Figures
Abstract
Whiteflies (Hemiptera: Aleyrodidae) are sap-sucking insect pests, and some cause serious damage in agricultural crops by direct feeding and by transmitting plant viruses. Whiteflies maintain close associations with bacterial endosymbionts that can significantly influence their biology. All whitefly species harbor a primary endosymbiont, and a diverse array of secondary endosymbionts. In this study, we surveyed 34 whitefly populations collected from the states of Sao Paulo, Bahia, Minas Gerais and Parana in Brazil, for species identification and for infection with secondary endosymbionts. Sequencing the mitochondrial Cytochrome Oxidase I gene revealed the existence of five whitefly species: The sweetpotato whitefly Bemisia tabaci B biotype (recently termed Middle East-Asia Minor 1 or MEAM1), the greenhouse whitefly Trialeurodes vaporariorum, B. tabaci A biotype (recently termed New World 2 or NW2) collected only from Euphorbia, the Acacia whitefly Tetraleurodes acaciae and Bemisia tuberculata both were detected only on cassava. Sequencing rRNA genes showed that Hamiltonella and Rickettsia were highly prevalent in all MEAM1 populations, while Cardinium was close to fixation in only three populations. Surprisingly, some MEAM1 individuals and one NW2 population were infected with Fritschea. Arsenopnohus was the only endosymbiont detected in T. vaporariorum. In T. acaciae and B. tuberculata populations collected from cassava, Wolbachia was fixed in B. tuberculata and was highly prevalent in T. acaciae. Interestingly, while B. tuberculata was additionally infected with Arsenophonus, T. acaciae was infected with Cardinium and Fritschea. Fluorescence in situ hybridization analysis on representative individuals showed that Hamiltonella, Arsenopnohus and Fritschea were localized inside the bacteriome, Cardinium and Wolbachia exhibited dual localization patterns inside and outside the bacteriome, and Rickettsia showed strict localization outside the bacteriome. This study is the first survey of whitely populations collected in Brazil, and provides further insights into the complexity of infection with secondary endosymionts in whiteflies.
Citation: Marubayashi JM, Kliot A, Yuki VA, Rezende JAM, Krause-Sakate R, Pavan MA, et al. (2014) Diversity and Localization of Bacterial Endosymbionts from Whitefly Species Collected in Brazil. PLoS ONE 9(9): e108363. https://doi.org/10.1371/journal.pone.0108363
Editor: Kostas Bourtzis, International Atomic Energy Agency, Austria
Received: May 2, 2014; Accepted: August 25, 2014; Published: September 26, 2014
Copyright: © 2014 Marubayashi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All relevant data are included within the paper.
Funding: JMM received a fellowship from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) scholarship number 9521/11-9. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: MG declares that they are a PLOS ONE editorial board member and that this does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials.
Introduction
The whitefly, Bemisia tabaci Gennadius (Hemiptera: Aleyrodidae) is one of the most devastating insect pests of the 20th century, being cosmopolitan and polyphagous [1]. In addition to the direct damage caused by feeding on the plant phloem and secretion of honeydew, B. tabaci is known as vector of more than 100 plant viruses from different genera including Begomovirus, Crinivirus, Carlavirus and others [2], [3].
B. tabaci is considered a complex of cryptic species, which are also sometimes termed “biotypes”, and are characterized as genetic variants or haplotypes that differ in molecular and biological characteristics [4]. Based on the molecular and biological aspects of B. tabaci it is classified into about 35 species [1], [5], [6], [7]. For example, biotypes B and B2 belong to the new termed Middle East-Asia Minor 1 (MEAM1) species; the biotypes Q, J, L, Sub-Saharan Africa, the Silver-leafing biotypes and Mediterranean all belong to the group termed Africa/Middle East/Asia Minor, and the biotypes known as A, C, D, F, Jatropha, N, R and Sida belong to the New World group that includes New World (NW) and New World 2 (NW2) species [1], [5]. Based on the new classification, the species MEAM1, NW and NW2 were recently investigated in Brazil [8]. In addition to B. tabaci, other whitefly species such as Bemisia tuberculata, Tetraleurodes acaciae and Trialeurodes vaporariorum are known to be present in Brazil. For example B. tuberculata has been shown to colonize cassava plants in the states of São Paulo, Mato Grosso and Rio de Janeiro [9], [10], [11], while the greenhouse whitefly T. vaporariorum, was associated with outbreaks in 2003 in horticultural and ornamental crops in the state of São Paulo [12].
Whiteflies, similar to many other arthropods, are usually infected with bacterial endosymbionts that may influence their biology and their interaction with other organisms or the environment [13]. Whiteflies harbor the primary obligatory endosymbiont Portiera aleyrodidarum [14], [15], which is essential for the species persistence and for complementing the insect’s unbalanced diet that consists mainly sugars from the plant phloem. Besides Portiera, whitefly populations from around the world were reported to harbor a diverse array of facultative secondary endosymbionts which are not essential for the species persistence and those include the Gammaproteobacteria Arsenophonus (Enterobacteriales), Hamiltonella (Enterobacteriales) [16], [17], Fritschea (Chlamydiales) [18], Cardinium (Bacteroidetes) [19], the alphaproteobacteria Rickettsia (Rickettsiales) [20], Wolbachia (Rickettsiales) [21], [22], and Orientia-like organism [23]. Several whitefly populations around the world were surveyed for infection with endosymbionts and a clear association between biotypes and secondary symbionts were often observed. For example, in populations tested from Israel Hamiltonella was detected only in the B biotype, Wolbachia and Arsenophonus only in the Q biotype, and Rickettsia in both biotypes [24]. None of the populations from Israel were infected with Fritschea or Cardinium. Fritschea has only been detected in the A biotype (NW2) from the United States [25], and only Arsenophonus has been associated with T. vaporariorum [16]. Cardinium was detected in B and Q biotype populations from China [26], Q populations from Croatia [27], [28], and France [29]. Additional T. vaporariorum populations were analyzed from Croatia and were reported to be infected with Portiera and Hamiltonella in addition to the previously reported infection with Arsenophonus [27]. Other whitefly species such as the ash whitefly Siphoninus phillyreae (Haliday) from Croatia were surveyed and the same endosymbionts were detected similar to other whitefly species [28].
