Open Access

Rickettsia parkeri colonization in Amblyomma maculatum: the role of superoxide dismutases

Parasites & Vectors20169:291

https://doi.org/10.1186/s13071-016-1579-1

Received: 12 April 2016

Accepted: 9 May 2016

Published: 20 May 2016

Abstract

Background

The Gulf Coast tick (Amblyomma maculatum) is an arthropod vector of Rickettsia parkeri, the causative agent of American boutonneuse fever and an infectious agent of public health significance. In this study, we evaluated the biological significance of the superoxide dismutases (SODs) of A. maculatum in hematophagy and R. parkeri colonization within the tick host.

Methods

An RNA interference approach was used to measure the functional roles of tick SODs (Cu/Zn-SOD and Mn-SOD) in R. parkeri colonization of the tick vector. Total microbial load, R. parkeri infection rate, and compensatory mechanisms by tick genes were examined using quantitative polymerase chain reaction (PCR) and quantitative reverse-transcriptase PCR assays. SOD enzymatic activity assays and malondialdehyde (MDA) lipid peroxidation were employed to determine the redox states in the tick tissues.

Results

Knockdown of the Cu/Zn-SOD gene caused the upregulation of Mn-SOD in transcript levels. Single and dual knockdowns of the SOD genes caused an increase in MDA lipid peroxidation while SOD enzymatic activities did not show a significant change. Mn-SOD knockdown resulted in a substantial increase in the microbial load; however, Cu/Zn-SOD transcript depletion prompted an upsurge in the midgut bacterial load, and significantly decreased the bacterial load in salivary gland tissues. Additionally, Cu/Zn-SOD transcript silencing led to significantly fewer R. parkeri DNA copy numbers in both tick tissues (midguts and salivary glands).

Conclusions

SOD enzymes play an important function in the regulation of bacterial communities associated with tick vectors and also in the defense mechanisms against the damage caused by reactive oxygen species within the tick. Knockdown experiments increased the levels of total oxidative stress in ticks, revealing the interplay between SOD isozymes that results in the transcriptional regulation of tick antioxidants. Moreover, the tick's Cu/Zn-SOD aids in the colonization of R. parkeri in tick tissues providing evidence of A. maculatum's vectorial success for a spotted fever group rickettsial pathogen.

Keywords

Amblyomma maculatum Rickettsia parkeri TickAmerican boutonneuse feverSuperoxide dismutaseReactive oxygen speciesSelenoproteinLipid peroxidationBacterial load

Background

The Gulf Coast tick, Amblyomma maculatum, is a recently emerged arthropod that is posing an increasingly significant risk to public health [1]. This tick covers a geographical range encompassing the coastal areas of the Eastern Atlantic and the Gulf of Mexico within the United States. It is an arthropod vector of the spotted fever group rickettsial pathogen, Rickettsia parkeri, which causes American boutonneuse fever, a similar but milder form of Rocky Mountain spotted fever. Vector competence in ticks (pathogen acquisition, colonization, and transmission) is a multifactorial process involving several genes and numerous gene networks within the tick organs (midgut and salivary glands).

Tick blood meal digestion elevates the reactive oxygen species (ROS) level, which in turn can severely harm cellular components, thereby promoting apoptosis. Hydroxyl radicals, superoxide anions (O2-), and hydrogen peroxide (H2O2) are generated through ROS. The manganese superoxide dismutase (Mn-SOD) enzyme catalyzes a small percentage of O2- to H2O2, as molecular oxygen is consecutively reduced to H2O by the electron transport chain complexes. Several other mitochondrial enzymes facilitate the additional reduction of H2O2 into H2O and molecular oxygen. Under normal circumstances, ROS partake in cell signaling by the intervention of select thiol residues in proteins, which have, among other capacities, a plausible role in regulating significant changes in transcriptional expression [2]. However, certain conditions can disturb the balance between the antioxidant capacity of the cell and an increase in the level of ROS. This condition, known as oxidative stress, causes permanent harm to macromolecules (proteins, lipids and DNA) and can eventually lead to cellular necrosis and cell death. Ticks must maintain homeostasis to survive, and they take blood meals of spectacular size, up to 100 times their unfed mass. Ticks must somehow avert the detrimental effects while promoting the beneficial aspects of ROS, and this suggests that there are specific factors for maintaining homeostasis within the tick itself and possibly at the tick–host interface. To achieve redox homeostasis in response to the detrimental effects of ROS, the tick antioxidant system acts through enzymes, such as catalase (Cat), superoxide dismutases (SODs), glutathione peroxide, glutathione-S-transferase, glutathione reductase (GSHR), selenoenzymes, and non-enzymatic molecules [36].

