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Article

The Genome of Arsenophonus sp. and Its Potential Contribution in the Corn Planthopper, Peregrinus maidis

by
Yu-Hui Wang
1,
Aram Mikaelyan
1,
Brad S. Coates
2 and
Marcé Lorenzen
1,*
1
Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC 27695, USA
2
USDA-ARS, Corn Insects & Crop Genetics Research Unit, Ames, IA 50011, USA
*
Author to whom correspondence should be addressed.
Insects 2024, 15(2), 113; https://doi.org/10.3390/insects15020113
Submission received: 2 January 2024 / Revised: 26 January 2024 / Accepted: 31 January 2024 / Published: 5 February 2024
(This article belongs to the Section Insect Molecular Biology and Genomics)
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Abstract

:

Simple Summary

Microbes play important roles in the biochemistry, physiology and survival of insects. An example is Arsenophonus sp. in the brown planthopper (Nilaparvata lugens), an endosymbiotic bacterium supplementing the nutritionally poor diet of its sap-feeding host. In this study, we use the genome of Nl Arsenophonus sp. as a reference to facilitate the genome assembly of a closely related Arsenophonus sp. found in the corn planthopper (Peregrinus maidis). Our assembly is one of the largest Arsenophonus genomes reported to date. We also investigated the role of Arsenophonus sp. in P. maidis, in which it appears to provide B vitamins and essential amino acids.

Abstract

The co-evolution between symbionts and their insect hosts has led to intricate functional interdependencies. Advances in DNA-sequencing technologies have not only reduced the cost of sequencing but, with the advent of highly accurate long-read methods, have also enabled facile genome assembly even using mixed genomic input, thereby allowing us to more easily assess the contribution of symbionts to their insect hosts. In this study, genomic data recently generated from Peregrinus maidis was used to assemble the genome of a bacterial symbiont, Pm Arsenophonus sp. This ~4.9-Mb assembly is one of the largest Arsenophonus genomes reported to date. The Benchmarking Universal Single-Copy Orthologs (BUSCO) result indicates that this Pm Arsenophonus assembly has a high degree of completeness, with 96% of the single-copy Enterobacterales orthologs found. The identity of the Pm Arsenophonus sp. was further confirmed by phylogenetic analysis. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis indicates a major contribution by Pm Arsenophonus sp. to the biosynthesis of B vitamins and essential amino acids in P. maidis, where threonine and lysine production is carried out solely by Pm Arsenophonus sp. This study not only provides deeper insights into the evolutionary relationships between symbionts and their insect hosts, but also adds to our understanding of insect biology, potentially guiding the development of novel pest control methods.

