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Current state of knowledge on Wolbachia infection among Coleoptera: a systematic review

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Current state of knowledge on Wolbachia infection among Coleoptera: a systematic review
Note that a Preprint of this article also exists, first published November 15, 2017.


The relations between the intracellular α-proteobacterium Wolbachia pipientis Hertig 1936 (hereafter Wolbachia) and its hosts from various groups of arthropods and nematodes have been the object of much research and numerous publications (O’Neill et al., 1992; Werren, Windsor & Guo, 1995; Weinert et al., 2015). The majority of these studies have focused on verifying endosymbiotic bacteria occurrence and diversity in various hosts at different levels: (i) among selected species sharing a geographic area (e.g., O’Neill et al., 1992; Werren, Windsor & Guo, 1995; 2000), (ii) among species inhabiting the same environment or that are ecologically-associated (e.g., Stahlhut et al., 2010), (iii) among species from particular taxonomic groups (e.g., Czarnetzki & Tebbe, 2004; Lachowska, Kajtoch & Knutelski, 2010; Sontowski et al., 2015), and (iv) within populations of selected taxa (e.g., Stenberg & Lundmark, 2004; Mazur et al., 2016). Another branch of research on the relations between Wolbachia and its hosts has focused on host species phylogenetics or population genetics, which is in some cases related to population differentiation and speciation (e.g., Kubisz et al., 2012; Montagna et al., 2014). In this research, Wolbachia is sometimes treated as an additional “marker”—a source of genetic data about the eco-evolutionary relations of its hosts. A third type of Wolbachia studies has concerned the direct or indirect effects of the infection on host fitness, development or survival at the individual and population levels (e.g., Weeks, Reynolds & Hoffmann, 2002; O’Neill, 2007). Moreover, in a separate branch of research (or in conjunction with the abovementioned types of studies), Wolbachia is often examined directly, mainly with respect to strain diversity, distribution and relations with other strains or different co-existing bacteria (Baldo & Werren, 2007). All these branches of research have substantially extended the knowledge about the relations between the most widespread intracellular endosymbiont—Wolbachia and its various hosts. Moreover, these studies have been expanded to encompass other bacteria with similar biologies and effects on hosts (like Cardinium, Spiroplasma, Rickettsia) (Zchori-Fein & Perlman, 2004; Goto, Anbutsu & Fukatsu, 2006; Duron et al., 2008; Weinert et al., 2015); however, a great majority of studies are still conducted on Wolbachia (Zug & Hammerstein, 2012). Recently, the various Wolbachia supergroups have been proposed to belong to several “Candidatus Wolbachia” species (Ramirez-Puebla et al., 2015); however, this approach has been criticized (Lindsey et al., 2016). Due to the uncertain species status of the “Candidatus Wolbachia” and because all previous studies considered these presumed different species as distant supergroups, in this review we have followed the previous Wolbachia taxonomy.

In summary, Wolbachia has been detected in 10–70% of examined hosts (Hilgenboecker et al., 2008; Zug & Hammerstein, 2012), depending on the geographical, ecological or taxonomical association of the selected species. Moreover, more detailed studies, at the population level, have shown that infection is not as straightforward as was assumed in the early stages of Wolbachia research. More and more species have been found to be only partially infected, e.g., in only some parts of their ranges or infection was associated with only some phylogenetic lineages (usually correlated with the distribution of mitochondrial lineages) (Clark et al., 2001; Roehrdanz et al., 2006). Furthermore, examples of multiply infected species and individuals have been reported, which has important consequences for the understanding of some of the effects of Wolbachia infection (Malloch, Fenton & Butcher, 2000). Wolbachia is known to have numerous effects on its hosts, among which the most interesting and important are those that disturb host reproduction, such as cytoplasmic incompatibility, thelytokous parthenogenesis, feminization of genetic males, male-killing, increased mating success of infected males via sperm competition and the host’s complete dependence on bacteria for egg production (for reviews see Werren, 1997; Werren & O’Neill, 1997; Stouthamer, Breeuwer & Hurst, 1999). Some of these effects are responsible for diversification of host populations and consequently Wolbachia have probably been involved in speciation (e.g., by the selective sweep of mtDNA or the whole genome of the infected host with the genome of bacteria; Keller et al., 2004; Mazur et al., 2016). This could be another major factor, additional to those already known, responsible for radiation of insects and particularly beetles.

There are several reviews summarizing the state of knowledge on Wolbachia infection among various taxonomic groups of nematodes and arthropods. Over the last years, such reviews have been prepared for the following groups: filarial nematodes (Filarioidea) (Taylor & Hoerauf, 1999; Casiraghi et al., 2001), crustaceans (Crustacea) (Cordaux, Bouchon & Greve, 2011), spiders (Araneae) (Goodacre et al., 2006; Yun et al., 2011), mites (Acari) (Chaisiri et al., 2015), springtails (Collembola) (Czarnetzki & Tebbe, 2004), Heteropteran Bugs (Heteroptera) (Kikuchi & Fukatsu, 2003), ants (Formicidae) (Russell, 2012), wasps (Hymenoptera: Apocrita) (Shoemaker et al., 2002) and butterflies (Lepidoptera) (Tagami & Miura, 2004). Surprisingly, there is no such review for beetles (Coleoptera), which include large number of diversified taxa, known from various habitats, and whose members belong to all major trophic guilds of animals. Some groups of beetles have been examined with respect to Wolbachia infection, but usually only with a limited coverage of species (e.g., weevils, Curculionidae, Lachowska, Kajtoch & Knutelski, 2010; leaf beetles; Chrysomelidae, Clark et al., 2001; Jäckel, Mora & Dobler, 2013; jewel beetles; Buprestidae, Sontowski et al., 2015 and minute moss beetles, Hydraenidae, Sontowski et al., 2015).

