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Latrocimicinae completes the phylogeny of Cimicidae: meeting old morphologic data rather than modern host phylogeny

Abstract

The family Cimicidae includes obligate hematophagous ectoparasites (bed bugs and their relatives) with high veterinary/medical importance. The evolutionary relationships of Cimicidae and their hosts have recently been reported in a phylogenetic context, but in the relevant study, one of the six subfamilies, the bat-specific Latrocimicinae, was not represented. In this study the only known species of Latrocimicinae, i.e., Latrocimex spectans, was analyzed with molecular and phylogenetic methods based on four (two nuclear and two mitochondrial) genetic markers. The completed subfamily-level phylogeny of Cimicidae showed that Latrocimicinae is most closely related to Haematosiphoninae (ectoparasites of birds and humans), with which it shares systematically important morphologic characters, but not hosts. Moreover, in the phylogenetic analyses, cimicid bugs that are known to infest phylogenetically distant bat hosts clustered together (e.g., Leptocimex and Stricticimex within Cacodminae), while cimicid subfamilies (Latrocimicinae, Primicimicinae) that are known to infest bat hosts from closely related superfamilies clustered distantly. In conclusion, adding Latrocimicinae significantly contributed to the resolution of the phylogeny of Cimicidae. The close phylogenetic relationship between Latrocimicinae and Haematosiphoninae is consistent with long-known morphologic data. At the same time, phylogenetic relationships of genera within subfamilies are inconsistent with the phylogeny of relevant hosts.

Graphical abstract

The family Cimicidae (Insecta: Hemiptera: Heteroptera) includes obligate hematophagous ectoparasites, with more than 110 described species in 24 genera and six subfamilies [1,2,3]. While the majority of extant cimicid species rely on bat hosts [4], several groups are adapted to other warm-blooded vertebrates, including birds and humans. In this respect, a few cimicids are generalists [3], although they have most likely evolved from host-specialist insects [5].

Even strictly host-specific permanent ectoparasites (such as blood-sucking lice) tend to show incongruent phylogenies in comparison with their hosts, probably as the result of a complex evolutionary history of host-switching events [6]. Cimicidae includes temporary ectoparasites which, in the course of their evolution, colonized bat hosts several times independently [5]. Thus, it can be expected that cimicid bugs and their bat hosts show independent phylogenetic clustering. Recently, when the host relationships of Cimicidae were analyzed in an evolutionary/phylogenetic context, one of the six subfamilies, Latrocimicinae, was not represented [5]. Here we complete the subfamily-level phylogeny of Cimicidae by adding Latrocimex spectans Lent, 1941, the only known species of Latrocimicinae, with Noctilio sp. bats as its specific hosts [1].

In this study, two male bugs were used, which were collected near the resting places of greater bulldog bats (Noctilio leporinus) in Belize (latitude 18.25677 and longitude −88.267594) in Central America on July 19, 2017. Both specimens were identified as L. spectans according to Usinger [1], and one of them was molecularly analyzed here.

The DNA was extracted from one leg of the bug with the QIAamp DNA Mini Kit (QIAGEN, Hilden, Germany) according to the manufacturer's instruction, including an overnight digestion in tissue lysis buffer and proteinase K at 56 °C.

Part of the cytochrome c oxidase subunit I (cox1) gene was amplified with a conventional PCR using the primers Lep1F (5′-ATT CAA CCA ATC ATA AAG ATA TTG G-3′), Lep1Fdeg (5′-ATT CAA CCA ATC ATA AAG ATA TNG G-3′), and Lep3R (5′-TAT ACT TCA GGG TGT CCG AAA AAT CA-3′) [7] as reported [8]. For the amplification of part of the 16S rRNA gene, the primers 16S LR-J (5′-TTA CGC TGT TAT CCC TAA-3′) and 16S LR-N (5′-CGC CTG TTT ATC AAA AAC AT-3′) were used [9, 10]. Two conventional PCRs were carried out with the primer pairs 18S-1 (5′-CTG GTT GAT CCT GCC AGT AGT-3′) and 18S-3 (5′-GGT TAG AAC TAG GGC GGT ATC T-3′), and 18S-2 (5′-AGA TAC CGC CCT AGT TCT AAC C-3′) and 18S-4 (5′-GAT CCT TCT GCA GGT TCA CC-3′) [11] to amplify approx. 1200 bp and 800 bp long fragments, respectively, of the 18S rRNA gene. In addition, the primers 1274 (5′-GAC CCG TCT TGA AAC ACG GA-3′) and 1275 (5′-TCG GAA GGA ACC AGC TAC TA-3′) [12] were used to amplify part of the 28S rRNA gene. In summary, amplified parts of the cox1, 16S, 18S, and 28S rRNA genes correspond to those reported in Roth et al. [5], where sequence lengths are also listed.