1. Introduction

The corn planthopper, Peregrinus maidis, is a notorious sap-feeding pest that targets corn and sorghum, and is known to vector the maize mosaic rhabdovirus and maize stripe tenuivirus [1]. The combination of insect damage and viral infection can significantly reduce crop yield [2]. Current management tactics mainly rely on insecticide applications, but effective control remains difficult because of the limited direct exposure of P. maidis under field conditions. Insecticides also have negative effects on ecosystems and human health. As such, new efficacious and sustainable methods are needed for the management of P. maidis and the viruses it transmits. Sequence-specificity-based RNA interference (RNAi) holds promise for the targeted control of pest species [3]. The efficacy of RNAi on P. maidis has been validated under laboratory conditions [4,5,6], but an efficient system for delivering double-stranded RNA (dsRNA) to P. maidis in the field is not yet available. Innovative solutions for delivery involve the modification of symbionts to express host-specific dsRNAs [7,8,9], but research into the symbionts of P. maidis is still limited. Therefore, we leveraged the genomic sequence data recently generated for P. maidis in order to assemble the genome of the Arsenophonus sp. associated with this hemipteran. We focused on Arsenophonus sp. because of its demonstrated nutritional importance in another planthopper, Nilaparvata lugens [10], which suggests it may play a similar role in P. maidis. Moreover, the fact that protocols have been worked out for culturing and genetically modifying other Arsenophonus spp. [11,12] bodes well for the development of similar methods for Pm Arsenophonus sp. and supports the potential of using this symbiont to deliver dsRNA to P. maidis.
The genus Arsenophonus, first proposed in 1991 for Arsenophonus nasoniae [13], derives its name from the Greek “Arsen” (male) and “phonus” (slayer), reflecting the ability of A. nasoniae to kill the male offspring of Nasonia vitripennis. Arsenophonus spp. have been found in many insect species with diverse lifestyles [14]. They serve as primary symbionts in Lipoptena cervi and Aleurodicus disperses [15,16], and as secondary symbionts in Aleurodicus floccissimus, Trialeurodes vaporariorum, N. lugens and triatomine bugs [10,16,17]. Such a stable association is not observed in the honeybee, Apis mellifera, as individuals can acquire Arsenophonus sp. from the environment or nestmates [18]. Although it is rare, Arsenophonus spp. can act as insect-vectored plant pathogens; for example, A. phytopathogenicus transmitted by Pentastiridius leporinus causes low sugar content in sugar beets [19].
In this study, we identified Arsenophonus-specific scaffolds within a newly generated P. maidis genome assembly. The ~4.9 Mb Pm Arsenophonus genome assembly was surveyed for genes involved in key biosynthetic pathways, and the role Pm Arsenophonus sp. plays in the production of B vitamins and essential amino acids was determined. The data presented here have the potential to assist with the development of novel pest control methods, both by increasing our understanding of P. maidis biology, and by providing a candidate for use in symbiont-mediated RNAi.

2. Materials and Methods

2.1. Insect Rearing

Corn planthoppers were reared on 5-week-old corn (cultivar Early Sunglow, Park Seed Company, Greenwood, SC, USA) and kept in 30 cm × 30 cm × 60 cm cages covered by nylon-mesh screens (BioQuip Products Inc., Compton, CA, USA) in a room at 25 ± 1 °C, ~70% RH and at a 14:10 (light:dark) photoperiod.

2.2. Genome Sequencing, Assembly and Annotation

We extracted genomic DNA from P. maidis using the Mag-Bind Blood and Tissue DNA HDQ 96 Kit (Omega Bio-tek, Norcross, GA, USA). The quality of genomic DNA was assessed and submitted to Eremid Genomic Services (North Carolina Research Campus, Kannapolis, NC, USA) for library preparation using SMRTbell Express Template Prep Kit 2.0 (Pacific Biosystems, Menlo Park, CA, USA) and subsequent high-fidelity (HiFi) read generation on a Sequel IIe system (Pacific Biosystems). Raw reads were converted to fastq format using BamTools v. 2.5.1 [20], filtered to remove reads < 8 kb, and the data was transferred to the USDA–ARS SCINet high-performance computing cluster, Ceres. A histogram of canonical k-mer counts was made at k  =  21 for filtered reads using Meryl [21], and was then applied as the maximum depth input for the R script, GenomeScope 2.0 [22,23]. Next, reads were assembled into contigs using hifiasm [24] with default assembly options but purging adjusted to [-I 3 (aggressive purging); -purge-max 14; -s 0.55; n-hap 2 (diploid)] on 40 cores with 768 GB DDR3 ECC RAM. Then, contigs were scaffolded using RagTag [25] on Galaxy Europe (https://usegalaxy.eu, accessed on 25 May 2022) [26]. RagTag uses whole-genome homology to scaffold, in which a reference genome is used to inform the order and orientation of query sequences. The genome of Arsenophonus sp. in N. lugens (accession number: GCA_000757905.1) was used as a reference to scaffold contigs [10]. Completeness of the Pm Arsenophonus assembly was compared to other Arsenophonus genome assemblies (accession number: GCA_004768525.1, GCA_020268605.1, GCA_001534665.1, GCA_900343015.1, GCA_900343025.1, GCA_002287155.1 and GCA_000757905.1) using Benchmarking Universal Single-Copy Orthologs (BUSCO) [27,28,29] on Galaxy Europe (https://usegalaxy.eu, accessed on 22 June 2022) [26]. Genes were then predicted from the genome assemblies above using Glimmer [30], and annotation of the resulting genes was conducted using the BLASTx algorithm against the non-redundant protein database (E-value cutoff of 10−5) through OmicsBox software (BioBam, Valencia, Spain) [31]. Then, criteria based on a previous study (E-value < 10−15 and similarity < 80%) [32] were applied to the predicted genes to roughly estimate the number of pseudogenes, and free-living bacteria Proteus mirabilis, Escherichia coli and Pseudomonas aeruginosa were included for comparison. Pathway analysis was then conducted on the genes predicted from the Pm Arsenophonus assembly and P. maidis transcriptome data [5] using the Kyoto Encyclopedia of Genes and Genomes (KEGG) [33] through OmicsBox.

2.3. RNA Polymerase β Subunit Gene (rpoB) Identification and Phylogenetic Analysis

The amino-acid sequence of rpoB (accession number: WP_000263098.1) was used as a query to search for rpoB orthologs in the predicted Arsenophonus genes exported from OmicsBox. The rpoB nucleotide sequences were then aligned using the MUSCLE algorithm [34] and evaluated against 24 nucleotide substitution models to find the most appropriate one for phylogenetic analysis in MEGAX [35]. The phylogenetic tree based on rpoB was constructed using the Maximum Likelihood method, with the best-fitting substitution model identified by the lowest Bayesian information criterion score. Tree topology was evaluated using bootstrap analysis with 1000 replications. The rpoB genes of Buchnera aphidicola and Riesia pediculicola were used as outgroups to root the phylogenetic tree. The predicted genes of B. aphidicola and R. pediculicola were generated from genome assemblies B. aphidicola JF99 (accession number: GCA_000183285.1) and R. pediculicola (accession number: GCA_014879315.1), and were queried for rpoB orthologs as described above.

3. Results and Discussion

Eleven Arsenophonus-specific scaffolds were identified within the P. maidis genomic data. Together these formed a genome assembly of ~4.9 Mb, which was then compared to data from Arsenophonus spp. whose genome assemblies and roles in their respective hosts were available. An exception was made for Arsenophonus sp. in the keeled treehopper (Entylia carinata), due to the closer relationship between its insect host and P. maidis. Our Pm Arsenophonus assembly is ~4.9 Mb in size, one of the largest reported to date. While the difference in genome size might be attributed to genuine biological variation among the genomes, it could also result from the different sequencing platforms. Notably, the larger Arsenophonus genome assemblies have been mostly generated using third-generation PacBio and/or Nanopore reads, which generate mean read lengths that are sufficient to span repetitive regions and facilitate more accurate and complete genome assemblies. In contrast, assemblies from short-read data often leave repetitive regions unassembled, resulting in gapped pseudomolecules [36]. Therefore, the comparatively larger-sized Pm Arsenophonus genome could be a consequence of our use of PacBio HiFi reads. De novo assembly of other Arsenophonus genomes with long-read data may alter the ranking based on genome size. The large size of the Pm Arsenophonus genome may contribute to it containing 423 of the 440 single-copy orthologs in the BUSCO Enterobacterales data set (Figure 1), which is among the highest compared to other Arsenophonus genomes. BUSCO results also suggest that some Arsenophonus genome assemblies may be incomplete and thus have underestimated sizes, particularly those that are not primary symbionts (A. triatominarum, Arsenophonus sp. in A. floccissimus and Arsenophonus sp. in N. lugens).
During symbiont evolution, characteristic changes manifest within the genomes of host-dependent bacteria, reflecting the adaptation to different symbiotic lifestyles and ongoing selection pressures. One commonly observed trend is genome size reduction, which leads to more host-restricted symbionts [37] and the accumulation of mutations. A prevalent mutational bias towards AT suggests that primary symbionts generally tend to have genomes with a lower GC content. This is reflected in our comparative genomic analysis (Table 1). Specifically, the primary symbionts A. lipopteni and Arsenophonus sp. in A. disperses (hereafter “Arsenophonus sp. (ARAD)”) have a lower GC content, with an estimated 29.4 and 32.2%, respectively. The high 41.3% GC content of the Pm Arsenophonus genome and the comparatively large genome size suggest that Pm Arsenophonus sp. is at a relatively early stage of symbiont evolution.
Pseudogenes, or putative non-functional remnants of once-active genes, serve as another indicator of evolutionary stage and degree of endosymbiotic specialization. In the process of the transition from a free-living bacterium to a primary symbiont, pseudogenes accumulate due to the changing selective pressures associated with the symbiotic lifestyle. In a free-living state, gene function is maintained to support the diverse requirements of independent life. As an organism enters into a symbiotic relationship, a subset of genes that were essential in a free-living state might become redundant, leading to the formation of pseudogenes. Once the symbiotic relationship is well established and the organism has become a primary symbiont, there could be a deletional bias whereby non-functional DNA (like pseudogenes) is removed from the genome [37,38]. This pattern may lead to relatively higher numbers of pseudogenes