected mice. These findings demonstrate that Nb-initiated FGT eosinophil recruitment promotes an eosinophil, IL-33, and IL-5 inflammatory circuit that enhances vaginal epithelial necrosis and pathology following HSV-2 infection. These findings identify a mechanistic framework as to how helminth infections can exacerbate viral-induced vaginal pathology.


Subject(s)
Eosinophils/immunology , Helminthiasis/immunology , Herpes Simplex/immunology , Receptors, Cell Surface/immunology , Vagina/immunology , Vaginal Diseases/immunology , Animals , Eosinophils/pathology , Female , Helminthiasis/complications , Helminths , Herpes Simplex/complications , Herpes Simplex/pathology , Herpes Simplex/virology , Herpesvirus 2, Human/immunology , Immunity , Interleukin-33 , Interleukin-5 , Necrosis , Nippostrongylus , Receptors, Cell Surface/genetics , Vagina/pathology , Vagina/virology , Vaginal Diseases/parasitology , Vaginal Diseases/virology
3.
BMC Infect Dis ; 20(1): 857, 2020 Nov 18.
Article in English | MEDLINE | ID: mdl-33208109

ABSTRACT

BACKGROUND: Human papillomavirus (HPV) is a common sexually transmitted pathogen and the cause of several cancers and of anogenital warts. With this study, we estimated the trend of hospitalizations for anogenital warts (AGWs) in the Veneto region (Italy) from 2007 to 2018. METHODS: The analysis included all the hospital discharge records of public and accredited private hospitals occurred in Veneto residents in the timespan 2007-2018. The ICD9-CM code 078.11 considered were those associated with condyloma acuminatum and those associated with surgical interventions for vulval/vaginal warts, penile warts anal warts. Annual total and sex- and age-specific hospitalization rates and trends were calculated and correlated with the different HPV vaccine coverage over the study period. RESULTS: We observed an overall reduction of hospitalization rates for AGWs: from 15.0 hospitalizations every 100,000 Veneto residents in years 2007-08 to 10.9 hospitalizations every 100,000 Veneto residents in year 2017-18 (- 37.4%; p < 0.05). Reduction has been caused by a drop in hospitalizations in females - from a rate of 20.4/100,000 in 2007-2008 to a rate of 10.8/100,000 in 2017-18 (AAPC: -7.1; 95%CI: - 10.6;-3.4); while in males, we observed a slight - but not statistically significant - increase in hospitalization rates. CONCLUSION: The marked decline in hospitalization rates for AGWs in Veneto Region is probably attributable to the high coverage rates of HPV vaccination programs implemented since 2008.


Subject(s)
Anus Diseases/prevention & control , Condylomata Acuminata/prevention & control , Hospitalization/trends , Papillomaviridae/immunology , Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/immunology , Penile Diseases/prevention & control , Sexually Transmitted Diseases, Viral/prevention & control , Vaccination , Vaginal Diseases/prevention & control , Vulvar Diseases/prevention & control , Adolescent , Adult , Anus Diseases/virology , Child , Child, Preschool , Cohort Studies , Condylomata Acuminata/epidemiology , Condylomata Acuminata/virology , Cross-Sectional Studies , Female , Humans , Infant , Infant, Newborn , Italy/epidemiology , Male , Middle Aged , Papillomavirus Infections/epidemiology , Papillomavirus Infections/virology , Penile Diseases/virology , Sexually Transmitted Diseases, Viral/epidemiology , Vaginal Diseases/virology , Vulvar Diseases/virology , Young Adult
4.
Am J Obstet Gynecol ; 223(3): B2-B6, 2020 09.
Article in English | MEDLINE | ID: mdl-32470457

ABSTRACT

Recent surveys have shown widespread lapses in the procedures used to reduce the risk of transmitting infection via medical devices. Transvaginal ultrasound examination has the potential to transmit vaginal infections, including human papillomavirus. Areas of particular concern are the use of probe covers with high rates of leakage, disinfectants that are not effective against human papillomavirus, and coupling gel from multiple-use containers. We reviewed these issues, and we recommend 4 steps to reduce the risk of transmitting infection. First, during every transvaginal ultrasound exam, the probe should be covered with a sterile, single-use "viral barrier" cover or a condom. Second, sterile, single-use ultrasound gel packets should be used. Third, after every examination, the probe should be cleaned to remove any visible gel or debris. Finally, after cleaning, the probe should undergo high-level disinfection using an agent with proven efficacy against the human papillomavirus, including hydrogen peroxide, hypochlorite, or peracetic acid. Glutaraldehyde, orthophthalaldehyde, phenols, and isopropyl alcohol have virtually no efficacy against the human papillomavirus.


