Transcriptional response of individual Hawaiian Culex quinquefasciatus mosquitoes to the avian malaria parasite Plasmodium relictum.


Journal

Malaria journal
ISSN: 1475-2875
Titre abrégé: Malar J
Pays: England
ID NLM: 101139802

Informations de publication

Date de publication:
29 Aug 2022
Historique:
received: 17 06 2022
accepted: 16 08 2022
entrez: 29 8 2022
pubmed: 30 8 2022
medline: 1 9 2022
Statut: epublish

Résumé

Plasmodium parasites that cause bird malaria occur in all continents except Antarctica and are primarily transmitted by mosquitoes in the genus Culex. Culex quinquefasciatus, the mosquito vector of avian malaria in Hawai'i, became established in the islands in the 1820s. While the deadly effects of malaria on endemic bird species have been documented for many decades, vector-parasite interactions in avian malaria systems are relatively understudied. To evaluate the gene expression response of mosquitoes exposed to a Plasmodium infection intensity known to occur naturally in Hawai'i, offspring of wild-collected Hawaiian Cx. quinquefasciatus were fed on a domestic canary infected with a fresh isolate of Plasmodium relictum GRW4 from a wild-caught Hawaiian honeycreeper. Control mosquitoes were fed on an uninfected canary. Transcriptomes of five infected and three uninfected individual mosquitoes were sequenced at each of three stages of the parasite life cycle: 24 h post feeding (hpf) during ookinete invasion; 5 days post feeding (dpf) when oocysts are developing; 10 dpf when sporozoites are released and invade the salivary glands. Differential gene expression analyses showed that during ookinete invasion (24 hpf), genes related to oxidoreductase activity and galactose catabolism had lower expression levels in infected mosquitoes compared to controls. Oocyst development (5 dpf) was associated with reduced expression of a gene with a predicted innate immune function. At 10 dpf, infected mosquitoes had reduced expression levels of a serine protease inhibitor, and further studies should assess its role as a Plasmodium agonist in C. quinquefasciatus. Overall, the differential gene expression response of Hawaiian Culex exposed to a Plasmodium infection intensity known to occur naturally in Hawai'i was low, but more pronounced during ookinete invasion. This is the first analysis of the transcriptional responses of vectors to malaria parasites in non-mammalian systems. Interestingly, few similarities were found between the response of Culex infected with a bird Plasmodium and those reported in Anopheles infected with human Plasmodium. The relatively small transcriptional changes observed in mosquito genes related to immune response and nutrient metabolism support conclusions of low fitness costs often documented in experimental challenges of Culex with avian Plasmodium.

Sections du résumé

BACKGROUND BACKGROUND
Plasmodium parasites that cause bird malaria occur in all continents except Antarctica and are primarily transmitted by mosquitoes in the genus Culex. Culex quinquefasciatus, the mosquito vector of avian malaria in Hawai'i, became established in the islands in the 1820s. While the deadly effects of malaria on endemic bird species have been documented for many decades, vector-parasite interactions in avian malaria systems are relatively understudied.
METHODS METHODS
To evaluate the gene expression response of mosquitoes exposed to a Plasmodium infection intensity known to occur naturally in Hawai'i, offspring of wild-collected Hawaiian Cx. quinquefasciatus were fed on a domestic canary infected with a fresh isolate of Plasmodium relictum GRW4 from a wild-caught Hawaiian honeycreeper. Control mosquitoes were fed on an uninfected canary. Transcriptomes of five infected and three uninfected individual mosquitoes were sequenced at each of three stages of the parasite life cycle: 24 h post feeding (hpf) during ookinete invasion; 5 days post feeding (dpf) when oocysts are developing; 10 dpf when sporozoites are released and invade the salivary glands.
RESULTS RESULTS
Differential gene expression analyses showed that during ookinete invasion (24 hpf), genes related to oxidoreductase activity and galactose catabolism had lower expression levels in infected mosquitoes compared to controls. Oocyst development (5 dpf) was associated with reduced expression of a gene with a predicted innate immune function. At 10 dpf, infected mosquitoes had reduced expression levels of a serine protease inhibitor, and further studies should assess its role as a Plasmodium agonist in C. quinquefasciatus. Overall, the differential gene expression response of Hawaiian Culex exposed to a Plasmodium infection intensity known to occur naturally in Hawai'i was low, but more pronounced during ookinete invasion.
CONCLUSIONS CONCLUSIONS
This is the first analysis of the transcriptional responses of vectors to malaria parasites in non-mammalian systems. Interestingly, few similarities were found between the response of Culex infected with a bird Plasmodium and those reported in Anopheles infected with human Plasmodium. The relatively small transcriptional changes observed in mosquito genes related to immune response and nutrient metabolism support conclusions of low fitness costs often documented in experimental challenges of Culex with avian Plasmodium.