in organisms that are neither fully free-living nor fully adapted as primary symbionts. Based on the criteria applied, 25 pseudogenes were estimated to be present in the genomes of P. mirabilis, one in E. coli and none in P. aeruginosa. Among Arsenophonus spp., the fewest number of pseudogenes was estimated to be present in the genomes of primary symbionts A. lipopteni and Arsenophonus sp. (ARAD) (Table 1). This was in line with expectations for free-living bacteria and primary symbionts. Interestingly, the Pm Arsenophonus genome appears to contain 1123 pseudogenes, which indicates that it is neither a free-living bacterium nor a primary symbiont. This fits well with the idea that Pm Arsenophonus sp. is at a relatively early stage of symbiont evolution.
The identity of Pm Arsenophonus sp. was further confirmed by phylogenetic analysis. The 16S ribosomal RNA (16S rRNA) gene, which produces the RNA component of the prokaryotic small ribosomal subunit, is commonly used for bacterial identification. The essential role of 16S rRNA results in its ubiquitous presence in almost all bacteria, making it a good molecular marker. Additionally, since the function of 16S rRNA has not changed, random changes in the sequence can be used to measure evolutionary time. Available 16S rRNA gene databases, such as Greengenes [39], Ribosomal Database Project [40] and SILVA [41], reflect the common use of the 16S rRNA gene. Despite the ease of using the 16S rRNA gene for bacterial identification, problems can arise [42]. For example, some species possess multiple copies of the 16S rRNA gene, and the sequences can differ by as much as 11.6% [43], which can cause identification issues. Since Arsenophonus spp. also possess multiple copies of the 16S rRNA gene, we used the single-copy gene, encoding the β subunit of RNA polymerase (rpoB) instead for phylogenetic analysis and the identification of Arsenophonus spp. (Figure 2). The rpoB gene was first used in 1997 [44], and it provides better phylogenetic resolution than the 16S rRNA gene at both the species and subspecies levels [43]. Although it was not investigated further, likely due to the lower completeness of the A. triatominarum genome assembly (Figure 1, 137 of 440 BUSCO, 31.1% predicted as missing), its rpoB could not be identified, and therefore was excluded from phylogenetic analysis. Regardless, the resultant phylogenetic tree provides strong support for the bacterial species (with bootstrap values ≥ 97%), and groups primary symbionts into a distinct clade. The tree topology also reflects the relatedness of their insect hosts.
To gain insights into the role Pm Arsenophonus sp. plays in P. maidis, we conducted KEGG pathway analysis on the Arsenophonus genome and previously reported P. maidis transcriptome [5]. Since some Arsenophonus spp. are reported to provide their insect hosts with B vitamins (Table 2) [10,15,16,45], we specifically interrogated components of the biosynthetic pathways for vitamins B1, B2, B5, B6, B7 and B9. Our KEGG pathway analysis suggests that Pm Arsenophonus sp. complements the biosynthetic pathways for vitamins B1, B2, B6, B7 and B9 in P. maidis (Figure 3). The nine enzymes for vitamin B7 production are encoded solely within Pm Arsenophonus sp., suggesting that the insect is dependent on the bacterium for B7 provisioning. We also examined components of biosynthetic pathways for essential amino acids, since symbionts in hemipterans are known for supplying essential amino acids to their insect hosts. KEGG analysis suggests that Pm Arsenophonus sp. provides components for the production of isoleucine, leucine, valine, threonine and lysine (Figure 4). The sole encoding of enzymes for threonine and lysine biosynthesis within the Pm Arsenophonus genome further emphasizes their symbiotic relationship. While such contributions of Arsenophonus spp. to essential amino acid provisioning in insect hosts have not been observed in previous studies (Table 2), our findings point to a potential novel aspect of the involvement of Arsenophonus sp. in the metabolism of P. maidis, meriting further investigation.
Whitten et al. [7] demonstrated the feasibility of symbiont-mediated RNAi in the kissing bug (Rhodnius prolixus) and the western flower thrips (Frankliniella occidentalis). They found that targeted insect genes were significantly knocked down by feeding the insects dsRNA-expressing symbiotic bacteria. Furthermore, the modified symbionts were able to successfully compete with the gut microbiota. While there is more to learn, the important role Pm Arsenophonus sp. plays in P. maidis and the availability of protocols for culturing and genetically modifying Arsenophonus spp. support Pm Arsenophonus sp. as an excellent candidate for use in symbiont-mediated RNAi.

Author Contributions

Conceptualization, Y.-H.W. and M.L.; methodology, Y.-H.W., A.M., B.S.C. and M.L.; validation, Y.-H.W.; investigation, Y.-H.W.; resources, B.S.C. and M.L.; writing—original draft preparation, Y.-H.W.; writing—review and editing, Y.-H.W., A.M., B.S.C. and M.L.; visualization, Y.-H.W.; supervision, M.L.; funding acquisition, M.L. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Defense Advanced Research Projects Agency (DARPA) Insect Allies Program.

Data Availability Statement

The data are available at NCBI with the BioProject ID PRJNA1060725.

Acknowledgments

This research was performed in cooperation with the United States Department of Agriculture (USDA), Agricultural Research Service (ARS) (CRIS Project 5030-22000-019-00D) “Ecologically-based Management of Arthropods in the Maize Agroecosystem”. This research used resources provided by the SCINet project of the USDA–ARS, project number 0500-00093-001-00-D. Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture. USDA–ARS is an equal opportunity employer and provider. Y.-H.W. is supported by a Taiwan Government Fellowship for Studying Abroad. Work by A.M. is supported by a National Institute of Food and Agriculture Hatch Project (accession number 1019324). The authors acknowledge the support of the Freiburg Galaxy Team: Person X and Björn Grüning, Bioinformatics, University of Freiburg (Germany), funded by the Collaborative Research Centre 992 Medical Epigenetics (DFG grant SFB 992/1 2012) and the German Federal Ministry of Education and Research BMBF grant 031 A538A de.NBI-RBC.

Conflicts of Interest

North Carolina State University, Department of Entomology and Plant Pathology, was part of a team supporting DARPA’s Insect Allies Program. The views, opinions and/or findings expressed are those of the authors and should not be interpreted as representing the official views or policies of the Department of Defense or the U.S. Government. The authors declare no competing interests.

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Figure 1. BUSCO assessment results. The completeness of genome assemblies was assessed using BUSCO on Galaxy Europe (https://usegalaxy.eu, accessed on 22 June 2022).
Figure 1. BUSCO assessment results. The completeness of genome assemblies was assessed using BUSCO on Galaxy Europe (https://usegalaxy.eu, accessed on 22 June 2022).
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Figure 2. Maximum likelihood-based phylogenetic tree of Arsenophonus spp. estimated from a consensus rpoB nucleotide sequence alignment. The proportion (%) of 1000 bootstrap replicates supporting each node is indicated. The rpoB gene of Pm Arsenophonus sp. is highlighted in blue, while those identified in primary symbionts are highlighted in orange. The scale bar represents an evolutionary distance of 0.10 nucleotide substitutions per site.
Figure 2. Maximum likelihood-based phylogenetic tree of Arsenophonus spp. estimated from a consensus rpoB nucleotide sequence alignment. The proportion (%) of 1000 bootstrap replicates supporting each node is indicated. The rpoB gene of Pm Arsenophonus sp. is highlighted in blue, while those identified in primary symbionts are highlighted in orange. The scale bar represents an evolutionary distance of 0.10 nucleotide substitutions per site.
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Figure 3. The biosynthetic pathway of B vitamins completed by Arsenophonus sp. and P. maidis. The KEGG pathway analysis was conducted, and enzyme commission numbers (EC numbers) are shown above. The EC numbers in red font within red boxes represent enzymes that were found in the P. maidis transcriptome; those in blue font within blue boxes represent enzymes that were found in the Pm Arsenophonus genome; and those in blue font within red boxes indicate enzymes that were found in both. B vitamins are shown in solid purple circles.
Figure 3. The biosynthetic pathway of B vitamins completed by Arsenophonus sp. and P. maidis. The KEGG pathway analysis was conducted, and enzyme commission numbers (EC numbers) are shown above. The EC numbers in red font within red boxes represent enzymes that were found in the P. maidis transcriptome; those in blue font within blue boxes represent enzymes that were found in the Pm Arsenophonus genome; and those in blue font within red boxes indicate enzymes that were found in both. B vitamins are shown in solid purple circles.
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Figure 4. The biosynthetic pathway of essential amino acids completed by Arsenophonus sp. and P. maidis. The KEGG pathway analysis was conducted, and EC numbers are shown above. The EC numbers in red font within red boxes represent enzymes that were found in the P. maidis transcriptome; those in blue font within blue boxes represent enzymes that were found in the Pm Arsenophonus genome; and those in blue font within red boxes indicate enzymes that were found in both. Essential amino acids are shown in solid green circles.
Figure 4. The biosynthetic pathway of essential amino acids completed by Arsenophonus sp. and P. maidis. The KEGG pathway analysis was conducted, and EC numbers are shown above. The EC numbers in red font within red boxes represent enzymes that were found in the P. maidis transcriptome; those in blue font within blue boxes represent enzymes that were found in the Pm Arsenophonus genome; and those in blue font within red boxes indicate enzymes that were found in both. Essential amino acids are shown in solid green circles.
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Table 1. Comparison between Arsenophonus genomes.
Table 1. Comparison between Arsenophonus genomes.
NameArsenophonus nasoniaeArsenophonus sp.Arsenophonus lipopteniArsenophonus
triatominarum
