Single-Cell Analysis Reveals Distinct Gene Expression and Heterogeneity in Male and Female Plasmodium falciparum Gametocytes.
Abstract
Sexual reproduction is an obligate step in the Plasmodium falciparum life cycle, with
mature gametocytes being the only form of the parasite capable of human-to-mosquito
transmission. Development of male and female gametocytes takes 9 to 12 days, and although
more than 300 genes are thought to be specific to gametocytes, only a few have been
postulated to be male or female specific. Because these genes are often expressed
during late gametocyte stages and for some, male- or female-specific transcript expression
is debated, the separation of male and female populations is technically challenging.
To overcome these challenges, we have developed an unbiased single-cell approach to
determine which transcripts are expressed in male versus female gametocytes. Using
microfluidic technology, we isolated single mid- to late-stage gametocytes to compare
the expression of 91 genes, including 87 gametocyte-specific genes, in 90 cells. Such
analysis identified distinct gene clusters whose expression was associated with male,
female, or all gametocytes. In addition, a small number of male gametocytes clustered
separately from female gametocytes based on sex-specific expression independent of
stage. Many female-enriched genes also exhibited stage-specific expression. RNA fluorescent
in situ hybridization of male and female markers validated the mutually exclusive
expression pattern of male and female transcripts in gametocytes. These analyses uncovered
novel male and female markers that are expressed as early as stage III gametocytogenesis,
providing further insight into Plasmodium sex-specific differentiation previously
masked in population analyses. Our single-cell approach reveals the most robust markers
for sex-specific differentiation in Plasmodium gametocytes. Such single-cell expression
assays can be generalized to all eukaryotic pathogens.IMPORTANCE Most human deaths
that result from malaria are caused by the eukaryotic parasite Plasmodium falciparum
The only form of this parasite that is transmitted to the mosquito is the sexual form,
called the gametocyte. The production of mature gametocytes can take up to 2 weeks
and results in phenotypically distinct males and females, although what causes this
gender-specific differentiation remains largely unknown. Here, we demonstrate the
first use of microfluidic technology to capture single gametocytes and determine their
temporal sex-specific gene expression in an unbiased manner. We were able to determine
male or female identity of single cells based on the upregulation of gender-specific
genes as early as mid-stage gametocytes. This analysis has revealed strong markers
for male and female gametocyte differentiation that were previously concealed in population
analyses. Similar single-cell analyses in eukaryotic pathogens using this method may
uncover rare cell types and heterogeneity previously masked in population studies.
Type
Journal articleSubject
Plasmodium falciparumRNA, Protozoan
In Situ Hybridization, Fluorescence
Microfluidics
Gene Expression
Life Cycle Stages
Single-Cell Analysis
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https://hdl.handle.net/10161/19667Published Version (Please cite this version)
10.1128/mSphere.00130-18Publication Info
Walzer, Katelyn A; Kubicki, Danielle M; Tang, Xiaohu; & Chi, Jen-Tsan Ashley (2018). Single-Cell Analysis Reveals Distinct Gene Expression and Heterogeneity in Male and
Female Plasmodium falciparum Gametocytes. mSphere, 3(2). 10.1128/mSphere.00130-18. Retrieved from https://hdl.handle.net/10161/19667.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Jen-Tsan Ashley Chi
Associate Professor in Molecular Genetics and Microbiology
We are using functional genomic approaches to investigate the nutrient signaling and
stress adaptations of cancer cells when exposed to various nutrient deprivations and
microenvironmental stress conditions. Recently, we focus on two areas. First, we are
elucidating the genetic determinants and disease relevance of ferroptosis, a newly
recognized form of cell death. Second, we have identified the mammalian stringent
response pathway which is highly similar to bacterial stringent response, but

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