Subject(s)
Disease Transmission, Infectious/prevention & control , Equipment Contamination/prevention & control , Ultrasonography, Prenatal/instrumentation , Vaginal Diseases/microbiology , Vaginal Diseases/prevention & control , Disinfectants , Disinfection/methods , Disposable Equipment , Female , Glutaral , Humans , Infection Control/methods , Papillomavirus Infections/prevention & control , Pregnancy , Sterilization/methods , Ultrasonography, Prenatal/adverse effects , Vaginal Diseases/virology , o-Phthalaldehyde
5.
Am J Trop Med Hyg ; 100(6): 1552-1555, 2019 06.
Article in English | MEDLINE | ID: mdl-30994102

ABSTRACT

Vaginal self-sampling and human papillomavirus (HPV) DNA testing can be useful tools for women with limited access to health care living in sub-Saharan Africa. To assess the feasibility and acceptability of vaginal self-sampling and high-risk HPV prevalence in two villages of central Senegal, women were asked to self-sample vaginal swabs for HPV detection in May, 2016. Vaginal swabs were collected from 133 women and were tested for HPV genotyping. The acceptability rate of vaginal self-sampling was 98.5%, and 99.2% of the women (133/134) used the device correctly. The quality of self-sampling was satisfactory in 100% of the samples; 10.5% of the samples were positive for HPV, including 6% with high-risk HPV types and 4% with low-risk HPV types. This preliminary study indicates that vaginal self-sampling is a valuable strategy for high-risk HPV detection and cervical cancer screening in a population of women not attending gynecologic screening in rural areas of Senegal.


Subject(s)
Papillomaviridae/isolation & purification , Papillomavirus Infections/diagnosis , Rural Population , Specimen Handling , Vaginal Diseases/virology , Vaginal Smears/standards , Adult , Early Detection of Cancer , Feasibility Studies , Female , Humans , Middle Aged , Papillomaviridae/classification , Papillomavirus Infections/epidemiology , Papillomavirus Infections/virology , Patient Acceptance of Health Care , Senegal/epidemiology , Vaginal Diseases/epidemiology
6.
Gynecol Oncol ; 154(1): 110-117, 2019 07.
Article in English | MEDLINE | ID: mdl-30982556

ABSTRACT

OBJECTIVE: Nine-valent human papillomavirus (9vHPV) vaccine efficacy against disease and cervical surgeries related to all nine vaccine components was assessed compared with a historic placebo population. This was not assessed in the 9vHPV vaccine efficacy trial since the trial was quadrivalent HPV (qHPV) vaccine-controlled, efficacy was measured for the five HPV types covered only by 9vHPV vaccine (HPV31/33/45/52/58), but not the four types covered by both vaccines (HPV6/11/16/18). METHODS: Three international, randomized, double-blind studies were conducted using the same methodology. In the 9vHPV vaccine study (NCT00543543), 7106 and 7109 women received 9vHPV or qHPV vaccine, respectively. In the historic qHPV vaccine studies (FUTURE I [NCT00092521] and II [NCT00092534]), 8810 and 8812 women received qHPV vaccine or placebo, respectively, based on the same eligibility criteria. Cervical cytological testing was performed regularly. Biopsy or definitive therapy specimens were assessed for HPV DNA. RESULTS: Among women negative for 14 HPV types prior to vaccination, incidence of high-grade cervical disease (9vHPV, n = 2 cases; placebo, n = 141 cases) and cervical surgery (9vHPV, n = 3 cases; placebo, n = 170 cases) related to the nine HPV types was reduced by 98.2% (95% confidence interval [CI], 93.6-99.7) and 97.8% (95% CI, 93.4-99.4), respectively. The 9vHPV vaccine did not prevent disease related to vaccine HPV types detected at baseline, but significantly reduced cervical, vulvar, and vaginal diseases related to other vaccine HPV types. CONCLUSIONS: Effective implementation of the 9vHPV vaccine may substantially reduce the burden of HPV-related diseases and related medical procedures. TRIAL REGISTRATIONS: clinicaltrials.gov: NCT00543543, NCT00092521, NCT00092534.


