<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kina UY</submitter><funding>NIAID NIH HHS</funding><funding>HHS | NIH | National Institute of Allergy and Infectious Diseases</funding><funding>TUBITAK</funding><pagination>e0016723</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10353352</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>91(7)</volume><pubmed_abstract>A frequent side effect of chemotherapy against malaria parasite blood infections is a dramatic induction of the sexual blood stages, thereby enhancing the risk of future malaria transmissions. The polyamine biosynthesis pathway has been suggested as a candidate target for transmission-blocking anti-malarial drug development. Herein, we describe the role of a bacterial-type amino acid decarboxylase (&lt;i>AAD&lt;/i>) in the life cycle of the malaria model parasite Plasmodium yoelii. Hallmarks of AAD include a conserved catalytic lysine residue and high-level homology to arginine/lysine/ornithine decarboxylases of pathogenic bacteria. By targeted gene deletion, we show that &lt;i>AAD&lt;/i> plays an essential role in the exflagellation of microgametes, resulting in complete absence of sporozoites in the</pubmed_abstract><journal>Infection and immunity</journal><pubmed_title>A Candidate Bacterial-Type Amino Acid Decarboxylase Is Essential for Male Gamete Exflagellation and Mosquito Transmission of the Malaria Parasite.</pubmed_title><pmcid>PMC10353352</pmcid><funding_grant_id>R21 AI111058</funding_grant_id><funding_grant_id>119Z409</funding_grant_id><funding_grant_id>1R21AI111058-01A1</funding_grant_id><pubmed_authors>Deveci G</pubmed_authors><pubmed_authors>Kina UY</pubmed_authors><pubmed_authors>Rafiqi AM</pubmed_authors><pubmed_authors>Matuschewski K</pubmed_authors><pubmed_authors>Aly ASI</pubmed_authors><pubmed_authors>Kamil M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Candidate Bacterial-Type Amino Acid Decarboxylase Is Essential for Male Gamete Exflagellation and Mosquito Transmission of the Malaria Parasite.</name><description>A frequent side effect of chemotherapy against malaria parasite blood infections is a dramatic induction of the sexual blood stages, thereby enhancing the risk of future malaria transmissions. The polyamine biosynthesis pathway has been suggested as a candidate target for transmission-blocking anti-malarial drug development. Herein, we describe the role of a bacterial-type amino acid decarboxylase (&lt;i>AAD&lt;/i>) in the life cycle of the malaria model parasite Plasmodium yoelii. Hallmarks of AAD include a conserved catalytic lysine residue and high-level homology to arginine/lysine/ornithine decarboxylases of pathogenic bacteria. By targeted gene deletion, we show that &lt;i>AAD&lt;/i> plays an essential role in the exflagellation of microgametes, resulting in complete absence of sporozoites in the</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jul</publication><modification>2025-05-29T21:47:21.437Z</modification><creation>2025-05-29T21:47:21.437Z</creation></dates><accession>S-EPMC10353352</accession><cross_references><pubmed>37260388</pubmed><doi>10.1128/iai.00167-23</doi></cross_references></HashMap>