A novel MALDI-TOF MS-based method for blood meal identification in insect vectors: A proof of concept study on phlebotomine sand flies
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu hodnotící studie, časopisecké články, práce podpořená grantem
PubMed
31498786
PubMed Central
PMC6733444
DOI
10.1371/journal.pntd.0007669
PII: PNTD-D-19-00170
Knihovny.cz E-zdroje
- MeSH
- biochemická analýza krve metody MeSH
- druhová specificita MeSH
- hemoglobiny chemie MeSH
- lidé MeSH
- ověření koncepční studie MeSH
- peptidy chemie MeSH
- Psychodidae chemie fyziologie MeSH
- spektrometrie hmotnostní - ionizace laserem za účasti matrice MeSH
- stravovací zvyklosti MeSH
- tandemová hmotnostní spektrometrie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- hemoglobiny MeSH
- peptidy MeSH
BACKGROUND: Identification of blood sources of hematophagous arthropods is crucial for understanding the transmission cycles of vector-borne diseases. Many different approaches towards host determination were proposed, including precipitin test, ELISA, DNA- and mass spectrometry-based methods; yet all face certain complications and limitations, mostly related to blood degradation. This study presents a novel method for blood meal identification, peptide mass mapping (PMM) analysis of host-specific hemoglobin peptides using MALDI-TOF mass spectrometry. METHODOLOGY/PRINCIPAL FINDINGS: To identify blood meal source, proteins from abdomens of engorged sand fly females were extracted, cleaved by trypsin and peptide fragments of host hemoglobin were sequenced using MALDI-TOF MS. The method provided correct host identification of 100% experimentally fed sand flies until 36h post blood meal (PBM) and for 80% samples even 48h PBM. In females fed on two hosts, both blood meal sources were correctly assigned for 60% of specimens until 36h PBM. In a validation study on field-collected females, the method yielded unambiguous host determination for 96% of specimens. The suitability of PMM-based MALDI-TOF MS was proven experimentally also on lab-reared Culex mosquitoes. CONCLUSIONS/SIGNIFICANCE: PMM-based MALDI-TOF MS analysis targeting host specific hemoglobin peptides represents a sensitive and cost-effective method with a fast and simple preparation protocol. As demonstrated here on phlebotomine sand flies and mosquitoes, it allows reliable and rapid blood source determination even 48h PBM with minimal material input and provides more robust and specific results than other currently used methods. This approach was also successfully tested on field-caught engorged females and proved to be a promising useful tool for large-scale screening of host preferences studies. Unlike other methods including MALDI-TOF protein profiling, it allows correct identification of mixed blood meals as was demonstrated on both experimentally fed and field-collected sand flies.
Department of Parasitology Faculty of Science Charles University Prague Czech Republic
Institute of Microbiology of the Czech Academy of Sciences Prague Czech Republic
USDA ARS European Biological Control Laboratory Thessaloniki Greece
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Maroli M, Feliciangeli MD, Bichaud L, Charrel RN, Gradoni L. Phlebotomine sandflies and the spreading of leishmaniases and other diseases of public health concern. Med Vet Entomol. 2013;27(2):123–147. 10.1111/j.1365-2915.2012.01034.x PubMed DOI
Alvar J, Vélez ID, Bern C, Herrero M, Desjeux P, Cano J, et al. Leishmaniasis worldwide and global estimates of its incidence. PLoS One. 2012;7(5):e35671 10.1371/journal.pone.0035671 PubMed DOI PMC
Killick-Kendrick R. The biology and control of phlebotomine sand flies. Clin Dermatol. 1999;17(3):279–289. PubMed
Lewis DJ, Ward RD. Transmission and vectors In: Peters W, Killick-Kendrick R, editors. The Leishmaniases in Biology and Medicine. Vol. 1 London: Academic Press; 1987. pp. 235–262.
Daba S, Daba A, Shehata MG, El Sawaf BM. A simple micro-assay method for estimating blood meal size of the sand fly, Phlebotomus langeroni (Diptera: Psychodidae). J Egypt Soc Parasitol. 2004;34(1):173–182. PubMed
Pruzinova K, Sadlova J, Seblova V, Homola M, Votypka J, Volf P. Comparison of blood meal digestion and the peritrophic matrix in four sand fly species differing in susceptibility to Leishmania donovani. PLoS One. 2015;10(6):e0128203 10.1371/journal.pone.0128203 PubMed DOI PMC
Dillon RJ, Lane P. Blood meal digestion in the midgut of Phlebotomus papatasi and Phlebotomus langeroni. Med Vet Entomol. 1993;7(3):225–232. PubMed
Benkova I, Volf P. Effect of temperature on metabolism of Phlebotomus papatasi (Diptera: Psychodidae). J Med Entomol. 2007;44(1):150–154. 10.1603/0022-2585(2007)44[150:eotomo]2.0.co;2 PubMed DOI
Bull CG, King WV. The identification of the blood meal of mosquitoes by means of the precipitin test. Am J Trop Med Hyg. 1923;3:491–496.