In the current study, different populations representing five whitefly species collected in four states in Brazil were surveyed for infection with secondary endosymbionts, and the identified endosymbionts were localized in adult individuals using fluorescence in situ hybridization (FISH) analysis. The results provide new infections with endosymbionts in whitefly species that have not been reported before, adding further complexity to the already known endosymbiont bacterial infections among whitefly populations around the world.
Results
Identification of whitefly species
Altogether 34 populations were analyzed in this study. The populations were collected from four states in Brazil between 2010–2012, from different locations and host plants as shown in Table 1. Varying numbers of individuals, depending on availability, from each population were analyzed for infection with six different secondary endosymbionts: Hamiltonella, Rickettsia, Cardinium, Wolbachia, Arsenophonus and Fritschea. PCR targeting Portiera, the primary endosymbionts, was performed as a positive control for the reaction. PCR and sequencing analyses were further performed for determining the whitefly species and biotypes using the COI gene amplification and sequencing and microsatellite primers as detailed in the methods section. Twenty two populations were identified as B. tabaci MEAM1 species (B biotype), while one population was identified as the NW2 (Table 1). Other whitefly species that were identified based on COI gene amplification are: four populations of B. tuberculata, three populations of T. acaciae and four populations of T. vaporariorum (Table 1).
B. tabaci infection with secondary endosymbionts
Individual whiteflies were analyzed for infection with the six secondary endosymbionts using genus-specific primers (Table 2), and each individual was tested for infection with Portiera, the primary endosymbionts, as a positive control. Figure 1 shows the infection with endosymbionts of all individuals that were tested from each population and the mixed infections with multiple endosymbionts within each individual. For example ten individuals from the population collected in Votuporanga from cabbage were tested, and all these individuals were co-infected with Hamiltonella and Rickettsia, while the other secondary endosymbionts were not detected. The most prevalent co-infection observed in the tested populations was individuals doubly infected with Hamiltonella and Rickettsia (64.20%). Most of the individuals from three populations collected in Itapeva, Dom Basilio and Londrina were simultaneously infected with Hamiltonella, Rickettsia and Cardinium, and the prevalence of triply infected individuals was 14.22%. Other single, double and triple infections from B. tabaci MEAM1 populations were also observed and those included individuals infected with only Rickettsia or only Hamiltonella, individuals infected with Hamiltonella and Fritschea (Patos de Minas) and two individuals infected with Hamiltonella, Rickettsia and Fritschea. Interestingly, only three individuals among total of 204 individuals that were analyzed were not infected with any secondary endosymbionts while the rest were infected with at least one endosymbiont (98.04% infection rate). 91.67% of the individuals were infected with Rickettsia, 87.25% with Hamiltonella, 14.22% with Cardinium, 4.90% with Fritschea. The four individuals in the only population that was identified as NW2 were infected with Hamiltonella, Cardinium and Fritschea.
Twenty two MEAM1 (B biotype) and one NW2 (A biotype) populations were collected and surveyed. Each box represents one population. Vertical columns represent the different symbionts tested as indicated in the base of each column, and each horizontal column represents one individual that was tested for the presence of the six different symbionts. Shaded boxes represent positive infection with the tested symbiont. The geographical origin of the populations, the species and the number of individuals tested are indicated at the top of each box (see Table 1 for full names).
T. vaporariorum, T. acacia and B. tuberculata infection with secondary endosymbionts
The prevalence of T. vaporariorum was much lower than B. tabaci in the surveyed regions. Thirty five T. vaporariurom individuals from four different regions of the State of Sao Paulo were tested for infection with the six different endosymbionts (Fig. 2). The primary endosymbiont Portiera was detected in all individuals, while among the secondary endosymbionts only Arsenophonus was detected as a single infection (94.28% of the tested individuals) in all individuals except one individual from Apiai and a second individual from Bom sucesso do itarare, both were uninfected with none of the secondary endosymbionts (Fig. 2). Two additional whitefly species were detected in the survey we performed. Both species, B. tuberculata and T. acaciae, were detected only on cassava plants (Table 1). Four B. tuberculata and three T. acacia populations were analyzed for infections with endosymbionts.
Four populations of T. vaporariorum (T. v.), 4 populations of B. tuberculata (B. tub.) and 3 populations of T. acaciae (T. a.) were collected and analyzed in this study (See legend to figure 2 for more details).
Among B. tuberculata tested individuals, 96.97% were infected with at least one endosymbiont, while only one individual was not infected with any secondary endosymbiont (Fig. 2). Wolbachia and Arsenophonus were detected in single or mixed infections in all four populations analyzed. Arsenophonus was the most prevalent endosymbiont with 81.82% infection rate and Wolbachia with 84.85% infection rate. Interestingly, Fritschea appeared in 15.15% infection rate, while Cardinium with 12.12%, and both appeared in single or mixed infections. One individual was infected with Fritschea, one individual with only Fritschea and Cardinium both collected in Votuporanga, and one individual collected from Assis was infected with the four endosymbionts detected in B. tuberculata: Wolbachia, Arsenophonus, Fritschea and Cardinium.
Among T. acaciae populations, three endosymbionts were detected: Wolbachia, Cardinium and Fritschea. All tested individuals were infected with at least one endosymbiont (Fig. 2). Wolbachia appears to be fixed in T. acaciae populations with all individuals harboring this endosymbiont. The triple infection with the three detected endosymbionts was the most prevalent infection pattern with 85.71% of the individuals showing this infection pattern. Among the 28 tested individuals only one individual showed single infection with Wolbachia, one individual showed double infection with Wolbachia and Cardinium and one individual showed double infection with Wolbachia and Fritschea (Fig. 2).