Identifiants

pubmed: 36038897
doi: 10.1186/s12936-022-04271-x
pii: 10.1186/s12936-022-04271-x
pmc: PMC9422152
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

249

Subventions

Organisme : National Science Foundation
ID : 2001213
Organisme : National Science Foundation
ID : 2001213
Organisme : National Science Foundation
ID : 2001213
Organisme : National Science Foundation
ID : 2001213
Organisme : National Science Foundation
ID : 2001213
Organisme : National Science Foundation
ID : 2001213

Informations de copyright

© 2022. The Author(s).

Références

Philos Trans R Soc Lond B Biol Sci. 2015 Aug 19;370(1675):
pubmed: 26150666
Nucleic Acids Res. 2015 Jan;43(Database issue):D707-13
pubmed: 25510499
EMBO Rep. 2005 Sep;6(9):891-7
pubmed: 16113656
Am Nat. 2020 Jun;195(6):1070-1084
pubmed: 32469658
Proc Natl Acad Sci U S A. 1998 May 12;95(10):5700-5
pubmed: 9576947
Infect Immun. 2003 Jun;71(6):3000-9
pubmed: 12761076
PLoS One. 2011;6(7):e21800
pubmed: 21789182
Mol Biol Evol. 2018 Feb 1;35(2):383-403
pubmed: 29126122
Bioinformatics. 2016 Oct 1;32(19):3047-8
pubmed: 27312411
BMC Evol Biol. 2009 Dec 22;9:298
pubmed: 20028549
J Biol Chem. 2003 Feb 28;278(9):7059-64
pubmed: 12496260
Am J Trop Med Hyg. 2006 Feb;74(2):284-9
pubmed: 16474085
Bioinformatics. 2015 Jan 15;31(2):166-9
pubmed: 25260700
Ecohealth. 2013 Dec;10(4):366-75
pubmed: 24430825
J Parasitol. 2005 Aug;91(4):843-9
pubmed: 17089752
Cell Host Microbe. 2009 May 8;5(5):498-507
pubmed: 19454353
Mol Ecol. 2006 Nov;15(13):3919-30
pubmed: 17054493
Nat Commun. 2021 May 20;12(1):2960
pubmed: 34017003
Bio Protoc. 2017 Sep 5;7(17):
pubmed: 29075656
Genome Res. 2018 Apr;28(4):547-560
pubmed: 29500236
Ecology. 2020 Jul;101(7):e03038
pubmed: 32129884
Trends Parasitol. 2022 Feb;38(2):124-135
pubmed: 34548252
J Med Entomol. 2018 Oct 25;55(6):1509-1516
pubmed: 30085189
Bioinformatics. 2014 Aug 1;30(15):2114-20
pubmed: 24695404
Genome Biol. 2014;15(12):550
pubmed: 25516281
Nat Biotechnol. 2019 Aug;37(8):907-915
pubmed: 31375807
Curr Biol. 2005 Jul 12;15(13):1185-95
pubmed: 16005290
EMBO J. 1998 Nov 2;17(21):6115-23
pubmed: 9799221
J Avian Med Surg. 2009 Mar;23(1):53-63
pubmed: 19530408
Proc Natl Acad Sci U S A. 2005 Feb 1;102(5):1531-6
pubmed: 15668377
J Parasitol. 2010 Apr;96(2):318-24
pubmed: 20001096
PLoS Negl Trop Dis. 2022 Aug 8;16(8):e0010689
pubmed: 35939523
Trends Parasitol. 2016 Dec;32(12):979-990
pubmed: 27639778
Genomics. 2021 Jul;113(4):2327-2337