All above PCRs were performed in a reaction volume of 25 μl, which included 5 μl of extracted DNA and 20 μl of reaction mixture containing 1 unit HotStarTaq Plus DNA polymerase (5 U/μl) (QIAGEN, Hilden, Germany), 200 μM PCR nucleotide mix, 1 μM each primer, and 2.5 μl of 10 × Coral Load PCR buffer (15 mM MgCl2 included). For amplification, an initial denaturation step at 95 °C for 5 min was followed by 40 cycles of denaturation at 94 °C for 40 s, annealing at 48 °C (in case of the cox1 PCR at 53 °C) for 1 min, and extension at 72 °C for 1 min. Final extension was performed at 72 °C for 10 min.

Purification and sequencing of the PCR products were performed by Biomi Ltd. (Gödöllő, Hungary). Representative sequences were submitted to GenBank (cox1: MW269881, 16S rRNA: MW270938, 18S rRNA: MZ378786, 28S rRNA: MW270939). All those species for which sequences of all four of the above genetic markers were retrievable from GenBank according to accession numbers in Roth et al. [5] were included in the phylogenetic analyses (Additional file 1: Fig. S1). The outgroup contained all taxa from Roth et al. [5], for which all four genetic markers analyzed here were available in GenBank.

The sequences were concatenated with Geneious Prime 2019.2.3 [13] and aligned with the MAFFT algorithm [14]. A Bayesian consensus tree was created from the previously concatenated, aligned sequences using the MrBayes [15, 16] Geneious plugin, GTR (General Time Reversible) model with gamma distribution and invariant sites (GTR + G + I). The chain length was set to 5,000,000, sampling frequency to 500, and burn-in length to 100,000. The gene partitions were treated as unlinked. The random seed was set to 3967. The final phylogenetic tree was loaded into MEGAX 10.0.5 [17] for analysis. An additional phylogenetic analysis was conducted with the maximum likelihood method and Tamura–Nei model with gamma distribution and invariant sites (bootstrap: 1000) in MEGAX (10.0.5.).

The Bayesian consensus tree (Fig. 1) showed that Latrocimicinae (represented by L. spectans) was most closely related to Haematosiphoninae (ectoparasites of birds and humans), with strong support. These two subfamilies formed a sister group to Cacodminae and Cimicinae (Fig. 1). The topology of the maximum likelihood tree was slightly different: while the close relationship between Latrocimicinae and Haematosiphoninae was confirmed, these two belonged to a sister group of Cimicinae (Fig. 2). In comparison with previous findings [5], the above results imply that by adding Latrocimicinae, the sister group position of Cacodminae and Haematosiphoninae changed.

Fig. 1
figure1

Bayesian consensus tree of Cimicidae (including all six subfamilies) based on concatenated sequences of the cytochrome c oxidase subunit 1 (cox1), 16S, 18S, and 28S rRNA genes. Cimicid subfamilies are collapsed for better overview. The outgroup contained all taxa from Roth et al. [5], for which all four genetic markers analyzed here were available in GenBank. The scale bar indicates the number of substitutions per site

Fig. 2
figure2

Maximum likelihood tree from concatenated sequences of the cytochrome c oxidase subunit 1 (cox1), 16S, 18S, and 28S rRNA genes. GenBank accession numbers are shown in parentheses. The phylogenetic tree was made with the Tamura–Nei model (with gamma distribution and invariant sites), based on 1000 bootstrap resamplings. The scale bar indicates the number of substitutions per site

Considering the hitherto enigmatic position of Latrocimicinae, these results confirm the morphologic tree [18] which was based on the relationships proposed by Usinger [1]. In particular, the genus Latrocimex belonged to the same cluster with (and next to) Haematosiphoninae, forming a sister group to Cimicinae together with Cacodminae [18]. Usinger [1] already noted that Latrocimicinae and Haematosiphoninae share systematically important morphologic characters, such as the prominent bristles on the hind angles of the pronotum, or the stout, spine-like bristles on the tibiae, as well as the right-ventral position of the paragenital sinus.