Localization of secondary endosymbionts in whitefly species collected in Brazil
All detected secondary endosymbionts in the populations collected in Brazil were localized in all developmental stages using FISH analysis. All the previously reported localization patterns for endosymbionts in whiteflies from complete confinement within the bacteriome to complete localization outside the bacteriome, and dual localization patterns inside and outside the bacteriome were observed.
Four endosymbionts were detected in B. tabaci: Hamiltonella, Rickettsia, Cardinium and Fritschea. Hamiltonella was detected only in B. tabaci MEAM1 and NW2 species (Fig. 1) and localization experiments showed that this bacterium is always confined in the bacteriosome cells, co-localizing with Portiera, the primary endosymbionts (Fig. 3). Hamiltonella cells were localized is small patches inside bacteriocyte cells and did not occupy the whole cavity of the cell. This localization pattern was observed in all developmental stages: eggs, nymphal stages and adults. Rickettsia was localized outside the bacteriome and occupied most of the body cavity, but not bacteriocyte cells. This localization pattern was observed in all developmental stages. Close inspection of Rickettsia localization patterns showed that it infects many organs.
A–B: FISH of Arsenophonus (yellow) and Portiera (red) in T. vaporariorum under bright field (A) and dark field (B). C–D: FISH of Fritschea (blue) and Portiera (red) in NW2 under bright field (C) and dark field (D). E–F: FISH of Hamiltonella (green) and Portiera (red) in MEAM1 under bright field (E) and dark field (F). G–H: FISH of Rickettsia (blue) and Portiera (red) in MEAM1 under bright field (G) and dark field (H). I–J: FISH of Cardinium (blue) and Portiera (red) in T. acaciae under bright field (I) and dark field (J). K–L: FISH of Wolbachia (blue) in B. tuberculata under bright field (K) and dark field (L). T: testicle.
Two additional endosymbionts that were localized inside the bacteriome are Arsenophonus and Fritschea. Arsenophonus, which was not detected from B. tabaci and T. acaciae, but was present in T. vaporariorum and B. tuberculate, localized in both species inside bacteriocyte cells with Portiera, the primary endosymbiont. Arsenophonus localized in patches and appeared in rod-shaped structures, unlike the other endosymbionts. Fritschea was localized in all tested whitefly species except in T. vaporariorum also inside bacteriocute cells, however, the localization signal was weak and the concentration of the bacterium seemed very low.
Two endosymbionts that were detected in this study, Wolbachia and Cardinium, exhibited dual localization pattern inside and outside the bacteriome (Fig. 3). These two bacteria were detected in B. tabaci, B. tuberculata and T. acaciae. The localization pattern in the three species did not differ for the two endosymbionts; however both symbionts appeared in very low concentration. As in previous reports, Wolbachia is localized on the circumference or within the bacteriocytes with the primary endosymbiont. Additionally, although Wolbachia can be found outside bacteriocyte cells, it is always localized adjacent to those cells in the abdomen and not seen in other parts of the insect such as the thorax and the head.
Discussion
This study presents, for the first time, a comprehensive survey of whitefly species that were detected in four states in eastern Brazil: São Paulo, Parana, Bahia and Minas Gerais. Altogether 34 populations were collected from different host plants and tested for whitefly species identity and infections with bacterial endosymbionts using PCR and sequencing (Tables 1 & 2). The majority of B. tabaci populations were collected in São Paulo while only few populations were collected in the remaining states. Twenty three of the collected populations in the four states were identified as MEAM1 species, four were T. vaporariorum, four B. tuberculate, three populations were identified as T. acaciae and one population as NW2. All other whitefly species that were not MEAM1 were collected only in São Paulo state. MEAM1 populations were collected from different host plants, suggesting that none of the host plants was a preferred host for this species, which emphasizes its known polyphagy.
B. tabaci populations collected in this study all belonged to the MEAM1 species and only one population collected from Euphorbia was identified as NW2 (Table 1). MEAM1 populations were found to harbor Hamiltonella, Rickettsia, Cardinium and surprisingly some individuals were also infected with Fritschea, which also infected all individuals from the only NW2 population. The identity of Fritschea was verified by sequencing the amplified 23 S rRNA gene fragments. Previous surveys of whitefly species in some parts of the world that included MEAM1, MED and others, such as in Israel [24], China [26], Croatia [27], [28] and some European and African countries [29], revealed that Fritschea does not infect any of the surveyed populations, and that this bacterium was only reported from the USA infecting the A biotype (NW) [18]. To assess the variability of the bacterial species infecting the surveyed populations tested in this study, the 16 S or 23 S rRNA gene sequences were obtained. The results revealed that for each bacterial species no variability was observed and it is likely that one strain from each bacterium was detected in the surveyed populations in this study, indicating that single infections, or single introductions of whiteflies infected with those endosymbionts are the origin of the observed bacterial populations. For example, sequences from Fritschea that was detected in MEAM1 and NW2 showed 100% homology, suggesting that the same strain of Fritschea colonize both whitefly species, which may indicate a horizontal transfer or ancestral single infection with Fritschea between the two species by sharing host plant [34], [35]. Endosymbionts can be injected into the plant vascular system from which they can be acquired and established in new arthropod hosts [36]. A recent study has shown that salivary glands can indeed be infected by endosymbionts, as in the case of Cardinium in Scaphoideus titanus [37], [38]. An additional study has shown that Rickettsia in whiteflies can be horizontally transmitted through the plant vascular system [39], presenting its ability to colonize distantly related insect species through common plant hosts.
