Antonym monogamous relationship and hpv

Cervical Cancer

(Also known as/Synonyms) The HPV is a very small microorganism that is transmitted sexually. . Avoid multiple partners; try to maintain monogamous relationships; If possible, avoid sexual contact with individuals having Genital Warts. Here's expert advice for reassuring those who test HPV-positive that they most surprise, to major concern about past and future sexual relationships. based on a patient's fears that HPV is synonymous with cervical cancer. (Note: Only 1 percent of women who contract HPV will get cancer.) should consider the vaccination if they are not in a monogamous, long-term relationship.

Our objective in the current study was to characterize type-specific genital HPV incidence among heterosexual partners across a broad age range and to investigate the effects of monogamy and relationship duration on incidence. Understanding more about the natural history of HPV within these couples may provide new insights into prevention strategies.

Its methods have been described in detail elsewhere [ 6 ]. Enrollment criteria for the HIM Study included an age of 18—70 years; no prior diagnosis of an HPV-associated cancer or genital warts; and no current sexually transmitted disease diagnosis, including human immunodeficiency virus HIV infection.

A total of men agreed to invite their partners, with female partners responding affirmatively. Thus, a total of female sexual partners of HIM Study participants were enrolled.

After the enrollment visit, couples returned to the clinic for a total of 4 semiannual follow-up visits during a 2-year period. Although couples were encouraged to attend each clinic visit with no more than 14 days between each other's visit, not all couples observed the day limit.

Although partners in couples were required to be each other's current primary sexual partners, they were not required to be monogamous nor to acknowledge sex with their primary partner in the recent past. Couples were instructed not to have sex for 48 hours before each clinic visit to avoid detection of superficial HPV.

Women were asked not to douche for 24 hours before an appointment. Participants received a nominal incentive for study involvement. Each partner independently consented to the study's protocol, which was approved by the Institutional Review Board of the University of South Florida.

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Procedure The clinical protocols were similar for both male and female partners and included a physical examination, collection of biological specimens, and collection of behavioral data with a computer-assisted self-interview which elicited information about participant demographics, substance use, and sexual behaviors. Women were also questioned about Papanicolaou screening and pregnancy histories. At all study visits, blood and urine samples were collected, and a clinician examined the external genitalia of each participant.

Then, with a separate swab, cells were collected from between the anal os and the anal canal dentate line. To sample the endo- and ectocervix, a swab moistened with normal saline was introduced into the cervical os, rotated once or twice, and then brushed back and forth across the ectocervix. The cervix was then swabbed to assess cytological status. A second swab was used to sample the entire surface of the penile shaft, and a third to sample the scrotum.

Hopefully, future efforts will be directed towards identifying additional types that are very distantly related to the known genera. An example of the large diversity of animal papillomaviruses are the two recently described types from birds, both of which lack traditional E6 and E7 ORFs Tachezy et al.

Several of the papillomavirus types that presently appear as single species within a genus have in the past been identified only because of the availability of lesions that harbour many viral particles or from which substantial amounts of circular double-stranded DNA could be purified.

This term originally had a different meaning, and was used when different isolates of the same type differed partially in their restriction enzyme cleavage patterns, such as HPV 2a, HPV 2b and HPV 2c. Other misclassifications, which were originally based on hybridization data, include the classification of papillomaviruses as types that now fall under the subtype classification.

The latter is therefore a subtype of the pygmy chimpanzee papillomavirus de Villiers et al. It is unclear why genomes that are intermediate to closely related papillomavirus types are so rare de Villiers et al. Most HPV types have been isolated repeatedly in a large number of clinical studies, and the sequences of these isolates have been compared. As may be expected, most of these isolates differ from one another. The phylogenetic implications of this, namely the slow, linked evolution of host and virus, have been discussed extensively while the clinical implications, i.

Evolution of papillomaviruses Papillomaviruses are an ideal model system for the study of the evolution of DNA viruses. On several levels, phylogenetic trees of papillomaviruses reflect the relationship of their hosts. One branch of HPVs includes one ape and two monkey papillomaviruses, possibly because the diversification of the viruses predated the separation of the infected-primate taxa.

This hypothesis predicts that the root of the evolution of some if not all HPV types should point to Africa, since humans evolved from non-human primates in this continent. This frequency of novel RhPVs suggests that rhesus monkeys may play host to papillomaviruses with a diversity similar to that of HPVs. In phylogenetic trees, all 12 novel RhPVs and the previously described type RhPV-1 were members of the genital HPV supergroup and formed three minor branches that were distinct from the 11 branches formed by genital HPVs.