By contrast, when comparing Latrocimex with Afrocimex, it was mentioned that the number of autosomes is the same, but the two groups are completely unlike in appearance and therefore probably have no close connection [1]. This is also well reflected by the concatenated phylogenetic tree (Fig. 1), on which the two subfamilies, Afrocimicinae and Latrocimicinae, are only distantly related. Thus, the above morphologic characters are in line with the results of phylogenetic analyses performed here when including Latrocimicinae.

On the other hand, completing the phylogenetic tree with Latrocimicinae also highlights inconsistencies between host and parasite phylogenies. For instance, regarding bug genera with bats as typical hosts, the two distantly related cimicid subfamilies, Latrocimicinae and Primicimicinae, have hosts from two bat superfamilies (Noctilionoidea and Vespertilionoidea, respectively) [1] which are closely related (sister groups: [19]). At the same time, closely related cimicid genera such as Leptocimex and Stricticimex (Fig. 2) have bat hosts [1] from the most distantly related bat superfamilies Vespertilionoidea, Emballonuroidea, and Rhinolophoidea [19].

Regarding geographical ranges on the subfamily level, the ancestral Primicimicinae is Nearctic-Neotropical, whereas the core of the phylogenetic tree is occupied by Old World groups, as well as by Cimicinae showing global distribution (Fig. 1). The sister groups Latrocimicinae and Haematosiphoninae both occur in the New World. This geographically consistent pattern might reflect that the temporary parasitism by cimicid bugs prevented them from frequent natural dispersal events, especially on a transcontinental scale [3]. Accordingly, while their hosts are highly mobile, cimicid populations tend to be genetically more isolated [20] (except for the common bed bug, C. lectularius, and the tropical bed bug, C. hemipterus, which became cosmopolitan in distribution as the result of artificial dispersal events, owing to their association with humans and man-made objects).

In summary, the complete phylogeny of Cimicidae reflects morphologic relationships, rather than host associations. However, the latter might be more relevant if approached in a geographical context.

Availability of data and materials

The sequences obtained and/or analyzed during the current study are deposited in GenBank (cox1: MW269881, 16S rRNA: MW270938, 18S rRNA: MZ378786, 28S rRNA: MW270939). All other relevant data are included in the manuscript and the references or are available upon request from the corresponding author.

Abbreviations

cox1:

Cytochrome c oxidase subunit 1

References

  1. 1.

    Usinger RL. Monograph of Cimicidae (Hemiptera-Heteroptera). Maryland, College Park: Entomological Society of America; 1966. p. 585.

    Google Scholar 

  2. 2.

    Henry TJ. Biodiversity of heteroptera. In: Foottit RG, Adler PH, editors. Insect biodiversity science and society, vol. 1. 2nd ed. Chichester: Wiley; 2017. p. 279–336.

    Chapter  Google Scholar 

  3. 3.

    Ossa G, Johnson JS, Puisto AIE, Rinne V, Sääksjärvi IE, Waag A, et al. The Klingon batbugs: morphological adaptations in the primitive bat bugs, Bucimex chilensis and Primicimex cavernis, including updated phylogeny of Cimicidae. Ecol Evol. 2019;9:1736–49.

    Article  Google Scholar 

  4. 4.

    Poulin R, Morand S. The diversity of parasites. Q Rev Biol. 2000;75:277–93.

    CAS  Article  Google Scholar 

  5. 5.

    Roth S, Balvín O, Siva-Jothy MT, Di Iorio O, Benda P, Calva O, et al. Bedbugs evolved before their bat hosts and did not co-speciate with ancient humans. Curr Biol. 2019;29:1847-53.e4.

    CAS  Article  Google Scholar 

  6. 6.

    Light JE, Smith VS, Allen JM, Durden LA, Reed DL. Evolutionary history of mammalian sucking lice (Phthiraptera: Anoplura). BMC Evol Biol. 2010;10:292.

    Article  Google Scholar 

  7. 7.

    Hajibabaei M, Janzen DH, Burns JM, Hallwachs W, Hebert PD. DNA barcodes distinguish species of tropical Lepidoptera. Proc Natl Acad Sci USA. 2006;103:968–71.

    Article  Google Scholar 

  8. 8.

    Hornok S, Szőke K, Boldogh SA, Sándor AD, Kontschán J, Tan TuV, et al. Phylogenetic analyses of bat-associated bugs (Hemiptera: Cimicidae: Cimicinae and Cacodminae) indicate two new species close to Cimex lectularius. Parasit Vectors. 2017;10:439.