T. vaporariorum populations collected from São Paulo were found to be infected only with Arsenophonus, unlike T. vaporariorum populations previously tested in Croatia that were shown to be infected with Hamiltonella and Arsenophonus [27], [28]. The only other whitefly species that was found to be infected with Arsenophonus in this study is B. tuberculata, which was found to colonize only cassava plants. It is hard to hypothesize how this symbiont infects these distantly related insects and again it might be a recent horizontal transfer or an infection of an ancient ancestor. Other symbiont strains that were shared between distantly related whitefly species collected in this study are Cardinium which was shared between MEAM1, NW2, B. tuberculata and T. acaciae, and Fritschea which was also shared between all whitefly species except for T. vaporariorum. Other examples included B. tuberculata infection with Wolbachia, Cardinium and Fritschea, infection of B. tabaci MEAM1 with Hamiltonella, Rickettsia, Cardinium and Fritschea, the infection of NW2 with Hamiltonella, Cardinium and Fritschea and the infection of T. acaciae with Wolbachia, Cardinium and Fritschea. Some populations showed very low infection rates with some of the symbionts such as the infection of some MEAM1 populations with Fritschea and Cardinium. This result can be attributed to recent introduction of new whitefly populations with specific symbiont infections into Brazil, or instability or rarity of some whitefly-endosymbiont combinations under certain conditions such as climate, predation, agricultural practices and more. Several internal factors may influence maximum infection rates in the same individuals. These factors include competition for space and resources among two or more endosymbionts [33], [40], or on the contrary, positive interaction, cooperation and dependence of one endosymbiont on the other [41]. Another important factor is the insect host response to the presence of these symbionts which in most cases will influence the bacterial community residing within this host. In general, infection with secondary symbionts, without reaching fixation suggests that those bacteria are not essential for the insect, while bacteria that reached fixation or close to fixation indicate mutualistic relationships. For example, Hamiltonella was shown to infect only 40% of the pea aphid individuals tested from California, while only 0–40% were infected with Rickettsia [42], [43], [44], [45], [46], [47]. Hamiltonella reached fixation in B. tabaci populations, like those tested from Israel [24], [27], [28], [29], indicating some mutualistic or obligatory relationships, with the insect or the primary endosymbiont as Hamiltonella was always localized inside bacteriome cells with the primary endosmbiont Portiera. Such interactions might be complementing the host’s diet, increasing its fitness or coping with environmental conditions such as resistance to extreme conditions.
B. tuberculata and T. acaciae were not previously surveyed with regard to infection with secondary endosymbionts. Both species strictly share the same host plant and can be found in sympatry on cassava, and were not detected on other plant hosts. Although it is not known when those two species became specialized on cassava in Brazil, it is not surprising that both species share some secondary endosymbionts including Wolbachia, Cardinium and Fritschea. Interestingly, Fritschea was previously reported only from the A biotype [18], and this is the first time that this Chlamydia is reported to be infecting other whitefly species with such a high prevalence, sometimes reaching fixation or near fixation, such as in the case of T. acaciae populations tested in this study. This high prevalence suggests intimate association between Fritschea and T. acaciae, and may hint on an important role that this chlamydia is playing in the biology of T. acaciae. In B. tuberculata, however, Fritschea appeared in only 14% of the tested individuals, and some populations did not harbor it, such is the populations collected from C. Mota and Cardoso (Fig. 2). Since T. acaciae and B. tuberculate share the same plant host, they are also likely to share common parasitoids. It has been previously shown that Rickettsia from B. tabaci was acquired by three whitefly parasitoids Eretmocerus emiratus, Eretmocerus eremicus and Encarsia pergandiella, however was not vertically transferred to offspring of these parasotoid species [48]. This study demonstrated the potential routes and barriers to horizontal transmission of symbionts across trophic levels, and suggests that the common symbionts between T. acaciae and B. tuberculate observed in our study might be also horizontally transferred via parasitization by common whitefly parasitoids, as the ones investigated in this study [48]. Similarly, Wolbachia has been shown to be transmitted to the parasitic wasp Leptopilina boulardi from its infected host Drosophila simulans, and subsequently undergo diminishing vertical transmission in this novel host species [49].
Arsenophonus was the only endosymbiont that infected B. tuberculata populations but did not appear in T. acaciae (Fig. 2). This bacterium was fixed in some populations such as in Assis, close to fixation such is in C. Mota and Cardoso, and appeared only in one individual such as in the case of the populations collected from Votup (Fig. 2). Arsenophonus have been implicated in reproductive manipulations in a wide range of insect species by inducing the male-killing phenotype [50], and might be acting like such in B. tuberculata. This bacterium was localizaed inside the bacteriosome cells by FISH analysis (Fig. 3), suggesting that it is strictly vertically transmitted and this might be the cause for its absence from T. acaciae that colonize the same host plants.
In addition to Arsenophonus which was localized to bacteriocyte cells, the other endosymbionts detected in this study were localized in representative specimens. Hamiltonella and Fritschea, in addition to Arsenophonus, were strictly localized inside bacteriocye cells (Fig. 3) in MEAM1, NW2, B. tuberculata and T. acaciae. Cardinium and Wolbachia were observed inside and outside bacteriocyte cells (Fig. 3), but appeared in very low concentrations. Only Rickettsia strictly appeared outside the bacteriome and was never observed inside (Fig. 3). These localization patterns appeared in all developmental stages: eggs, nymphs and adults. Endosymbionts that are strictly localized to the bacteriocytes are vertically transmitted and thus they may contribute to their host’s fitness [54], similar to effects induced by symbionts localized outside bacteriocytes such as Wolbachia and Rickettsia. However, those endosymbionts are less likely to manipulate their host’s reproduction since this requires invading reproductive organs outside the bacteriome. Wolbachia and Cardinium showed dual localization patterns. They can be found in many insect orders at various different frequencies, and were indeed associated with reproductive disorders [51], [53]. Additionally Wolbachia is an extensively studied symbiont that has been shown to induce many effects on its arthropod hosts, including effects on mosquito species hosts, an effect that has been recently employed in controlling the spread of the Dengue virus [55], [56]. The low concentration of Wolbachia and its dual localization pattern in B. tuberculata and T. acaciae suggests that it may play a role in reproductive manipulation; however, other effects cannot be ruled out and more research is required to confirm this assumption.
