Malaria, a potentially life-threatening disease caused
by the mosquito-borne
parasitic infection of human red blood cells, still accounts for over
half a million deaths worldwide every year. Accurate early-stage diagnosis
of malaria is indispensable for quick medical intervention and the
avoidance of any potential complications leading to fatality. In this
regard, DNA-specific fluorescent probes coupled with flow cytometry
techniques emerged as a promising cost-effective diagnostic platform
for highly sensitive rapid detection of malaria. However, ideal DNA-specific
fluorescent probes that can be efficiently employed for both fluorescence
microscopic studies as well as flow cytometric analysis to enable
precise, high-quality clinical diagnosis of malaria are inadequate.
In this context, we have reported a rationally designed hemicyanine
dye MR-1 with blue absorption and red emission that can
exhibit a turn-on fluorescence response upon effective binding with
the AT-rich segments of dsDNA. The rationale behind designing the
fluorescent probe MR-1 was well explained with the help
of control compounds MR-2 and MR-3. The
DNA-specific fluorescent probe MR-1 revealed excellent
cell permeability and localized in the cellular nucleus of both live
and fixed cells. A marked enhancement in fluorescence intensity was
observed when malaria parasite-infected red blood cells were incubated
with MR-1, and the detection limit was found to be ∼20/μL.
Further, the flow cytometric analysis of clinical malaria parasite-infected
red blood cells incubated with MR-1 not only demonstrated
precise detection and classification of various malaria parasites
but also smartly enabled the differentiation of malaria from Babesia-parasite
infection with similar clinical symptoms.