Localized ROS generation has been described in arthropods as the first line of defense against infectious agents [7, 8]. Tick-borne pathogens manipulate the gene expression of their host vector to ensure their survival, replication, and transmission to the mammalian host. Evidence of a well-organized tick antioxidant system lends support to the idea that tick-borne pathogens manipulate the system so that it is beneficial for their survival and colonization within the tick before inoculation into the mammalian host. While the role of ROS and antioxidants in the vectorial competence of ticks has not yet been explained, the redox balance and the growth and survival of R. parkeri in the tick host is an enigma. Hence, in this study, the biological implications of SODs in R. parkeri colonization within the A. maculatum vector are examined.

Methods

Ethics statement

All animal experiments were conducted in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health, USA. The protocol for tick blood feeding on sheep was approved by the Institutional Animal Care and Use Committee of the University of Southern Mississippi (protocol #15101501 and #15011402). All efforts were made to minimize animal suffering.

Ticks and other animals

Gulf Coast ticks (A. maculatum) were maintained at the University of Southern Mississippi according to established methods [9]. Unfed adult ticks were obtained from Oklahoma State University’s Tick Rearing Facility (Stillwater, OK, USA). Rickettsia parkeri-infected A. maculatum ticks were maintained in the laboratory after collection from the field [10]. Adult ticks were kept at room temperature with approximately 90 % relative humidity under a photoperiod of 14 h light/10 h dark before infestation on sheep. Ticks were blood-fed on sheep and were either allowed to feed to repletion or were removed at 3–10 days after attachment, depending on the experimental protocol. Adult ticks were fed on sheep and immature ticks were fed on hamsters (specifically used for this study), and the animal studies were performed in accordance with protocols approved by the Institutional Animal Care and Use Committee (IACUC) at the University of Southern Mississippi.

Bioinformatics analyses

The coding sequences of SODs for A. maculatum genes used in this study were obtained from an A. maculatum sialotranscriptome study [3]. Nucleotide sequences were conceptually translated and initially aligned using ClustalX2 [11, 12] and graphically presented using Jalview [13]. Phylogenetic relationships were inferred by MEGA 6 [14] using maximum likelihood method using JTT matrix-based model [15].

Tick midgut and salivary gland preparation

The unfed and partially blood-fed female adult ticks were dissected within 4 h of removal from the sheep. The remarkable contribution of midgut and salivary gland tissues in tick’s hematophagy, and potential role of these tissues in pathogen colonization, propagation, and saliva-assisted transmission to the vertebrate host led us to focus on these tissues in this study [16]. The tick midgut and salivary gland tissues were dissected in ice-cold M-199 buffer as described by Morgan et al. [17, 18]. After removal, the midguts and salivary glands were washed gently in the same ice-cold buffer. The tick tissues were either stored immediately after dissection in RNAlater (Invitrogen, Carlsbad, CA, USA) prior to mRNA extraction, or in protein extraction buffer.

RNA preparation, cDNA synthesis, and quantitative reverse-transcriptase (qRT)-PCR

Extraction of total RNA, cDNA synthesis, and qRT-PCR were conducted as previously described [19]. Briefly, the tick midguts and salivary gland tissues stored in RNAlater were used for total RNA extraction using an Illustra™ RNAspin Mini Isolation kit (GE Healthcare, Piscataway, NJ, USA) according to the manufacturer’s instructions. The RNA concentration was determined using a Nanodrop spectrophotometer (Thermo Fisher Scientific, Wilmington, DE, USA). Total RNA (1 μg) was reverse transcribed into cDNA using iScript cDNA synthesis kit (Bio-Rad Inc., Hercules, CA, USA) according to the manufacturer’s instructions . The gene-specific primer sequences designed to amplify specific cDNA fragments from A. maculatum tissues are listed in the Table. Transcriptional gene expression of the SODs in uninfected (naïve) ticks was normalized against the β-actin gene, while glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used to normalize gene expression in R. parkeri-infected tick tissues. The selection of β-actin and GAPDH reference genes was based on their stable gene expression levels in uninfected and rickettsial-infected ticks [19]. All genes used in this study were first amplified using gene-specific primers (Table 1), and their sequences were confirmed by sequencing prior to dsRNA synthesis or gene expression studies. First-strand cDNA was used to measure mRNA levels using qRT-PCR. SYBR Green qPCR Master Mix (Bio-Rad Inc., Hercules, CA, USA), 25 ng of cDNA, and 150 nM of gene-specific primers were used in each reaction mixture [6]. The qRT-PCR mixtures were subjected to 10 min at 95 °C, followed by 35 cycles of 15 s at 95 °C, 30 s at 60 °C, and 30 s at 72 °C using the CFX96 Real Time System (Bio-Rad Inc.).
Table 1

Gene-specific quantitative reverse-transcriptase PCR primers used in the experiments

Gene

Accession number

Forward primer 5′-3′

Reverse primer 5′-3′

Size (bp)

TrxR

JO843723

TGTGACTACACCAACGTGCCTACA

AGTAGCCTGCATCCGTTCCTCTTT

175

Catalase

JO843741

AAAGGACGTCGACATGTTCTGGGA

ACTTGCAGTAGACTGCCTCGTTGT

173

GSHR

JO844062

ACCTGACCAAGAGCAACGTTGAGA

ATCGCTTGTGATGCCAAACTCTGC

170

MnSOD (SOD3)

JO843979

GCATCTACTGGACAAACCTCTC

GCAGACATCAGGCCTTTGA

115

Cu/ZnSOD (SOD1)

JO844140

GGAACCGAAGACAGCAAGAA

GAGAAGAGGCCGATGACAAA

143

Duox

N/A

ATGACGCACAGCCTGTATATT

TGTCCAGAGTGAAGACGATTG

123

16S rRNA

N/A

AGAGTTTGATCCTGGCTCAG

CATGCTGCCTCCCGTAGGAGT

N/A

Actin

JO842238

TGGCTCCTTCCACCATGAAGATCA

TAGAAGCACTTGCGGTGCACAATG

169

GAPDH

JO842341

CACCCATCACAAACATGGGTGCAT

TTTCAGGAAATGAAGCCTGCCAGC

175

OmpB

AF123717

CAAATGTTGCAGTTCCTCTAAATG

AAAACAAACCGTTAAAACTACCG

96

Probe: 6-FAM-CGCGAAATTAATACCCTTATGAGCAGCAGTCGCG-BHQ-1

SelM

JO842653

ATGATACCTGAATGGCCATCCGCA

TGATCGCGGGTCATCTTCTCCAAA

171

eEFSec (SEF)

KC989559

TGGCTCCAGAAATGCTGCTCATTG

ACGCCTTTGCGACTCTTCTCCTTA

157

SelS

JO842687

AGAACAAGTGCACCACAACAGCAG

ATTTCTTGCATCCTTCGACGTGCC

107

SelN

KC989560

TTAGTTTGGACACTGTGGACGGGT

AGGCTTCTCTAACAACGGCACTCA

150

SelK

JO843326

AGTTCCAGCAGGTCATCAGTGTCA

TCCAGGAATAGGGCAGTCCATTGT

132

Salp25D

JO843645

TGCCGCGCTGTCTTTATTATTGGC

AGTTGCACGGAGAACCTCATCGAA

102

Double-stranded RNA (dsRNA) synthesis, tick injections, and hematophagy

Synthesis of dsRNA for SOD analysis and tick manipulations was performed according to the methods described previously [20, 21]. Briefly, PCR product, purified using a QIAquick PCR purification kit (Qiagen, Valencia, CA, USA), was used in a secondary PCR using the same primers with SOD-specific sequences (Table 1), but with the addition of flanking T7 sequences that allow for the binding of reverse transcriptase and the generation of dsRNA. After confirming the T7-flanked SOD gene sequence, the secondary PCR product was reverse transcribed into RNA using a T7 Quick High Yield RNA synthesis kit (New England Biolabs, Ipswich, MA, USA) by incubating the PCR product with T7 polymerase overnight at 37 °C. The resulting dsRNA was purified by ethanol precipitation and its concentration measured spectrophotometrically using a Nanodrop device (Thermo Fisher Scientific). The product was visualized by gel electrophoresis using a 2 % agarose gel. The dsRNAs (dsMn-SOD and dsCu/Zn-SOD) were diluted to working concentrations of 1 μg/μl. The same protocol was used to synthesize dsRNA-LacZ to be used as a dsRNA control. Forty-five unfed adult female ticks (uninfected or R. parkeri-infected) were microinjected with 1 μl of dsRNA-SOD or dsLacZ using a 27-gauge needle, after which they were kept overnight at 37 °C to alleviate needle trauma and promote survival. The surviving ticks were used to infest a sheep and allowed to blood feed in the presence of male ticks. For sample collection, 10 partially fed experimental control ticks were removed on days 5 and 7 post-tick infestation, and the remaining ticks were allowed to remain attached and blood feed until repletion. The feeding success of the individual ticks was evaluated by recording their attachment duration, repletion weight, and the ability to oviposition [22]. Partially fed ticks removed from the dsLacZ or dsSOD groups were dissected to obtain their midguts and salivary gland tissues.

Quantification of total bacterial load

The bacterial load in each tick tissue was estimated as described previously [6, 23]. Briefly, 25 ng of cDNA from the tick tissues, 200 μM 16sRNA gene primers, and 2× iTaq Universal SYBR green mix (Bio-Rad Inc.) in a 25-μl volume reaction was used with the following thermocycler parameters: 94 °C for 5 min followed by 35 cycles at 94 °C for 30 s, 60 °C for 30 s and 72 °C for 30 s. Standard curves were used to estimate the copy numbers of each gene. The bacterial copy numbers were normalized against A. maculatum actin copy numbers in the uninfected ticks and GAPDH in the R. parkeri-infected ticks. All samples were run in triplicate.