In this review we have summarized the current state of knowledge on the relations between beetles and Wolbachia by referring to all the abovementioned aspects of research. Moreover, we have highlighted future research directions concerning Wolbachia relationships with their diverse Coleopteran hosts.

Survey Methodology

We searched the scientific literature with Web of Knowledge databases, using the following combination of keywords linked by AND (the Boolean search term to stipulate that the record should contain this AND the next term): “Wolbachia” AND “Coleoptera” and “Wolbachia” AND “beetles”. Our final literature search for this analysis was conducted on December 22, 2017. This produced 322 results. Each result was inspected to determine whether or not it contained information on the subject matter. Articles that had no relevance (e.g., any reports that were not about Wolbachia-Coleoptera relations, including those that only had some references to either beetles or bacteria in the citations) were excluded. After the removal of duplicates, 65 were excluded from the remaining articles (n = 239) for not being direct reports about Wolbachia-Coleoptera relations, 44 were excluded because they examined other hosts and only referred to publications on Coleoptera, and 44 others were excluded because they referred to data already presented in previous publications on Coleoptera. Each document was read critically for the information that it contained on Wolbachia-Coleoptera relations, with special reference to answering the study questions listed below. Figure 1 shows a flow diagram for the systematic review following Prisma guidelines (Moher et al., 2009). We intended to also use data from The National Center for Biotechnology Information database (GenBank) but the majority of hits (if “Wolbachia” AND “Coleoptera” or “beetle” were used) led to either studies not related with Wolbachia infection in beetles (which only included references to some other studies on either bacteria or beetles), or to Wolbachia sequences submitted to GenBank but without any references to published (and reviewed) articles. Searches in NCBI (GenBank) resulted only in the finding of some beetle hosts, which have been already described in papers found via Web of Science searches.

Prisma flow-diagram (see Moher et al., 2009) for literature on Wolbachia-Coleoptera relations included in this study

Figure 1: Prisma flow-diagram (see Moher et al., 2009) for literature on Wolbachia-Coleoptera relations included in this study

We examined the collected data on various aspects of Wolbachia infection in Coleoptera with respect to the following: the (i) characteristics of the publications (to determine the scope and progress of studies on Wolbachia) (n = 86), (ii) geographic distribution of infected beetle species and populations (n = 84), (iii) sampling design (how many sites and individuals were examined) (n = 63), (iv) characteristics of the markers (genes) used for genotyping the bacteria (n = 82) and their hosts (n = 34), (v) numbers and frequencies of species found to be infected in particular beetle families and genera (n = 58), (vi) supergroup prevalence in examined taxonomic groups (n = 43), (vii) strain distribution and diversity in populations and individuals (n = 30), (vii) effects of Wolbachia on its beetle hosts (n = 39). Statistical analyses (Spearman correlation for number of publication across years and for the number of examined and number of infected species, Chi2 test for frequency of supergroups and infected taxa in particular taxonomic groups, Chi2 ANOVA for comparison of single/double/multiple infected taxa, Kruskal–Wallis Z test for infection frequency in Chrysomelidae and Curculionidae) were done in Statistica 11 (Statsoft).

Finally, we downloaded from GenBank ( and the Wolbachia MLST database ( all available sequences of Wolbachia genes found in any species of beetle. We restricted further analyses to the most widely used bacteria genes, i.e., 16S rDNA and cell division protein gene ftsZ. Because of the different lengths and spans of available sequences, the long parts of the 3′ and 5′ ends of each gene were trimmed, which resulted in alignments of length 663 bp for 16S rDNA and 241 bp for ftsZ. The length of the ftsZ alignment was particularly short as two different sets of primers have been used for its amplification, and its amplicons only overlapped across a relatively short part of the gene. Phylogenetic trees were only reconstructed for unique gene variants found in particular host taxa. Trees were inferred using Maximum Likelihood (ML) implemented in the IQ-TREE web server ( (Trifinopoulos et al., 2016) under the following settings Auto selection of substitution model, ultrafast bootstrap approximation (UFBoot) (Minh, Nguyen & Von Haeseler, 2013) with 10,000 iterations, maximum correlation coefficient = 0.99, single branch test with use of the approximate Likelihood-Ratio Test (SH-aLRT) (Anisimova & Gascuel, 2006; Guindon et al., 2010) and other default options.

The nomenclature of host taxa and their systematic positions throughout the paper follow the articles from which the data was derived.

Characterization of Wolbachia Infection Among Coleoptera


The final list of publications concerning data about Wolbachia infection in Coleoptera comprised 86 papers (Table S1). The oldest articles with relevant information about Wolbachia infection in beetles were published in 1992 (Campbell, Bragg & Turner, 1992; O’Neill et al., 1992), and the number of articles since then has increased significantly year by year (Spearman correlation = 0.841; Fig. 2). The majority of these articles (60%) concerned infection in only single beetle species, whereas 19% discussed infection in multiple species belonging to the same genus, 6%—multiple species from the same family, 6%—various species of Coleoptera et al., and a further 9%—studies on geographic groups of insects that included some, usually random species of beetles (O’Neill et al., 1992; Werren, Windsor & Guo, 1995; Weinert et al., 2015.

Change in the number of publications considering Wolbachia infection among Coleoptera.

Figure 2: Change in the number of publications considering Wolbachia infection among Coleoptera.