In contrast to the rest of the detected endosymbionts in this study, only Rickettsia showed a scattered localization pattern and was observed outside the bacteriome infecting tissues in the abdomen, thorax and head as was recently shown [57]. Rickettsia was shown to manipulate host reproduction in many arthropods [50], [52], and this fits well with its localization pattern in B. tabaci. Previously, Rickettsia has been shown to exhibit two different localization phenotypes: scattered throughout the body and confined to the bacteriome [33]. These two phenotypes were never observed together in the same individuals; however, one study that tested populations from Croatia showed that those two phenotypes were observed in the same individual [27]. Our FISH results showed the presence of only the scattered phenotype in MEAM1 populations where Rickettsia was detected (Fig. 2). This phenotype is different from the obligatory Rickettsia in booklice, in which it was found to appear with both phenotypes in the same individual [58]. A recent study has demonstrated that Rickettsia is transovarially transmitted to B. tabaci subsequent generation by invading developing oocytes and follicular cells, thus being included in individuals that develop from those oocytes [57]. Rickettsia has been shown to reach high prevalence and near fixation in natural populations as was recently shown in Arizona [59]. The later study has further shown that Rickettsia-infected B. tabaci females exhibit high fitness benefits such as increased fecundity, a greater rate of survival, and host reproduction manipulation via the production of a higher proportion of daughters [59]. A recent study has shown that Rickettsia is horizontally transmitted between individuals through the host plant [39]. Additional studies have shown that the presence of Rickettsia in B. tabaci populations influenced the whitefly’s response to heat stress by benefitting its host under high temperatures [60], and has also shown to increase the whitefly’s susceptibility to chemical insecticides [61]. Studies on Rickettsia from other invertebrates have revealed diverse effects of the bacteria on their hosts. For example, in the pea aphid Acyrthosiphon pisum, Rickettsia-infected individuals showed lower fresh body weight, reduced fecundity and significantly suppressed densities of Buchnera, suggesting a negative effect of Rickettsia [62], [63]. Reproductive manipulation and Rickettsia-associated parthenogenesis have been shown in the endoparasitoid Neochrysocharis formosa [64], and in the parasitoid wasp Pnigalio soemius [65], as has Rickettsia-associated male-killing in beetles [66], [67], and involvement in oogenesis of booklice [68]. Although none of the later phenomena associated with Rickettsia have been investigated in this study, it will be interesting to investigate such interactions of Rickettsia with whitefly populations in Brazil.
Materials and Methods
Collection of whiteflies
Most of the whitefly samples tested in this study were collected from the state of São Paulo and some samples were collected from the states of Bahia, Minas Gerais and Paraná in eastern Brazil during the years 2010 to 2012. No specific permissions were required for collecting all the samples in this study in all locations presented in Table 1, and this study did not involve endangered or protected species. The insects were collected as adults using a hand-held aspirator and immediately preserved in 100% ethanol or fixative solution (See below) until further processing for endosymbiont or biotype genotyping, or for FISH analysis. Table 1 summarizes the whitefly populations collected and analyzed in this study.
DNA Extraction and PCR for B and Q biotype identification
DNA was extracted from individual whiteflies as previously described [28]. Four to ten individual adults per population were analyzed for initial species identification using the Bem23 primer pair: Bem23F (5′-CGGAGCTTGCGCCTTAGTC-3′) and Bem23R (5′-CGGCTTTATCATAGCTCTCGT-3′) [30] that distinguish the biotypes B based and Q based on PCR fragment size.
Whitefly species identity confirmation for MEAM1, NW2, B. tuberculata and T. acaciae was performed by PCR and sequencing using the primer pair C1-J-2195 (5′-TTGATTTTTTGGTCATCCAGAAGT-3′) and L2-N-3014 (5′-TCCAATGCACTAATCTGCCATATTA-3′) that amplify a fragment from the mitochondrial cytochrome oxidase I gene (mtCOI) [31]. For T. vaporariorum the primer pair Tvap-F (5′-GGCATTATTTCTCATCTTATTAGTGCT-3′) and Tvap-R (5′-GTGAYTAAGRGMTGGYTTATT-3′) that amplify mtCOI from this species [32] were used. The sequences obtained were verified using BLAST tool in NCBI. Obtained sequences from the different whitefly species were deposited in GenBank and assigned the accession numbers KM368235, KM368236, KM368246–KM368249 and KM368251–KM368255.
Bacterial endosymbiont
The same DNA originated from each individual was used for the screening of all six secondary endosymbionts Hamiltonella, Rickettsia, Wolbachia, Arsenophonus, Cardinium and Fritschea using genus-specific primers (Table 2) targeting the 16 S or 23 S rDNA genes. PCR cycling was performed as previously described [27], [28]. Confirmation of the presence of the endosymbiont was performed by sequencing the amplified sequences from representative individuals. Obtained sequences from symionts in the different whitefly species were deposited in GenBank and assigned the accession numbers KM368237–KM368245 and KM368250.
Localization of endosymbionts using Fluorescence in situ Hybridization (FISH)
For endosymbiont localization in adult whiteflies, FISH analysis was used. Generally the methods used in this protocol were previously described [27], [28], [33]. After collecting the insect samples detailed in Table 1, they were immediately transferred to Carnoy’s fixative (Chloroform:Ethanol:Acetic acid = 6∶3∶1) for overnight fixation. The samples were then bleached with 6% H2O2 in ethanol for 2 hours and hybridized overnight in hybridization buffer (20 mM Tris-HCl [pH 8.0], 0.9 M NaCl, 0.01% SDS, 30% Formamide) containing 10 pmol/ml of fluorescent probes specifically targeting the different symbionts as detailed in Table 3. The specimens were then mounted whole and viewed under an Olympus IX81 Fluoview 500 confocal microscope (Olympus, Tokyo, Japan). At least twenty specimens were analyzed for each endosymbiont in each developmental stage.
Acknowledgments
We wish to thank members of the Department of Entomology, Institute Plant Protection, the Volcani Center for their helpful suggestion throughout this work.