Quantification of R. parkeri copy numbers in tick tissues

The level of infection with R. parkeri within the tick tissues (midguts and salivary glands) was quantified using a probe-based qPCR method described previously [10]. Briefly, 0.4 μM of probe, 0.7 μM of each forward and reverse primer (Rpa129F, Rpa224R) (Table 1) and 8 mM of MgSO4 reaction mixture was subjected to one cycle each of 50 °C for 2 min and 95 °C for 2 min, then 45 cycles of 95 °C for 15 s and 60 °C for 30 s. A standard curve was used to calculate the R. parkeri copy numbers in the tick samples. All samples were run in triplicate.

Quantification of total oxidative stress levels

A malondialdehyde (MDA) lipid peroxidation assay was used to quantify the total oxidative stress levels in the tick tissues. Degradation of lipids as a result of oxidative damage was estimated by quantification of MDA through the use of a Lipid Peroxidation MDA Assay Kit (Sigma-Aldrich, St. Louis, MO, USA) following the manufacturer provided protocol. Twenty milligrams of midgut tissue from individual ticks was filtered through a 0.2 μm filter before the assay was performed according to the manufacturer’s instructions.

Quantification of SOD activity

Superoxide enzymatic activity was quantified in individual midgut and salivary gland tissues using the Superoxide Dismutase Assay Kit (Cayman Chemical Co, Ann Arbor, MI, USA). The tissues were processed according to the manufacturer’s instructions.

Data analysis

All data are expressed as mean ± SEM unless otherwise stated. Statistical significance between the two experimental groups or their respective controls was determined by the t-test). Comparative differences amongst the multiple experimental groups were determined by analysis of variance with statistically significant P-values of < 0.05 (Graphpad Prism 6.05, La Jolla, CA, USA). Transcriptional expression levels were determined using Bio-Rad software (Bio-Rad CFX MANAGER v.3.1), and the expression values were considered significant if the P-value was 0.05 when compared with the control.

Results

Bioinformatic analyses

In this study, the functional role of A. maculatum superoxide dismustases (SODs) in hematophagy, and bacterial colonization of endosymbionts and pathogenic microbe R. parkeri was determined. Two gene sequences of tick superoxide dismutases cytosolic with signal peptide (Cu/ZnSOD) and intramitrocondrial scavenger (Mn-SOD) were selected to analyze for the presence of secretory signal peptide using SignalP [24] server (http://www.cbs.dtu.dk/services/SignalP/). The amino acid residues deduced from the transcripts of two SODs identified earlier [3] were translated and visualized using Jalview and observed six histidine residues in each sequences showing metal-binding sites (Additional file 1: Figure S2A, B). The four histidine imidazoles are coordinated to Cu(II) while two other and including one common histidine imadazoles binds to Zn(II) metal in Cu/Zn-SOD dismutase [25]. The Mn-SOD localized in mitochondria in eukaryotes, and found in cytoplasm in prokaryotes shares common structural properties with Fe-SOD [26]. The phylogenetic tree was built in MEGA software version 6 [14] to provide evolutionary significance between mitochondrial and cytoplasmic superoxide dismutases (Additional file 1: Figure S1). Phylogenetically Mn-SOD and Cu/Zn-SOD fit in two different clades, sharing common node with corresponding SODs from another Amblyomma ticks (Additional file 1: Figure S1).
Fig. 1

Time-dependent Cu/Zn-SOD and Mn-SOD transcriptional expression levels in uninfected (naïve) tick midgut and salivary gland tissues during the blood meal. The relative transcript levels of the SODs during the blood meal were measured by comparing the SOD expression levels in the midgut (Gut) and salivary gland (SG) tissues of the unfed-stage ticks. The changes in transcriptional activity of (a) Cu/Zn-SOD and (b) Mn-SOD in the A. maculatum midgut and salivary gland tissues were normalized to the unfed developmental stage using β-actin as a reference gene

Time-dependent transcriptional gene expression analysis

The time-dependent transcriptional expression of the Cu/Zn-SOD and Mn-SOD genes was examined in unfed and partially blood-fed tick tissues (midguts and salivary glands) (Fig. 1). The time-dependent expression of the Cu/Zn-SOD gene in the tick midgut tissues showed its highest transcript level during the unfed phase followed by significant depletion after attachment, and the transcript level remained down-regulated as the tick blood feeding switched from day 2 to day 8 (Fig. 1a). Interestingly, the transcript level of the Cu/Zn-SOD gene in the tick salivary glands was up-regulated during the slow and fasting feeding phases of tick blood feeding, signifying a potential functional role in tick hematophagy (Fig. 1a). By contrast, the transcript level of the Mn-SOD gene in the tick midgut tissues upon blood feeding was up-regulated and remained 2-fold higher than in the unfed tissues in the 2- and 6 day-fed ticks (Fig. 1b); however, the salivary glands showed a 2- to 6-fold increase in the transcript level on days 4 and 6 post-attachment to the vertebrate host (Fig. 1b). Surprisingly, the transcript level of Mn-SOD decreased in the fast-feeding phase (8 days post-infestation), implying compensation by Cu/Zn-SOD or a reduced biological need in the cell.

