Evaluation of matrix-assisted laser desorption/ionization time of flight mass spectrometry for the identification of ceratopogonid and culicid larvae

• Published in: Parasitology Vol. 140; no. 3; pp. 318 - 327
• Main Authors: STEINMANN, I. C., PFLÜGER, V., SCHAFFNER, F., MATHIS, A., KAUFMANN, C.
• Format: Journal Article
• Language: English
• Published: Cambridge, UK Cambridge University Press 01.03.2013
• Subjects: Aedes aegypti; Animals; Ceratopogonidae - chemistry; Ceratopogonidae - classification; Culicidae - chemistry; Culicidae - classification; Culicoides nubeculosus; Dasyhelea; Desorption; Insect Proteins - chemistry; Insect Vectors - chemistry; Insect Vectors - classification; Insect Vectors - parasitology; Insects; Ionization; Larva - chemistry; Larva - classification; Larvae; Mass spectrometry; Mosquitoes; Parasitology - methods; Sample preparation; Species Specificity; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods; MALDI-TOF MS; identification; Ceratopogonidae; Culicidae; insect; larvae; vector; Culicoides
• ISSN: 0031-1820; 1469-8161; 1469-8161
• DOI: 10.1017/S0031182012001618

Matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF MS) was evaluated for the rapid identification of ceratopogonid larvae. Optimal sample preparation as evaluated with laboratory-reared biting midges Culicoides nubeculosus was the homogenization of gut-less larvae in 10% formic acid, and analysis of 0·2 mg/ml crude protein homogenate mixed with SA matrix at a ratio of 1:1·5. Using 5 larvae each of 4 ceratopogonid species (C. nubeculosus, C. obsoletus, C. decor, and Dasyhelea sp.) and of 2 culicid species (Aedes aegypti, Ae. japonicus), biomarker mass sets between 27 and 33 masses were determined. In a validation study, 67 larvae belonging to the target species were correctly identified by automated database-based identification (91%) or manual full comparison (9%). Four specimens of non-target species did not yield identification. As anticipated for holometabolous insects, the biomarker mass sets of adults cannot be used for the identification of larvae, and vice versa, because they share only very few similar masses as shown for C. nubeculosus, C. obsoletus, and Ae. japonicus. Thus, protein profiling by MALDI-TOF as a quick, inexpensive and accurate alternative tool is applicable to identify insect larvae of vector species collected in the field.