Author Contributions
Conceived and designed the experiments: JMM MG RKS. Performed the experiments: JMM AK. Analyzed the data: JMM MG AK. Contributed reagents/materials/analysis tools: JMM MG RKS MAP. Contributed to the writing of the manuscript: MG JMM RKS MAP VAY JAMR.
References
- 1. De Barro PJ, Liu SS, Boykin LM, Dinsdale AB (2011) Bemisia tabaci: a statement of species status. Ann Rev Entomol 56: 1–19.
- 2. Jones CM, Gorman K, Denholm I, Williamson MS (2008) High-throughput allelic discrimination of B and Q biotypes of the whitefly, Bemisia tabaci, using TaqMan allele selective PCR. Pest Manag Sci 64: 12–15.
- 3. Navas-Castillo J, Fiallo-Olivé, E.; Sánchez-Campos S (2011) Emerging virus diseases transmitted by whiteflies. Ann Rev Phytopathol 49: 219–248.
- 4. Ueda S, Brown JK (2006) First report of the Q biotype of Bemisia tabaci in Japan by mitochondrial cytochrome oxidase I sequence analysis. Phytoparasitica 34: 405–411.
- 5. Dinsdale A, Cook L, Riginos C, Buckley YM, Barro P (2010) Refined Global Analysis of Bemisia tabaci (Hemiptera: Sternorrhyncha: Aleyrodoidea: Aleyrodidae) Mitochondrial Cytochrome Oxidase I to Identify Species Level Genetic Boundaries. Ann Entomol Soc Am 103: 197–208.
- 6. Alemandri V, De Barro P, Bejerman N, Argüello-Caro EB, Dumón AD, et al. (2012) Species within the Bemisia tabaci (Hemiptera: Aleyrodidae) complex in soybean and bean crops in Argentina. J Econ Entomol 105: 48–53.
- 7. Firdaus S, Vosman B, Hidayati N, Supena E, Visser R, et al. (2013) The Bemisia tabaci species complex: Additions from different parts of the world. Insect Sci. 20: 723–33.
- 8. Marubayashi JM, Yuki VA, Rocha KCG, Mituti T, Pelegrinotti FM, et al. (2013) At least two indigenous species of the Bemisia tabaci complex are present in Brazil. J Appl Entomol 137: 113–121.
- 9. Marubayashi JM, Pelegrinotti FM, Ferreira FZ, Yuki VA, Mituti T, et al. (2010) Bemisia tuberculata identification on cassava (Manihot esculenta) by the analysis of the mitocondrial gene (Cytochrome oxidase, mtCOI). Revista Raízes e Amidos Tropicais 6: 92–98 Available: http://www.cerat.unesp.br/Home/RevistaRAT/volume6/artigos/artigo17.
- 10. Rabello AR, Queiroz PR, Simões KCC, Hiragi CO, Lima LHC, et al. (2008) Diversity analysis of Bemisia tabaci biotypes: RAPD, PCR-RFLP and sequencing of the ITS1 rDNA region. Genet Mol Biol 31: 585–590.
- 11. Alonso RS, Racca-Filho F, Lima AF (2012) Occurrences of Whiteflies (Hemiptera: Aleyrodidae) on Cassava (Manihot esculenta Crantz) Crops Under Field Conditions in the State of Rio de Janeiro, Brazil. EntomoBrasilis 5: 78–79 Available: http://www.periodico.ebras.bio.br/ojs/index.php/ebras/article/view/170.
- 12. Lourenção AL, Alves AC, Fugi CGQ, Matos ES (2008) Outbreaks of Trialeurodes vaporariorum (West.) (Hemiptera: Aleyrodidae) under field conditions in the State of São Paulo, Brazil. Neotrop Entomol 37: 89–91.
- 13. Gottlieb Y, Ghanim M, Gueguen G, Kontsedalov S, Vavre F, et al. (2008) Inherited intracellular ecosystem: symbiotic bacteria share bacteriocytes in whiteflies. FASEB J 22: 2591–2599.
- 14. Thao ML, Baumann P (2004) Evolutionary relationships of primary prokaryotic endosymbionts of whiteflies and their hosts. Appl Environ Microbiol 70: 401–3406.
- 15. Sloan DB, Moran NA (2012) Endosymbiotic bacteria as a source of carotenoids in whiteflies. Biol Lett 8: 986–9.
- 16. Thao MLL, Baumann P (2004) Evidence for multiple acquisition of Arsenophonus by whitefly species (Sternorrhyncha: Aleyrodidae). Curr Microbiol 48: 140–144.
- 17. Moran NA, Degnan PH, Santos SR, Dunbar HE, Ochman H (2005) The players in a mutualistic symbiosis: insects, bacteria, viruses, and virulence genes. Proc Natl Acad Sci USA 102: 16919–16926.
- 18. Everett KDE, Thao ML, Horn M, Dyszynski GE, Baumann P (2005) Novel chlamydiae in whiteflies and scale insects: endosymbionts ‘Candidatus Fritschea bemisiae’ strain Falk and ‘Candidatus Fritschea eriococci’ strain Elm. Int J Syst Evol Microbiol 55: 1581–1587.
- 19. Weeks AR, Velten R, Stouthamer R (2003) Incidence of a new sex-ratio-distorting endosymbiotic bacterium among arthropods. Proc R Soc Lond B Biol Sci 270: 1857–1865.
- 20. Gottlieb Y, Ghanim M, Chiel E, Gerling D, Portnoy V, et al. (2006) Identification and localization of a Rickettsia sp in Bemisia tabaci (Homoptera: Aleyrodidae). Appl Environ Microbiol 72: 3646–3652.
- 21. Zchori-Fein E, Brown JK (2002) Diversity of prokaryotes associated with Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae). Ann Entomol Soc Am 95: 711–718.
- 22. Nirgianaki A, Banks GK, Frohlich DR, Veneti Z, Braig HR, et al. (2003) Wolbachia infections of the whitefly Bemisia tabaci. Curr Microbiol 47: 93–101.