It appears that the evolution of primate lineages that lead to the genus Macaca and to humans created transmission barriers for papillomaviruses, which resulted in a viral evolution that was closely linked to the host. Additional support for the hypothesis of linked evolution derives from the phylogenetic association of two other ape and monkey viruses with genital HPVs: Portions of the genome from two different papillomaviruses of the Abyssinian Colobus monkey were sequenced and analysed phylogenetically.

This revealed that the major evolutionary separation between genital and EV-associated papillomaviruses, hitherto found only in humans, also exists in animals. Although isolated from the same monkey species, the other Colobus monkey virus, CgPV-1, is a typical genital virus as shown by comparison of E and L gene sequences. The presence of these two major phylogenetic divisions of papillomaviruses in both human and monkey hosts strongly suggests that this diversification predated the evolutionary split between monkeys and apes.

Human Papillomavirus (HPV) Infection - Human Papillomaviruses - NCBI Bookshelf

This would imply that at least two different groups of papillomavirus have evolved separately in their respective primate hosts for more than 22 million years with only moderate sequence changes since their genesis Chan, S. The specimens were taken from patients in Brazil, Germany, Singapore and Tanzania.

The sequence of a bp fragment of the LCR of the virus revealed 38 variants, most of which differed by one or several point mutations. In the phylogenetic trees that were constructed, two branches could be distinguished. Nearly all of the variants from Tanzania were assigned to one African branch and all of the German and most of the Singaporean variants were assigned to the other Eurasian branch. While some German and Singaporean variants were identical, each group also contained variants that formed unique branches.

In contrast to the internal homogeneity within the groups of the Singaporean, German and Tanzanian variants, the Brazilian variants were clearly divided between the two branches. Exceptions to this were the seven Singaporean isolates with mutational patterns typical of the Tanzanian isolates.

HPV & Relationships

Representatives of both branches may have been transferred to Brazil through past colonial immigration. The comparable efficiencies of transfer of the African and the Eurasian variants to South America suggest the pandemic spread of HPV 16 in past centuries. Representatives of the African branch were possibly transferred to the Far East along old Arab and Indonesian sailing routes.

The small amount of divergence in any one geographical location and the lack of marked divergence between the Tanzanian and Brazilian African genome variants two centuries after their probable introduction into South America suggest a very slow rate of viral evolution.

The phylogenetic tree, therefore, probably represents a minimum of several centuries of evolution, if not an age equal to that of the respective human races. The diversity of a hypervariable bp segment from the HPV 16 LCR genome was investigated in virus isolates collected from 25 different ethnic groups and geographical locations.

Altogether, 48 variants could be distinguished that had diversified from one another along five phylogenetic branches. Variants from two of these branches were nearly completely confined to Africa. Variants from a third branch were the only variants identified in Europeans but occurred at lower frequency in all other ethnic groups.

A fourth branch was specific for Japanese and Chinese isolates. A small fraction of all isolates from Asia and from indigenous as well as immigrant populations in the Americas formed a fifth branch. Important patterns of HPV 16 phylogeny suggested coevolution of the virus with people of the three major human races, namely, Africans, Caucasians and East Asians.

However, several minor patterns are indicative of smaller bottlenecks of viral evolution and spread, which may correlate with the migration of ethnic groups in prehistoric times. The HPV 16 genomes of today represent a degree of diversity that may have evolved over a large time span, probably exceeding years, from a precursor genome that may have originated in Africa Ho et al.

In a similar study, the genomic sequences of HPV type 18 isolates from four continents were compared. Diversity within HPV 18 correlates with patterns of human evolution and the spread of Homo sapiens: HPV 18 variants, similarly to HPV 16 variants, are specific for the major human races, with maximal diversity in Africa. African HPV 18 variants are at the root of the phylogenetic tree. HPV 18 variants from Amazonian Indians are the closest relatives to those from Japanese and Chinese patients and suggest that a single point mutation in the phylogenetically evaluated genomic segment represents at least 12 years of evolution.

Human Papillomavirus - HPV - Nucleus Health

The diversity within HPV 18, and probably within other HPV types, is estimated to have evolved over a period of more than years and diversity between HPV types may have evolved over several million years Ong et al. The host specificity and the benign nature of most papillomavirus infections suggest that these viruses are extremely well adapted parasites. It has been proposed that this could be indicative of host—virus co-evolution Chan et al.

Function of viral proteins The functions of the papillomavirus proteins are discussed below and summarized in Table 3. Unless otherwise stated, the description of protein functions refers to HPV proteins. Functions of papillomavirus proteins.