Accession No.GCA_004768525.1GCA_020268605.1GCA_001534665.1GCA_001640365.1
HostNasonia vitripennisApis melliferaLipoptena fortisetosaTriatoma infestans
SequencingOxford Nanopore MinION;
PacBio RS II;
Illumina MiSeq		Oxford Nanopore MinION;
Illumina MiSeq		IlluminaPacBio
Genome size (bp)4,987,1073,639,254836,7243,858,720
GC content (%)38.1 137.7 124.9 138.3
Pseudogene 21086720104523
NameArsenophonus sp. (ARAD)Arsenophonus sp. (ARAF)Arsenophonus sp. (ENCA)Arsenophonus sp.Arsenophonus sp.
(this study)
Accession No.GCA_900343015.1GCA_900343025.1GCA_002287155.1GCA_000757905.1
HostAleurodicus dispersesAleurodicus floccissimusEntylia carinataNilaparvata lugensPeregrinus maidis
SequencingIllumina HiSeq 2000Illumina HiSeq 2000Illumina MiSeqIllumina HiSeq 2000PacBio
Genome size (bp)663,1253,001,8753,228,5332,953,8634,888,380
GC content (%)32.2 13739.537.641.3
Pseudogene 2293824304691123
1 Plasmid sequence was not included in the calculation of GC content. 2 The number of pseudogenes was roughly estimated by applying the criteria based on a previous study (E value < 10−15 and similarity < 80%) [32] to the predicted genes.
Table 2. Comparison among Arsenophonus spp.
Table 2. Comparison among Arsenophonus spp.
NameHostRole and Function 1TransmissionReference
Arsenophonus phytopathogenicusPentastiridius leporinusPlant pathogen of sugar
beets vectored
by P. leporinus		Maternal and horizontal (major) transmission
by infecting the same
sugar beet		[19]
Arsenophonus nasoniaeNasonia vitripennis
Nasonia longicornis		Reproductive parasite
Killing sons, 80% of sons die		Maternal and horizontal
transmission by infecting
the same pupa host		[46]
Arsenophonus sp.Apis melliferaProviding B vitamins
(B2, B6, B7, B9)		Horizontal transmission
by social interactions
(trophallaxis and/or general
contact) and environmental
acquisition		[18,45]
Arsenophonus lipopteniLipoptena cerviPrimary endosymbiont
Providing B vitamins
(B2, B6, B7)		Unclear[15]
Arsenophonus triatominarumtriatomine bugsSecondary endosymbiont
No apparent effect on host fitness or reproduction		Vertical transmission
(transovarially)		[17]
Arsenophonus sp. (ARAD)Aleurodicus dispersesARAD as primary endosymbiont
ARAF and ARTV as
secondary endosymbiont
ARAD providing cofactors
and B vitamins
(B1, B2, B6, B7, B9)		Unclear[16]
Arsenophonus sp. (ARAF)Aleurodicus floccissimus
Arsenophonus sp. (ARTV)Trialeurodes vaporariorum
Arsenophonus sp.Nilaparvata lugensSecondary endosymbiont
Providing B vitamins		Maternal transmission[10,47]
1 B vitamins in bold indicate that Arsenophonus sp. possesses all the genes in the biosynthetic pathway; B vitamins with an underline indicate that genes from both the Arsenophonus sp. and the host are required to complete the biosynthetic pathway; the remainder are not specified in references.
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Wang, Y.-H.; Mikaelyan, A.; Coates, B.S.; Lorenzen, M. The Genome of Arsenophonus sp. and Its Potential Contribution in the Corn Planthopper, Peregrinus maidis. Insects 2024, 15, 113. https://doi.org/10.3390/insects15020113

AMA Style

Wang Y-H, Mikaelyan A, Coates BS, Lorenzen M. The Genome of Arsenophonus sp. and Its Potential Contribution in the Corn Planthopper, Peregrinus maidis. Insects. 2024; 15(2):113. https://doi.org/10.3390/insects15020113

Chicago/Turabian Style

Wang, Yu-Hui, Aram Mikaelyan, Brad S. Coates, and Marcé Lorenzen. 2024. "The Genome of Arsenophonus sp. and Its Potential Contribution in the Corn Planthopper, Peregrinus maidis" Insects 15, no. 2: 113. https://doi.org/10.3390/insects15020113

APA Style

Wang, Y.-H., Mikaelyan, A., Coates, B. S., & Lorenzen, M. (2024). The Genome of Arsenophonus sp. and Its Potential Contribution in the Corn Planthopper, Peregrinus maidis. Insects, 15(2), 113. https://doi.org/10.3390/insects15020113

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