Jonathan J. Juliano

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Jonathan James Juliano is an American physician/scientist. He currently works at UNC School of Medicine.

Contents

Biography

Jonathan Juliano is Professor of Medicine, Division of Infectious Diseases at UNC School of Medicine, where he also is Associate Director, UNC Infectious Diseases Fellowship Training Program. [1] He has been on faculty since 2009. In addition, he is an adjunct assistant professor in the Department of Epidemiology at the UNC Gillings School of Global Public Health and an instructor in the Curriculum of Genetics and Molecular Biology.

He received his BSc from University of Toronto, Toronto, Canada in 1994. He completed a MSPH at the UNC Gillings School of Global Public Health (1997) and his MD at the UNC School of Medicine in 2001. [1]

He trained in Internal Medicine and Pediatrics at the University of Minnesota, Minneapolis, MN from 2001 to 2005. Following this, he completed his Infectious Disease Fellowship at University of North Carolina, Chapel Hill, NC in 2008. [1] He is board certified in Internal Medicine and Infectious Diseases.

Research

Jonathan Juliano has led research efforts in infectious diseases and genetics, with the goal of improving our understanding of how infections cause disease, how infectious agents evolve, and how the genetic diversity impacts our understanding of drug resistance. His work has focused on malaria; however he has worked with other agents as well. [2] [3] In particular, he is interested in understanding within host genetic diversity of malaria infections, as each infection may contain multiple genetically different parasite strains, and the impact of this diversity on drug and vaccine efficacy. [4] [5] His work in this area has called into question some of the current practices of how clinical trials for malaria are conducted. [6] [7] [8] [9]

He has been the recipient of several awards including the Merle A. Sande/Pfizer Fellowship Award in International Diseases and the Terry Lee Award from the North Carolina Infectious Disease Society. [10] He has also authored articles and a book chapter concerning the clinical care of malaria. [11] [12] Juliano collaborates with Dr. Carla Cerami at the University of North Carolina and Dr. Steve M. Taylor at Duke University School of Medicine. [13]

In 2019, he was elected to the American Society for Clinical Investigation. [14] In 2022 he was named a Fellow of the American Society of Tropical Medicine and Hygiene [15] and the Infectious Diseases Society of America. [16]

Related Research Articles

<span class="mw-page-title-main">Malaria</span> Mosquito-borne infectious disease

Malaria is a mosquito-borne infectious disease that affects vertebrates and Anopheles mosquitoes. Human malaria causes symptoms that typically include fever, fatigue, vomiting, and headaches. In severe cases, it can cause jaundice, seizures, coma, or death. Symptoms usually begin 10 to 15 days after being bitten by an infected Anopheles mosquito. If not properly treated, people may have recurrences of the disease months later. In those who have recently survived an infection, reinfection usually causes milder symptoms. This partial resistance disappears over months to years if the person has no continuing exposure to malaria. The mosquito vector is itself harmed by Plasmodium infections, causing reduced lifespan.

<span class="mw-page-title-main">Mefloquine</span> Pharmaceutical drug

Mefloquine, sold under the brand name Lariam among others, is a medication used to prevent or treat malaria. When used for prevention it is typically started before potential exposure and continued for several weeks after potential exposure. It can be used to treat mild or moderate malaria but is not recommended for severe malaria. It is taken by mouth.

<i>Plasmodium falciparum</i> Protozoan species of malaria parasite

Plasmodium falciparum is a unicellular protozoan parasite of humans, and the deadliest species of Plasmodium that causes malaria in humans. The parasite is transmitted through the bite of a female Anopheles mosquito and causes the disease's most dangerous form, falciparum malaria. P. falciparum is therefore regarded as the deadliest parasite in humans. It is also associated with the development of blood cancer and is classified as a Group 2A (probable) carcinogen.