Most studies were done on Curculionidae (34) and Chrysomelidae (34), following Coccinellidae (10), Tenebrionidae (9), and Sylvanidae (3) (Table S1). The members of all other families were investigated in only 1–2 studies. Consequently, 2.5 and 1.6 Curculionidae and Chrysomelidae species were respectively examined per article. All species of Hydraenidae and Buprestidae were included in only single article (Sontowski et al., 2015), whereas limited numbers of species of Coccinellidae and Tenebrionidae were examined in several articles (Hurst et al., 19991; Hurst et al., 1999b; Fialho & Stevens, 1996; Fialho & Stevens, 1997; Fialho & Stevens, 2000; Majerus & Majerus, 2000; Weinert et al., 2007; Elnagdy et al., 2013; Ming et al., 2015; Goodacre, Fricke & Martin, 2015; Kageyama et al., 2010; Li et al., 2015; Li et al., 2016b; Dudek et al., 2017). Wolbachia infection was only studied more than once in 20 species.

Sampling design

The majority of species investigated with respect to Wolbachia infection were from Europe, and a relatively high number of species were from Asia and both Americas, whereas only ten infected species were from Africa, and three from Australia-Oceania (Fig. 3). A number of publications describing Wolbachia infection in Coleoptera had similar geographic coverages (Fig. 3).

Number of publications that described Wolbachia infection among Coleoptera and number of infected beetle species.

Figure 3: Number of publications that described Wolbachia infection among Coleoptera and number of infected beetle species.

Both are shown with respect to the zoogeography of the examined hosts (from which continent the host was collected).

Studies were done on samples collected from an average of 5.2 sites and concerned on average 53.0 specimens, or if excluding the most widely studied families Curculionidae and Chrysomelidae, 6.0 sites and 65.1 individuals (Fig. 4). For Curculionidae and Chrysomelidae, these numbers were on average 4.4 and 6.0 sites, respectively, and 40.7 and 70.2 individuals, respectively (Fig. 4). The numbers of sites and individuals examined in particular groups were insignificantly different, with the exception of the numbers of examined individuals in Curculionidae and Chrysomelidae (Fig. 4).

Number of sites (A) and number of individuals (B) of beetles examined with respect to Wolbachia infection.

Figure 4: Number of sites (A) and number of individuals (B) of beetles examined with respect to Wolbachia infection.

P—Mann-Whitney test p-values.

Examined genetic markers

The most often used Wolbachia gene for studies on Coleoptera was ftsZ, followed by hcpA, wsp and 16S rDNA (Fig. 5). Most studies using hcpA also used other MLST genes, including ftsZ. On the other hand, many species were only investigated with either 16S rDNA or wsp or ftsZ alone. Single studies used groEL (Monochamus alternatus, Aikawa et al., 2009; Tribolium madens, Fialho & Stevens, 2000) or ITS genes (Tribolium madens, Fialho & Stevens, 2000). So far, only five studies have used next-generation sequencing technology (Illumina or 454) to detect Wolbachia; two used 16S rDNA for metabarcoding of microbiota (Sitona obsoletus, Steriphus variabilis, White et al., 2015; Aleochara bilineata and Aleochara bipustulata, Bili et al., 2016; Hylobius abietis, Berasategui et al., 2016; Brontispa longissimi, Takano et al., 2017; Harmonia axyridis, Dudek et al., 2017) and one used shotgun genomic sequencing (Amara alpine, Heintzman et al., 2014). For genotyping of hosts, 52.4% of studies utilized fragments of COI from mtDNA (usually a barcode fragment of this gene). Fewer studies (23.1%) analyzed rDNA (usually ITS1 and/or ITS2 spacers), EF1α (14.0%), Wingless (2.2%), Histone H3 (2.2%) and microsatellites (6.1%). In Wolbachia-related studies, host genes have been used for several purposes like (i) using host DNA as a control for genetic material quality, (ii) barcoding for host species identification, (iii) phylogenetics, phylogeography and population genetics, (iv) estimating co-evolutionary relations between the bacteria and host, and (v) detecting some of the effects of Wolbachia on its hosts (like linkage disequilibrium, selective sweep, cytoplasmic incompatibility).

Shares of Wolbachia genes used in studies on Wolbachia infection among Coleoptera.

Figure 5: Shares of Wolbachia genes used in studies on Wolbachia infection among Coleoptera.

Taxonomic coverage

The beetles examined with respect to Wolbachia infection belong to 23 families (Micromalthidae, Gyrinidae, Haliplidae, Noteridae, Dytiscidae, Carabidae, Staphyllinidae, Hydrophilidae, Hydraenidae, Anobiidae, Dermestidae, Buprestidae, Byturidae, Cleridae, Lampyridae, Coccinellidae, Tenebrionidae, Scarabeidae, Meloidae, Sylvanidae, Cerambycidae, Chrysomelidae, Curculionidae). In total 204 beetle species were found to harbor Wolbachia infection; however, the distribution of infected species among families varied markedly. The highest numbers of infected beetle species were found for the Curculionidae (81 species), Chrysomelidae (49 species), Hydraenidae (14 species), Buprestidae (13 species), Coccinellidae (12 species) and Dytiscidae (8 species) (Fig. 6). In all other families only 1–3 species were reported to harbor Wolbachia (Table S1). However, these numbers are biased by the low number of articles (studies) dealing with members of particular beetle families (see above).

Shares of Wolbachia infected beetle species across the examined families of Coleoptera.

Figure 6: Shares of Wolbachia infected beetle species across the examined families of Coleoptera.

