The performance of a new point-of-care HIV virus load technology to identify patients failing antiretroviral treatment

2020 ◽  
Vol 122 ◽  
pp. 104212
Author(s):  
Diana Mariani ◽  
Marcelo C.V.M. de Azevedo ◽  
Isabelle Vasconcellos ◽  
Luiz Ribeiro ◽  
Cassia Alves ◽  
...  
2020 ◽  
Vol 24 (1) ◽  
pp. 30-33
Author(s):  
Isabelle Vasconcellos ◽  
Diana Mariani ◽  
Marcelo C.V.M. de Azevedo ◽  
Orlando C. Ferreira ◽  
Amilcar Tanuri

2019 ◽  
Vol 8 (1) ◽  
Author(s):  
Shun-Xian Zhang ◽  
Fen-Yan Kang ◽  
Jia-Xu Chen ◽  
Li-Guang Tian ◽  
Lan-Lan Geng

Abstract Background Blastocystis is a widespread zoonotic protozoan of mammalian species, especially in HIV/AIDS individuals. The aim of this study was to analyze the prevalence and risk factors related with Blastocystis infection among HIV/AIDS patients in Southwest China. Methods The cross-sectional study was performed in 311 HIV/AIDS cases in Tengchong City, Yunnan Province from July 2016 to March 2017. For each subject, stool specimen was collected to detect the Blastocystis, and the blood sample was used to detect HIV virus load and CD4+ T cell count, in addition, structured questionnaire was used to collect the basic information and risk factors. Findings The result showed that the detection rate of Blastocystis was 3.86% (95% CI: 2.22–6.62) among HIV/AIDS patients. Both raising animal (OR = 12.93, 95% CI: 1.54–108.36) and drinking un-boiled water (OR = 8.17, 95% CI: 1.76–37.90) were risk factors for Blastocystis infection in HIV/AIDS individuals. In addition, the interaction of CD4+ T cell count and HIV virus load was also contribution to Blastocystis infection (P = 0.007). Conclusions A high prevalence of Blastocystis infection was found in HIV/AIDS patients in Tengchong. Poor hygienic habits, the interaction of HIV virus load and CD4+ T cell count were identified as main risk factors for infection. These results will help us to develop efficient control strategies to intervene with and prevent the occurrence of Blastocystis among HIV-infected individuals.


Author(s):  
Xiong Ding ◽  
Kun Yin ◽  
Ziyue Li ◽  
Changchun Liu

AbstractA recent outbreak of novel coronavirus (SARS-CoV-2), the causative agent of COVID-19, has spread rapidly all over the world. Human immunodeficiency virus (HIV) is another deadly virus and causes acquired immunodeficiency syndrome (AIDS). Rapid and early detection of these viruses will facilitate early intervention and reduce disease transmission risk. Here, we present an All-In-One Dual CRISPR-Cas12a (termed “AIOD-CRISPR”) assay method for simple, rapid, ultrasensitive, one-pot, and visual detection of coronavirus SARS-CoV-2 and HIV virus. In our AIOD CRISPR assay, a pair of crRNAs was introduced to initiate dual CRISPR-Cas12a detection and improve detection sensitivity. The AIOD-CRISPR assay system was successfully utilized to detect nucleic acids (DNA and RNA) of SARS-CoV-2 and HIV with a sensitivity of few copies. Also, it was evaluated by detecting HIV-1 RNA extracted from human plasma samples, achieving a comparable sensitivity with real-time RT-PCR method. Thus, our method has a great potential for developing next-generation point-of-care molecular diagnostics.


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