Subject(s)
Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/administration & dosage , Uterine Cervical Dysplasia/prevention & control , Vaginal Diseases/prevention & control , Vulvar Diseases/prevention & control , Adult , DNA, Viral/isolation & purification , Double-Blind Method , Female , Humans , Papillomaviridae/genetics , Papillomaviridae/immunology , Papillomavirus Infections/pathology , Papillomavirus Vaccines/adverse effects , Papillomavirus Vaccines/immunology , Uterine Cervical Dysplasia/pathology , Uterine Cervical Dysplasia/surgery , Uterine Cervical Dysplasia/virology , Vaginal Diseases/pathology , Vaginal Diseases/virology , Vulvar Diseases/pathology , Vulvar Diseases/virology , Young Adult
7.
Mil Med ; 183(5-6): e270-e271, 2018 05 01.
Article in English | MEDLINE | ID: mdl-29415160

ABSTRACT

Introduction: Smallpox, or vaccinia, has been eradicated worldwide as a disease; however, it may be weaponized and is thus a required immunization when military members deploy to certain parts of the world. Materials and Methods: We report two unusual cases of genital autoinoculation following smallpox vaccination. Results: Both patients' lesions resolved without sequelae within 20 d. Conclusions: We advocate for thorough education on this potential vaccination adverse event. These cases highlight the importance of a broad differential diagnosis when dealing with vulvar lesions, particularly in our military population.


Subject(s)
Smallpox Vaccine/adverse effects , Vaccinia/etiology , Vaginal Diseases/etiology , Adult , Female , Humans , Military Personnel , Smallpox/drug therapy , Smallpox/prevention & control , Smallpox Vaccine/therapeutic use , Vaccination/adverse effects , Vaccinia/virology , Vaginal Diseases/virology
8.
Sex Transm Infect ; 94(4): 277-283, 2018 06.
Article in English | MEDLINE | ID: mdl-29180538

ABSTRACT

OBJECTIVES: Cervical cancer is a largely preventable disease, and the strategic implementation of a cervical cancer prevention programme is partly dependent on the impact of human papillomavirus (HPV) infection interpreted within the context of the country's sociodemographic attributes. The objective of this study is to determine the prevalence of cervicovaginal HPV infection among a healthy, community-based, multiethnic Malaysian population. The HPV prevalence was subsequently correlated to the individual's sociodemographics and sexual/reproductive history. Of significance, the observed prevalence captured was in a birth cohort not included in the national school-based HPV vaccination programme. METHODS: This was a cross-sectional study where 1293 healthy women aged between 18 and 60 years were recruited via convenience sampling from five community-based clinics in Selangor, Malaysia. Cervicovaginal self-samples were obtained and DNA was extracted for HPV detection and genotyping. A comprehensive questionnaire was administered to determine the sociodemographics and behavioural patterns of participants. RESULTS: The median age at enrolment was 37 years old (IQR: 30-47). In total, 86/1190 (7.2%) of the samples collected were positive for HPV infection, with the highest HPV prevalence (11.9%) detected in the subgroup of 18-24 years old. The top three most prevalent HPV genotypes were HPV 16, 52 and 58. The independent risk factors associated with higher rates of HPV infection included Indian ethnicity, widowed status and women with partners who are away from home for long periods and/or has another sexual partner. CONCLUSIONS: The overall prevalence of HPV infection in this Malaysian multiethnic population was 7.2%, with 6.5% being high-risk genotypes. The top three most common high-risk HPV types were HPV 16, 52 and 58. This information is important for the planning of primary (HPV vaccination) and secondary (screening) cervical cancer prevention programmes in Malaysia.


Subject(s)
Papillomavirus Infections/ethnology , Uterine Cervical Neoplasms/ethnology , Vaginal Diseases/ethnology , Adolescent , Adult , China/ethnology , Cross-Sectional Studies , DNA, Viral/isolation & purification , Female , Genotype , Genotyping Techniques , Humans , India/ethnology , Malaysia/epidemiology , Malaysia/ethnology , Middle Aged , Papillomaviridae/genetics , Papillomaviridae/isolation & purification , Prevalence , Risk Factors , Sexual Behavior/ethnology , Socioeconomic Factors , Specimen Handling/methods , Uterine Cervical Neoplasms/virology , Vaginal Diseases/virology , Vaginal Smears/methods , Young Adult
9.
J Infect Chemother ; 23(12): 814-819, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28923300