Impact of single and multiple SOD knockdowns in uninfected ticks

Transcriptional gene expression: To investigate the functional role(s) of the secreted extracellular and mitochondrial SOD enzymes, genes were disrupted using RNA interference, and the effects of the single and dual knockdowns upon the transcriptional gene expression of Cat, dual oxidase (Duox), GSHR and thioredoxin reductase, as well as oxidative stress, bacterial load, and enzymatic activity was investigated (Figs. 2, 3 and 4). A Cu/Zn-SOD gene silencing efficiency of 77 and 76 % was achieved in 5 dpi tick midgut and salivary gland tissues respectively (Fig. 2a). On the contrary, Mn-SOD transcript silencing efficiency of 76 and 94 % was obtained in tick midgut and salivary tissues respectively (Fig. 2b). Intriguingly, simultaneous gene silencing of Cu/Zn-SOD and Mn-SOD showed 90 and 98 % silencing efficiency of Cu/Zn-SOD verses 63 and 71 % of Mn-SOD in midgut and salivary gland tissues respectively (Fig. 2c). Regardless of the single (Cu/Zn-SOD or Mn-SOD) and dual (Cu/Zn-SOD and Mn-SOD) knockdowns, there were no significant changes in tick behavior or phenotype in terms of the tick engorgement weight, the attachment duration (Additional file 1: Figure S3). Surprisingly, knockdown of tick SODs did not translate into the depletion of SOD enzymatic activity in midgut tissues but salivary glands showed a decrease in Cu/Zn-SOD and dual knockdown tissues, dsMn-SOD (P = 0.002), and dual SOD injected (P = 0.036) (one-way ANOVA using multiple comparison with Tukey test) (Fig. 3a, b). The lack of correlation between Cu/Zn-SOD level may be due to the residual amount of proteins already present in the tissues. Cu/Zn-SOD silencing in the partially blood-fed tick tissues up-regulated Mn-SOD gene expression; however, Cat, Duox, and GSHR gene expression in the salivary glands remained unchanged (Fig. 2a). By contrast, Mn-SOD silencing in uninfected (naïve) ticks showed a 4–35-fold increase in Cu/Zn-SOD expression and, intriguingly, Duox expression in the salivary glands was significantly down-regulated (P < 0.05), suggesting an interplay between Duox and Mn-SOD in the salivary glands (Fig. 2b). Simultaneous silencing of Cu/Zn-SOD and Mn-SOD in naïve ticks only impacted the expression of selected genes in the salivary gland tissues (Fig. 2c), suggesting the tissue-specific expression of antioxidant genes during blood feeding.
Fig. 2

Knockdown of tick SODs in naïve (uninfected) A. maculatum and the effect on tick antioxidants. aCu/Zn-SOD, bMn-SOD, cCu/Zn-SOD + Mn-SOD dual knockdowns. Gene expression in naïve ticks was normalized against tick β-actin, used as the reference gene. The transcript levels of the target genes in dsLacZ injected tick tissues were made equal to 1 and represented by a dashed line in the graphs. KD; Knockdowns

Fig. 3

Quantification of the SOD activity and total oxidative stress levels in superoxide dismutase-silenced naïve tick midguts. a Cytosolic and b mitochondrial SOD enzymatic activities in tick midgut and salivary gland tissues were estimated using Superoxide Dismutase Assay Kit (Cayman Chemical Co, Ann Arbor, MI, USA). The tissue cytosolic fraction was used for determining the enzymatic activity of Cu/Zn-SOD, and mitochondrial fraction was reconstituted to assess Mn-SOD activity. c A Lipid Peroxidation (MDA) Assay Kit (Sigma-Aldrich, St. Louis, MO, USA) was used for estimating total oxidative stress in the tick midgut tissues. The MDA-TBA adduct was spectrometrically estimated at 532 nm in each control and knockdown tick midgut

Fig. 4

Impact of SOD knockdown on microbiota load in naïve tick tissues. The bacterial load in the tick tissues (measured in copy numbers) was calculated by qRT-PCR using the bacterial 16 s rRNA gene and was normalized against the tick β-actin gene (copy number) in tick midguts and salivary glands each knockdown; Mn-SOD (a, b); Cu/Zn-SOD (c, d); and Dual SODs knockdown (e, f)

