in

Myzomyia and Pyretophorus series of Anopheles mosquitoes acting as probable vectors of the goat malaria parasite Plasmodium caprae in Thailand

  • Asada, M. et al. Close relationship of Plasmodium sequences detected from South American pampas deer (Ozotoceros bezoarticus) to Plasmodium spp. in North American white-tailed deer. Int. J. Parasitol. 7, 44–47. https://doi.org/10.1016/j.ijppaw.2018.01.001 (2018).

    Article 

    Google Scholar 

  • Boundenga, L. et al. Haemosporidian parasites of antelopes and other vertebrates from Gabon, Central Africa. PLoS ONE 11, e0148958. https://doi.org/10.1371/journal.pone.0148958 (2016).

    Article 
    CAS 

    Google Scholar 

  • Martinsen, E. S., Perkins, S. L. & Schall, J. J. A three-genome phylogeny of malaria parasites (Plasmodium and closely related genera): Evolution of life-history traits and host switches. Mol. Phylogen. Evol. 47, 261–273. https://doi.org/10.1016/j.ympev.2007.11.012 (2008).

    Article 
    CAS 

    Google Scholar 

  • Templeton, T. J. et al. Ungulate malaria parasites. Sci. Rep. 6, 23230. https://doi.org/10.1038/srep23230 (2016).

    Article 
    ADS 
    CAS 

    Google Scholar 

  • Templeton, T. J., Martinsen, E., Kaewthamasorn, M. & Kaneko, O. The rediscovery of malaria parasites of ungulates. Parasitology 143, 1501–1508. https://doi.org/10.1017/s0031182016001141 (2016).

    Article 

    Google Scholar 

  • Bruce, D., Harvey, D., Hamerton, A. E. & Bruce, L. Plasmodium cephalophi, sp. nov. Proc. R. Soc. B. 87, 45–47 (1913).

    ADS 

    Google Scholar 

  • Sheather, A. L. A malarial parasite in the blood of a buffalo. J. Comp. Pathol. 32, 223–229 (1919).

    Article 

    Google Scholar 

  • Kandel, R. C. et al. First report of malaria parasites in water buffalo in Nepal. Vet. Parasitol. Reg. Stud. Rep. 18, 100348. https://doi.org/10.1016/j.vprsr.2019.100348 (2019).

    Article 

    Google Scholar 

  • de Mello, F. & Paes, S. Sur une plasmodiae du sang des chèvres. C. R. Séanc. Soc. Biol 88, 829–830 (1923).

    Google Scholar 

  • Kaewthamasorn, M. et al. Genetic homogeneity of goat malaria parasites in Asia and Africa suggests their expansion with domestic goat host. Sci. Rep. 8, 5827. https://doi.org/10.1038/s41598-018-24048-0 (2018).

    Article 
    ADS 
    CAS 

    Google Scholar 

  • Garnham, P. C. & Edeson, J. F. Two new malaria parasites of the Malayan mousedeer. Riv. Malariol. 41, 1–8 (1962).

    CAS 

    Google Scholar 

  • Garnham, P. C. & Kuttler, K. L. A malaria parasite of the white-tailed deer (Odocoileus virginianus) and its relation with known species of Plasmodium in other ungulates. Proc. R. Soc. Lond. B 206, 395–402. https://doi.org/10.1098/rspb.1980.0003 (1980).

    Article 
    ADS 
    CAS 

    Google Scholar 

  • Martinsen, E. et al. Hidden in plain sight: Cryptic and endemic malaria parasites in North American white-tailed deer (Odocoileus virginianus). Sci. Adv. 2, e1501486. https://doi.org/10.1126/sciadv.1501486 (2016).

    Article 
    ADS 
    CAS 

    Google Scholar 

  • Rattanarithikul, R. et al. Illustrated keys to the mosquitoes of Thailand. IV. Anopheles. Southeast Asian. Trop. Med. Public Health 37, 1–128 (2006).

    Google Scholar 

  • Walter Reed Biosystematics Unit. Systematic catalogue of Culicidae. http://mosquitocatalog.org (2021).

  • Manguin, S., Garros, C., Dusfour, I., Harbach, R. E. & Coosemans, M. Bionomics, taxonomy, and distribution of the major malaria vector taxa of Anopheles subgenus Cellia in Southeast Asia: An updated review. Infect. Genet. Evol. 8, 489–503. https://doi.org/10.1016/j.meegid.2007.11.004 (2008).