ABSTRACT

AIM: Human papillomaviruses (HPV) infection is a primary cause of the development of cervical precancerous lesions and cervical cancer. However, the influence of other infections on intraepithelial neoplasia (CIN) development has not been fully elucidated. We evaluated the association between co-infection and CIN development in subjects with atypical squamous cells of undetermined significance (ASCUS). METHOD: Data for ASCUS subjects who had undergone testing for high risk HPV (HR-HPV) and pathological diagnosis were analyzed. From the CIN grade, HR-HPV and vaginal infection (VI) data, both the relationship between HPV infection and CIN development and the influence of co-infection on CIN were retrospectively evaluated. RESULTS: Data for 56 ASCUS subjects who had undergone HR-HPV testing and cytological diagnosis were analyzed. Positive rates were HPV (73.2%), HPV16 (21.4%), HPV18 (7.1%), and HPV16 and/or 18 (26.8%). Seventeen of the subjects were diagnosed as having one or more VI pathogen; the major pathogens found were Candida spp., Gardnerella vaginalis, group B streptococcus, coagulase negative Staphylococcus, and Chlamydia trachomatis. The rate of CIN 2 or worse (≥CIN 2) was significantly higher in subjects positive for HPV16 compared with HPV negative subjects, and was significantly higher in subjects with a VI complicated with HPV compared to those without a VI. Univariate and multivariate logistic regression analysis identified positive for HPV16 and/or 18 and positive for VI to be significant variables for ≥ CIN 2. CONCLUSION: Our results indicate that having a vaginal infection complicated with HR-HPV affects the development of CIN in subjects with ASCUS cytology.


Subject(s)
Atypical Squamous Cells of the Cervix/microbiology , Coinfection/microbiology , Papillomavirus Infections/complications , Uterine Cervical Dysplasia/microbiology , Uterine Cervical Neoplasms/microbiology , Vaginal Diseases/microbiology , Adult , Atypical Squamous Cells of the Cervix/virology , Coinfection/virology , Female , Humans , Logistic Models , Papillomaviridae/genetics , Papillomavirus Infections/virology , Retrospective Studies , Uterine Cervical Neoplasms/virology , Vaginal Diseases/virology , Uterine Cervical Dysplasia/virology
10.
Clin Ther ; 38(12): 2567-2577, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27836494

ABSTRACT

PURPOSE: Infection with and persistence of high-risk human papillomavirus (HR HPV) are the strongest risk factors for cervical cancer. Little is known about the prevalence and role of concurrent sexually transmitted infections (STIs) found in HPV-infected female sex workers (FSW) in Africa. This study purports to test our a priori hypotheses that STIs are associated with genotypes pertaining to the α-group species 9. The objectives were to determine the prevalence of bacterial vaginosis (BV), Trichomonas vaginalis, and Candida spp in FSW, the association between these STIs and the prevalence of any potential HR and HR HPV genotypes in FSWs. METHODS: A cross-sectional study design of 616 FSW from Western Kenya aged between 18 and 61 years during 2009-2015 using a peer recruitment sampling strategy. Inclusion criteria for the study entailed female sex and >18 years of age and having engaged in transactional sex in exchange for money, goods, services, or drugs in the last 3 months. Women were excluded if they were pregnant, <18 years of age, had a history of cervical dysplasia or cancer, had current abnormal bleeding, or had a hysterectomy. FINDINGS: Of the FSW, 33.3% had HIV and 57.7% harbored a potential HR and HR HPV genotype. The 2 most prevalent potential HR and HR genotypes were HPV 16 (16.10%) and HPV 59 (12.20%). BV was the most common infection (48.3%), followed by Trichomonas vaginalis (31.4%) and Candida spp (19.9%). A multivariate regression revealed significant associations with both α-group 9 and 6; BV and HPV 58 (adjusted odds ratio [aOR] = 2.3; 95% CI, 1.0-5.2; P = 0.05), Trichomonas vaginalis and HPV 31 and HPV 35 (aOR = 2.0; 95% CI, 1.0-3.8; P = 0.04 and aOR = 1.8; 95% CI, 1.0-3.3, P = 0.05 respectively); and between Candida spp and HPV 53 (aOR = 2.0; 95% CI, 1.1-4.0; P = 0.03) and 16 (aOR = 1.9; 95% CI, 1.1-3.3; P = 0.03). IMPLICATIONS: Snowball sampling may have inadvertently excluded FSW less likely to benefit from a social network. Significant associations between BV and HPV 58 and between Candida spp and HPV 16 and 53 suggest the need for sexually transmitted disease management within a cervical cancer prevention program. The probable synergistic effects of the vaginal microbiota should be elucidated, especially within this vulnerable population. Given the potential for FSW to transmit STIs, robust epidemiologic sampling methods are urgently required that account for the heterogeneity of the FSW population.


Subject(s)
Papillomaviridae/genetics , Papillomavirus Infections/virology , Uterine Cervical Dysplasia/virology , Uterine Cervical Neoplasms/virology , Vaginal Diseases/virology , Adolescent , Adult , Cross-Sectional Studies , Female , Genotype , Human papillomavirus 16/genetics , Human papillomavirus 16/isolation & purification , Humans , Kenya/epidemiology , Papillomaviridae/isolation & purification , Papillomavirus Infections/epidemiology , Prevalence , Risk Factors , Sex Workers , Uterine Cervical Neoplasms/epidemiology , Vaginal Diseases/epidemiology , Vaginal Diseases/microbiology , Vaginosis, Bacterial/epidemiology , Vaginosis, Bacterial/microbiology , Uterine Cervical Dysplasia/epidemiology
11.
BMC Infect Dis ; 16: 293, 2016 06 14.
Article in English | MEDLINE | ID: mdl-27301867

ABSTRACT

BACKGROUND: Human papillomavirus (HPV) vaccines were designed to prevent cervical cancer in women and their provision remains a major public health need. However, HPV is also a major cause of non-cervical anogenital and oropharyngeal cancers and the potential benefit of vaccination likely extends beyond cervical cancer. METHODS: A systematic literature search of PubMed (1995-2014) identified publications assessing the incidence, persistence, and clearance of non-cervical anogenital/oral HPV infections. Comparability with cervical HPV was assessed by identifying articles assessing the same or similar populations. RESULTS: Available data suggest high incidence rates of non-cervical HPV infection in men and women, with HPV-16 predominating in all sites. The incidence of high risk HPV per 100 person-years ranged from 11.4 to 72.9 for penile infections, 6.7-47.9 at other male genital sites, and 4.4-36.7 and 5.3-23.4 for anal infections in men and women, respectively. The incidence per 100 person-years of oral infection with any HPV type ranged from 5.7 to 6.7 in men and 6.8-39.6 in women. Within the limitations of the data, there was a general pattern of higher incidence and clearance of non-cervical genital HPV infections, compared to cervical infections. HIV status, circumcision, number of sex partners and partner HPV status significantly influenced high-risk HPV incidence/clearance at male anogenital sites. Few studies assessed risk factors for oral HPV. CONCLUSIONS: Parallels appear to exist between the epidemiology of cervical and non-cervical HPV infections in terms of incidence, HPV-type distribution, and risk factors for infection. Available data suggest that non-cervical genital HPV infections may occur more frequently, with higher clearance rates, than cervical infections. More extensive studies could provide useful information for estimating vaccine impact, the wider cost-benefit of HPV vaccination, and guiding vaccination policy. TRIAL REGISTRATION: Not applicable, as systematic review of the literature.


Subject(s)
Anus Diseases/epidemiology , Genital Diseases, Male/epidemiology , Mouth Diseases/epidemiology , Papillomavirus Infections/epidemiology , Vaginal Diseases/epidemiology , Anus Diseases/virology , Female , Genital Diseases, Male/virology , Human papillomavirus 16 , Humans , Incidence , Male , Mouth Diseases/virology , Papillomavirus Infections/virology , Papillomavirus Vaccines , Sexual Partners , Sexually Transmitted Diseases/epidemiology , Sexually Transmitted Diseases/virology , Vaginal Diseases/virology
12.
Cell Host Microbe ; 19(6): 788-99, 2016 Jun 08.
Article in English | MEDLINE | ID: mdl-27281569

ABSTRACT

Herpes simplex virus 1 (HSV-1), a leading cause of genital herpes, infects oral or genital mucosal epithelial cells before infecting the peripheral sensory nervous system. The spread of HSV-1 beyond the sensory nervous system and the resulting broader spectrum of disease are not well understood. Using a mouse model of genital herpes, we found that HSV-1-infection-associated lethality correlated with severe fecal and urinary retention. No inflammation or infection of the brain was evident. Instead, HSV-1 spread via the dorsal root ganglia to the autonomic ganglia of the enteric nervous system (ENS) in the colon. ENS infection led to robust viral gene transcription, pathological inflammatory responses, and neutrophil-mediated destruction of enteric neurons, ultimately resulting in permanent loss of peristalsis and the development of toxic megacolon. Laxative treatment rescued mice from lethality following genital HSV-1 infection. These results reveal an unexpected pathogenesis of HSV associated with ENS infection.


Subject(s)
Enteric Nervous System/virology , Herpes Genitalis/virology , Herpesvirus 1, Human/pathogenicity , Megacolon, Toxic/virology , Neurons/virology , Vaginal Diseases/virology , Animals , Disease Models, Animal , Enteric Nervous System/pathology , Female , Ganglia/pathology , Ganglia/ultrastructure , Ganglia/virology , Ganglia, Spinal/pathology , Ganglia, Spinal/virology , Genome, Viral , Herpes Genitalis/pathology , Herpesvirus 1, Human/genetics , Herpesvirus 1, Human/physiology , Intestines/virology , Megacolon, Toxic/pathology , Mice , Mice, Inbred C57BL , Neurons/pathology , Neutrophils/virology , Nociceptors/virology , Vagina/virology , Vaginal Diseases/pathology , Virus Replication/physiology
13.
Sci Rep ; 6: 26817, 2016 05 26.
Article in English | MEDLINE | ID: mdl-27226349