<span class="mw-page-title-main">Artemisinin</span> Group of drugs used against malaria

Artemisinin and its semisynthetic derivatives are a group of drugs used in the treatment of malaria due to Plasmodium falciparum. It was discovered in 1972 by Tu Youyou, who shared the 2015 Nobel Prize in Physiology or Medicine for her discovery. Artemisinin-based combination therapies (ACTs) are now standard treatment worldwide for P. falciparum malaria as well as malaria due to other species of Plasmodium. Artemisinin is extracted from the plant Artemisia annua an herb employed in Chinese traditional medicine. A precursor compound can be produced using a genetically engineered yeast, which is much more efficient than using the plant.

<span class="mw-page-title-main">Tropical medicine</span> Interdisciplinary branch of medicine

Tropical medicine is an interdisciplinary branch of medicine that deals with health issues that occur uniquely, are more widespread, or are more difficult to control in tropical and subtropical regions.

<span class="mw-page-title-main">Chloroquine</span> Medication used to treat malaria

Chloroquine is an antiparasitic medication that treats malaria. It works by increasing the levels of haeme in the blood, a substance toxic to the malarial parasite. This kills the parasite and stops the infection from spreading. Certain types of malaria, resistant strains, and complicated cases typically require different or additional medication. Chloroquine is also occasionally used for amebiasis that is occurring outside the intestines, rheumatoid arthritis, and lupus erythematosus. While it has not been formally studied in pregnancy, it appears safe. It was studied to treat COVID-19 early in the pandemic, but these studies were largely halted in the summer of 2020, and the NIH does not recommend its use for this purpose. It is taken by mouth.

<i>Plasmodium vivax</i> Species of single-celled organism

Plasmodium vivax is a protozoal parasite and a human pathogen. This parasite is the most frequent and widely distributed cause of recurring malaria. Although it is less virulent than Plasmodium falciparum, the deadliest of the five human malaria parasites, P. vivax malaria infections can lead to severe disease and death, often due to splenomegaly. P. vivax is carried by the female Anopheles mosquito; the males do not bite.

<span class="mw-page-title-main">Amodiaquine</span> Chemical compound

Amodiaquine (ADQ) is a medication used to treat malaria, including Plasmodium falciparum malaria when uncomplicated. It is recommended to be given with artesunate to reduce the risk of resistance. Due to the risk of rare but serious side effects, it is not generally recommended to prevent malaria. Though, the World Health Organization (WHO) in 2013 recommended use for seasonal preventive in children at high risk in combination with sulfadoxine and pyrimethamine.

<span class="mw-page-title-main">History of malaria</span>

The history of malaria extends from its prehistoric origin as a zoonotic disease in the primates of Africa through to the 21st century. A widespread and potentially lethal human infectious disease, at its peak malaria infested every continent except Antarctica. Its prevention and treatment have been targeted in science and medicine for hundreds of years. Since the discovery of the Plasmodium parasites which cause it, research attention has focused on their biology as well as that of the mosquitoes which transmit the parasites.

Merle Alden Sande was a leading American infectious-diseases expert whose early recognition of the looming public health crisis posed by AIDS led to the development of basic protocols for how to handle infected patients. He graduated from Washington State University and received his MD degree from the University of Washington, School of Medicine in Seattle.

<span class="mw-page-title-main">Pyronaridine</span> Chemical compound

Pyronaridine is an antimalarial drug. It was first made in 1970 and has been in clinical use in China since the 1980s.

Pregnancy-associated malaria (PAM) or placental malaria is a presentation of malaria in pregnancy which is life-threatening to both pregnant women and unborn fetuses. PAM occurs when a pregnant woman contracts malaria, generally as a result of Plasmodium falciparum infection, and because she is pregnant, is at greater risk of associated complications such as placental malaria. Placental malaria interferes with the transmission of vital substances through the fetal placenta, which can result in stillbirths, miscarriages, and dangerously low birth weights.

<span class="mw-page-title-main">Intermittent fever</span> Pattern of fever

Intermittent fever is a type or pattern of fever in which there is an interval where temperature is elevated for several hours followed by an interval when temperature drops back to normal. This type of fever usually occurs during the course of an infectious disease. Diagnosis of intermittent fever is frequently based on the clinical history but some biological tests like complete blood count and blood culture are also used. In addition radiological investigations like chest X-ray, abdominal ultrasonography can also be used in establishing diagnosis.

<span class="mw-page-title-main">Abdoulaye Djimdé</span>

Abdoulaye Djimdé is an associate professor of Microbiology and Immunology in Mali. He works on the genetic epidemiology of antimalarial drug resistance and is a Wellcome Sanger Institute International Fellow. He is Chief of the Molecular Epidemiology and Drug Resistance Unit at the University of Bamako Malaria Research and Training Centre.

<span class="mw-page-title-main">Elizabeth A. Winzeler</span> American microbiologist

Elizabeth Ann Winzeler is an American microbiologist and geneticist. She is a professor in the Division of Host-Microbe Systems and Therapeutics of the School of Medicine at the University of California at San Diego. Although she works in a variety of different disease areas, most research focuses on developing better medicines for the treatment and eradication of malaria.

Silvie Huijben is an evolutionary biologist and assistant professor at Arizona State University. The Huijben Lab uses fieldwork, lab experiments, and mathematical modeling to study antimalarial and insecticide resistance in parasites, such as disease-transmitting mosquitoes. Her work is focused on applying evolutionary theory to produce resistance management strategies to best combat malaria.

Claire B. Panosian Dunavan is an emeritus Professor of Medicine at the University of California, Los Angeles. Her research considered global health and diseases, including parasitic infections, tuberculosis and malaria. Panosian served as president of the American Society of Tropical Medicine and Hygiene in 2008. She is also a science writer, reporter and television presenter.

Lyda Elena Osorio Amaya is a Colombian physician, epidemiologist and infectious disease specialist. She is an associate professor at the Universidad del Valle, and a researcher at the Centro Internacional de Entrenamiento e Investigaciones Médicas (CIDEIM) in Cali, Valle del Cauca. Osorio's research has focused mainly on vector-borne diseases like malaria, leishmaniasis, Zika and dengue fever. She has also played a role in Colombia's response against COVID-19.

Joseph Michael Vinetz is a Professor of Medicine and Anthropology at Yale University, Research Professor at the Universidad Peruana Cayetano Heredia and Associate Investigator of the Alexander von Humboldt Institute of Tropical Medicine at the Universidad Peruana Cayetano Heredia.

<span class="mw-page-title-main">David A. Fidock</span>

David A. Fidock, is the CS Hamish Young Professor of Microbiology and Immunology and Professor of Medical Sciences at Columbia University Irving Medical Center in Manhattan.

