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Interaction of Arsenophonus with Wolbachia in Nilaparvata lugens



Co-infection of endosymbionts in the same host is ubiquitous, and the interactions of the most common symbiont Wolbachia with other symbionts, including Spiroplasma, in invertebrate organisms have received increasing attention. However, the interactions between Wolbachia and Arsenophonus, another widely distributed symbiont in nature, are poorly understood. We tested the co-infection of Wolbachia and Arsenophonus in different populations of Nilaparvata lugens and investigated whether co-infection affected the population size of the symbionts in their host.


A significant difference was observed in the co-infection incidence of Wolbachia and Arsenophonus among 5 populations of N. lugens from China, with nearly half of the individuals in the Zhenjiang population harbouring the two symbionts simultaneously, and the rate of occurrence was significantly higher than that of the other 4 populations. The Arsenophonus density in the superinfection line was significantly higher only in the Maanshan population compared with that of the single-infection line. Differences in the density of Wolbachia and Arsenophonus were found in all the tested double-infection lines, and the dominant symbiont species varied with the population only in the Nanjing population, with Arsenophonus the overall dominant symbiont.


Wolbachia and Arsenophonus could coexist in N. lugens, and the co-infection incidence varied with the geographic populations. Antagonistic interactions were not observed between Arsenophonus and Wolbachia, and the latter was the dominant symbiont in most populations.


Symbiotic associations between prokaryotic and eukaryotic organisms are ubiquitous in natural communities, and bacterial symbiosis has played a fundamental role in the evolution of eukaryotes, which range from parasitism to mutualism [2, 20, 32]. Many invertebrate hosts have been found to harbour multiple inherited symbionts within a single host [21, 27, 3034, 40]. Other than co-infection of different symbiont species, co-infections with multiple strains of the same symbiont species have also been found [7, 28].

Wolbachia is an intracellular symbiont that infects between 20 and 76% of arthropod species [14, 38]. Wolbachia has been known to coinfect and interact with various symbionts in the same host, and the superinfections vary with the species of symbionts and are also affected by many other factors, including the species of insect host, environmental conditions, etc. [7, 8, 21, 28]. In Bemisia tabaci, Wolbachia was found to be present with Hamiltonella or Cardinium or both genera [8]. Co-infection of Wolbachia and Cardinium was also found in Encarsia inaron [39], and superinfection with combination of Wolbachia and Spiroplasma occurs in Drosophila melanogaster, whereas an asymmetrical interaction occurs between Wolbachia and Spiroplasma in which the population of Wolbachia organisms is negatively affected by Spiroplasma organisms while the population of Spiroplasma organisms is not influenced by Wolbachia organisms [7]. The genus Arsenophonus is an emerging clade of symbiotic bacteria with a vast host distribution that includes parasitic wasps, triatomine bugs, psyllids, whiteflies, aphids, ticks, planthoppers, etc. [6, 8, 10, 24, 26, 35]. However, interactions among Arsenophonus and Wolbachia are poorly understood.

Brown planthopper Nilaparvata lugens Stål (Homoptera: Delphacidae) is a monophagous insect herbivore of rice that causes serious damage to rice crops. N. lugens has been known to harbour symbionts, including Wolbachia and Arsenophonus, and previous detection has shown that although Wolbachia and Arsenophonus were present in all 15 brown planthopper populations collected from China and Southeast Asian countries, coexistence was not observed in the same individuals from Laos [26]. In this study, we investigated the co-infection of Wolbachia and Arsenophonus in different populations of N. lugens collected from 5 sites in China, and then we established a single-infected line (infected with only Wolbachia) and a double-infected line (infected with both Wolbachia and Arsenophonus). Subsequently, we examined Wolbachia and Arsenophonus titres in the double- and single-infected N. lugens to assess whether these two symbionts interacted mutually or competitively.


Field collection of Nilaparvata lugens

All geographic populations of brown planthopper were collected from rice paddies in different locations of China. The details of each population were listed in Table 1. The planthoppers were maintained on rice seedlings at a constant temperature of 27 (± 1) °C and a light period of 14:10 h light:dark.