Oxidative stress levels and SOD enzymatic activity: The cytosolic and mitochondrial SOD enzymatic activities were determined in the uninfected single- and simultaneously gene-silenced tick midgut and salivary gland tissues. Knockdown of Cu/Zn-SOD resulted in slightly decreased enzyme activity, while Mn-SOD silencing lowered the activity in the midgut and salivary gland tissue fractions compared with the control (Fig. 3a). Simultaneous silencing of Cu/Zn-SOD and Mn-SOD produced lower Cu/Zn-SOD activity in the midgut and salivary gland tissues; while the salivary glands experienced a slight decrease in Mn-SOD activity as compared with the irrelevant dsRNA-treated tick tissues (Fig. 3b). Additionally, the level of oxidative stress, as quantified by MDA, showed a 5–6-fold increase in oxidative stress upon knockdown of Cu/Zn-SOD (t = 2.847, P = 0.0465) and Mn-SOD (t = 10, P = 0.0004) in the midgut tissues; however, simultaneous knockdown of the expression of both genes produced only a 2-fold increase (t = 0.6904, P = 0.529) in the oxidative stress level (Fig. 3c). Quantification of the oxidative stress level in the salivary gland tissues was hampered by the insufficiently high protein concentration needed for this assay.

Native microbial load: To further understand the role of SODs in the native microbial load within the tick tissues, we calculated the overall bacterial load by quantifying the 16S rRNA gene. We observed that when Mn-SOD was knocked down in the uninfected tick tissues the total bacterial load in the midgut and salivary gland tissues increased (F (3, 36) = 9.636, P < 0.0001) (Fig. 4a and b). By contrast, Cu/Zn-SOD gene silencing significantly depleted the colonization of microbiota in the tick salivary glands (t = 2.794, P = 0.0190) (Fig. 4d), suggesting a hypothetical role for this gene in the colonization of microbes in tick salivary glands before saliva-assisted transmission to the host (Fig. 4b). Intriguingly, Cu/Zn-SOD gene silencing resulted in no significant difference in the microbial load in the tick midgut tissues (t = 2.151, P = 0.0570) (Fig. 4c). The bacterial load in tick tissues was significantly altered in dual knockdown of SODs in tick tissues (F (3, 20) =7.493, P = 0.0015) (Fig. 4e, f).

Impact of Cu/Zn-SOD knockdown in R. parkeri-infected ticks

SOD expression was assessed in the tissues (midgut and salivary glands) of uninfected and R. parkeri-infected partially blood-fed adult ticks (Fig. 5a). Interestingly, the Mn-SOD transcript level was up-regulated 8-fold while Cu/Zn-SOD was down-regulated in the R. parkeri-infected tick midgut tissues (Fig. 5a). Rickettsia parkeri infection in the partially blood-fed salivary glands caused up-regulation of the expression of both SODs (2–8-fold, P < 0.05), suggesting their potential role in pathogen colonization within the tick host (Fig. 5a). To further understand the proposed role of Cu/Zn-SOD in R. parkeri colonization in A. maculatum, Cu/Zn-SOD was silenced using RNAi, and its effect on the native microbial load and R. parkeri colonization was examined (Fig. 5c, d). As anticipated, the Cu/Zn-SOD transcript in the knockdown showed 77 and 99 % silencing efficiency in midgut and salivary gland tissues respectively in 5 dpi ticks (Fig. 5b) (P < 0.05). Predictably, the transcriptional expression of Mn-SOD exhibited a 6.5–7-fold up-regulation upon silencing of Cu/Zn-SOD in the partially blood-fed infected tissues (Fig. 5b). The transcript level of selected antioxidant genes (Cat, Duox, GSHR, and TrxR) decreased slightly in the Cu/Zn-SOD-silenced R. parkeri-infected tick tissues. Intriguingly, Cu/Zn-SOD silencing up-regulated the transcript level of selenoprotein O, Mn-SOD, and glutathione peroxidase (Salp25D) in the tick midguts, while Mn-SOD and Salp25D expression in the salivary gland tissues increased by 6–8-fold, indicating the existence of a compensatory mechanism (Fig. 5b). Interestingly, quantification of R. parkeri in the gene-silenced partially blood-fed tick tissues revealed a significant decrease in the rickettsial copy numbers in midguts (t = 7.5, P < 0.0001) and in salivary gland tissues (t = 8.419, P < 0.0001) (Fig. 5c), suggesting a potential role for Cu/Zn-SOD in R. parkeri colonization within the tick host. Surprisingly, the total bacterial load in Cu/Zn-SOD knockdown midgut (t = 0.5079, P = 0.6225) and salivary gland tissues (t = 0.03569, P = 0.09722) remained unchanged (Fig. 5d).
Fig. 5