The numbers presented after the family names indicate the number of infected species.
Table 1:
Share of Wolbachia infected species among families and genera of examined beetles.
Only taxonomic groups for which at least two species were tested are presented.
N of examined % of infected Genus N of examined % of infected genus N of examined % of infected
Buprestidae 61 23.0 Barypeithes 9 11.0 Julodis 2 0.0
Chrysomelidae 84 45.2 Brachysomus 4 0.0 Koreoculio 2 50.0
Curculionidae 137 41.6 Brumoides ‘2 0.0 Laccophilus 2 0.0
Dytiscidae 36 16.7 Buprestis 3 0.0 Limnebius 7 28.6
Gyrinidae 3 33.3 Byturus 3 33.0 Longitarsus 3 100.0
Haliplidae 2 50.0 Callosbruchus 3 33.3 Meliboeus 2 0.0
Hydraenidae 27 63.0 Callosobruchus 7 33.0 Micraspis 2 0.0
Hydrophilidae 12 16.7 Capnodis 3 33.3 Naupactus 16 69.0
Noteridae 2 100.0 Charidotella 2 50.0 Neoglanis 2 0.0
Tenebrionidae 11 9.1 Chlaenius 7 14.3 Ochthebius 12 41.7
Subfamily Chrysobothris 3 33.3 Ophionea 3 0.0
Bruchinae 24 16.7 Coccinella 2 50.0 Oreina 5 80.0
Galerucinae 12 25.0 Crioceris 5 40.0 Otiorhynchus 4 50.0
Curculionidae 36 16.7 Curculio 23 17.4 Paederus 3 0.0
Scolytinae 23 34.8 Cyanapion 6 50.0 Pantomorus 3 100.0
Genus Deronectes 11 45.4 Polydrosus 4 75.0
Acalymma 2 100.0 Diabrotica 12 25.0 Rhantus 2 0.0
Acmaeodera 5 0.0 Dorytomus 3 67.0 Rhinusa 3 33.3
Acmaeoderella 4 0.0 Epilachna 2 0.0 Sciaphobus 2 50.0
Agabus 6 16.7 Eurymetopus 2 100.0 Sitophilus 3 100.0
Agrilus 34 17.6 Gyrinus 3 33.0 Sphenoptera 11 9.1
Altica 16 88.0 Haliplus 3 33.0 Strophosoma 3 67.0
Anthaxia 6 16.7 Helophorus 3 0.0 Trachypteris 2 0.0
Aramigus 3 100.0 Hydraena 24 33.3 Trachys 6 16.7
Archarius 6 16.7 Hydroporus 5 0.0 Tribolium 8 12.5
Atrichonotus 2 50.0 Hygrotus 5 20.0
Aulacophora 3 0.0 Ilybius 2 0.0
DOI: 10.7717/peerj.4471/table-1

Considering infection across beetle genera, the most richly infected genera were Altica (Chrysomelidae, 17 species), Naupactus (Curculionidae, 11 species), Hydraena (Hydraenidae, eight species) and Agrilus (Buprestidae, 6 species) (Table S1). In total, 49 genera were found to have infected members (Table S1, Table 1). The infection in Coleoptera was estimated at 38.3% of examined species; however, the proportion of infected species varied greatly between families and genera. At the family level the infection frequency was from 10.5% (Tenebrionidae) to 100% (Noteridae) (Goodacre, Fricke & Martin, 2015; Sontowski et al., 2015); however when considering only families for which more than 30 species were investigated (e.g., Clark et al., 2001; Lachowska, Kajtoch & Knutelski, 2010; Rodriguero et al., 2010a; Kondo et al., 2011; Jäckel, Mora & Dobler, 2013; Sontowski et al., 2015; Kawasaki et al., 2016), infection was found in up to 63% of species (Hydraenidae) (Table 1). At lower taxonomic levels, Wolbachia was found in 25% of Diabroticite (Chrysomelidae; Clark et al., 2001), 14.3–16.7% of Bruchina (Chrysomelidae; Kondo et al., 2011), 34.8% of Scolytinae (Curculionidae, Kawasaki et al., 2016) and 16.7% of Curculioninii (Toju et al., 2013). Among 54 genera in which Wolbachia infection was examined for at least two species, 12 genera were completely uninfected, while six genera were completely infected (Table 1). If considering only genera with at least five verified species, Wolbachia was found in 0% (Acmaeodera; Buprestidae; Sontowski et al., 2015) to 88% of species (Altica, Chrysomelidae; Jäckel, Mora & Dobler, 2013). There was only a marginally negative and insignificant correlation between the number of examined and number of infected species (R =  − 0.078). If considering only the most widely examined families, Chrysomelidae and Curculionidae, the difference in infection frequency between these two groups was insignificant (Z =  − 1.656, P = 0.098). Geographic studies on Wolbachia prevalence in insects have found much lower frequencies of infection in Coleoptera species: the bacterium was found in only 10.5% of beetles from Panama and 13.5% of beetles from North America (Werren, Windsor & Guo, 1995).