    Article  Google Scholar 

  9. 9.

    Kambhampati S, Smith PT. PCR primers for the amplification of four insect mitochondrial gene fragments. Insect Mol Biol. 1995;4:233–6.

    CAS  Article  Google Scholar 

  10. 10.

    Simon C, Frati F, Beckenbach A, Crespi B, Liu H, Flook P. Evolution, weighting and phylogenetic utility of mitochondrial gene sequences and compilation of conserved polymerase chain reaction primers. Ann Ent Soc Am. 1994;87:651–701.

    CAS  Article  Google Scholar 

  11. 11.

    Tian Y, Zhu W, Li M, Xie Q, Bu W. Influence of data conflict and molecular phylogeny of major clades in Cimicomorphan true bugs (Insecta: Hemiptera: Heteroptera). Mol Phylogenet Evol. 2008;47:581–97.

    CAS  Article  Google Scholar 

  12. 12.

    Markmann M, Tautz D. Reverse taxonomy: an approach towards determining the diversity of meiobenthic organisms based on ribosomal RNA signature sequences. Philos Trans R Soc Lond B Biol Sci. 2005;360(1462):1917–24.

    CAS  Article  Google Scholar 

  13. 13.

    Kearse M, Moir R, Wilson A, Stones-Havas S, Cheung M, Sturrock S, et al. Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics. 2012;28:1647–9.

    Article  Google Scholar 

  14. 14.

    Katoh K, Misawa K, Kuma K, Miyata T. MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Res. 2002;30:3059–66.

    CAS  Article  Google Scholar 

  15. 15.

    Ronquist F, Huelsenbeck JP. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003;19:1572–4.

    CAS  Article  Google Scholar 

  16. 16.

    Huelsenbeck JP, Ronquist F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics. 2001;17:754–5.

    CAS  Article  Google Scholar 

  17. 17.

    Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol. 2018;35:1547–9.

    CAS  Article  Google Scholar 

  18. 18.

    Reinhardt K, Siva-Jothy MT. Biology of the bed bugs (Cimicidae). Ann Rev Entomol. 2007;52:351–74.

    CAS  Article  Google Scholar 

  19. 19.

    Teeling EC, Springer MS, Madsen O, Bates P, O’brien SJ, Murphy WJ. A molecular phylogeny for bats illuminates biogeography and the fossil record. Science. 2005;307(5709):580–4.

    CAS  Article  Google Scholar 

  20. 20.

    Talbot B, Vonhof MJ, Broders HG, Fenton B, Keyghobadi N. Range-wide genetic structure and demographic history in the bat ectoparasite Cimex adjunctus. BMC Evol Biol. 2016;16:268.

    Article  Google Scholar 

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Acknowledgements

Not applicable.

Funding

Molecular work was supported by NKFI K 130216 and project no. TKP2020-NKA-01. The latter has been implemented with the support provided from the National Research, Development and Innovation Fund of Hungary, financed under the “Tématerületi Kiválósági Program 2020 (2020-4.1.1-TKP2020)” funding scheme. The project was also supported by the European Union and co-financed by the European Social Fund (grant agreement no. EFOP-3.6.3-VEKOP-16-2017-00005, project title: “Strengthening the scientific replacement by supporting the academic workshops and programs of students, developing a mentoring process”).

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SH initiated the study, identified the species, extracted the DNA, supervised molecular and phylogenetic analyses, and wrote the manuscript. NF and TS provided the samples. TS, OG, PC, and NF significantly contributed to manuscript writing. NT carried out molecular work. ÁBK and MG performed concatenated phylogenetic analyses. JK supervised taxonomic work and performed individual phylogenetic analyses. All authors read and approved the final manuscript.

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Correspondence to Sándor Hornok.

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No vertebrate animals were caught or restrained for bug collection, and therefore no ethical permission was needed.

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Supplementary Information

Additional file 1: Figure S1

. The original, detailed phylogenetic tree corresponding to Fig. 1. GenBank accession numbers are shown in parentheses.

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Hornok, S., Szentiványi, T., Takács, N. et al. Latrocimicinae completes the phylogeny of Cimicidae: meeting old morphologic data rather than modern host phylogeny. Parasites Vectors 14, 441 (2021). https://doi.org/10.1186/s13071-021-04932-x

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Keywords

  • Latrocimex spectans
  • Heteroptera
  • Bug
  • Ectoparasite