Table 1 Information for the different geographic populations of brown planthopper

Investigation of Wolbachia and Arsenophonus infection

To compare the co-infection of Wolbachia and Arsenophonus among different geographic populations of N. lugens, approximately 80 (64–88) adults were randomly collected from each population for a diagnostic PCR analysis. Extraction of DNA was the same as previously described, and only DNA samples with a ratio of OD260/OD280 ranging from 1.6 to 1.9 were used for the PCR detection [18]. The presence of Wolbachia and Arsenophonus was checked as previously described (Wolbachia: [41], Arsenophonus [31]).

Preparation of single-infected (Wolbachia) line and double-infected line (Wolbachia and Arsenophonus)

Geographic populations were set up as mass bred lines. The single-infected (Wolbachia) line and double-infected lines (Wolbachia and Arsenophonus) were developed from each geographic population of N. lugens. To minimize variation in the genetic background within populations, a pair of newly emerged female and male adults was randomly selected from the same population.

To ensure that only the single infection or the double infection was being considered, at first, newly emerged brown planthoppers from each line were screened for the presence of all the known symbionts in planthoppers, which consisted of Wolbachia, Arsenophonus, Cardinium hertigii, Acinetobacter, Chryseobaterium, Serratia and Arthrobacter as previously described (Wolbachia: [41], Arsenophonus [31]; Cardinium: [23]; Acinetobacter: [33]; Chryseobaterium: [1]; Serratia: [43]; Arthrobacter: [15]). Then female and male parents and their offspring that were only infected with Wolbachia or only infected with Wolbachia and Arsenophonus were kept for subsequent experiments.

Analysis of Wolbachia and Arsenophonus density

In order to measure the density of Wolbachia and Arsenophonus, the real-time quantitative PCR was performed with an ABI StepOne Real-Time PCR System (Applied Biosystems Inc, Foster City, CA, USA). For each line, a total of 10 female and male adults was collected as one sample, and the DNA was extracted with a Wizard® Genomic DNA Purification Kit (Promega, USA). The primers of Wolbachia and Arsenophonus for the reaction were as follows: (Wsp-F) 5′-ATGTAACTCCAGAAATCAAACTC-3′, (Wsp-R) 5′-GATACCAGCATCATCCTTAGC-3′; (ARS16S-F) 5′-TTCGGTCGGAACTCAAAGG-3′ (ARS16S-R) 5′-TCTGAGTTCCGCTTCCCATC-3′. The 20 µL quantitative PCR (qPCR) reaction system included 10 µL SYBR® Premix Ex Taq (Tli RNaseH Plus) (2X) (Takara, Japan), 0.4 µL forward and 0.4 µL reverse primers, 0.4 µL ROX Reference Dye, 2 µL DNA and 6.8 µL ddH2O. The RT-PCR program were as follows: 95 °C for 30 s, followed by 40 cycles of 95 °C for 5 s and 60 °C for 31 s, and then 95 °C for 15 s, 60 °C for 1 min, and a final step at 95 °C for 15 s. A standard curve using real-time fluorescent quantitative PCR of the Wolbachia wsp gene or the Arsenophonus ARS16S rDNA gene was performed to determine accurate Wolbachia or Arsenophonus gene copy numbers as described previously [42]. For each sample, there was three technical replicates, and for each line, there was three biological replicates.


The infection incidence of Arsenophonus and Wolbachia among different populations were compared using the Chi-square test, and the density of Arsenophonus between the double-infected line and single-infected line were compared using Student’s t test, the density of Wolbachia among different populations were tested by ANOVAs. IBM Statistics (SPSS 19.0) software was used for these statistical analyses.


Co-infection of Wolbachia and Arsenophonus varies with the population of Nilaparvata lugens

The symbionts Wolbachia and Arsenophonus were detected in all the 5 populations of N. lugens from China (Fig. 1). Compared to Wolbachia infection, Arsenophonus infection was more common in N. lugens, with the infection incidence of Arsenophonus ranging from 88.9 to 100%. In the MS and NJ populations, all the tested individuals were infected with Arsenophonus, and the infection incidence was significantly higher than that in the NT population (88.9%) (\(\chi_{4}^{2}\) = 17.196, P = 0.002, Fig. 1).