Wolbachia diversity

Among the various beetle species, Wolbachia strains belonged to three supergroups (A, B and F). However, they occurred at very different proportions in different groups of beetles, and these differences were significant (Chi2 = 98.78, P = 0.000). Overall, the proportion of beetle species found to be infected with Wolbachia strains belonging to supergroups A or B was similar, with approximately 12% of all species harboring either supergroup (either as single infections in different species or populations or as multiple infections within individuals) (Fig. 7), whereas supergroup F was found in only three beetle species: Agrilus araxenus and Lamprodila mirifica (both Buprestidae; Sontowski et al., 2015) and Rhinocyllus conicus (Curculionidae; Campbell, Bragg & Turner, 1992). In the four groups of beetles with the highest numbers of examined and infected species, the distributions of supergroups varied: in Buprestidae, a similar numbers of species were infected by supergroups A and B (all singly infected), with a relatively high proportion of F infected species (Sontowski et al., 2015). In contrast, in Hydraenida, supergroup A dominated over supergroup B (Sontowski et al., 2015). This was also the case in Chrysomelidae, with some species infected by both strains (Kondo et al., 2011; Jäckel, Mora & Dobler, 2013; Kolasa et al., 2017). The most varied infections were observed in Curculionidae, with supergroup B dominating, a presence of taxa infected by both A and B supergroups, and a single species infected by F supergroup (Lachowska, Kajtoch & Knutelski, 2010; Rodriguero et al., 2010a; Kawasaki et al., 2016) (Fig. 7). Considering the frequency of infected specimens in the examined beetle species represented by the available data (n = 106), 63 species were reported to be totally infected (all individuals possessed Wolbachia), whereas 43 species had this bacterium in only some individuals (if exclude Chrysomelidae and Curculionidae: 8 and 15 species, respectively) (Fig. 8). The same calculated for Chrysomelidae resulted in 17 and 10 species, respectively, and for Curculionidae in 38 and 18 species, respectively (Fig. 8). These differences between these values (between these groups of species) were significant (Ch2 = 72.03, P = 0.000). A single Wolbachia strain was observed in 43 species (species with available data n = 62), whereas two strains were reported in 10 species (Byturus tomentosus, Malloch, Fenton & Butcher, 2000; Altica quercetorum, Jäckel, Mora & Dobler, 2013; Callosobruchus chinensis, Okayama et al., 2016; Chelymorpha alternans, Keller et al., 2004; Crioceris quaterdecimpunctata and Crioceris quinquepunctata, Kolasa et al., 2017; Adalia bipunctata, Majerus & Majerus, 2000; Polydrusus inustus, Kajtoch, Korotyaev & Lachowska-Cierlik, 2012; Cyanapion afer and C. spencii, Kajtoch, Montagna & Wanat, 2018) and multiple infection in a further nine species (Callosobruchus chinensis, Kondo et al., 2002; Diabrotica barberi, Roehrdanz & Levine, 2007; Conotrachelus nenuphar, Zhang et al., 2010; Pityogenes chalcographus, Arthofer et al., 2009; Xyleborus dispar and Xylosandrus germanus, Kawasaki et al., 2016) (Fig. 8). In Chrysomelidae (n = 22) these numbers were 12, 5 and five, respectively and in Curculionidae (n = 37), 30, 3 and four, respectively (Fig. 8). The numbers of single, double and multiple infected individuals in these groups of beetles differed insignificantly (Chi2 ANOVA = 2.364, P = 0.307).

Shares of beetles infected by Wolbachia supergroups (A, B, F).

Figure 7: Shares of beetles infected by Wolbachia supergroups (A, B, F).

(Beetle photographs are from ICONOGRAPHIA COLEOPTERORUM POLONIAE (©Copyright by Prof. Lech Borowiec).
Diversity of Wolbachia infection in Coleoptera with respect to shares of infected individuals within species and numbers of strains found in beetles.

Figure 8: Diversity of Wolbachia infection in Coleoptera with respect to shares of infected individuals within species and numbers of strains found in beetles.

(Beetle photographs are from ICONOGRAPHIA COLEOPTERORUM POLONIAE (©Copyright by Prof. Lech Borowiec).

Effects on hosts

Wolbachia affected beetle hosts in several ways. Linkage disequilibrium and/or selective sweep between bacteria and host genomes (usually with host mtDNA) were detected in six species (3% or 9% if excluding Chrysomelidae and Curculionidae): two (4%) Chrysomelidae (Altica lythri, Jäckel, Mora & Dobler, 2013; Aphthona nigriscutis, Roehrdanz et al., 2006) and four (5%) Curculionidae (Eusomus ovulum, Mazur et al., 2016; Naupactus cervinus, Rodriguero, Lanteri & Confalonieri, 2010b, Polydrusus inustus, Polydrusus pilifer, Kajtoch, Korotyaev & Lachowska-Cierlik, 2012). Cytoplasmic incompatibility was detected or suspected but unconfirmed in 12 (6% or 18% if excluding Chrysomelidae and Curculionidae) Coleoptera: six (13%) Chrysomelidae (Chelymorpha alternans, Keller et al., 2004, Diabrotica barberi, Roehrdanz & Levine, 2007, et al., Diabrotica virgifera virgifera, Giordano, Jackson & Robertson, 1997; Callosobruchus chinensis, Kondo et al., 2002; Callosobruchus analis, Numajiri, Kondo & Toquenaga, 2017; Brontispa longissimi, Takano et al., 2017), three (4%) of Curculionidae (Cossomus sp., Zhang et al., 2010; Hypothenemus hampei, Mariño, Verle Rodrigues & Bayman, 2017, Xylosandrus germanus, Kawasaki et al., 2016), one of Sylvanidae (Oryzaephilus surinamensis, Sharaf et al., 2010) and one of Tenebrionidae (Tribolium confusum, Li et al., 2016b; Ming et al., 2015). Horizontal transfer of Wolbachia was detected or suspected in 26 species of Coleoptera (13% or 39% if excluding Chrysomelidae and Curculionidae)—16 (33%) species of Chrysomelidae (several species of Altica, Jäckel, Mora & Dobler, 2013, Crioceris quaterdecimpunctata and Crioceris quinquepunctata, Kolasa et al., 2017) and 10 (14%) species of Curculionidae (members of Euwallacea, Xyleborus, Xylosandrus, Xyleborinus schaufussi and Taphrorychus bicolor, Kawasaki et al., 2016, Polydrusus and Parafoucartia squamulata, Kajtoch, Korotyaev & Lachowska-Cierlik, 2012; Sitophilus oryzae and S. zaemais, Carvalho et al., 2014). Other effects of Wolbachia on beetles included the following: (i) transfer of bacteria genes to the autosomes of the host (so far detected only for Monochamus alternatus, Cerambycidae, Aikawa et al., 2009 and Callosobruchus chinensis, Chrysomelidae, Nikoh et al., 2008); (ii) coexistence of Wolbachia with Rickettsia (Calvia quattuordecimguttata, Coccidula rufa, Coccinella septempunctata, Halyzia sedecimguttata, Rhizobius litura, Weinert et al., 2007; Sitona obsoletus, White et al., 2015; Micromalthus debilis, Perotti, Young & Braig, 2016) in the host or with Spiroplasma (Chilocorus bipustulatus, Weinert et al., 2007; Aleochara bipustulata, Bili et al., 2016) or with both (Adalia bipunctata, Majerus & Majerus, 2000, Harmonia axyridis, Dudek et al., 2017; Curculio sikkimensis, Toju & Fukatsu, 2011; Aleochara bilineata, Bili et al., 2016); (iii) induction and reinforcement of parthenogenesis, however this effect had weak support and had other possible alternative explanations (numerous species of Naupactini, Rodriguero et al., 2010a and Eusomus ovulum, Mazur et al., 2016; all Curculionidae; Micromalthus debilis, Perotti, Young & Braig, 2016); (iv) possible induction of haplodiploidy (Euwallacea interjectus, Euwallacea validus, Curculionidae, Kawasaki et al., 2016); (v) male-killing (Tribolium madens, Tenebrionidae, Fialho & Stevens, 2000); (vi) necessity of infection for egg development (Otiorhynchus sulcatus, Curculionidae, Son et al., 2008; Coccotrypes dactyliperda, Zchori-Fein, Borad & Harari, 2006); (vii) populations evolving towards endosymbiont loss and repeated intraspecific horizontal transfer of Wolbachia (Pityogenes chalcographus, Curculionidae, Arthofer et al., 2009), (viii) fitness decline in infected beetles (Callosobruchus analis, Numajiri, Kondo & Toquenaga, 2017), (ix) modification of sperm (Chelymorpha alternans, Clark et al., 2008), (x) down-regulation of defense genes in host plants (Diabrotica virgifera virgifera on maize, Barr et al., 2010).