    Article 
    CAS 

    Google Scholar 

  • Brosseau, L. et al. A multiplex PCR assay for the identification of five species of the Anopheles barbirostris complex in Thailand. Parasit. Vectors 12, 223. https://doi.org/10.1186/s13071-019-3494-8 (2019).

    Article 

    Google Scholar 

  • Paredes-Esquivel, C., Donnelly, M. J., Harbach, R. E. & Townson, H. A molecular phylogeny of mosquitoes in the Anopheles barbirostris Subgroup reveals cryptic species: implications for identification of disease vectors. Mol. Phylogen. Evol. 50, 141–151. https://doi.org/10.1016/j.ympev.2008.10.011 (2009).

    Article 
    CAS 

    Google Scholar 

  • Taai, K. & Harbach, R. E. Systematics of the Anopheles barbirostris species complex (Diptera: Culicidae: Anophelinae) in Thailand. Zool. J. Linn. Soc. 174, 244–264. https://doi.org/10.1111/zoj.12236 (2015).

    Article 

    Google Scholar 

  • Garros, C., Van Bortel, W., Trung, H. D., Coosemans, M. & Manguin, S. Review of the Minimus Complex of Anopheles, main malaria vector in Southeast Asia: From taxonomic issues to vector control strategies. Trop. Med. Int. Health 11, 102–114. https://doi.org/10.1111/j.1365-3156.2005.01536.x (2006).

    Article 
    CAS 

    Google Scholar 

  • Dahan-Moss, Y. et al. Member species of the Anopheles gambiae complex can be misidentified as Anopheles leesoni. Malar. J. 19, 89. https://doi.org/10.1186/s12936-020-03168-x (2020).

    Article 
    CAS 

    Google Scholar 

  • Van Bortel, W. et al. Confirmation of Anopheles varuna in Vietnam, previously misidentified and mistargeted as the malaria vector Anopheles minimus. Am. J. Trop. Med. Hyg. 65, 729–732. https://doi.org/10.4269/ajtmh.2001.65.729 (2001).

    Article 

    Google Scholar 

  • Wharton, R. H., Eyles, D. E., Warren, M., Moorhouse, D. E. & Sandosham, A. A. Investigations leading to the identification of members of the Anopheles umbrosus group as the probable vectors of mouse deer malaria. Bull. 29, 357–374 (1963).

    CAS 

    Google Scholar 

  • Nugraheni, Y. R. et al. Myzorhynchus series of Anopheles mosquitoes as potential vectors of Plasmodium bubalis in Thailand. Sci. Rep. 12, 5747. https://doi.org/10.1038/s41598-022-09686-9 (2022).

    Article 
    ADS 
    CAS 

    Google Scholar 

  • Tu, H. L. C. et al. Development of a novel multiplex PCR assay for the detection and differentiation of Plasmodium caprae from Theileria luwenshuni and Babesia spp. in goats. Acta Trop. 220, 105957. https://doi.org/10.1016/j.actatropica.2021.105957 (2021).

    Article 
    CAS 

    Google Scholar 

  • Cywinska, A., Hunter, F. F. & Hebert, P. D. Identifying Canadian mosquito species through DNA barcodes. Med. Vet. Entomol. 20, 413–424. https://doi.org/10.1111/j.1365-2915.2006.00653.x (2006).

    Article 
    CAS 

    Google Scholar 

  • Hebert, P. D., Cywinska, A., Ball, S. L. & de Waard, J. R. Biological identifications through DNA barcodes. Proc. R. Soc. Lond. B 270, 313–321. https://doi.org/10.1098/rspb.2002.2218 (2003).

    Article 
    CAS 

    Google Scholar 

  • Ogola, E. O., Chepkorir, E., Sang, R. & Tchouassi, D. P. A previously unreported potential malaria vector in a dry ecology of Kenya. Parasit. Vectors 12, 80. https://doi.org/10.1186/s13071-019-3332-z (2019).

    Article 

    Google Scholar 

  • Maquart, P. O., Fontenille, D., Rahola, N., Yean, S. & Boyer, S. Checklist of the mosquito fauna (Diptera, Culicidae) of Cambodia. Parasite 28, 60. https://doi.org/10.1051/parasite/2021056 (2021).

    Article 

    Google Scholar 

  • Tainchum, K. et al. Diversity of Anopheles species and trophic behavior of putative malaria vectors in two malaria endemic areas of northwestern Thailand. J. Vector. Ecol. 39, 424–436. https://doi.org/10.1111/jvec.12118 (2014).

