LETTER
In an article by Junaid et al. (1), the considerable work that three of my students (Drs. Baro, Pooput, and Callaghan) performed in inventing and perfecting approaches used in this paper that are important for its conclusions was not cited. I write to note this out of respect for the years of work that those students devoted to developing those approaches. In particular, the back-translation of the amino acid sequence to yield a yeast codon-optimized Plasmodium gene, expression of those back-translated membrane transporter genes in S. cerevisiae yeast, subsequent quantitative analysis of those strains vs. antimalarial drugs by spotting of yeast, and then quantitative growth analysis +/− drug to reveal possible roles of membrane transporter isoforms in antimalarial drug resistance phenomena were first published by Nick Baro, Chaya Pooput, and Paul Callaghan from my laboratory starting in 2011 (2–4). Reference to their collective creativity, hard work, and conclusions should have been included.
I also write to mention that although the paper does a wonderful job in identifying new intraerythrocytic digestive vacuolar (DV) membrane transport proteins putatively involved in antimalarial drug resistance phenomena, at least one known to fall within this category and that is known to reside in the DV (e.g., PfAAT) (5) is not found by the methods used in the study and not mentioned in the paper.
Contributor Information
Paul D. Roepe, Email: roepep@georgetown.edu.
Audrey Odom John, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
REFERENCES
- 1. Junaid IT, Panda A, Deshmukh A, Sardar R, Narwal M, Agrawal P, Prakash N, Akhtar A, Dey AK, Singh SS, Mridha S, Mochi J, Parveen S, Kumar M, Nagar R, Gaur N, Gupta D, Mohmmed A, Kaur I, Karmodiya K, Malhotra P. 2025. Role of novel mutations in food vacuole transporters beyond K13-mediated artemisinin resistance in Plasmodium falciparum Antimicrob Agents Chemother 69:e00293-25. doi: 10.1128/aac.00293-25 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2. Baro Nicholas K, Pooput C, Roepe PD. 2011. Analysis of chloroquine resistance transporter (CRT) isoforms and orthologues in S. cerevisiae yeast. Biochemistry 50:6701–6710. doi: 10.1021/bi200922g [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Baro N.K., Callaghan P, Roepe PD. 2013. Analysis of naturally occurring P. falciparum Chloroquine Resistance Transporter (PfCRT) isoforms in S. cerevisiae yeast. Biochemistry 52:4242–4249 doi: 10.1021/bi400557x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Callaghan PS, Hassett MR, Roepe PD. 2015. Functional comparison of 45 naturally occurring isoforms of the Plasmodium falciparum chloroquine resistance transporter (PfCRT). Biochemistry 54:5083–5094. doi: 10.1021/acs.biochem.5b00412 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Amambua-Ngwa A, Button-Simons KA, Li X, Kumar S, Brenneman KV, Ferrari M, Checkley LA, Haile MT, Shoue DA, McDew-White M, et al. 2023. Chloroquine resistance evolution in Plasmodium falciparum is mediated by the putative amino acid transporter AAT1. Nat Microbiol 8:1213–1226. doi: 10.1038/s41564-023-01377-z [DOI] [PMC free article] [PubMed] [Google Scholar]