Phylogenetic relations

The tree reconstructed for 16S rDNA included 52 sequences from bacteria found in 45 host beetle species. This tree included three major lineages, with separate clusters of Wolbachia sequences belonging to A, B and F supergroups (Fig. S1). F supergroup was represented by a single sequence from Rhinocyllus conicus (Curculionidae) (Fig. S1). Sequences assigned to supergroup A (based on information available in the articles) were found to be polyphyletic. Some 16S sequences from Xylosandrus spp. and Curculio spp. (Curculionidae), or Oreina cacaliae and Galeruca tanaceti (Chrysomelidae) clustered as a sister lineage to all other A and B sequences (Fig. S1). Overall, the diversity of 16S sequences assigned to supergroup B was much greater than those assigned to supergroup A (Fig. S1).

The tree reconstructed for ftsZ included 131 sequences found in 114 host beetle species. The ftsZ phylogenetic tree resulted in a topology similar to that of 16S rDNA—it included groups of sequences belonging to A, B and F supergroups (Fig. S2). Supergroup F was represented by Agrilus araxenus and Sphaerobothris aghababiani (both Buprestidae). Moreover, the supergroup B clade was divided into two clusters, among which one included a small group of sequences found in four beetle hosts: Chelymorpha alternans (Chrysomelidae), Eurymetopus fallax, Sitophilus oryzae and Conotrachelus nenuphar (all three Curculionidae) (Fig. S2). Also in this gene, the genetic variation of sequences belonging to supergroup A was much lower, and only a few sequences were highly diverged (e.g., strains of Callosobruchus chinensis, Chrysomelidae; Tribolium confusum, Tenebrionidae or Polydrosus pilosus, Curculionidae) (Fig. S2). There was also one slightly distinct clade that mainly consisted of bacteria sequences found in some Hydraenidae, Curculionidae and Chrysomelidae (Fig. S2).

The abovementioned phylogenetic reconstructions of the relations among Wolbachia strains identified on the basis of polymorphism of two genes show that there is no strict correlation between host phylogeny and bacterial strain relationships. Even in studies that covered multiple related species (e.g., those belonging to the same genus), evidence for direct inheritance of Wolbachia strains from common ancestors is restricted to Hydraenidae (Sontowski et al., 2015) and some species of Oreina (Montagna et al., 2014) or Curculio (Toju et al., 2013). In the case of Altica, the data show that cospeciation was rare and restricted to a few recently diverged species (Jäckel, Mora & Dobler, 2013). In contrast, there are numerous examples of phylogenetically related beetle species possessing different Wolbachia strains (e.g., Lachowska, Kajtoch & Knutelski, 2010). It is also often the case among related species that some are infected, whereas others not (Crioceris, Kubisz et al., 2012; Oreina, Montagna et al., 2014; Cyanapion, Kajtoch, Montagna & Wanat, 2018); so any assumption that the bacteria were inherited from a common ancestor would also need to consider multiple losses of infection. The latter phenomenon is probable; however, there is no direct evidence from natural populations, at least in studies on beetles, of Wolbachia disappearing over time. Some exemplary studies that found Wolbachia present in related species, after detailed examination, rejected the idea that bacteria was inherited from a common ancestor. This was because different host species harbored unrelated stains (e.g., among weevils, Lachowska, Kajtoch & Knutelski, 2010) or in cases where strains were identical or similar, the hosts were not phylogenetically close to each other (e.g., Crioceris, Kubisz et al., 2012). Finally, there is evermore proof of horizontal Wolbachia transmission via different mechanisms, such as via predators, parasitoids, common habitat or foraging on the same host plants (Huigens et al., 2004; Stahlhut et al., 2010; Caspi-Fluger et al., 2012; Ahmed et al., 2015; Kolasa et al., 2017). Studies on beetles have mainly provided indirect evidence of such transmissions. There are known groups of species that inhabit the same environments and share the same or very similar Wolbachia strains, e.g., steppic weevils from East-central Europe (Mazur, Kubisz & Kajtoch, 2014) and bark beetles in Japan (Kawasaki et al., 2016). Recently, evidence for has also appeared for the role of host plants in bacteria spread—Wolbachia DNA was detected in two species of Crioceris leaf beetles and in their host plant—Asparagus spp. (Kolasa et al., 2017).

