A prophylactic quadrivalent (types 6/11/16/18) vaccine against oncogenic and warts-causing genital Human papillomavirus (HPV)
types was approved by the US Food and Drug Administration in 2006. This paper presents a nonlinear, deterministic, age-structured,
mathematical model of the transmission dynamics of HPV and disease occurrence in a US population stratified by gender and
sexual activity group. The model can assess both the epidemiologic consequences and cost effectiveness of alternative vaccination
strategies in a setting of organized cervical cancer screening in the United States. Inputs for the model were obtained from
public data sources, published literature, and analyses of clinical trial data. The results suggest that a prophylactic quadrivalent
HPV vaccine can: (i) substantially reduce the incidence of disease, (ii) increase survival among females, (iii) improve quality
of life for both males and females, (iv) be cost-effective when administered to females age 12–24 years, and (v) be cost-effective
when implemented as a strategy that combines vaccination of both females and males before age 12 vaccination with a 12 to
24 years of age catch-up vaccination program. 相似文献
Market crop wastes of banana (Musa acuminata) leaves and pseudo-stem sheaths, sweet potato (Ipomoea batatas) vines and Solanum aethiopicum (traditionally known as nakati) were collected from three major markets in Kampala (Uganda). The wastes were evaluated for chemical composition during the dry and wet seasons, rumen degradation using three cannulated indigenous mature ewes, and digestibility using 12 indigenous intact growing male goats, 4–6 months old and weighing 15.8 kg (S.D. 2.1). The goats in the digestibility study were kept in metabolism cages and fed the wastes as sole diets, either fresh or wilted.
Mean dry matter (DM) content was 97, 121, 197 and 216 g/kg for pseudo-stem sheaths, nakati, sweet potato vines and banana leaves, respectively. Crude protein (CP) was 34, 109, 112 and 114 g/kg DM for pseudo-stem sheaths, banana leaves, sweet potato vines and nakati, respectively. The chemical composition was similar among seasons and markets for the banana based wastes. However, for sweet potato vines and nakati, the wet season wastes had significantly higher CP and lower NDFom and ADFom. Chemical composition was different (P<0.05) among the markets for nakati. Effective degradability differed (P<0.05) between the wastes, averaging 0.43 (banana leaves), 0.47 (pseudo-stem sheaths) and 0.56 (nakati) to 0.69 g/g DM incubated (sweet potato vines). DM intake, N retention and digestibility were not significantly affected by wilting. Average DM intake was 176, 270 and 559 g/day; CP intake was 26, 30 and 63 g/day, while metabolizable energy (ME) intake was 1.3, 1.7 and 5.1 MJ/day for nakati, banana leaves and sweet potato vines, respectively. N retention (as a fraction of N intake) was −0.51 (banana leaves), 0.62 (nakati) and 0.39 (sweet potato vines). The organic matter (OM) and CP digestibilities of banana leaves were low, averaging 0.52 and 0.49, respectively. The high moisture content of nakati wastes resulted in low intake, whereas banana leaves had a low degradation rate and a low N retention. Market sweet potato vine wastes were sufficient to provide the CP and ME required by growing goats under tropical conditions. 相似文献
The importance of the emerging genus Gordonia in industrial and environmental biotechnology is evidenced by the recent increase in associated publications and patents. But, investigations into potentially valuable Gordonia members are restricted by the limitations of current isolation and detection techniques. This motivated us to design a genus-specific oligonucleotide primer pair which could assist in rapid detection of species of the genus Gordonia by means of PCR-specific amplification. The Gordonia-specific 16S rDNA fragment (829 bp) was successfully amplified for all the reference Gordonia species with the designed primer pair G268F/G1096R. No amplification was noted for closely related species from other genera. The genus specificity was validated with 47 strains including wild-type isolates. Interestingly, two strains assigned earlier as Gordonia nitida (DSM 777) and Gordonia rubripertinctus (ATCC 21930) failed to produce a Gordonia-specific fragment with this primer pair. Further analysis of these two isolates based on 16S rDNA sequencing and phylogenetic analysis classified them to the genus Rhodococcus. Preliminary screening of soil samples with the Gordonia-specific primers was successful in terms of the rapid detection of nine Gordonia wild-type isolates. 相似文献
