Evidence map›Paper›PMID 32448128›Full record

ArticleBMC evolutionary biology2020

The puzzling mitochondrial phylogeography of the black soldier fly (Hermetia illucens), the commercially most important insect protein species.

Gunilla Ståhls, Rudolf Meier, Christoph Sandrock, Martin Hauser, Ljiljana Šašić Zorić, Elina Laiho, Andrea Aracil, Jovana Doderović, Rozane Badenhorst, Phira Unadirekkul and 7 more

Abstract read
In one paragraph

Article in BMC evolutionary biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Gunilla StåhlsFinnish Museum of Natural History Luomus, Zoology unit, University of Helsinki, PO Box 17, FI-00014, Helsinki, Finland. Gunilla.stahls@helsinki.fi.ORCID 0000-0003-0505-0691
Rudolf MeierDepartment of Biological Sciences, National University of Singapore, Block S3 #05-01, 14 Science Dr 4, Singapore, 117543, Singapore.ORCID 0000-0002-4452-2885
Christoph SandrockDepartment of Livestock Sciences, Research Institute of Organic Agriculture (FiBL), Ackerstrasse 113, 5070, Frick, Switzerland.ORCID 0000-0002-2054-2216
Martin HauserCalifornia Department of Food and Agriculture, Plant Pest Diagnostics Branch, 3294 Meadowview Road, Sacramento, California, 95832-1448, USA.ORCID 0000-0002-6368-3529
Ljiljana Šašić ZorićBioSense Institute, Dr Zorana Đinđića 1, Novi Sad, 21000, Serbia.
Elina LaihoFinnish Museum of Natural History Luomus, Zoology unit, University of Helsinki, PO Box 17, FI-00014, Helsinki, Finland.
Andrea AracilDepartment of Environmental Sciences & Natural Resources, University of Alicante, PO Box 99, E-03080, Alicante, Spain.
Jovana DoderovićDepartment of Biology and Ecology, Faculty of Sciences, University of Novi Sad, Novi Sad, 2100, Serbia.
Rozane BadenhorstAgriprotein, 1 Rochester Road, Cape Town, South Africa.
Phira UnadirekkulDepartment of Biological Sciences, National University of Singapore, Block S3 #05-01, 14 Science Dr 4, Singapore, 117543, Singapore.
Nur Arina Binte Mohd AdomDepartment of Biological Sciences, National University of Singapore, Block S3 #05-01, 14 Science Dr 4, Singapore, 117543, Singapore.
Leo WeinProtenga, 302 Ang Mo Kio Ave 3, #01-1840 560302, Singapore, Singapore.
Cameron RichardsAgriprotein, 1 Rochester Road, Cape Town, South Africa.
Jeffery K TomberlinDepartment of Entomology, Texas A&M University, TAMU 2475, College Station, TX, 77843-2475, USA.
Santos RojoDepartment of Environmental Sciences & Natural Resources, University of Alicante, PO Box 99, E-03080, Alicante, Spain.
Sanja VeselićDepartment of Biology and Ecology, Faculty of Sciences, University of Novi Sad, Novi Sad, 2100, Serbia.
Tuure ParviainenVTT Technical Research Centre of Finland Ltd, TT2 Tietotie 2, P.O. Box 1000, FI-02044 VTT, Espoo, Finland.

Funding

H2020 Marie Skłodowska-Curie Actions 645636National Research Foundation Singapore R-154-000-A94-592National Research Foundation Singapore R-154-000-B46-114
6 · The paper itself

Abstract

backgroundThe black soldier fly (Diptera: Stratiomyidae, Hermetia illucens) is renowned for its bioconversion ability of organic matter, and is the worldwide most widely used source of insect protein. Despite varying extensively in morphology, it is widely assumed that all black soldier flies belong to the same species, Hermetia illucens. We here screened about 600 field-collected and cultured flies from 39 countries and six biogeographic regions to test this assumption based on data for three genes (mitochondrial COI, nuclear ITS2 & 28S rDNA) and in order to gain insights into the phylogeography of the species.

resultsOur study reveals a surprisingly high level of intraspecific genetic diversity for the mitochondrial barcoding gene COI (divergences up to 4.9%). This level of variability is often associated with the presence of multiple species, but tested nuclear markers (ITS2 and 28S rDNA) were invariant and fly strain hybridization experiments under laboratory conditions revealed reproductive compatibility. COI haplotype diversity is not only very high in all biogeographic regions (56 distinct haplotypes in total), but also in breeding facilities and research centers from six continents (10 haplotypes: divergences up to 4.3%). The high genetic diversity in fly-breeding facilities is mostly likely due to many independent acquisitions of cultures via sharing and/or establishing new colonies from field-collected flies. However, explaining some of the observed diversity in several biogeographic regions is difficult given that the origin of the species is considered to be New World (32 distinct haplotypes) and one would expect severely reduced genetic diversity in the putatively non-native populations in the remaining biogeographic regions. However, distinct, private haplotypes are known from the Australasian (N = 1), Oriental (N = 4), and the Eastern Palearctic (N = 4) populations. We reviewed museum specimen records and conclude that the evidence for introductions is strong for the Western Palearctic and Afrotropical regions which lack distinct, private haplotypes.

conclusionsBased on the results of this paper, we urge the black soldier fly community to apply molecular characterization (genotyping) of the fly strains used in artificial fly-breeding and share these data in research publications as well as when sharing cultures. In addition, fast-evolving nuclear markers should be used to reconstruct the recent invasion history of the species.

Indexed as

PhylogeographyAnimalsBreedingDipteraGenetic VariationInsect ProteinsLarvaMitochondriaReproductionInsect ProteinsBlack soldier flyHermetia illucensmtDNA COI haplotypesNuclear rDNA

Identifiers

PMID32448128
PMCPMC7247124

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.