Quartan fever

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Quartan fever
P malariae schizont4.jpg
P. malariae schizont in a thick blood smear
Specialty Infectious disease
Symptoms Fever
DurationFever in 72 hour intervals
CausesPlasmodium spread by mosquitos
Diagnostic method Blood tests
Medication Chloroquine

Quartan fever is one of the four types of malaria which can be contracted by humans. [1]

Contents

It is specifically caused by the Plasmodium malariae species, one of the six species of the protozoan genus Plasmodium . Quartan fever is a form of malaria where an onset of fever occurs in an interval of three to four days, hence the name "quartan". [2] It is transmitted by bites of infected female mosquitoes of the genus Anopheles . Symptoms include fevers which range from approximately 40–41 °C (104–106 °F) and occur periodically in 72 hour intervals. Although cases of malaria have occurred throughout the world, quartan fever typically occurs in the subtropics. Quartan fever is considered to be a less severe form of malaria fever that can be cured by anti-malarial medication, and prevention methods can be taken in order to avoid infection. [3]

Signs and symptoms

Early indications of quartan fever include having irritated spots, welts, hives and burning skin, however this is dependent on individual's tolerance to mosquito bites and may not be evident on some people. With the Anopheles malaria mosquitoes, the welts are most likely to not appear unless there are severe allergic reactions. [4]

Cause

The female Anopheles mosquito is a vector which transmits quartan fever to people. Mature mosquitoes carry uninucleate sporozoites in their salivary glands; these sporozoites enter a human's bloodstream when mosquitoes puncture human flesh during feeding.  Sporozoites attack and inhabit liver parenchymal cells, called hepatocytes, in order to develop further. Once the uninucleate sporozoites have matured, the sporozoites then develop into uninucleate merozoites. Uninucleated merozoites mature into an erythrocytic stage called schizonts which contain merozoites. The schizonts, an infected erythrocyte, then rupture to release these merozoites; leading to more infections in the red blood cells. Uninucleated merozoites can also mature into uninucleate gametocytes which can invade and infect other female Anopheles mosquitoes during feeding, thus spreading the disease onto a wider population of humans. [3]

Anopheles Mosquito feeding (video taken County Durham, UK.)

Diagnosis

Fevers in intervals of 72 hours distinguish quartan fever from other forms of malaria where fevers range in 48 hour intervals or fever spikes that occur sporadically. [3]

The prepatent period is the time interval for when parasites infect a host and when they can be detected on a thick blood film. For quartan fever, P. malariae has a prepatent period ranging from 16 to 59 days. Specifically in the case of quartan fever, the rupturing of liver stage schizonts releases merozoites. This stage of the P. malariae life cycle is known as the "ring stages" and are the first stages which can be detected in human blood for diagnosis. [5]

Medical procedures that diagnose quartan fever

Prevention

Ways to minimise exposure to the Anopheles mosquito include:

Anopheles mosquito larvae, taken by Steffen Dietzel

Treatment

Related Research Articles

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References

  1. Garcia, Célia R. S.; Markus, Regina P.; Madeira, Luciana (2001). "Tertian and Quartan Fevers: Temporal Regulation in Malarial Infection". Journal of Biological Rhythms. 16 (5): 436–443. doi:10.1177/074873001129002114. ISSN   0748-7304. PMID   11669417. S2CID   6409247.
  2. "quartan". English Oxford living Dictionaries. 2019. Archived from the original on April 14, 2019. Retrieved 29 March 2019.
  3. 1 2 3 Crutcher, James M. (1996). Medical Microbiology. 4th edition. Galveston: The University of Texas Medical Branch at Galveston.
  4. "Insect Bite Prevention". IAMAT. 25 January 2019. Retrieved 13 May 2019.
  5. 1 2 3 Collins, William E. (2007). "Plasmodium malariae: Parasite and Disease". Clinical Microbiology Reviews. 20 (4): 579–592. doi:10.1128/CMR.00027-07. PMC   2176047 . PMID   17934075.
  6. 1 2 3 "Rapid Diagnostic Tests: How They Work". CDC. 2018. Retrieved 9 May 2019.
  7. "AIDS info". HIV/AIDS Glossary. Retrieved 9 May 2019.
  8. 1 2 3 4 5 6 7 Tizifa, Tinashe A (8 February 2018). "Prevention Efforts for Malaria". Current Tropical Medicine Reports. 5 (1): 41–50. doi:10.1007/s40475-018-0133-y. PMC   5879044 . PMID   29629252.
  9. 1 2 Kayentao, K (23 February 2012). "Intermittent preventive therapy for malaria during pregnancy using 2 vs 3 or more doses of sulfadoxine-pyrimethamine and risk of low birth weight in Africa: systematic review and meta-analysis". JAMA. 309 (6): 594–604. doi:10.1001/jama.2012.216231. PMC   4669677 . PMID   23403684.
  10. "Mosquito Life Cycle". EPA. 13 March 2017. Retrieved 3 May 2019.
  11. C Beier, John (1 February 2012). "Attractive toxic sugar bait (ATSB) methods decimate populations of Anopheles malaria vectors in arid environments regardless of the local availability of favoured sugar-source blossoms". Malaria Journal. 11: 31. doi: 10.1186/1475-2875-11-31 . PMC   3293779 . PMID   22297155.
  12. "LABEL: CHLOROQUINE- chloroquine phosphate tablet". DAILY MED. 8 July 2010. Retrieved 10 May 2019.
  13. 1 2 "Malaria". 2019. Retrieved 10 May 2019.