Finally, in light of the proposed “Candidatus Wolbachia” species, the summarized phylogenetic relations among Wolbachia strains infecting various beetles indicate that the taxonomic distinctiveness of supergroups is inconclusive (Ramirez-Puebla et al., 2015; Lindsey et al., 2016). First, beetles generally harbor members of supergroups A and B, and only occasionally members of supergroup F. Therefore, it is not possible to make any conclusions about broader Wolbachia taxonomy based only on Wolbachia strains found in Coleoptera. However, there are numerous examples of beetle hosts harboring both supergroups, including beetles in which some Wolbachia genes are of supergroup A origin, while others are of supergroup B origin; this indicates that recombination between strains belonging to different supergroups is quite frequent. This is evidence against the designation of the “Candidatus Wolbachia” species, at least with respect to members of supergroup A and B.

Current Gaps and Future Endeavors

The present knowledge on Wolbachia infection across beetle species and populations is very uneven. Even the basic data about infection statuses in species and frequencies of infected species across genera and families is superficial, as there are only c. 200 beetle species known to be infected. This means that if 38% is the average frequency of infection among beetle species, then only c. 530 species have been tested so far. This is merely c. 0.15% of the total number of beetles, which is estimated to be around 360,000 species (Farrell, 1998; Bouchard et al., 2009). We know even less at the population level, as the majority of beetle species have only had single individuals tested for Wolbachia infection (e.g., Lachowska, Kajtoch & Knutelski, 2010; Sontowski et al., 2015). These very basic screens have probably underestimated the number of infected species because of false-negative results obtained for species with low or local infection in populations. There is also another and important cause that should be mentioned—low titer infections that are under the detection limit of conventional PCR (e.g., Arthofer et al., 2009; Schneider et al., 2013). On the other hand, these preliminary estimates could have overestimated the real number infected beetles, as sampling in these studies was rarely random and most often focused on specific groups, e.g., on genera for which preliminary data suggested the presence of Wolbachia infection. Indeed, an intensive search of Wolbachia infection across hundreds of beetle species from Europe suggested a lower infection rate—c. 27% to be infected (Ł Kajtoch et al., 2018, unpublished data). Also, knowledge about infection at the geographic scale is very uneven, and only Europe and Asia (basically China and Japan) have been relatively well investigated. There is a huge gap in the knowledge for African, Australian and Oceanian beetles, where a high diversity of beetles exists and probably a similar diversity of Wolbachia could be expected (e.g., compared to preliminary data available from Central and South America (Werren, Windsor & Guo, 1995; Rodriguero et al., 2010a).

Little is known about Wolbachia diversity in beetle hosts, as the majority of studies used only single genetic markers, and often different genes were sequenced for different taxa. This precludes complex analysis of Wolbachia diversity across all tested beetle hosts. This has changed since 2006, since Baldo et al. (2006) proposed Multilocus Sequence Typing (MLST), which is based on the genotyping of five housekeeping genes, usually in conjunction with wsp sequencing. MLST is and should remain a sufficient way to understand basic Wolbachia diversity. On the other hand, to fully understand Wolbachia relations among strains and supergroups (or presumed species), between Wolbachia and its hosts and especially between Wolbachia and other microorganisms, amplicon-sequencing (e.g., 16S rDNA) or genome-sequencing are needed. This could be achieved thanks to the development of next-generation sequencing technologies (NGS). Surprisingly, despite fast development of NGS in the last years, very few studies have used this technology for studying Wolbachia in beetle populations. For example, five studies sequenced 16S amplicons generated from microbiota and detected Wolbachia (White et al., 2015; Bili et al., 2016; Berasategui et al., 2016; Takano et al., 2017; Dudek et al., 2017). The only study that utilized shotgun sequencing was executed for other purposes and only accidentally showed Wolbachia genes in examined species (Heintzman et al., 2014). NGS is probably the best prospect for studies on Wolbachia infection and diversity, and will help to answer most current riddles and issues.

The big challenge is to understand the impact of infection on beetle biology, physiology and ecology. It is known that Wolbachia has several effects on host reproduction, but relatively few studies prove or suggest e.g., cytoplasmic incompatibility, male-killing or other effects on the development of selected beetles (Clark et al., 2001; Keller et al., 2004; Roehrdanz et al., 2006; Roehrdanz & Levine, 2007; Sharaf et al., 2010; Zhang et al., 2010; Jäckel, Mora & Dobler, 2013; Ming et al., 2015; Kawasaki et al., 2016; Li et al., 2016b; Mariño, Verle Rodrigues & Bayman, 2017; Numajiri, Kondo & Toquenaga, 2017; Takano et al., 2017). It is very probable that this bacteria has large and frequent effects on beetle reproduction and is consequently partially responsible for beetle radiation, at least in some taxonomic groups, geographic areas or habitats. Also, very few studies have shown data on linkage disequilibrium and selective sweep between bacteriium and host genomes (Roehrdanz et al., 2006; Rodriguero, Lanteri & Confalonieri, 2010b; Kajtoch, Korotyaev & Lachowska-Cierlik, 2012; Jäckel, Mora & Dobler, 2013; Mazur et al., 2016). These effects could also have probably been involved in speciation of numerous beetles. Moreover, this phenomenon could have serious implications for beetle barcoding, as selective sweep is known to reduce mitochondrial diversity in its hosts and therefore could decrease the number of identified species (Hurst & Jiggins, 2005). On the other hand, cytoplasmic incompatibility can lead to the origin of highly diverged phylogenetic mitochondrial lineages within species, which would increase the number of identified taxa (Smith et al., 2012). Also here, NGS technologies will enable more sophisticated analyses of these genetic relations and their effects (e.g., by the sequencing of transcriptomes for physiological studies or by genotyping-by-sequencing for phylogenetic studies). Genotyping with NGS should also verify whether the recent assumption that different supergroups are indeed “Candidatus Wolbachia” species is correct or not (Ramirez-Puebla et al., 2015; Lindsey et al., 2016).