References

  1. 1 2 3 "Jonathan Juliano, MD, MSPH". Department of Medicine. Retrieved 2022-11-14.
  2. Carter, YL; Juliano, JJ; Montgomery, SP; Qvarnstrom, Y (2012). "Acute chagas disease in a returning traveler". The American Journal of Tropical Medicine and Hygiene. 87 (6): 1038–40. doi:10.4269/ajtmh.2012.12-0354. PMC   3516071 . PMID   23091192.
  3. Bratton, EW; El Husseini, N; Chastain, CA; Lee, MS; Poole, C; Stürmer, T; Juliano, JJ; Weber, DJ; Perfect, JR (2012). "Correction: Comparison and Temporal Trends of Three Groups with Cryptococcosis: HIV-Infected, Solid Organ Transplant, and HIV-Negative/Non-Transplant". PLOS ONE. 7 (10): 10.1371/annotation/a94bc542-6682-4579-a315-57019cef7e0e. doi: 10.1371/annotation/a94bc542-6682-4579-a315-57019cef7e0e . PMC   3507528 . Open Access logo PLoS transparent.svg
  4. Juliano, JJ; Porter, K; Mwapasa, V; Sem, R; Rogers, WO; Ariey, F; Wongsrichanalai, C; Read, A; Meshnick, SR (2010). "Exposing malaria in-host diversity and estimating population diversity by capture-recapture using massively parallel pyrosequencing". Proceedings of the National Academy of Sciences of the United States of America. 107 (46): 20138–43. Bibcode:2010PNAS..10720138J. doi: 10.1073/pnas.1007068107 . PMC   2993407 . PMID   21041629.
  5. Bailey, JA; Mvalo, T; Aragam, N; Weiser, M; Congdon, S; Kamwendo, D; Martinson, F; Hoffman, I; Meshnick, SR; Juliano, JJ (2012). "Use of massively parallel pyrosequencing to evaluate the diversity of and selection on Plasmodium falciparum csp T-cell epitopes in Lilongwe, Malawi". The Journal of Infectious Diseases. 206 (4): 580–7. doi:10.1093/infdis/jis329. PMC   3491736 . PMID   22551816.
  6. Juliano, JJ; Taylor, SM; Meshnick, SR (2009). "Polymerase chain reaction adjustment in antimalarial trials: Molecular malarkey?". The Journal of Infectious Diseases. 200 (1): 5–7. doi:10.1086/599379. PMC   2803033 . PMID   19469704.
  7. Juliano, JJ; Ariey, F; Sem, R; Tangpukdee, N; Krudsood, S; Olson, C; Looareesuwan, S; Rogers, WO; Wongsrichanalai, C; Meshnick, SR (2009). "Misclassification of drug failure in Plasmodium falciparum clinical trials in southeast Asia". The Journal of Infectious Diseases. 200 (4): 624–8. doi:10.1086/600892. PMC   2761972 . PMID   19591576.
  8. Juliano, JJ; Gadalla, N; Sutherland, CJ; Meshnick, SR (2010). "The perils of PCR: Can we accurately 'correct' antimalarial trials?". Trends in Parasitology. 26 (3): 119–24. doi:10.1016/j.pt.2009.12.007. PMC   2844636 . PMID   20083436.
  9. Porter, KA; Burch, CL; Poole, C; Juliano, JJ; Cole, SR; Meshnick, SR (2011). "Uncertain outcomes: Adjusting for misclassification in antimalarial efficacy studies". Epidemiology and Infection. 139 (4): 544–51. doi:10.1017/S0950268810001652. PMC   4829077 . PMID   20619072.
  10. Merle Sande: http://www.idsociety.org/Merle_A._Sande_Pfizer_Fellowship_Award/%5B%5D
  11. Taylor, SM; Molyneux, ME; Simel, DL; Meshnick, SR; Juliano, JJ (2010). "Does this patient have malaria?". JAMA: The Journal of the American Medical Association. 304 (18): 2048–56. doi:10.1001/jama.2010.1578. PMID   21057136.
  12. Book chapter: Netter’s Internal medicine, 2e. Saunders. ISBN   978-1416044178 [ page needed ]
  13. Taylor, S. M.; Messina, J. P.; Hand, C. C.; Juliano, J. J.; Muwonga, J.; Tshefu, A. K.; Atua, B.; Emch, M.; Meshnick, S. R. (2011). Braga, Erika Martins (ed.). "Molecular Malaria Epidemiology: Mapping and Burden Estimates for the Democratic Republic of the Congo, 2007". PLOS ONE. 6 (1): e16420. Bibcode:2011PLoSO...616420T. doi: 10.1371/journal.pone.0016420 . PMC   3031549 . PMID   21305011. Open Access logo PLoS transparent.svg
  14. "Jonathan James Juliano, MD, MSPH". American Society for Clinical Investigation. Archived from the original on 2022-10-18. Retrieved 2022-11-14.
  15. "ASTMH - Fellows of ASTMH (FASTMH)". www.astmh.org. Retrieved 2022-11-14.
  16. "IDSA Honors 175 Distinguished Physicians, Scientists with FIDSA Designation". www.idsociety.org. Retrieved 2022-11-14.