pubmed: 34023365
PLoS One. 2018 Feb 5;13(2):e0192315
pubmed: 29401525
J Innate Immun. 2017;9(4):333-342
pubmed: 28494453
Cell Microbiol. 2016 Jul;18(7):905-18
pubmed: 27111866
Cell Microbiol. 2007 Mar;9(3):708-24
pubmed: 17054438
Mol Ecol. 2019 Feb;28(3):568-583
pubmed: 30298567
Malar J. 2017 Mar 3;16(1):101
pubmed: 28253926
Ecol Evol. 2021 Mar 27;11(9):4935-4944
pubmed: 33976860
Parasitology. 2020 Apr;147(4):441-447
pubmed: 31965951
Exp Parasitol. 2013 Apr;133(4):454-61
pubmed: 23337824
Mol Ecol. 2000 Nov;9(11):1803-14
pubmed: 11091316
Cell Host Microbe. 2012 Oct 18;12(4):521-30
pubmed: 23084919
Malar J. 2016 Mar 11;15:154
pubmed: 26969510
Proc Biol Sci. 2012 Oct 7;279(1744):4033-41
pubmed: 22859589
Bioinformatics. 2009 Aug 15;25(16):2078-9
pubmed: 19505943
J Anim Ecol. 2014 Jul;83(4):850-7
pubmed: 24286465
J Parasitol. 2004 Aug;90(4):797-802
pubmed: 15357072
Cell Microbiol. 2008 Apr;10(4):891-8
pubmed: 18005239
Dev Comp Immunol. 2010 Apr;34(4):387-95
pubmed: 20026176
Int J Parasitol. 2010 Sep;40(11):1229-35
pubmed: 20621627
Int J Parasitol. 2007 May;37(6):673-81
pubmed: 17275826

Auteurs

Francisco C Ferreira (FC)

Center for Conservation Genomics, Smithsonian Conservation Biology Institute, Washington, DC, USA. franciscocarlosfj@gmail.com.
Center for Vector Biology, Entomology Department, Rutgers University, New Brunswick, NJ, 08901, USA. franciscocarlosfj@gmail.com.

Elin Videvall (E)

Center for Conservation Genomics, Smithsonian Conservation Biology Institute, Washington, DC, USA.
Department of Ecology, Evolution and Organismal Biology, Brown University, Providence, RI, USA.
Institute at Brown for Environment and Society, Brown University, Providence, RI, USA.
Animal Ecology, Department of Ecology and Genetics, Uppsala University, Uppsala, Sweden.

Christa M Seidl (CM)

Department of Ecology and Evolutionary Biology, University of California, Santa Cruz, CA, USA.

Nicole E Wagner (NE)

Center for Vector Biology, Entomology Department, Rutgers University, New Brunswick, NJ, 08901, USA.

A Marm Kilpatrick (AM)

Department of Ecology and Evolutionary Biology, University of California, Santa Cruz, CA, USA.

Robert C Fleischer (RC)

Center for Conservation Genomics, Smithsonian Conservation Biology Institute, Washington, DC, USA.

Dina M Fonseca (DM)

Center for Vector Biology, Entomology Department, Rutgers University, New Brunswick, NJ, 08901, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH