New insights into the DNA extraction and PCR amplification of minute ascomycetes in the genus Laboulbenia (Pezizomycotina, Laboulbeniales)

. 2024 Jun 11 ; 15 (1) : 14. [epub] 20240611

Status PubMed-not-MEDLINE Jazyk angličtina Země Bulharsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid38863065

Grantová podpora
DEB-2127290 Directorate for Biological Sciences
Senior Postdoctoral Fellowship 1206024N Research Foundation Flanders

Odkazy

PubMed 38863065
PubMed Central PMC11167896
DOI 10.1186/s43008-024-00146-9
PII: 10.1186/s43008-024-00146-9
Knihovny.cz E-zdroje

Molecular studies of fungi within the order Laboulbeniales (Ascomycota, Pezizomycotina) have been hampered for years because of their minute size, inability to grow in axenic culture, and lack of reliable and cost-efficient DNA extraction protocols. In particular, the genus Laboulbenia is notorious for low success with DNA extraction and polymerase chain reaction (PCR) amplification. This is attributed to the presence of melanin, a molecule known to inhibit PCR, in the cells. We evaluated the efficacy of a standard single cell-based DNA extraction protocol by halving the recommended amount of reagents to reduce the cost per extraction and adding bovine serum albumin (BSA) during the multiple displacement amplification step to reverse the effect of melanin. A total of 196 extractions were made, 111 of which were successful. We found that halving the reagents used in the single cell-based extraction kit did not significantly affect the probability of successful DNA extraction. Using the halved protocol reduces cost and resource consumption. Moreover, there was no significant difference in the probability of successfully extracting DNA based on whether BSA was added or not, suggesting that the amount of melanin present in cells of the thallus has no major inhibitory effect on PCR. We generated 277 sequences from five loci, but amplification of the internal transcribed spacer region, the mitochondrial small subunit rDNA, and protein-coding genes remains challenging. The probability of successfully extracting DNA from Laboulbeniales was also impacted by specimen storage methods, with material preserved in > 95% ethanol yielding higher success rates compared to material stored in 70% ethanol and dried material. We emphasize the importance of proper preservation of material and propose the design of Laboulbeniales-specific primers to overcome the problems of primer mismatches and contaminants. Our new insights apply not only to the genus Laboulbenia; Laboulbeniales generally are understudied, and the vast majority of species remain unsequenced. New and approachable molecular developments will benefit the study of Laboulbeniales, helping to elucidate the true diversity and evolutionary relationships of these peculiar microfungi.

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Bakken LR, Olsen RA. Buoyant densities and dry-matter contents of microorganisms: conversion of a measured biovolume into biomass. Appl Environ Microbiol. 1983;45(4):1188–1195. doi: 10.1128/aem.45.4.1188-1195.1983. PubMed DOI PMC

Bates D, Maechler M, Bolker B, Walker S (2015) Fitting linear mixed-effects models using lme4. J Stat Softw 67(1):1–48. 10.18637/jss.v067.i01

Bellemain E, Carlsen T, Brochmann C, Coissac E, Taberlet P, Kauserud H. ITS as an environmental DNA barcode for fungi: an in silico approach reveals potential PCR biases. BMC Microbiol. 2010;10:189. doi: 10.1186/1471-2180-10-189. PubMed DOI PMC

Blackwell M, Haelewaters D, Pfister DH. Laboulbeniomycetes: Evolution, natural history, and Thaxter’s final word. Mycologia. 2020;112(6):1048–1059. doi: 10.1080/00275514.2020.1718442. PubMed DOI

Bridge PD, Arora DK, Reddy CA, Elander RP. Applications of PCR in mycology. Wallingford: CAB International; 1998.

Bridge PD, Spooner BM, Roberts PJ. The impact of molecular data in fungal systematics. Adv Bot Res. 2005;42:33–67. doi: 10.1016/S0065-2296(05)42002-9. DOI

Bruns TD, Fogel R, Taylor JW. Amplification and sequencing of DNA from fungal herbarium specimens. Mycologia. 1990;82(2):175–184. doi: 10.2307/3759846. DOI

Butler MJ, Day AW. Fungal melanins: a review. Can J Microbiol. 1998;44(12):1115–1136. doi: 10.1139/w98-119. DOI

Cao B, Haelewaters D, Schoutteten N, Begerow D, Boekhout T, Giachini AJ, Gorjón SP, Gunde-Cimerman N, Hyde KD, Kemler M, Li GJ, Liu DM, Liu XZ, Nuytinck J, Papp V, Savchenko A, Savchenko K, Tedersoo L, Theelen B, Thines M, Tomšovský M, Toome-Heller M, Urón JP, Verbeken A, Vizzini A, Yurkov AM, Zamora JC, Zhao RL. Delimiting species in Basidiomycota: a review. Fungal Divers. 2021;109:181–237. doi: 10.1007/s13225-021-00479-5. DOI

Chernomor O, von Haeseler A, Minh BQ. Terrace aware data structure for phylogenomic inference from supermatrices. Syst Biol. 2016;65(6):997–1008. doi: 10.1093/sysbio/syw037. PubMed DOI PMC

Crous PW, Wingfield MJ, Richardson DM, Leroux JJ, Strasberg D, Edwards J, Roets F, Hubka V, Taylor PWJ, Heykoop M, Martín MP, Moreno G, Sutton DA, Wiederhold NP, Barnes CW, Carlavilla JR, Gené J, Giraldo A, Guarnaccia V, Guarro J, Hernández-Restrepo M, Kolařík M, Manjón JL, Pascoe IG, Popov ES, Sandoval-Denis M, Woudenberg JHC, Acharya K, Alexandrova AV, Alvarado P, Barbosa RN, Baseia IG, Blanchette RA, Boekhout T, Burgess TI, Cano-Lira JF, Čmoková A, Dimitrov RA, Dyakov MYu, Dueñas M, Dutta AK, Esteve-Raventós F, Fedosova AG, Fournier J, Gamboa P, Gouliamova DE, Grebenc T, Groenewald M, Hanse B, Hardy GEStJ, Held BW, Jurjević Ž, Kaewgrajang T, Latha KPD, Lombard L, Luangsa-ard JJ, Lysková P, Mallátová N, Manimohan P, Miller AN, Mirabolfathy M, Morozova OV, Obodai M, Oliveira NT, Ordóñez ME, Otto EC, Paloi S, Peterson SW, Phosri C, Roux J, Salazar WA, Sánchez A, Sarria GA, Shin HD, Silva BDB, Silva GA, Smith MTh, Souza-Motta CM, Stchigel AM, Stoilova-Disheva MM, Sulzbacher MA, Telleria MT, Toapanta C, Traba JM, Valenzuela-Lopez N, Watling R, Groenewald JZ, Fungal Planet description sheets: 400–468. Persoonia. 2016;36:316–458. doi: 10.3767/003158516X692185. PubMed DOI PMC

De Kesel A, Gerstmans C, Haelewaters D. Catalogue of the Laboulbeniomycetes of Belgium. Sterbeeckia. 2020;36:3–143.

De Weggheleire S. Biodiversity of the genus Laboulbenia: are there cryptic species? Antwerp: MSc thesis. University of Antwerp; 2019. pp. 1–48.

Eckhart L, Bach J, Ban J, Tschachler E. Melanin binds reversibly to thermostable DNA polymerase and inhibits its activity. Biochem Biophys Res Commun. 2000;271(3):726–730. doi: 10.1006/bbrc.2000.2716. PubMed DOI

Flournoy LE, Adam RP, Pandy RN. Interim and archival preservation of plant specimens in alcohols for DNA studies. Biotechniques. 1996;20(4):657–660. doi: 10.2144/19962004657. PubMed DOI

Gardes M, Bruns TD. ITS primers with enhanced specificity for basidiomycetes - application to the identification of mycorrhizae and rusts. Mol Ecol. 1993;2(2):113–118. doi: 10.1111/j.1365-294X.1993.tb00005.x. PubMed DOI

Giambernardi TA, Rodeck U, Klebe RJ. Bovine serum albumin reverses inhibition of RT-PCR by melanin. Biotechniques. 1998;25(4):564–566. doi: 10.2144/98254bm03. PubMed DOI

Gibson JL. Ultrastructural observations of the Laboulbeniales. Syracuse: Master thesis. State University of New York; 2012. pp. 1–70.

Goldmann L, Weir A. Position specificity in Chitonomyces (Ascomycota, Laboulbeniomycetes) on Laccophilus (Coleoptera, Dytiscidae): a molecular approach resolves a century-old debate. Mycologia. 2012;104(5):1143–1158. doi: 10.3852/11-358. PubMed DOI

Goldmann L, Weir A. Molecular phylogeny of the Laboulbeniomycetes (Ascomycota) Fungal Biol. 2018;122(2–3):87–100. doi: 10.1016/j.funbio.2017.11.004. PubMed DOI

Goldmann L, Weir A, Rossi W. Molecular analysis reveals two new dimorphic species of Hesperomyces (Ascomycota, Laboulbeniomycetes) parasitic on the ladybird Coleomegilla maculata (Coleoptera, Coccinellidae) Fungal Biol. 2013;117(11–12):807–813. doi: 10.1016/j.funbio.2013.10.004. PubMed DOI

Groenewald M, Lombard L, de Vries M, Lopez AG, Smith M, Crous PW (2018) Diversity of yeast species from Dutch garden soil and the description of six novel Ascomycetes. FEMS Yeast Res 18(7):foy076. 10.1093/femsyr/foy076 PubMed

Haelewaters D. Studies of the Laboulbeniomycetes: Diversity, evolution, and patterns of speciation. Cambridge, Massachusetts: Ph.D. dissertation. Harvard University; 2018. pp. 1–287.

Haelewaters D, De Kesel A. Checklist of thallus-forming Laboulbeniomycetes from Belgium and the Netherlands, including Hesperomyces halyziae and Laboulbenia quarantenae spp. nov. MycoKeys. 2020;71:23–86. doi: 10.3897/mycokeys.71.53421. PubMed DOI PMC

Haelewaters D, De Kesel A, Gorczak M, Bao K, Gort G, Zhao SY, Pfister DH. Laboulbeniales (Ascomycota) of the Boston Harbor Islands II (and other localities): species parasitizing Carabidae, and the Laboulbenia flagellata species complex. Northeast Nat. 2019;25(Sp9):110–149. doi: 10.1656/045.025.s906. DOI

Haelewaters D, De Kesel A, Pfister DH. Integrative taxonomy reveals hidden species within a common fungal parasite of ladybirds. Sci Rep. 2018;8(1):15966. doi: 10.1038/s41598-018-34319-5. PubMed DOI PMC

Haelewaters D, Gorczak M, Kaishian P, De Kesel A, Blackwell M (2021) Laboulbeniomycetes, enigmatic fungi with a turbulent taxonomic history. In: Encyclopedia of mycology, vol 1. Elsevier, Oxford, pp 263–283. 10.1016/B978-0-12-819990-9.00049-4

Haelewaters D, Gorczak M, Pfliegler WP, Tartally A, Tischer M, Wrzosek M, Pfister DH. Bringing Laboulbeniales into the 21st century: enhanced techniques for extraction and PCR amplification of DNA from minute ectoparasitic fungi. IMA Fungus. 2015;6(2):363–372. doi: 10.5598/imafungus.2015.06.02.08. PubMed DOI PMC

Haelewaters D, Matthews TJ, Wayman JP, Cazabonne J, Heyman F, Quandt CA, Martin TE. Laboulbeniomycetes as a case study for biodiversity shortfalls in poorly studied groups. J Biogeogr. 2024;51(1):29–39. doi: 10.1111/jbi.14725. DOI

Haelewaters D, Okrasińska A, Gorczak M, Pfister DH (2020) Draft genome sequence of the globally distributed cockroach-infecting fungus Herpomyces periplanetae strain D. Haelew. 1187d. Microbiol Resour Announc 9(6):e01458–19. 10.1128/MRA.01458-19 PubMed PMC

Haelewaters D, Page RA, Pfister DH. Laboulbeniales hyperparasites (Fungi, Ascomycota) of bat flies: independent origins and host associations. Ecol Evol. 2018;8(16):8396–8418. doi: 10.1002/ece3.4359. PubMed DOI PMC

Haelewaters D, Pfister DH. Morphological species of Gloeandromyces (Ascomycota, Laboulbeniales) evaluated using single-locus species delimitation methods. Fungal Syst Evol. 2019;3:19–34. doi: 10.3114/fuse.2019.03.03. PubMed DOI PMC

Haelewaters D, Pfliegler WP, Gorczak M, Pfister DH. Birth of an order: Comprehensive molecular phylogenetic study excludes Herpomyces (Fungi, Laboulbeniomycetes) from Laboulbeniales. Mol Phylogenet Evol. 2019;133:286–301. doi: 10.1016/j.ympev.2019.01.007. PubMed DOI

Haelewaters D, Van Caenegem W, De Kesel A (2022) Hesperomyces harmoniae, a new name for a common ectoparasitic fungus on the invasive alien ladybird Harmonia axyridis. Sydowia 75:53–74. 10.12905/0380.sydowia75-2023-0053

Hartig F (2022) DHARMa: Residual Diagnostics for Hierarchical (Multi-Level / Mixed) Regression Models. https://cran.r-project.org/package=DHARMa

Hoang DT, Chernomor O, von Haeseler A, Minh BQ, Vinh LS. UFBoot2: Improving the ultrafast bootstrap approximation. Mol Biol Evol. 2018;35(2):518–522. doi: 10.1093/molbev/msx281. PubMed DOI PMC

Hopple JS. Phylogenetic investigations in the genus Coprinus based on morphological and molecular characters. Durham, North Carolina: Ph.D. dissertation. Duke University; 1994. pp. 1–402.

Hu Q, Liu Y, Yi S, Huang D. A comparison of four methods for PCR inhibitor removal. Forensic Sci Int Genet. 2015;16:94–97. doi: 10.1016/j.fsigen.2014.12.001. PubMed DOI

Kalyaanamoorthy S, Minh B, Wong T, von Haeseler A, Jermiin LS. ModelFinder: Fast model selection for accurate phylogenetic estimates. Nat Methods. 2017;14(6):587–589. doi: 10.1038/nmeth.4285. PubMed DOI PMC

Kates HR, Doby JR, Siniscalchi CM, et al. The effects of herbarium specimen characteristics on short-read NGS sequencing success in nearly 8000 specimens: Old, degraded samples have lower DNA yields but consistent sequencing success. Front Plant Sci. 2021;12:669064. doi: 10.3389/fpls.2021.669064. PubMed DOI PMC

Katoh K, Rozewicki J, Yamada KD. MAFFT online service: multiple sequence alignment, interactive sequence choice and visualization. Brief Bioinform. 2019;20(4):1160–1166. doi: 10.1093/bib/bbx108. PubMed DOI PMC

Kudo R, Masuya H, Endoh R, Kikuchi T, Ikeda H. Gut bacterial and fungal communities in ground-dwelling beetles are associated with host food habit and habitat. ISME J. 2019;13(3):676–685. doi: 10.1038/s41396-018-0298-3. PubMed DOI PMC

Kuraku S, Zmasek CM, Nishimura O, Katoh K. aLeaves facilitates on-demand exploration of metazoan gene family trees on MAFFT sequence alignment server with enhanced interactivity. Nucleic Acids Res. 2013;41:22–28. doi: 10.1093/nar/gkt389. PubMed DOI PMC

Kurtzman CP. Chapter 59 - Priceomyces M. Suzuki and Kurtzman 2010. In: Kurtzman CP, Fell JW, Boekhout T, editors. The yeasts. 5. London: Elsevier; 2011. pp. 719–724.

Kurtzman CP, Robnett CJ. Identification of clinically important ascomycetous yeasts based on nucleotide divergence in the 5’ end of the large-subunit (26S) ribosomal DNA gene. J Clin Microbiol. 1997;35:1216–1223. doi: 10.1128/jcm.35.5.1216-1223.1997. PubMed DOI PMC

Lahuf AA, Jaafar OH, Hameed ZL. A simple, rapid, safe and low-cost method to extract DNA from phytopathogenic fungi. Asian J Agric Biol. 2019;7(2):197–203.

Landvik S, Egger KN, Schumacher T. Towards a subordinal classification of the Pezizales (Ascomycota): phylogenetic analyses of SSU rDNA sequences. Nord J Bot. 1997;17:403–418. doi: 10.1111/j.1756-1051.1997.tb00337.x. DOI

Lenth RV, Bolker B, Buerkner P, Giné-Vázquez I, Herve M, Jung M, Love J, Miguez F, Riebl H, Singmann H (2024) emmeans: Estimated Marginal Means, aka Least-Squares Means. https://cran.r-project.org/package=emmeans

Lickfeldt D, Hofmann NE, Jones JD, Hamblin AM, Voigt TB (2002) Comparing three DNA extraction procedures for cost, efficiency, and DNA yield. HortScience 37(5):822–825. 10.21273/HORTSCI.37.5.822

Liu J, Haelewaters D, Pfliegler WP, Page RA, Dick CW, Aime MC. A new species of Gloeandromyces from Ecuador and Panama revealed by morphology and phylogenetic reconstruction, with a discussion of secondary barcodes in Laboulbeniomycetes taxonomy. Mycologia. 2020;112(6):1192–1202. doi: 10.1080/00275514.2020.1781496. PubMed DOI

Long N, Qiao Y, Xu Z, Tu J, Lu Z. Recent advances and application in whole-genome multiple displacement amplification. Quant Biol. 2020;8(4):279–294. doi: 10.1007/s40484-020-0217-2. DOI

Lubbers M. Peculiar parasites: on the ecology and genetics of Laboulbeniales. Master thesis. Leiden: Leiden University; 2021. pp. 1–28.

Lubbers M, Lamers G, De Kesel A, Nedvěd O, Schilthuizen M, Haelewaters D (2022) Bacterial biofilms on thalli of Laboulbeniales: a community uncovered. Sydowia 74:335–342. 10.12905/0380.sydowia74-2022-0335

Maharachchikumbura SSN, Chen Y, Ariyawansa HA, Hyde KD, Haelewaters D, Perera RH, Samarakoon MC, Wanasinghe DN, Bustamante DE, Liu JK, Lawrence DP, Cheewangkoon R, Stadler M. Integrative approaches for species delimitation in Ascomycota. Fungal Divers. 2021;109:155–179. doi: 10.1007/s13225-021-00486-6. DOI

Majewski T. The Laboulbeniales of Poland. Polish Botanical Studies. 1994;7:3–466.

Marquina D, Buczek M, Ronquist F, Łukasik P. The effect of ethanol concentration on the morphological and molecular preservation of insects for biodiversity studies. PeerJ. 2021;9:e10799. doi: 10.7717/peerj.10799. PubMed DOI PMC

Miadlikowska J, Lutzoni F. Phylogenetic revision of the genus Peltigera (lichen-forming Ascomycota) based on morphological, chemical, and large subunit nuclear ribosomal DNA data. Int J Plant Sci. 2000;161(6):925–958. doi: 10.1086/317568. DOI

Muilwijk J, Felix R, Dekoninck W, Bleich O. De loopkevers van Nederland en België (Carabidae) Entomol Tabellen. 2015;9:1–215.

Nagy ZT. A hands-on overview of tissue preservation methods for molecular genetic analyses. Org Divers Evol. 2010;10:91–105. doi: 10.1007/s13127-010-0012-4. DOI

Nguyen LT, Schmidt HA, von Haeseler A, Minh BQ. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol Biol Evol. 2015;32(2):268–274. doi: 10.1093/molbev/msu300. PubMed DOI PMC

Paloi S, Luangsa-ard JJ, Mhuantong W, Stadlet M, Kobmoo N. Intragenomic variation in nuclear ribosomal markers and its implication in species delimitation, identification and barcoding in fungi. Fungal Biol Rev. 2022;42:1–33. doi: 10.1016/j.fbr.2022.04.002. DOI

Perkins DD, Raju NB. Neurospora discreta, a new heterothallic species defined by its crossing behavior. Exp Mycol. 1986;10(4):323–338. doi: 10.1016/0147-5975(86)90019-8. DOI

Pincus DH, Orenga S, Chatellier S. Yeast identification—past, present, and future methods. Med Mycol. 2007;45(2):97–121. doi: 10.1080/13693780601059936. PubMed DOI

R Core Team (2021) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. http://www.R-project.org

Romanelli AM, Fu J, Herrera ML, Wickes BL. A universal DNA extraction and PCR amplification method for fungal rDNA sequence-based identification. Mycoses. 2014;57(10):612–622. doi: 10.1111/myc.12208. PubMed DOI

Rychlik W, Spencer WJ, Rhoads RE. Optimization of the annealing temperature for DNA amplification in vitro. Nucleic Acids Res. 1990;18(21):6409–6412. doi: 10.1093/nar/18.21.6409. PubMed DOI PMC

Santamaria S, Balazuc J, Tavares II. Distribution of the European Laboulbeniales (Fungi, Ascomycotina): an annotated list of species. Treb Inst Bot Barcelona. 1991;14:1–123.

Santamaria S, Pedersen J. Laboulbeniomycetes (Fungi, Ascomycota) of Denmark. Eur J Taxon. 2021;781:1–425. doi: 10.5852/ejt.2021.781.1583. DOI

Schmitt I, Crespo A, Divakar PK, Fankhauser JD, Herman-Sackett E, Kalb K, Nelsen MP, Nelson NA, Rivas-Plata E, Shimp AD, Widhelm T, Lumbsch HT. New primers for promising single-copy genes in fungal phylogenetics and systematics. Persoonia. 2009;23:35–40. doi: 10.3767/003158509X470602. PubMed DOI PMC

Schoch C, Seifert K, Huhndorf SM, Robert V, Spouge JL, Levesque CA, Chen W, Fungal Barcoding Consortium Nuclear ribosomal internal transcribed spacer (ITS) region as a universal DNA barcode marker for Fungi. Proc Natl Acad Sci U S A. 2012;109(16):6241–6246. doi: 10.1073/pnas.1117018109. PubMed DOI PMC

Stielow B, Lévesque CA, Seifert K, Meyer W, Irinyi L, Smits D, Renfurm R, Verkley GJM, Groenewald M, Chaduli D, Lomascolo A, Welti S, Lesage-Meessen L, Favel A, Al-Hatmi AMS, Damm U, Yilmaz N, Houbraken J, Lombard L, Quaedvlieg W, Binder M, Vaas LAI, Vu D, Yurkov A, Begerow D, Roehl O, Guerreiro M, Fonseca A, Samerpitak K, van Diepeningen AD, Dolatabadi S, Moreno LF, Casaregola S, Mallet S, Jacques N, Roscini L, Egidi E, Bizet C, Garcia-Hermoso D, Martín MP, Deng S, Groenewald JZ, Boekhout T, de Beer ZW, Barnes I, Duong TA, Wingfield MJ, de Hoog GS, Crous PW, Lewis CT, Hambleton S, Moussa TAA, Al-Zahrani HS, Almaghrabi OA, Louis-Seize G, Assabgui R, McCormick W, Omer G, Dukik K, Cardinali G, Eberhardt U, de Vries M, Robert V. One fungus, which genes? Development and assessment of universal primers for potential secondary fungal DNA barcodes. Persoonia. 2015;35:242–263. doi: 10.3767/003158515X689135. PubMed DOI PMC

Sundberg H, Ekman S, Kruys Å. A crush on small fungi: An efficient and quick method for obtaining DNA from minute ascomycetes. Methods Ecol Evol. 2018;9(1):148–158. doi: 10.1111/2041-210X.12850. DOI

Sundberg H, Kruys Å, Bergsten J, Ekman S. Position specificity in the genus Coreomyces (Laboulbeniomycetes, Ascomycota) Fungal Syst Evol. 2018;1:217–228. doi: 10.3114/fuse.2018.01.09. PubMed DOI PMC

Thaxter R. Contributions towards a monograph of the Laboulbeniaceae: Part I. Mem Am Acad Arts Sci N S. 1896;12:189–429.

Theelen B, Cafarchia C, Gaitanis G, Bassukas ID, Boekhout T, Dawson TL., Jr Malassezia ecology, pathophysiology, and treatment. Med Mycol. 2018;56:S10–S25. doi: 10.1093/mmy/myx134. PubMed DOI

Van Caenegem W, Blondelle A, Dumolein I, Santamaria B, Dick CW, Hiller T, Liu J, Quandt CA, Villarreal Saucedo RV, Verbeken A, Haelewaters D. Five new species of Gloeandromyces (Fungi, Laboulbeniales) from tropical American bat flies (Diptera, Streblidae), revealed by morphology and phylogenetic reconstruction. Mycologia. 2023;115(5):714–737. doi: 10.1080/00275514.2023.2230114. PubMed DOI

Van Caenegem W, Ceryngier P, Romanowski J, Pfister DH, Haelewaters D. Hesperomyces (Fungi, Ascomycota) associated with Hyperaspis ladybirds (Coleoptera, Coccinellidae): rethinking host specificity. Front Fungal Biol. 2023;3:1040102. doi: 10.3389/ffunb.2022.1040102. PubMed DOI PMC

Vicente ALSA, Bianchini RA, Laus AC, Macedo G, Reis RM, Vasquez VL (2019) Comparison of protocols for removal of melanin from genomic DNA to optimize PCR amplification of DNA purified from highly pigmented lesions. Histol Histopathol 34(9):1089–1096. 10.14670/hh-18-112 PubMed

Vilgalys R, Hester M. Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species. J Bacteriol. 1990;172(8):4238–4246. doi: 10.1128/jb.172.8.4238-4246.1990. PubMed DOI PMC

Walker MJ, Dorrestein A, Camacho JJ, Hiller T, Meckler LA, Silas KA, Haelewaters D. A tripartite survey of hyperparasitic fungi associated with ectoparasitic flies on bats (Mammalia: Chiroptera) in a neotropical cloud forest in Panama. Parasite. 2018;25:19. doi: 10.1051/parasite/2018017. PubMed DOI PMC

Weir A, Blackwell M. Extraction and PCR amplification of DNA from minute ectoparasitic fungi. Mycologia. 2001;93(4):802–806. doi: 10.1080/00275514.2001.12063212. DOI

White TJ, Bruns TD, Lee SB, Taylor JW. Analysis of phylogenetic relationships by amplification and direct sequencing of ribosomal RNA genes. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ, editors. PCR protocols: a guide to methods and applications. San Diego: Academic Press; 1990. pp. 315–322.

Wickham H (2016) ggplot2: elegant graphics for data analysis. Springer, New York, pp 1–213. 10.1007/978-0-387-98141-3

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