ABSTRACT

Evolutionary approaches are powerful tools for understanding human disorders. The composition of vaginal microbiome is important for reproductive success and has not yet been characterized in the contexts of social structure and vaginal pathology in non-human primates (NHPs). We investigated vaginal size, vulvovaginal pathology and the presence of the main human subtypes of Lactobacillus spp./ BV-related species in the vaginal microflora of baboons (Papio spp.). We performed morphometric measurements of external and internal genitalia (group I, n = 47), analyzed pathology records of animals from 1999-2015 (group II, n = 64 from a total of 12,776), and evaluated vaginal swabs using polymerase chain reaction (PCR) (group III, n = 14). A total of 68 lesions were identified in 64 baboons. Lactobacillus iners, Gardnerella vaginalis, Atopobium vaginae, Megasphaera I, and Megasphaera II were not detected. L. jensenii, L. crispatus, and L. gasseri were detected in 2/14 (14.2%), 1/14 (7.1%), and 1/14 (7.1%) samples, respectively. BVAB2 was detected in 5/14 (35.7%) samples. The differences in the vaginal milieu between NHP and humans might be the factor associated with human-specific pattern of placental development and should be taken in consideration in NHP models of human pharmacology and microbiology.


Subject(s)
Biological Evolution , Dysbiosis/microbiology , Dysbiosis/veterinary , Lactobacillus/isolation & purification , Microbiota , Papio/microbiology , Primate Diseases/microbiology , Vagina/microbiology , Vaginal Diseases/veterinary , Vulvar Diseases/veterinary , Animals , Female , Lactobacillus/physiology , Organ Size , Primate Diseases/pathology , Primate Diseases/virology , Simplexvirus/isolation & purification , Species Specificity , Vagina/anatomy & histology , Vaginal Diseases/microbiology , Vaginal Diseases/pathology , Vaginal Diseases/virology , Vulva/anatomy & histology , Vulva/microbiology , Vulvar Diseases/microbiology , Vulvar Diseases/pathology , Vulvar Diseases/virology
14.
JAMA Otolaryngol Head Neck Surg ; 142(5): 457-65, 2016 05 01.
Article in English | MEDLINE | ID: mdl-27010384

ABSTRACT

IMPORTANCE: Human papillomavirus (HPV) is a common infection in adults, with tropism for sites in the head and neck and the genital tracts. To date, few studies have addressed concurrent infection in these sites. OBJECTIVE: To understand the prevalence, characteristics, and concordance of HPV infections in the oral and vaginal regions. DESIGN, SETTING, AND PARTICIPANTS: This study was a retrospective analysis of cross-sectional survey data from the National Health and Nutrition Examination Survey, 2009-2012. The database was reviewed for all women aged 18 to 69 years with available oral and vaginal HPV DNA screening data. The study was performed from August 1, 2014, to November 1, 2014. Data analysis was performed from November 1, 2014, to June 30, 2015. MAIN OUTCOMES AND MEASURES: Logistic regression models were constructed to identify factors associated with infection. Covariates for multivariate analysis included age, income to poverty ratio, number of prior sexual partners, number of prior oral sex partners, and having recent oral sex partners. Dual infection was defined as having an infection of any serotype in both the oral and vaginal HPV regions. Concordant infection was defined as an infection of matching serotype in both locations. RESULTS: A total of 3463 women were identified (mean [SD] age, 37.5 [12.1] years). Racial distribution was 1341 white (38.7%), 786 black (22.7%), 554 Mexican American (16.0%), 378 other Hispanic (10.9%), and 404 self-identified as other (11.7%). Vaginal HPV infection was present in 1586 (45.2%) and oral HPV infection in 141 (4.1%). Dual infection was identified in 107 (3.0%) of all patients, and concordant infection was observed in 41 (1.1%). The prevalence of dual infection was 75.9% in those with oral infection and 6.8% in those with vaginal infection. On multivariate analysis, age (30-50 years) and higher income to poverty ratios had negative associations with dual and concordant infections. A new sexual partner within the last year was positively associated with dual infection (odds ratio, 2.28; 95% CI, 1.03-5.02; P = .04). More than 2 oral sex partners in the past year was positively associated with concordant infection (odds ratio, 3.43; 95% CI, 1.06-11.06; P = .04). CONCLUSIONS AND RELEVANCE: This analysis reveals the importance of several demographic factors (age and socioeconomic status) and behavioral factors (oral sex practices) in the development of dual and concordant HPV infection in women. Notably, other sexual behaviors, other sexually transmitted infections, sexual orientation, and number of lifetime sexual partners did not demonstrate any significant associations. Women with multiple oral sex partners and oral HPV infection have a high likelihood of having concurrent vaginal HPV infection.