Fig. 1
figure 1

Co-infection incidences of the symbiont Arsenophonus and Wolbachia in 5 populations of N. lugens. A refers to all infections of Arsenophonus including single and double infections, and AW refers to double infections of Arsenophonus and Wolbachia. NN, MS, NJ, ZJ and NT refer to the Nanning, Maanshan, Nanjing, Zhenjiang and Nantong populations from China, respectively

In all 5 tested populations, Wolbachia infection always coexisted with Arsenophonus infection, and the co-infection incidence of Wolbachia and Arsenophonus was the equivalent to the incidence of Wolbachia infection. The co-infection incidence in the ZJ population was 50%, which was the highest value among the 5 populations, whereas the co-infection incidence in the MS and NJ populations was rare at only 2.3% and 1.5%, respectively, while this value in the NN and NT populations was 15.5% and 25%, respectively, and a significant difference was observed among populations (\(\chi_{4}^{2}\) = 75.457, P < 0.001, Fig. 1).

Coexistence of Wolbachia does not negatively affect the density of Arsenophonus in most populations of Nilaparvata lugens

When Arsenophonus coexisted with Wolbachia in N. lugens, Arsenophonus density between the double-infected line and single-infected line varied based on the population (Fig. 2). In double-infected lines established from the NN, NJ, ZJ and NT populations, the Arsenophonus density was not significantly different from that in the single-infected lines (NN: t = 0.813, df = 4, P = 0.462; NJ: t = 0.661, df = 4, P = 0.545; ZJ: t = 1.61, df = 4, P = 0.183; NT: t = 0.803, df = 4, P = 0.467), whereas in double-infected lines established from the MS population, the Arsenophonus density was significantly higher than that in single-infected line (MS: t = 5.66, df = 4, P = 0.005).

Fig. 2
figure 2

Comparison of Arsenophonus density in the double-infected and single-infected lines of N. lugens. A: single-infected line of Arsenophonus; and AW: double-infected line of Arsenophonus and Wolbachia. For each population, 60 adults including 30 females and 30 males were used for the analysis, and they divided into three biological replicates with 10 females and 10 males in each replicate. Significant differences between the double-infected and single-infected lines are marked by asterisks (**P < 0.01)

Dominance of Wolbachia and Arsenophonus varies with the population of Nilaparvata lugens

The Wolbachia density in the double-infection lines varied with the population (Fig. 3). In the line established from the ZJ population, the Wolbachia density was significantly higher than that in the lines from the MS, NJ, and NT populations (F4,14 = 8.832, P = 0.003).

Fig. 3
figure 3

Comparison of the Wolbachia density in the superinfection lines of N. lugens established from 5 populations. There are three biological replicates, and 10 females and 10 males were used in each replicate. Values were the mean ± SE (n = 3). The same lower-case letter above the bars indicated there was no significant difference among populations at the 5% level (based on Tukey’s multiple comparison test)

The relative ratio of Wolbachia and Arsenophonus quantity in the double-infected lines of N. lugens also varied with the geographic population (Fig. 4). In the double-infected lines from the NN, ZJ and NT populations, the ratio of Wolbachia quantity was nearly 100% while that of Arsenophonus quantity was all less than 0.4%; however, in the line from the NJ population, Arsenophonus was the dominant symbiont and its ratio was 91.7%, and in the double-infected line from the MS population, the ratio of Arsenophonus quantity was 8.3%.

Fig. 4
figure 4

Relative ratio of Wolbachia and Arsenophonus in the double-infection lines of N. lugens varied among geographic populations


When different symbionts are simultaneously present within the same host, interactions between them will take place, which might affect the dynamics of the microbial population. The interaction of the common endosymbiont Wolbachia with other symbionts has received increasing attention. An asymmetrical interaction has been found between Wolbachia and Spiroplasma [7]. Our aim in this study was to test whether interactions between Wolbachia and another popular symbiont, Arsenophonus, in the same host could affect the titre of the symbionts. We established 5 double-infected lines from different natural populations of N. lugens, and they were stable co-infections.