Only very preliminary results suggest Wolbachia was not only transmitted vertically, but that it could also have spread horizontally (Jäckel, Mora & Dobler, 2013; Carvalho et al., 2014; Kawasaki et al., 2016; Kolasa et al., 2017; Mazur et al., 2016). Horizontal transmission was considered as an event that happens in evolutionary timescales. Only recently, Schuler et al. (2013) showed that such a transfer can happen within a few years after arrival of a new strain. In light of the general lack of cospeciation between bacteria and beetles, horizontal transmission must be a highly underestimated phenomenon. Horizontal transmission of Wolbachia among beetles cannot be confirmed without considering other coexisting insects that can mediate transmission, such as predators, parasitoids or beetle prey. Moreover, other arthropods that share habitats with beetles, e.g., phoretic ticks (Hartelt et al., 2004) and nematodes (Casiraghi et al., 2001), need to be examined. Finally, host plants are promising objects of studies on Wolbachia transmission across beetle populations (Kolasa et al., 2017), as phloem is probably an important mediator of this bacteria’s spread across insect populations (DeLay et al., 2012; Li et al., 2016a). Concerning transmission—another very interesting topic is the transfer of Wolbachia genes into host genomes (Dunning Hotopp et al., 2007; Koutsovoulos et al., 2014; Funkhouser-Jones et al., 2015). This issue has only been reported twice for beetle hosts so far (Nikoh et al., 2008; Aikawa et al., 2009). This problem could be important as if such transfers are frequent, simple testing of Wolbachia presence in a host based on single or even several gene sequencing could overestimate the number of truly infected species, populations or individuals.

Finally, a very interesting topic for future studies is the examination of the presence of other intracellular and symbiotic bacteria (like Cardinium, Spiroplasma, Rickettsia) in Coleoptera and their relations, both with the host and Wolbachia. So far, only seven studies have found Wolbachia with Rickettsia and/or Spiroplasma together in beetle hosts (Majerus & Majerus, 2000; Weinert et al., 2007; Toju & Fukatsu, 2011; White et al., 2015; Perotti, Young & Braig, 2016; Bili et al., 2016; Dudek et al., 2017). Preliminary results suggest that there is some balance in the number of these bacteria, probably caused by competition within host cells (Goto, Anbutsu & Fukatsu, 2006). A recent summary of the presence of these bacteria in insects showed that Rickettsia has been found in single species of Micromalthidae, Staphylinidae, Buprestidae, Coccinellidae and Curculionidae (Werren et al., 1994; Lawson et al., 2001; Weinert et al., 2007; Toju & Fukatsu, 2011; White et al., 2015; Perotti, Young & Braig, 2016; Bili et al., 2016), Spiroplasma in some species of Staphylinidae, Coccinellidae and Curculionidae (Majerus et al., 1998; Hurst et al., 1999a; Hurst et al., 1999b; Tinsley & Majerus, 2006; Weinert et al., 2007; Toju & Fukatsu, 2011; Bili et al., 2016), and Cardinium has not been detected so far in any beetle species (Zchori-Fein & Perlman, 2004). The coexistence of different endosymbiotic bacteria and their effects on hosts should also be investigated with NGS technologies, which are able to detect bacteria in numerous hosts (e.g., individuals) at once and estimate prevalence of bacteria in various hosts or different tissues. NGS has already been proven to be a powerful tool for detecting undescribed bacteria (e.g., it allowed the identification of new Alphaproteobacteria in Brontispa longissimi; Takano et al., 2017). Different endosymbiotic bacteria could have either similar or contrasting effects on beetle species, populations and individuals and could be the greatest overlooked phenomenon in the evolution and ecology of Coleoptera.

In our opinion, beetles are still an insufficiently examined group of Wolbachia hosts, especially considering their systematic and ecological diversity. All issues in studies on Wolbachia in Coleoptera are generally the same as in other hosts of these bacteria, or vice versa; there is no issue that has been or is being studied on Wolbachia infection in other (non-beetle) hosts that could not also be examined in beetle hosts. Also, the extraordinary diversity of beetles (with respect to their diverse systematics at various taxonomic levels, complex phylogenetic relations and extensive ecological relations with each other and numerous other species) makes this group an excellent target for Wolbachia studies. The presented summary about Wolbachia infection in beetles shows that despite numerous studies, there are still many issues that need to be investigated. We hope that this systematic review will facilitate various future studies on Wolbachia infection among beetles.

Supplemental Information

Image of characterization of Wolbachia infection across beetle species and populations based on data in the literature

DOI: 10.7717/peerj.4471/supp-1

Image of phylogenetic tree reconstructed based on Wolbachia 16S rDNA gene sequences obtained from hosts belonging to various species of Coleoptera

Maximum likelihood phylogenetic tree reconstructed based on Wolbachia 16S rDNA gene sequences obtained from hosts belonging to various species of Coleoptera (data downloaded from NCBI GenBank Statistical supports (bootstrap values) are presented above the branches (shown only if >0.50).

DOI: 10.7717/peerj.4471/supp-2

Image of phylogenetic tree reconstructed based on Wolbachia ftsZ gene sequences obtained from hosts belonging to various species of Coleoptera

Maximum likelihood phylogenetic tree reconstructed based on Wolbachia ftsZ gene sequences obtained from hosts belonging to various species of Coleoptera (data downloaded from NCBI GenBank Statistical supports (bootstrap values) are presented above the branches (shown only if >0.50).

DOI: 10.7717/peerj.4471/supp-3

PRISMA checklist

DOI: 10.7717/peerj.4471/supp-4