Publications by authors named "Madhu Puri"

Article Synopsis
  • - Atherosclerosis is an inflammatory disease leading to heart issues, and enhancing the process of efferocytosis (cell removal by macrophages) is being explored as a potential treatment.
  • - Blocking CD47, which signals cells not to be engulfed, reduces plaque buildup but can also cause anemia due to red blood cell clearance.
  • - A new macrophage-specific nanotherapy was developed to promote efferocytosis without causing anemia, proving effective in early atherosclerosis models in pigs, showing promise for future treatments.
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Leishmaniasis is one of the major parasitic diseases, caused by obligate intracellular protozoa having high mortality as well as morbidity rate. As there is no human licensed vaccine available against leishmaniasis, chemotherapy remains the major way of combating this disease. Many disadvantages are known to be associated with the current drug regime including severe side effects and toxicity, long duration and expensive treatment, and the emergence of resistance.

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LAMP diagnosis of malaria is simple and cost-effective with acceptable sensitivity and specificity as compared to standard diagnostic modules such as microscopy, RDTs and nested PCR, and thus its deployment for onsite screening of malaria in resource-limited regions is under consideration. However, the requirement of an electricity-operated dry bath and bulky read-out unit is still a major concern. In an effort to simplify this limitation, we have developed a portable LAMP device and fluorescence readout unit which can be used in the rapid point-of-care diagnosis of malaria.

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is an intracellular protozoan parasite, that causes visceral leishmaniasis (VL), and consequently, post-kala azar dermal leishmaniasis (PKDL). Diagnosis and treatment of leishmaniasis is crucial for decreasing its transmission. Various diagnostic techniques like microscopy, enzyme-linked immunosorbent assays (ELISA) and PCR-based methods are used to detect leishmaniasis infection.

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Article Synopsis
  • Arginine balance in lysosomes is crucial for the growth and metabolism of mammalian cells, particularly within macrophages where the protozoan parasite causing leishmaniasis resides.
  • When infected, the parasite detects low arginine levels through a surface sensor, activating a response that increases the abundance and activity of an arginine transporter, necessary for its survival.
  • Disruption of this response through gene editing demonstrated that while the mutants could grow normally in lab settings, they were significantly less effective at developing and infecting within host macrophages and mice, highlighting the importance of arginine sensing for the parasite's pathogenicity.
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The intracellular protozoan parasite Leishmania donovani causes human visceral leishmaniasis. Intracellular L. donovani that proliferate inside macrophage phagolysosomes compete with the host for arginine, creating a situation that endangers parasite survival.

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Autophagy, a well-established defense mechanism, enables the elimination of intracellular pathogens including . Host cell recognition results in ubiquitination of . and interaction with autophagy adaptors p62/SQSTM1 and NDP52, which target bacteria to autophagosomes by binding to microtubule-associated protein 1 light chain 3 (LC3).

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Listeria monocytogenes is a ubiquitously occurring gram-positive bacterium in the environment that causes listeriosis, one of the deadliest foodborne infections known today. It is a versatile facultative intracellular pathogen capable of growth within the host's cytosolic compartment. Following entry into the host cell, L.

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