Da Rocha Nery LC, Lorosa ES, Ramos Franco AM. Feeding preference of the sand flies Lutzomyia umbratilis and L. spathotrichia (Diptera: Psychodidae, Phlebotominae) in an urban forest patch in the City of Manaus, Amazonas, Brazil. Mem Inst Oswaldo Cruz. 2004;99(6):571–574. 10.1590/s0074-02762004000600006 PubMed DOI
Bongiorno G, Habluetzel A, Khoury C, Maroli M. Host preferences of phlebotomine sand flies at a hypoendemic focus of canine leishmaniasis in central Italy. Acta Trop. 2003;88(2):109–116. PubMed
Svobodova M, Sadlova J, Chang KP, Volf P. Short report: distribution and feeding preference of the sand flies Phlebotomus sergenti and P. papatasi in a cutaneous leishmaniasis focus in Sanliurfa, Turkey. Am J Trop Med Hyg. 2003;68(1):6–9. PubMed
Jimenez M, Gonzalez E, Iriso A, Marco E, Alegret A, Fuster F, et al. Detection of Leishmania infantum and identification of blood meals in Phlebotomus perniciosus from a focus of human leishmaniasis in Madrid, Spain. Parasitol Res. 2013;112(7):2453–2459. 10.1007/s00436-013-3406-3 PubMed DOI
Chaskopoulou A, Giantsis IA, Demir S, Bon MC. Species composition, activity patterns and blood meal analysis of sand fly populations (Diptera: Psychodidae) in the metropolitan region of Thessaloniki, an endemic focus of canine leishmaniasis. Acta Trop. 2016;158:170–176. 10.1016/j.actatropica.2016.03.006 PubMed DOI
Kent RJ. Molecular methods for arthropod blood meal identification and applications to ecological and vector-borne disease studies. Mol Ecol Resour. 2009;9(1):4–18. 10.1111/j.1755-0998.2008.02469.x PubMed DOI
Onder O, Shao W, Kemps BD, Lam H, Brisson D. Identifying sources of tick blood meals using unidentified tandem mass spectral libraries. Nat Commun. 2013;4:1746 10.1038/ncomms2730 PubMed DOI PMC
Keller JI, Ballif BA, St. Clair RM, Vincent JJ, Monroy MC, Stevens L. Chagas disease vector blood meal sources identified by protein mass spectrometry. PLoS One. 2017;12(12):e0189647 10.1371/journal.pone.0189647 PubMed DOI PMC
Yssouf A, Almeras L, Raoult D, Parola P. Emerging tools for identification of arthropod vectors. Future Microbiol. 2016;11(4):549–566. 10.2217/fmb.16.5 PubMed DOI
Dvorak V, Halada P, Hlavackova K, Dokianakis E, Antoniou M, Volf P. Identification of phlebotomine sand flies (Diptera: Psychodidae) by matrix-assisted laser desorption/ionization time of flight mass spectrometry. Parasit Vectors. 2014;7(1):21. PubMed PMC
Niare S, Berenger JM, Dieme C, Doumbo O, Raoult D, Parola P, et al. Identification of blood meal sources in the main African malaria mosquito vector by MALDI-TOF MS. Malar J. 2016;15(1):87. PubMed PMC
Tandina F, Niare S, Laroche M, Kone AK, Diarra AZ, Ongoiba A, et al. Using MALDI-TOF MS to identify mosquitoes collected in Mali and their blood meals. Parasitology. 2018;145(9):1170–1182. 10.1017/S0031182018000070 PubMed DOI
Steen H, Mann M. The ABC's (and XYZ's) of peptide sequencing. Nat Rev Mol Cell Biol. 2004;5(9):699–711. 10.1038/nrm1468 PubMed DOI
Volf P, Volfova V. Establishment and maintenance of sand fly colonies. J Vector Ecol. 2011;36 Suppl 1:S1–9. PubMed
Svobodova M, Alten B, Zidková L, Dvorak V, Hlavacková J, Mysková J, et al. Cutaneous leishmaniasis caused by Leishmania infantum transmitted by Phlebotomus tobbi. Int J Parasitol. 2009;39(2):251–256. 10.1016/j.ijpara.2008.06.016 PubMed DOI
Lewis D. A taxonomic review of the genus Phlebotomus (Diptera: Psychodidae). Bull Br Mus nat Hist Ent. 1982;45(2):121–209.