Subject(s)
Coinfection/epidemiology , Mouth Diseases/epidemiology , Papillomavirus Infections/epidemiology , Vaginal Diseases/epidemiology , Adult , Age Factors , Coinfection/virology , Cross-Sectional Studies , Female , Health Surveys , Humans , Income , Middle Aged , Mouth Diseases/virology , Multivariate Analysis , Racial Groups/statistics & numerical data , Retrospective Studies , Sexual Partners , United States/epidemiology , Vaginal Diseases/virology
15.
Int J Gynaecol Obstet ; 132(1): 20-4, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26463081

ABSTRACT

OBJECTIVE: To determine the predictive factors for progression and recurrence of vulvovaginal condyloma (VVC), with a specific focus on high-risk HPV (HR-HPV) infections. METHODS: Retrospective data were collected from 48 patients who were diagnosed with VVC and treated with topical trichloroacetic acid application or laser therapy during 2003-2014 at a hospital in South Korea. The diagnoses were made based on the presence of exophytic condylomatous lesions as assessed by direct visual inspection regardless of whether a biopsy was performed. RESULTS: Overall, 18 patients (50.0% of those with a test result) were positive for HR-HPV. Three-quarters of the patients with a poor treatment response had abnormal cytologies, and abnormal cytology was a risk factor for a poor response (odds ratio, 4.33 [95% confidence interval, 1.05-17.84]). During a median follow-up of 24months, VVC recurred in seven (14.6%) patients. A high viral load (more than 50 relative light units) of HR-HPV was significantly associated with recurrence (odds ratio, 7.42, 95% confidence interval, 1.19-46.18). CONCLUSION: A high HR-HPV load is a risk factor for recurrence, but is not related to treatment response. A poor treatment response is more related to abnormal cytology than it is to viral load.


Subject(s)
Condylomata Acuminata/virology , Papillomavirus Infections/complications , Vaginal Diseases/virology , Vulvar Diseases/virology , Administration, Topical , Adult , Aged , Caustics/administration & dosage , Condylomata Acuminata/pathology , Condylomata Acuminata/therapy , Female , Humans , Laser Therapy , Middle Aged , Odds Ratio , Papillomaviridae , Papillomavirus Infections/virology , Recurrence , Republic of Korea , Retrospective Studies , Risk Factors , Treatment Failure , Trichloroacetic Acid/administration & dosage , Vaginal Diseases/pathology , Vaginal Diseases/therapy , Viral Load , Vulvar Diseases/pathology , Vulvar Diseases/therapy
16.
Nat Prod Res ; 30(5): 605-7, 2016.
Article in English | MEDLINE | ID: mdl-25835328

ABSTRACT

The latex of Ficus carica Linn. (Moraceae) has been shown to interfere with the replication of caprine herpesvirus (CpHV)-1 in vitro. The present study was undertaken to determine the efficacy of vaginal administration of fig latex in goats experimentally infected with CpHV-1. The fig latex reduced the clinical signs of the herpetic disease although it slightly influenced the titres of CpHV-1 shed. Thus, the fig latex maintained a partial efficacy in vivo.


Subject(s)
Ficus/chemistry , Goat Diseases/drug therapy , Goats , Herpesviridae Infections/drug therapy , Latex/therapeutic use , Vaginal Diseases/drug therapy , Vaginal Diseases/veterinary , Varicellovirus , Animals , Female , Goat Diseases/virology , Herpesviridae Infections/virology , Treatment Outcome , Vaginal Diseases/virology
17.
J Infect Dis ; 210 Suppl 3: S616-21, 2014 Dec 15.
Article in English | MEDLINE | ID: mdl-25414415

ABSTRACT

Vaginal microbiota and sexually transmitted infections (STIs) are likely to influence the transmission of cell-associated human immunodeficiency virus (HIV). Lactic acid produced by Lactobacillus-dominated microbiota (Nugent score 0-3) will likely inhibit transmission, especially female-to-male transmission. In contrast, polymicrobial microbiota (Nugent score 4-10), community state types IV-A and IV-B, and STIs will likely increase transmission of cell-associated HIV.


