Background: Herpes simplex virus Type 2 (HSV-2) has been associated with HIV infection. More recently, HSV-2 incidence has been linked to HIV acquisition. A few studies have suggested that the fishing communities have...Background: Herpes simplex virus Type 2 (HSV-2) has been associated with HIV infection. More recently, HSV-2 incidence has been linked to HIV acquisition. A few studies have suggested that the fishing communities have a high HSV-2 prevalence but there is limited knowledge on HSV-2 incidence and associated risk factors among fishermen. Methods: Three hundred fishermen were consented, and evaluated for baseline HSV-2 serology status and again after 12 months among those negative at baseline. Sexual behavior and socio-demographic data were collected at enrolment and exit visits using a structured questionnaire. Baseline HIV serology and Human papillomavirus (HPV) DNA genotyping were also performed. Multivariate logistic regression was used to determine independent factors associated with HSV-2 acquisition. Results: Baseline HSV-2 prevalence was 56.3% (95% CI: 50.7 - 62.0). Factors associated with HSV-2 prevalence were, older age (aOR = 1.96;95% CI: 1.16 - 2.85), history of STI (aOR 2.12;95% CI: 1.19 - 3.91), infection with HIV (aOR 2.22;95% CI: 1.17 - 4.22), ever married (aOR = 3.80;95% CI: 1.42 - 11.90), most recent sexual act with sex worker/casual partner (OR= 3.56;95% CI: 1.49 - 8.62) and inconsistent condom use with new sexual partner (aOR = 6.34;95% CI: 2.24 - 13.04). The HSV-2 incidence was 23.6 (95% CI = 15.4 - 31.8)/100 pyr. Infection with persistent high-risk (HR) HPV (aIRR = 3.35;95% CI: 1.21 - 11.37), multiple (≥2) partners in 12 months prior to study participation (aIRR = 4.77;95% CI: 1.12 - 11.38), inconsistent condom use with new partner (aIRR =2.53;95% CI: 1.12 - 7.38) and most recent sexual act with sex worker/casual partner (OR = 3.03;95% CI: 1.17 - 8.58) were independent risk factors for HSV-2 acquisition. Conclusion: The incidence of HSV-2 is very high among fishermen. It is associated with persistent HR HPV infection and high-risk sexual behavior. Intervention strategies targeting these men with high risk sexual behavior are urgently needed to stop new HSV-2 acquisition and subsequently prevent HIV infection.展开更多
Microscopic examination and AFLP molecular markers were employed to determine the incidence and related markers of 2n pollen (unreduced pollen) in Populus tomentosa Carr. The parallel and tripolar spindle at metaphase...Microscopic examination and AFLP molecular markers were employed to determine the incidence and related markers of 2n pollen (unreduced pollen) in Populus tomentosa Carr. The parallel and tripolar spindle at metaphase Ⅱ and the absence of cytokinesis at telophase Ⅱ led to the formation of 2n pollen. A group of 298 clones came from their indigenous areas was investigated for the production of 2n pollen based on the pollen size differences, within a clone and between n and 2n pollen. Pollen grains of 224 clones were collected, six of them only produced normal pollen, and the rest produced 2n pollen at different frequencies (0.6% -21.9%). Clones producing six normal and 22 2n pollen were selected for AFLP analysis. Following an initial screening with 55 primer combinations, the E50-M38 (CAT/ACT) primer was identified, which generated a PCR fragment (246 bp) from the normal clones, but not from the 2n pollen producers. In addition, the E31-M50 (AAA/CAT) amplified DNA fragment (204 bp) that was present in 2n pollen producers, and absent in normal clones. Two polymorphic bands were found and they were distinguished between normal and 2n pollen clones. They are very useful as AFLP markers for molecular-assisted selection in triploid breeding of 2n gametes in P.tomentosa.展开更多
文摘Background: Herpes simplex virus Type 2 (HSV-2) has been associated with HIV infection. More recently, HSV-2 incidence has been linked to HIV acquisition. A few studies have suggested that the fishing communities have a high HSV-2 prevalence but there is limited knowledge on HSV-2 incidence and associated risk factors among fishermen. Methods: Three hundred fishermen were consented, and evaluated for baseline HSV-2 serology status and again after 12 months among those negative at baseline. Sexual behavior and socio-demographic data were collected at enrolment and exit visits using a structured questionnaire. Baseline HIV serology and Human papillomavirus (HPV) DNA genotyping were also performed. Multivariate logistic regression was used to determine independent factors associated with HSV-2 acquisition. Results: Baseline HSV-2 prevalence was 56.3% (95% CI: 50.7 - 62.0). Factors associated with HSV-2 prevalence were, older age (aOR = 1.96;95% CI: 1.16 - 2.85), history of STI (aOR 2.12;95% CI: 1.19 - 3.91), infection with HIV (aOR 2.22;95% CI: 1.17 - 4.22), ever married (aOR = 3.80;95% CI: 1.42 - 11.90), most recent sexual act with sex worker/casual partner (OR= 3.56;95% CI: 1.49 - 8.62) and inconsistent condom use with new sexual partner (aOR = 6.34;95% CI: 2.24 - 13.04). The HSV-2 incidence was 23.6 (95% CI = 15.4 - 31.8)/100 pyr. Infection with persistent high-risk (HR) HPV (aIRR = 3.35;95% CI: 1.21 - 11.37), multiple (≥2) partners in 12 months prior to study participation (aIRR = 4.77;95% CI: 1.12 - 11.38), inconsistent condom use with new partner (aIRR =2.53;95% CI: 1.12 - 7.38) and most recent sexual act with sex worker/casual partner (OR = 3.03;95% CI: 1.17 - 8.58) were independent risk factors for HSV-2 acquisition. Conclusion: The incidence of HSV-2 is very high among fishermen. It is associated with persistent HR HPV infection and high-risk sexual behavior. Intervention strategies targeting these men with high risk sexual behavior are urgently needed to stop new HSV-2 acquisition and subsequently prevent HIV infection.
文摘Microscopic examination and AFLP molecular markers were employed to determine the incidence and related markers of 2n pollen (unreduced pollen) in Populus tomentosa Carr. The parallel and tripolar spindle at metaphase Ⅱ and the absence of cytokinesis at telophase Ⅱ led to the formation of 2n pollen. A group of 298 clones came from their indigenous areas was investigated for the production of 2n pollen based on the pollen size differences, within a clone and between n and 2n pollen. Pollen grains of 224 clones were collected, six of them only produced normal pollen, and the rest produced 2n pollen at different frequencies (0.6% -21.9%). Clones producing six normal and 22 2n pollen were selected for AFLP analysis. Following an initial screening with 55 primer combinations, the E50-M38 (CAT/ACT) primer was identified, which generated a PCR fragment (246 bp) from the normal clones, but not from the 2n pollen producers. In addition, the E31-M50 (AAA/CAT) amplified DNA fragment (204 bp) that was present in 2n pollen producers, and absent in normal clones. Two polymorphic bands were found and they were distinguished between normal and 2n pollen clones. They are very useful as AFLP markers for molecular-assisted selection in triploid breeding of 2n gametes in P.tomentosa.