Previous studies have shown that the brown planthopper population from Laos was extensively infected by Wolbachia or Arsenophonus and the two bacteria may be exclusive in each host individual [26]. We found that Arsenophonus and Wolbachia could coexist in the same individual of brown planthopper in all the tested populations from China and differences among populations might result from differences in population resources.

The double-infection incidence of Wolbachia and Arsenophonus in brown planthopper varied with the geographical populations in China. In the ZJ population, the double-infection incidence was the highest, with half of the individuals simultaneously harbouring Wolbachia and Arsenophonus, whereas in the NJ and MS populations, less than 3% were infected with the two symbionts. The variance in double infection has been found in small brown planthopper, with a significantly higher co-infection incidence of Wolbachia and Serratia observed in the buprofezin-resistant strain compared with that of the buprofezin-susceptible strain [18].

Interactions between coexisting symbionts may affect infection densities because the symbionts may compete for available resources and space in the host body or they may share the resources and habitats by regulating their own exploitation to avoid damaging the whole symbiotic system [3, 12, 16, 29]. In pea aphids, the density of the primary symbiont Buchnera aphidicola is depressed when the insect is co-infected with Serratia symbiotica [16] or Rickettsia [29]. An antagonistic interaction between Hamiltonella and Cardinium has also been found in Bemisia tabaci, and the density of Cardinium increased across time and led to a decrease of Hamiltonella density [40]. Asymmetrical interactions have been found between the reproductive parasites Spiroplasma and Wolbachia in Drosophila melanogaster in which the population of Wolbachia organisms was affected by Spiroplasma while the population of Spiroplasma was not affected by Wolbachia [7]. Other than the interaction between different species of symbionts, interactions are also observed between different strains of the same symbiont. When multiple Wolbachia strains were observed in the same host, the density of each strain was specifically regulated [13, 17], which limited the segregation of symbionts through inefficient transmission by maintaining a sufficiently high density of each symbiont [4].

In our study, we found that in brown planthopper, co-infection with Wolbachia did not negatively affect eh Arsenophonus population and did not lead to lower net bacterial densities. In addition, the relative ratio of Wolbachia and Arsenophonus quantity in the double-infected lines of N. lugens varied with the geographic population. In the double-infected lines from the NN, ZJ, NT and MS populations, Wolbachia was the dominant symbiont, whereas in the double-infected line from the NJ population, Arsenophonus was the dominant symbiont and had a significantly higher density than that of Wolbachia. The difference in Arsenophonus density among lines might be related to the period of maintenance in the lab because the NJ population has been maintained for more than 14 years before investigation, which is at least 7 years longer than the other populations. This longer period of maintenance may possibly benefit the accumulation of Arsenophonus.

Wolbachia can provide protection against environmental stress, including RNA viruses and insecticides [11, 18, 19, 36], and this genus also confers certain fitness benefits to their hosts [22, 37]; however, Wolbachia can also have deleterious effects on the life history of their hosts [5, 9]. Arsenophonus was also found to provide protection against environmental stress, such as protection against the entomopathogenic fungi Metarhizium anisopliae [44], although it also induced negative effects on their hosts, such as decreasing the chemical insecticide (imidachloprid) resistance of rice brown planthopper [25]. Co-infection of Wolbachia and Arsenophonus is stable in brown planthopper, which raises the question of how these genera evolve and the effect that they have on the phenotype of their host.


Interactions of Wolbachia, the most common symbiont, with Arsenophonus, another widely distributed symbiont in nature has not been reported previously. Present study indicated that Wolbachia and Arsenophonus could coexist in N. lugens, and the co-infection incidence varied with the geographic populations. Antagonistic interactions were not observed between Arsenophonus and Wolbachia, and Wolbachia was the dominant symbiont in most populations.

Availability of data and materials

The datasets used and analysed during the current study are available from the corresponding author on reasonable request.