Subject(s)
HIV Infections/transmission , Sexually Transmitted Diseases/complications , Vaginal Diseases/complications , Female , Humans , Lactic Acid/metabolism , Lactobacillus/physiology , Leukocytes/physiology , Male , Microbiota/physiology , Vagina/microbiology , Vagina/virology , Vaginal Diseases/microbiology , Vaginal Diseases/virology
18.
Sex Transm Dis ; 40(7): 534-8, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23965766

ABSTRACT

BACKGROUND: Information on genital wart incidence in adolescents and young adults before human papillomavirus (HPV) vaccination is important for understanding the impact of the vaccine on the epidemiology of this early outcome of HPV infection. METHODS: The study population included 11- to 29-year-old enrollees of Northern California Kaiser Permanente between July 1, 2000, and July 1, 2005, before the availability of the HPV vaccine. We identified genital warts with an algorithm combining genital wart-specific International Classification of Diseases, Ninth Revision, Clinical Modification codes (078.10, 078.11, and 078.19) with physician-recorded anatomic locations. We calculated sex- and age-specific incidence rates of genital warts and described the specific anatomic location of presentation, as well as recurrences of genital warts. RESULTS: We identified 1,682 cases of genital warts among 181,264 individuals. The incidence rate was highest among women (6.3/1000 person-years) and men (2.9/1000 person-years) aged 20 to 24 years old. Among women (n = 96,792), 63.4% of the 1240 incident genital wart cases occurred on the vulva and 21.1% on the cervix. Among men (n = 84,472), 91.6% of the 442 incident genital wart cases did not have a specific anatomic location recorded. Most people with an incident genital wart diagnosis (87.2%) did not have a recurrence during the observation period. CONCLUSIONS: Our study found that the incidence of genital warts was highest among persons aged 20 to 24 years using a unique method to identify the location of the wart. Information on incidence of genital warts before vaccine use provides baseline data that can be used to measure HPV vaccine impact.


Subject(s)
Condylomata Acuminata/prevention & control , Papillomaviridae/immunology , Penile Diseases/prevention & control , Urethral Diseases/prevention & control , Uterine Cervical Diseases/prevention & control , Vaginal Diseases/prevention & control , Vulvar Diseases/prevention & control , Adolescent , Adult , California/epidemiology , Child , Cohort Studies , Condylomata Acuminata/classification , Condylomata Acuminata/epidemiology , Condylomata Acuminata/virology , Delivery of Health Care, Integrated , Female , Humans , Incidence , Male , Papillomavirus Vaccines , Penile Diseases/classification , Penile Diseases/virology , Sexually Transmitted Diseases, Viral/classification , Sexually Transmitted Diseases, Viral/epidemiology , Sexually Transmitted Diseases, Viral/prevention & control , Sexually Transmitted Diseases, Viral/virology , Urethral Diseases/classification , Urethral Diseases/virology , Uterine Cervical Diseases/classification , Uterine Cervical Diseases/virology , Vaccination , Vaginal Diseases/classification , Vaginal Diseases/virology , Vulvar Diseases/classification , Vulvar Diseases/virology , Young Adult
20.
Obstet Gynecol Clin North Am ; 40(2): 359-76, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23732036

ABSTRACT

Human papilloma virus is associated with a multitude of lower genital tract diseases in women in addition to cervical cancer, including genital warts, vulvar intraepithelial neoplasia, vaginal intraepithelial neoplasia, and some vulvar, vaginal, and anal cancers that are associated with oncogenic subtypes. The degree to which HPV manifests pathology depends on viral type, host immune response, and local environmental factors. This article reviews the evaluation and management of the following vulvar and vaginal human papilloma virus diseases: condyloma, vulvar intraepithelial neoplasia, and vaginal intraepithelial neoplasia. Included is a brief discussion of the association with vulvar and vaginal cancer.


Subject(s)
Papillomavirus Infections , Vaginal Diseases/virology , Vulvar Diseases/virology , Adolescent , Adult , Aged , Aminoquinolines/therapeutic use , Antineoplastic Agents , Carcinoma in Situ/diagnosis , Carcinoma in Situ/therapy , Carcinoma in Situ/virology , Colposcopy , Condylomata Acuminata/drug therapy , Condylomata Acuminata/surgery , Condylomata Acuminata/virology , Female , Human papillomavirus 11 , Human papillomavirus 6 , Humans , Imiquimod , Interferon Inducers , Middle Aged , Neoplasm Recurrence, Local , Papillomavirus Infections/drug therapy , Papillomavirus Infections/prevention & control , Papillomavirus Infections/surgery , Papillomavirus Vaccines , Podophyllotoxin/therapeutic use , Pregnancy , Pregnancy Complications, Infectious , Sexually Transmitted Diseases/virology , Trichloroacetic Acid/therapeutic use , Vaginal Neoplasms/diagnosis , Vaginal Neoplasms/therapy , Vaginal Neoplasms/virology , Vaginal Smears , Vulvar Neoplasms/diagnosis , Vulvar Neoplasms/therapy , Vulvar Neoplasms/virology , Young Adult
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