    Article 

    Google Scholar 

  • Vantaux, A. et al. Anopheles ecology, genetics and malaria transmission in northern Cambodia. Sci. Rep. 11, 6458. https://doi.org/10.1038/s41598-021-85628-1 (2021).

    Article 
    ADS 
    CAS 

    Google Scholar 

  • Chookaew, S. et al. Anopheles species composition in malaria high-risk areas in Ranong Province. Dis. Control J. 46, 483–493. https://doi.org/10.14456/dcj.2020.45 (2020).

    Article 

    Google Scholar 

  • Makanga, B. et al. Ape malaria transmission and potential for ape-to-human transfers in Africa. Proc. Natl. Acad. Sci. USA. 113, 5329–5334. https://doi.org/10.1073/pnas.1603008113 (2016).

    Article 
    ADS 
    CAS 

    Google Scholar 

  • Ariey, F., Gay, F. & Ménard, R. Malaria Control and Elimination Vol. 254 (Springer, 2020).

    Google Scholar 

  • Williams, J. & Pinto, J. Training Manual on Malaria Entomology (Springer, 2012).

    Google Scholar 

  • Rigg, C. A., Hurtado, L. A., Calzada, J. E. & Chaves, L. F. Malaria infection rates in Anopheles albimanus (Diptera: Culicidae) at Ipetí-Guna, a village within a region targeted for malaria elimination in Panamá. Infect. Genet. Evol. 69, 216–223. https://doi.org/10.1016/j.meegid.2019.02.003 (2019).

    Article 

    Google Scholar 

  • Torres-Cosme, R. et al. Natural malaria infection in anophelines vectors and their incrimination in local malaria transmission in Darién Panama. PLoS ONE 16, e0250059. https://doi.org/10.1371/journal.pone.0250059 (2021).

    Article 
    CAS 

    Google Scholar 

  • Beebe, N. W. & Saul, A. Discrimination of all members of the Anopheles punctulatus complex by polymerase chain reaction-restriction fragment length polymorphism analysis. Am. J. Trop. Med. Hyg. 53, 478–481. https://doi.org/10.4269/ajtmh.1995.53.478 (1995).

    Article 
    CAS 

    Google Scholar 

  • Perkins, S. L. & Schall, J. J. A molecular phylogeny of malarial parasites recovered from cytochrome b gene sequences. J. Parasitol. 88, 972–978. https://doi.org/10.1645/0022-3395(2002)088[0972:AMPOMP]2.0.CO;2 (2002).

    Article 
    CAS 

    Google Scholar 

  • Snounou, G. et al. High sensitivity of detection of human malaria parasites by the use of nested polymerase chain reaction. Mol. Biochem. Parasitol. 61, 315–320. https://doi.org/10.1016/0166-6851(93)90077-B (1993).

    Article 
    CAS 

    Google Scholar 

  • Hall, T. A. BioEdit: A user-friendly biological sequence alignment editor and analysis program for windows 95/98/NT. Nucleic. Acids. Symp. Ser. 41, 95–98 (1999).

    CAS 

    Google Scholar 

  • Huelsenbeck, J. P. & Ronquist, F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 17, 754–755 (2001).

    Article 
    CAS 

    Google Scholar 

  • Rambaut, A., Drummond, A. J., Xie, D., Baele, G. & Suchard, M. A. Posterior summarization in Bayesian phylogenetics using tracer 1.7. Syst. Biol. 67, 901–904. https://doi.org/10.1093/sysbio/syy032 (2018).

    Article 
    CAS 

    Google Scholar 

  • Nguyen, L. T., Schmidt, H. A., von Haeseler, A. & Minh, B. Q. IQ-TREE: A fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol. Biol. Evol. 32, 268–274. https://doi.org/10.1093/molbev/msu300 (2015).

    Article 
    CAS 

    Google Scholar 

  • Ventim, R. et al. Avian malaria infections in western European mosquitoes. Parasitol. Res. 111, 637–645. https://doi.org/10.1007/s00436-012-2880-3 (2012).

    Article 

    Google Scholar 


  • Source: Ecology - nature.com

    Methane emissions offset atmospheric carbon dioxide uptake in coastal macroalgae, mixed vegetation and sediment ecosystems

    Strengthening electron-triggered light emission