  1. Alonso C, Warnecke F, Amann R, Pernthaler J. High local and global diversity of Flavobacteria in marine plankton. Environ Microbiol. 2007;9:1253–66.

    Article  CAS  Google Scholar 

  2. Bright M, Bulgheresi S. A complex journey: transmission of microbial symbionts. Nat Rev Microbiol. 2010;8:218–30.

    Article  CAS  Google Scholar 

  3. Choisy M, de Roode JC. Mixed infections and the evolution of virulence: effects of resource competition, parasite plasticity, and impaired host immunity. Am Nat. 2010;175:E105–18.

    Article  Google Scholar 

  4. Engelstadter J, Hammerstein P, Hurst GDD. The evolution of endosymbiont density in doubly infected host species. J Evol Biol. 2007;20:685–95.

    Article  CAS  Google Scholar 

  5. Fleury F, Vavre F, Ris N, Fouillet P, Boulétreau M. Physiological cost induced by the maternally-transmitted endosymbiont Wolbachia in the Drosophila parasitoid Leptopilina heterotoma. Parasitology. 2000;121:493–500.

    Article  Google Scholar 

  6. Gherna RL, Werren JH, Weisburg W, Cote R, Woese CR, Mandelco L, Brenner DJ. Arsenophonus nasoniae gen. nov., sp. nov., the causative agent of the son-killer trait in the parasitic wasp Nasonia vitripennis. Internation. J Syst Evol Microbiol. 1991;41:563–5.

  7. Goto S, Anbutsu H, Fukatsu T. Asymmetrical Interactions between Wolbachia and Spiroplasma endosymbionts coexisting in the same insect host. Appl Environ Microbiol. 2006.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Guo HF, Qu YF, Liu XD, Zhong WF, Fang JC. Female-biased symbiont and tomato yellow leaf curl virus infection in Bemisia tabaci. PLoS ONE. 2014.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Hale LR, Hoffmann AA. Mitochondrial DNA polymorphism and cytoplasmic incompatibility in natural populations of Drosophila simulans. Evolution. 1990;44:1383–6.

    Article  Google Scholar 

  10. Hansen AK, Jeong G, Paine TD, Stouthamer R. Frequency of secondary symbiont infection in an invasive psyllid relates to parasitism pressure on a geographic scale in California. Appl Environ Microbiol. 2007;73:7531–5.

    Article  CAS  Google Scholar 

  11. Hedges LM, Brownlie JC, O’Neill SL, Johnson KN. Wolbachia and virus protection in insects. Science. 2008;322:702.

    Article  CAS  Google Scholar 

  12. Hughes WOH, Petersen KS, Ugelvig LV, Pedersen D, Thomsen L, Poulsen M, Boomsma JJ. Density-dependence and within-host competition in a semelparous parasite of leaf-cutting ants. BMC Evol Biol. 2004;4:45.

    Article  CAS  Google Scholar 

  13. Ikeda T, Ishikawa H, Sasaki T. Regulation of Wolbachia density in the Mediterranean flour moth, Ephestia kuehniella, and the almond moth Cadra cautella. Zoolog Sci. 2003;20:153–7.

    Article  Google Scholar 

  14. Jeyaprakash A, Hoy MA. Long PCR improves Wolbachia DNA amplification: wsp sequences found in 76% of sixty-three arthropod species. Insect Mol Biol. 2000;9:393–405.

    Article  CAS  Google Scholar 

  15. Koch C, Rainey FA, Stackebrandt E. 16S rDNA studies on members of Arthrobacter and Micrococcus: an aid for their future taxonomic restructing. FEMS Microbiol Lett. 1994;123:167–71.

    Article  CAS  Google Scholar 

  16. Koga R, Tsuchida T, Fukatsu T. Changing partners in an obligate symbiosis: a facultative endosymbiont can compensate for loss of the essential endosymbiont Buchnera in an aphid. Proc Biol Sci. 2003;270:2543–50.