- 23. Bing XL, Yang J, Zchori-Fen E, Wang XW, Liu SS (2013) Characterization of a newly discovered symbiont of the whitefly Bemisia tabaci (Hemiptera Aleyrodidae). Appl Environ Microbiol 72: 569–575.
- 24. Chiel E, Gottlieb Y, Zchori-Fein E, Mozes-Daube N, Katzir N, et al. (2007) Biotype-dependent secondary symbiont communities in sympatric populations of Bemisia tabaci. Bull Entomol Res 97: 407–413.
- 25. Thao ML, Baumann L, Hess JM, Falk BW, Ng JC, et al. (2003) Phylogenetic evidence for two new insect-associated Chlamydia of the family Simkaniaceae. Curr Microbiol 47: 46–50.
- 26. Chu D, Gao C, De Barro PJ, Zhang Y, Wan F, et al. (2011) Further insights into the strange role of bacterial endosymbionts in whitefly, Bemisia tabaci: Comparison of secondary symbionts from biotypes B and Q in China. Bull Entomol Res 101: 477–486.
- 27. Skaljac M, Zanic K, Ban SG, Kontsedalov S, Ghanim M (2010) Co-infection and localization of secondary symbionts in two whitefly species. BMC Microbiology 10: 142
- 28. Skaljac M, Zanic K, Hrncic S, Radonjic S, Perovic T, et al. (2013) Diversity and localization of bacterial symbionts in three whitefly species (Hemiptera: Aleyrodidae) from the east coast of the Adriatic Sea. Bull Entomol Res 103: 48–59.
- 29. Gueguen G, Vavre F, Gnankine O, Peterschmit M, Charif D, et al. (2010) Endosymbiont metacommunities, mtDNA diversity and the evolution of the Bemisia tabaci (Hemiptera: Aleyrodidae) species complex. Mol Ecol 19: 4365–4376.
- 30. De Barro PJ, Scott KD, Graham GC, Lange CL, Schutze MK (2003) Isolation and characterization of microsatellite loci in Bemisia tabaci. Mol Ecol Notes 3: 40–43.
- 31. Frohlich D, Torres-Jerez I, Bedford ID, Markham PG, Brown JK (1999) A phylogeographic analysis of the Bemisia tabaci species complex based on mitochondrial DNA markers. Mol Ecol 8: 1593–1602.
- 32. Scott IAW, Workman PJ, Drayton GM, Burnip GM (2007) First record of Bemisa Tabaci biotype Q in New Zealand. N Z Plant Protect 60: 264–270.
- 33. Gottlieb Y, Ghanim M, Gueguen G, Kontsedalov S, Vavre F, et al. (2008) Inherited intracellular ecosystem: symbiotic bacteria share bacteriocytes in whiteflies. FASEB J 22: 2591–2599.
- 34. Mitsuhashi W, Saiki T, Wei W, Kawakita H, Sato M (2002) Two novel strains of Wolbachia coexisting in both species of mulberry leafhoppers. Insect Mol Biol 11: 577–584.
- 35. Sintupachee S, Milne JR, Poonchaisri S, Baimai V, Kittayapong P (2006) Closely related Wolbachia strains within the pumpkin arthropod community and the potential for horizontal transmission via the plant. Microb Ecol 51: 294–301.
- 36. Gray SM, Banerjee N (1999) Mechanisms of Arthropod transmission of plant and animal viruses. Microbiol Mol Biol Rev 63: 128–148.
- 37. Zchori-Fein E, Gottlieb Y, Kelly SE, Brown JK, Wilson JM, et al. (2001) A newly-discovered bacterium associated with parthenogenesis and a change in host selection behavior in parasitoid wasps. Proc Natl Acad Sci USA 98: 12555–12560.
- 38. Bigliardi E, Sacchi L, Genchi M, Alma A, Pajoro M, et al. (2006) Ultrastructure of a novel Cardinium sp. symbiont in Scaphoideus titanus (Hemiptera: Cicadellidae). Tissue Cell 38: 257–261.
- 39. Caspi-Fluger A, Inbar M, Mozes-Daube N, Katzir N, Portnoy V, et al. (2012) Horizontal transmission of the insect symbiont Rickettsia is plant-mediated. Proc R Soc Lond B Biol Sci 279: 1791–1796.
- 40. Vautrin E, Vavre F (2009) Interactions between vertically transmitted symbionts: cooperation or conflict? Trends Microbiol 17: 95–99.
- 41. Vautrin E, Genieys S, Charles S, Vavre F (2008) Do vertically-transmitted symbionts co-existing in a single host compete or cooperate? A modeling approach. J Evol Biol 21: 145–161.
- 42. Chen DQ, Montllor CB, Purcell AH (2000) Fitness effects of two facultative endosymbiotic bacteria on the pea aphid, Acyrthosiphon pisum, and the blue alfalfa aphid, A. kondoi. Entomol Exp Appl 95: 315–323.
- 43. Darby AC, Birkle LM, Turner SL, Douglas AE (2001) An aphid-borne bacterium allied to the secondary symbionts of whitefly. FEMS Microb Ecol 36: 43–50.
- 44. Darby AC, Tosh CR, Walters KFA, Douglas AE (2003) The significance of a facultative bacterium to natural populations of the pea aphid Acyrthosiphon pisum. Ecol Entomol 28: 145–150.
- 45. Tsuchida T, Koga R, Shibao H, Matsumoto T, Fukatsu T (2002) Diversity and geographic distribution of secondary endosymbiotic bacteria in natural populations of the pea aphid, Acyrthosiphon pisum. Mol Ecol 11: 2123–2135.
- 46. Haynes S, Darby AC, Daniell TJ, Webster G, Van Veen FJF, et al. (2003) Diversity of bacteria associated with natural aphid populations. Appl Environ Microbiol 69: 7216–7223.
- 47. Ferrari J, Darby AC, Daniell TJ, Godfray HCJ, Douglas AE (2004) Linking the bacterial community in pea aphids with host-plant use and natural enemy resistance. Ecol Entomol 29: 60–65.
