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无血清培养基比传统含血清培养基更能诱导疟原虫感染性配子体的产生。

A human-serum-free medium can induce more infectious P. falciparum gametocytes than a conventional human-serum-containing medium.

机构信息

Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, 20852, USA.

Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 12735 Twinbrook Parkway, Rockville, MD, 20852, USA.

出版信息

Sci Rep. 2024 Sep 27;14(1):22052. doi: 10.1038/s41598-024-73843-5.

Abstract

Malaria remains a global health problem, and the standard membrane feeding assay (SMFA) is a key functional assay for development of new interventions to stop malaria transmission from human to mosquito. For SMFA, media with ~ 10% of human serum has been used for infectious gametocyte cultures, however, there are multiple challenges to obtain a suitable human serum. Here we show a human-serum-free culture medium (HSF), which was a mixture of two stem cell culture media and AlbuMAX, supported infectious gametocyte growth. Moreover, the HSF-induced gametocytes elicited significantly higher numbers of oocysts compared to gametocytes cultured with conventional human serum medium (Conv). While some caution is required when comparing percent transmission reducing activity data generated from HSF-SMFA and Conv-SMFA, the HSF method can facilitate the establishment of gametocyte cultures or SMFA by bypassing the need for human serum. Thus, this study will support future development of P. falciparum transmission-blocking interventions.

摘要

疟疾仍然是一个全球性的健康问题,标准膜喂食分析(SMFA)是开发新的干预措施以阻止疟疾从人类传播到蚊子的关键功能分析。对于 SMFA,已经使用含有约 10%人血清的培养基来培养感染性配子体,但是获得合适的人血清存在多种挑战。在这里,我们展示了一种无血清的培养基(HSF),它是两种干细胞培养基和 AlbuMAX 的混合物,支持感染性配子体的生长。此外,与用常规人血清培养基(Conv)培养的配子体相比,HSF 诱导的配子体产生的卵囊数量明显更高。虽然在比较从 HSF-SMFA 和 Conv-SMFA 生成的传播减少活性数据时需要谨慎,但 HSF 方法可以通过避免使用人血清来促进配子体培养或 SMFA 的建立。因此,本研究将支持未来开发疟原虫传播阻断干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bb9/11436888/fdd126f02d02/41598_2024_73843_Fig1_HTML.jpg

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