    Article  Google Scholar 

  17. Kondo N, Shimada M, Fukatsu T. Infection density of Wolbachia endosymbiont affected by co-infection and host genotype. Biol Lett. 2005;1:488–91.

    Article  Google Scholar 

  18. Li Y, Liu X, Guo H. Variations in endosymbiont infection between buprofezin-resistant and susceptible strains of Laodelphax striatellus (Fallén). Curr Microbiol. 2018.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Liu XD, Guo HF. Correlation between insecticide resistance and endosymboints Wolbachia and Rickettsia. Cur Opin Insect Sci. 2019;33:84–90.

    Article  Google Scholar 

  20. Łukasik P, van Asch M, Guo H, Ferrari J, Godfray HCJ. Unrelated facultative endosymbionts protect aphids against a fungal pathogen. Ecol Lett. 2013;16:214–8.

    Article  Google Scholar 

  21. McLean AHC, Benjamin JP, Hrček J, Kavanagh JC, Wellham PAD, Godfray HCJ. Consequences of symbiont co-infections for insect host phenotypes. J Anim Ecol. 2018;87:478–88.

    Article  Google Scholar 

  22. Moriyama M, Nikoh N, Hosokawa T, Fukatsu T. Riboflavin provisioning underlies Wolbachia’s fitness contribution to its insect host. mBio. 2015.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Nakamura Y, Kawai S, Yukuhiro F, Ito S, Gotoh T, Kisimoto R, Yanase T, Matsumoto Y, Kageyama D, Noda H. Prevalence of Cardinium bacteria in planthoppers and spider mites and taxonomic revision of “Candidatus Cardinium hertigii” based on detection of a new Cardinium group from biting midges. Appl Environ Microbiol. 2009;75:6757–63.

    Article  CAS  Google Scholar 

  24. Nováková E, Hypša V, Moran NA. Arsenophonus, an emerging clade of intracellular symbionts with a broad host distribution. BMC Microbiol. 2009;9:143.

    Article  Google Scholar 

  25. Pang R, Chen M, Yue L, Xing K, Li T, Kang K, Liang Z, Yuan L, Zhang W. A distinct strain of Arsenophonus symbiont decrease insecticide resistance in its insect host. PLoS Genet. 2018;14:e1007725.

    Article  Google Scholar 

  26. Qu LY, Lou YH, Fan HW, Ye YX, Huang HJ, Hu MQ, Zhu YN, Zhang CX. Two endosymbiotic bacteria, Wolbachia and Arsenophonus, in the brown planthopper Nilaparvata lugens. Symbiosis. 2013;61:47–53.

    Article  Google Scholar 

  27. Read AF, Taylor LH. The ecology of genetically diverse infections. Science. 2001;292:1099–102.

    Article  CAS  Google Scholar 

  28. Russell JA, Weldon S, Smith AH, Kim KL, Hu Y, Łukasik P, Doll S, Anastopoulos I, Novin M, Oliver KM. Uncovering symbiont-driven genetic diversity across North American pea aphids. Mol Ecol. 2013;22:2045–59.

    Article  Google Scholar 

  29. Sakurai M, Koga R, Tsuchida T, Meng XY, Fukatsu T. Rickettsia symbiont in the pea aphid Acyrthosiphon pisum: novel cellular tropism, effect on host fitness, and interaction with the essential symbiont Buchnera. Appl Environ Microbiol. 2005;71:4069–75.

    Article  CAS  Google Scholar 

  30. Skaljac M, Zanic K, Ban SG, Kontsedalov S, Ghanim M. Co-infection and localization of secondary symbionts in two whitefly species. BMC Microbiol. 2010;10:142.

    Article  Google Scholar 

  31. Thao ML, Baumann P. Evidence for multiple acquisition of Arsenophonus by whitefly species (Sternorrhyncha: Aleyrodidae). Curr Microbiol. 2004;48:140–4.

    Article  CAS  Google Scholar 

  32. Toft C, Andersson SG. Evolutionary microbial genomics: insights into bacterial host adaptation. Nat Rev Genet. 2010;11:465–75.