Knockdown of Cu/Zn-SOD in R. parkeri-infected A. maculatum. a Tissue-specific SOD transcriptional gene expression in uninfected and R. parkeri-infected partially blood-fed female adults tissues. A. maculatum GAPDH was used as a reference gene to normalize the gene expression data. Target gene expression in uninfected tick tissues was adjusted to 1. b Transcriptional gene expression of selected antioxidant genes in Cu/Zn-SOD-silenced partially fed tick tissues. The transcript level of each target gene in the tissues injected with control LacZ-dsRNA was set to 1.0 as a reference point. Expression was normalized against the tick GAPDH gene. c R. parkeri was quantified using a real-time PCR assay designed for specific detection of the R. parkeri ompB gene in A. maculatum midgut and salivary gland in dsLacZ and dsCu/Zn-SOD injected tick tissues, and (d), the bacterial load estimation in R. parkeri-infected ticks knocked down with Cu/ZnSOD. Tick GAPDH was used as a reference gene for estimating the total bacterial load in R. parkeri-infected ticks. KD; Knockdowns

Discussion

Ixodid ticks are arthropods dependent on hematophagy for transition to each life stage and for maintaining their reproductive fitness. Hematophagy in ixodid tick is a phase-dependent process, starting with host attachment and establishment of the feeding site, followed by slow feeding and transition into fast feeding until repletion. At this point in the feeding process, the tick can weigh over 100 times its pre-engorgement weight as a result of the imbibed blood meal. The entire process of tick feeding is dependent on the tick’s secreted salivary components that mechanistically facilitate successful transition of each feeding phase over the course of multiple days to weeks. Tick saliva, as shown by sialotranscriptome analysis, is composed of ~5000 putative secreted salivary proteins containing dozens of protein families [3, 27], many of which exhibit pharmacological properties capable of disarming the host’s attempts to establish hemostasis or to mount a specific immune response and, ultimately, enhancing the tick’s ability to blood-feed. At the same time, ticks face elevated oxidative stress both on and off the mammalian host and they must neutralize the harmful effect. The ability of ticks to counterbalance nutritional stress (starvation) and blood feeding-related stress (heme digestion) indicates the likely development of a proactive detoxification system. Complete studies of the antioxidant systems of blood-sucking arthropods are presently unavailable; nonetheless the scientific literature shows that ticks have an extensive arsenal of antioxidants and selenoproteins that allow them to survive extreme variations in redox homeostasis, with prolonged periods of starvation, the digestion of huge blood meals, and exposure to blood-related products [46, 20, 27]. Hence, an insight into the tick’s antioxidant repertoire should offer a glimpse of its defenses against elevated levels of oxidative stress. It should also broaden our understanding of tick–pathogen interactions. Although, A. maculatum is a recognized arthropod vector of R. parkeri, this vector-pathogen pair remains the most poorly studied vector-borne disease. Here, we investigated the functional role of two tick SODs (extracellular and mitochondrial) in tick hematophagy and pathogen colonization within the arthropod vector. Bioinformatic analysis of the Cu/Zn-SOD (cytosolic) and Mn-SOD proteins showed amino acid sequence similarity with arthropod and vertebrate proteins (Additional file 1: Figures S1 and S2).