- 48. Chiel E, Zchori-Fein E, Inbar M, Gottlieb Y, Adachi-Hagimori T, et al. (2009) Almost There: Transmission Routes of Bacterial Symbionts between Trophic Levels. PLoS ONE 4: e4767.
- 49. Heath BD, Butcher RDJ, Whitefield WGF, Hubbard SF (1999) Horizontal transfer of Wolbachia between phylogenetically distant insect species by a naturally occurring mechanism. Curr Biol 9: 313–316.
- 50. Balas MT, Lee MH, Werren JH (1996) Distribution and fitness effects of the sonkiller bacterium in nasonia. Evol Ecol 10: 593–607.
- 51. Stouthamer R, Breeuwer JAJ, Hurst GDD (1999) Wolbachia pipientis: Microbial manipulator of Arthropod reproduction. Annu Rev Microbiol 53: 71–102.
- 52. Lawson ET, Mousseau TA, Klaper R, Hunter MD, Werren JH (2001) Rickettsia associated with male-killing in a buprestid beetle. Heredity 86: 497–505.
- 53. Hunter MS, Perlman SJ, Kelly SE (2003) A bacterial symbiont in the Bacteroidetes induces cytoplasmic incompatibility in the parasitoid wasp Encarsia pergandiella. Proc R Soc Lond B Biol Sci 270: 2185–2190.
- 54. Wernegreen JJ (2004) Endosymbiosis: lessons in conflict resolution. PLoS Biol 2: 307–311.
- 55. Bouchery T, Lefoulon E, Karadjian G, Nieguitsila A, Martin C (2013) The symbiotic role of Wolbachia in Onchocercidae and its impact on filariasis. Clin Microbiol Infect 19: 131–40.
- 56. Ricci I, Damiani C, Capone A, DeFreece C, Rossi P, et al. (2012) Mosquito/microbiota interactions: from complex relationships to biotechnological perspectives. Curr Opin Microbiol 15: 278–84.
- 57. Brumim M, Levy M, Ghanim M (2012) Transovarial Transmission of Rickettsia spp. and Organ-Specific Infection of the Whitefly Bemisia tabaci.. Appl Environ Microbiol 78: 5565–5574.
- 58. Perotti MA, Clarke HK, Turner BD, Braig HR (2006) Rickettsia as obligate and mycetomic bacteria. FASEB J 20: 1646–1656.
- 59. Himler AG, Adachi-Hagimori T, Bergen JE, Kozuch A, Kelly SE, et al. (2011) Rapid spread of a bacterial symbiont in an invasive whitefly is driven by fitness benefits and female bias. Science 332: 254–256.
- 60. Brumin M, Kontsedalov S, Ghanim M (2011) Rickettsia influences thermotolerance in the whitefly Bemisia tabaci B biotype. Insect Sci 18: 57–66.
- 61. Kontsedalov S, Zchori-Fein E, Chiel E, Gottlieb Y, Inbar M, et al. (2008) The presence of Rickettsia is associated with increased susceptibility of Bemisia tabaci (Homoptera: Aleyrodidae) to insecticides. Pest Manag Sci 64: 789–792.
- 62. Chen DQ, Montllor CB, Purcell AH (2000) Fitness effects of two facultative endosymbiotic bacteria on the pea aphid, Acyrthosiphon pisum, and the blue alfalfa aphid, A. kondoi. Entomol Exp Appl 95: 315–323.
- 63. Sakurai M, Koga R, Tsuchida T, Meng XY, Fukatsu T (2005) Rickettsia symbiont of the pea aphid Acyrthosiphon pisum: novel cellular tropism, effect on the host fitness, and interaction with the essential symbiont Buchnera. Appl Environ Microbiol 71: 4069–4075.
- 64. Hagimori T, Abe Y, Date S, Miura K (2006) The first finding of a Rickettsia bacterium associated with parthenogenesis induction among insects. Curr Microbiol 52: 97–101.
- 65. Giorgini M, Bernardo U, Monti MM, Nappo AG, Gebiola M (2010) Rickettsia symbionts cause parthenogenetic reproduction in the parasitoid wasp Pnigalio soemius (Hymenoptera: Eulophidae). Appl Environ Microbiol 76: 2589–2599.
- 66. Werren JH, Hurst GDD, Zhang W, Breeuwer JAJ, Stouthamer R, et al. (1994) Rickettsial relative associated with male killing in the ladybird beetle (Adalia bipunctata). J Bacteriol 176: 388–394.
- 67. von der Schulenburg JHG, Habig M, Sloggett JJ, Webberley KM, Bertrand D, et al. (2001) Incidence of male-killing Rickettsia spp. (α-proteobacteria) in the ten-spot ladybird beetle Adalia decempunctata L. (Coleoptera: Coccinellidae). Appl Environ Microbiol. 67: 270–277.
- 68. Yusuf M, Turner B (2004) Characterisation of Wolbachia-like bacteria isolated from the parthenogenetic stored-product pest psocid Liposcelis bostrychophila (Badonnel) (Psocoptera). J Stored Prod Res 40: 207–225.
- 69.
Muyzer G, Hottentrager S, Teske A, Wawer C (1996) Denaturing gradient gel electrophoresis of PCR amplified 16s rDNA–a new molecular approach to analyze the genetic diversity of mixed microbial communities. In Akkermans ADL, van Elsas JD, Bruijn FJ, editors. Molecular microbial ecology manual 3.4.4. Dordrecht The Netherlands. Kluwer Academic Publishers. 1–23.
- 70. Heddi A, Grenier AM, Khatchadourian C, Charles H, Nardon P (1999) Four intracellular genomes direct weevilbiology: Nuclear, mitochondrial, principal endosymbiont,and Wolbachia. Proc Natl Acad Sci USA 96: 6814–6819.
- 71. Matalon Y, Katzir N, Gottlieb Y, Portnoy V, Zchori-Fein E (2007) Cardinium in Plagiomerus diaspidis (Hymenoptera: Encyrtidae). J Invert Pathol 96: 106–108.