    Article  CAS  Google Scholar 

  33. Vanbroekhoven K, Ryngaert A, Wattiau P, Mot RD, Springael D. Acinetobacter diversity in environmental samples assessed by 16S rRNA gene PCR–DGGE fingerprinting. FEMs Microbiol Ecol. 2004;50:37–50.

    Article  CAS  Google Scholar 

  34. Vautrin E, Vavre F. Interactions between vertically transmitted symbionts: cooperation or conflict? Trends Microbiol. 2009;17:95–9.

    Article  CAS  Google Scholar 

  35. Wagner SM, Martinez AJ, Ruan Y, Kim KL, Lenhart PA, Dehnel AC, Oliver KM, White JA. Facultative endosymbionts mediate dietary breadth in a polyphagous herbivore. Funct Ecol. 2015;29:1402–10.

    Article  Google Scholar 

  36. Walker T, Johnson PH, Moreira LA, Iturbe-Ormaetxe I, Frentiu FD, McMeniman CJ, Leong YS, Dong Y, Axford J, Kriesner P, Lloyd AL, Ritchie SA, O’Neill SL, Hoffmann AA. The wMel Wolbachia strain blocks dengue and invades caged Aedes aegypti populations. Nature. 2011;476:450–3.

  37. Weeks AR, Turelli M, Harcombe WR, Reynolds KT, Hoffmann AA. From parasite to mutualist: rapid evolution of Wolbachia in natural populations of Drosophila. PLoS Biol. 2007.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Werren JH, Baldo L, Clark ME. Wolbachia: master manipulators of invertebrate biology. Nat Rev Microbiol. 2008;6:741–51.

    Article  CAS  Google Scholar 

  39. White JA, Kelly SE, Cockburn SN, Perlman SJ, Hunter MS. Endosymbiont costs and benefits in a parasitoid infected with both Wolbachia and Cardinium. Heredity. 2011;106:585–91.

    Article  CAS  Google Scholar 

  40. Zhao DX, Hoffmann AA, Zhang ZC, Niu HT, Guo HF. Interaction between facultative symbionts Hamiltonella and Cardinium in Bemisia tabaci: cooperation or conflict? J Econ Entomol. 2018;111:2660–6.

    Article  Google Scholar 

  41. Zhou WG, Rousset F, O’Neill S. Phylogeny and PCR–based classification of Wolbachia strains using wsp gene sequences. Proc R Soc Lond B. 1998;265:509–15.

    Article  CAS  Google Scholar 

  42. Zhou LL, Zhang KJ, Song ZW, Hong XY. Relationship of WO phage and Wolbachia infection in Laodelphax striatellus (Fallén) (Hemiptera: Delphacidae). Acta Entomol Sin. 2010; 53:978–84 (in Chinese).

  43. Zhu H, Sun SJ, Dang HY. PCR detection of Serratia spp. using primers targeting pfs and luxS genes involved in AI-2-dependent quorum sensing. Curr Microbiol. 2008;57:326–30.

    Article  CAS  Google Scholar 

  44. Zhu HH, Chen Y, Wan PJ, Wang WX, Lai FX, Fu Q. Influence of symbiotic bacteria Arsenophonus, rice variety and temperature on the incidence rate of Nilaparvata lugens to Metarhizium flavoviride. Chin J Rice Sci. 2017;31:643–51 ((in Chinese)).

    Google Scholar 

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This research was supported by grants from the National Natural Science Foundation of China (Grant Nos. 31972265, 31672027). The funding body had no role in the design of the experiment; the collection, analysis, and interpretation of the data; or the writing of the manuscript.

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HG analyzed the infection incidence of symbionts, and was a major contributor in writing the manuscript. NA established most of the lines and analyzed the quantity of symbionts. HN collected part of the samples from fields. DZ established part of the lines. ZZ collected part of the samples from fields. All authors read and approved the final manuscript.

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Correspondence to Huifang Guo.

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Guo, H., Wang, N., Niu, H. et al. Interaction of Arsenophonus with Wolbachia in Nilaparvata lugens. BMC Ecol Evo 21, 31 (2021).

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