Weed RI, Reed CF, Berg G. Is hemoglobin an essential structural component of human erythrocyte membranes? J Clin Invest. 1963;42:581–588. 10.1172/JCI104747 PubMed DOI PMC
Wilkins MR, Lindskog I, Gasteiger E, Bairoch A, Sanchez JC, Hochstrasser DF, et al. Detailed peptide characterisation using PEPTIDEMASS—a World-Wide Web accessible tool. Electrophoresis. 1997;18(3–4):403–408. 10.1002/elps.1150180314 PubMed DOI
Garlapati RB, Abbasi I, Warburg A, Poche D, Poche R. Identification of blood meals in wild caught blood fed Phlebotomus argentipes (Diptera: Psychodidae) using cytochrome b PCR and reverse line blotting in Bihar, India. J Med Entomol. 2012;49(3):515–521. 10.1603/me11115 PubMed DOI
Maia C, Parreira R, Cristovao JM, Freitas FB, Afonso MO, Campino L. Molecular detection of Leishmania DNA and identification of blood meals in wild caught phlebotomine sand flies (Diptera: Psychodidae) from southern Portugal. Parasit Vectors. 2015;8(1):173. PubMed PMC
Paternina LE, Verbel-Vergara D, Romero-Ricardo L, Perez-Doria A, Paternina-Gomez M, Martinez L, et al. Evidence for anthropophily in five species of phlebotomine sand flies (Diptera: Psychodidae) from northern Colombia, revealed by molecular identification of blood meals. Acta Trop. 2016;153:86–92. 10.1016/j.actatropica.2015.10.005 PubMed DOI
Carvalho GML, Rego FD, Tanure A, Silva ACP, Dias TA, Paz GF, et al. Blood meal identification in field-collected sand flies from Casa Branca, Brazil, using the cytochrome b PCR method. J Med Entomol. 2017;54(4):1049–1054. 10.1093/jme/tjx051 PubMed DOI
Onder O, Shao W, Kemps BD, Lam H, Brisson D. Tracking the sources of blood meals of parasitic arthropods using shotgun proteomics and unidentified tandem mass spectral libraries. Nat Protoc. 2014; 9(4):842–850. 10.1038/nprot.2014.048 PubMed DOI PMC
Martinez-de la Puente J, Ruiz S, Soriguer R, Figuerola J. Effect of blood meal digestion and DNA extraction protocol on the success of blood meal source determination in the malaria vector Anopheles atroparvus. Malar J. 2013;12(1):109. PubMed PMC
Baum M, de Castro EA, Pinto MC, Goulart TM, Baura W, do Rocio Klisiowicz D, da Costa-Ribeiro MCV. Molecular detection of the blood meal source of sand flies (Diptera: Psychodidae) in a transmission area of American cutaneous leishmaniasis, Paraná State, Brazil. Acta Trop. 2015;143:8–12. 10.1016/j.actatropica.2014.11.006 PubMed DOI
Song Y, Laskay ÜA, Vilcins IM, Barbour AG, Wysocki VH. Top-down-assisted bottom-up method for homologous protein sequencing: hemoglobin from 33 bird species. J Am Soc Mass Spectrom. 2015;26(11):1875–1884. 10.1007/s13361-015-1185-z PubMed DOI PMC
Oshaghi MA, Chavshin AR, Vatandoost H, Yaaghoobi F, Mohtarami F, Noorjah N. Effects of post-ingestion and physical conditions on PCR amplification of host blood meal DNA in mosquitoes. Exp Parasitol. 2006;112(4):232–236. 10.1016/j.exppara.2005.11.008 PubMed DOI
Reeves LE, Holderman CJ, Gillett-Kaufman JL, Kawahara AY, Kaufman PE. Maintenance of host DNA integrity in field-preserved mosquito (Diptera: Culicidae) blood meals for identification by DNA barcoding. Parasit Vectors. 2016;9(1):503 10.1186/s13071-016-1791-z PubMed DOI PMC
Noguera P, Rondon M, Nieves E. Effect of blood source on the survival and fecundity of the sandfly Lutzomyia ovallesi Ortiz (Diptera: Psychodidae), vector of Leishmania. Biomedica. 2006;26 Suppl 1:57–63. PubMed
Lafri I, Almeras L, Bitam I, Caputo A, Yssouf A, Forestier CL, et al. Identification of Algerian field-caught phlebotomine sand fly vectors by MALDI-TOF MS. PLoS Negl Trop Dis. 2016;10(1):1–19. PubMed PMC
Phlebotomus perniciosus response to volatile organic compounds of dogs and humans