The two A. maculatum SODs we characterized showed quite different expression patterns. The transcriptional activity of Cu/Zn-SOD was 2-fold up-regulated throughout the blood meal in the salivary tissues, whereas it declined in the midgut tissues upon blood meal consumption (Fig. 1a). Mn-SOD expression was up-regulated 3–6-fold in the salivary glands on days 4 and 6; however, the midgut maintained a steady expression level (Fig. 1b). Furthermore, while we obtained both single and dual gene transcriptional knockdowns, significant differences in the tick phenotype (tick engorgement weight, attachment duration, egg mass, egg conversion ratio, and hatchability) (Additional file 1: Figure S3) were lacking, a result that is similar to previous studies reporting the existence of a strong compensatory mechanism in the tick host for detoxifying superoxide and H2O2 [20]. The tick salivary glands undergo tremendous biochemical and physiological changes as soon as a tick attaches itself to the host, followed by engorgement and repletion [28]. In ticks, breakdown of the huge blood meal generates toxic levels of heme leading to elevated ROS production. The gut bacterial community is strongly shaped by the ROS levels upon a blood meal, resulting in a decrease in diversity and an increase in Enterobacteriaceae [6]. The establishment of vector competence (pathogen survival, colonization, and transmission) is highly specific: R. parkeri can only be vectored by A. maculatum, Ehrlichia chaffeensis by Amblyomma americanum, and Borrelia burgdorferi by Ixodes scapularis. It is postulated that these vector-borne disease agents have developed an antioxidant capacity that aids them to survive and multiply by balancing oxidative tissue-specific homeostasis. Tick-borne pathogens are vulnerable to a high level of oxidative stress; consequently, disrupting the redox metabolism offers a promising approach for the prevention of tick-borne disease agents and for disturbing tick microbiota. Our recent work highlighted the biological implication of thioredoxin reductase (TrxR, a selenoprotein) in preserving the natural microbiota of ticks [6], and a link between selenocysteine elongation factor and R. parkeri survival in the midgut tissues [4]. It has been shown that elimination of ROS is required to conserve fertility in Anopheles, Drosophila, A. maculatum, and mammals [20, 2931]. To neutralize the damaging effects of ROS and attain homeostasis, tick SODs and Cat enzymes act together to catalyze the conversion of superoxide and H2O2. Superoxide and hydrogen peroxide facilitate the generation of the hydroxyl radical, the most reactive oxygen free radical, in the presence of iron metal [32, 33]. Interestingly, lipid peroxidation assays showed higher total oxidative stress levels for single knockdown tick midguts, while dual knockdown revealed only a slight change in the oxidative stress level, suggesting the presence of a strong compensatory mechanism, as has been reported previously (Fig. 3c) [20]. Estimation of the total oxidative stress levels in individual tick salivary glands was not successful because of the low protein concentrations required for this assay. Intriguingly, gene knockdown of Cu/Zn-SOD or Mn-SOD significantly increased the total bacterial load in the midgut tissues (Fig. 4a, c), whereas Cu/Zn-SOD knockdown in the salivary glands significantly reduced the total bacterial load (Fig. 4d). The total bacterial load in the dual SOD knockdown remained at a decreased level in both tissues. The interplay between ROS levels and survival and the colonization of intracellular bacteria has not been elucidated. Our results indicate that the microbes associated with ticks are dependent on maintaining redox homeostasis while also producing ROS within the tick cells, and they use the ROS as a signaling molecule to regulate the bacterial density [34]. Another possible interpretation is that Cu/Zn-SOD gene knockdown also affected the enzymatic activity of Mn-SOD (Fig. 3a, b), and the increased generation of superoxide in the salivary glands significantly reduced the total bacterial load. Intriguingly, redox homeostasis is routinely attained by counterbalancing ROS and antioxidants by regulating oxidative stress-induced genes [35], including Cat. The transcriptional expression of Cat was up-regulated slightly in the midgut tissues upon Cu/Zn-SOD knockdown; however, a compensatory role for Cat in increasing the bacterial load cannot be ruled out (Figs. 2a and 4). SOD facilitates the breakdown of O2− to H2O2 and molecular oxygen. Mn-SOD (SOD2) from Drosophila mutants show an increased herbicide (Paraquat) sensitivity, elevated endogenous oxidative stress, and reduced longevity [36]. A significant decrease in the total bacterial load upon Cu/Zn-SOD knockdown led us to a follow-up experiment to study the functional role of Cu/Zn-SOD gene depletion on R. parkeri colonization within the tick host.

ROS provide protection against a variety of pathogens by eliciting immune responses in organisms as diverse as mammals and arthropods, including tick responses against R. parkeri [4]. Fascinatingly, the interactions between A. maculatum and R. parkeri determine the ability of these ticks to become colonized by and transmit rickettsial agents. In tick-transmitted infections, the infectious agents manipulate gene expression of the vector host to ensure their colonization and onward transmission to the mammalian host. In the current study, Cu/Zn-SOD and Mn-SOD transcript levels in the R. parkeri-infected ticks showed differential gene expression. Interesting, the transcript level of Mn-SOD significantly upregulated (P < 0.05) in R. parkeri-infected partially blood fed tick tissues and Cu/Zn-SOD transcript level increased only in salivary glands (P < 0.05) and remained down-regulated in gut tissues (Fig. 5a). It suggests that tick protects herself from the elevated level of super-oxides generated and released upon rickettsial infection by regulating the expression of superoxide dismutase [37] (Fig. 5a). Interestingly, downregulation of Cu/Zn-SOD level in R. parkeri infected midguts co-related with alleviated Cu/Zn-SOD transcript abundance in partially blood-fed tissues (Fig. 1a). As expected, the Cu/Zn-SOD knockdown up-regulated Mn-SOD (~6.5-fold) expression in the midgut and salivary glands. Surprisingly, the expression levels of Salp25D and SelM were 9-fold and 3-fold up-regulated, respectively. It is established that A. maculatum eEFSec, I. scapularis glutathione peroxidase (Salp25D), and Dermacentor variabilis SelM offer a survival advantage to R. parkeri, B. burgdorferi, and Anaplasma marginale [4, 38, 39].

Conclusions

This is the first study to show that the silencing of Cu/Zn-SOD decreases the level of R. parkeri colonization in tick tissues. The A. maculatum antioxidants, Mn-SOD and Cu/Zn-SOD play a role in maintaining redox homeostasis within the tick and facilitate the colonization of human pathogenic bacteria, R. parkeri. Our findings provide a strong foundation for future research to elucidate the molecular determinants of vector competence. The relationship between ROS, vector competence, and R. parkeri-induced antioxidants is undergoing further investigation in our laboratory.

Declarations

Acknowledgments

This work was supported by grants from the National Institute of Allergy and Infectious Diseases (award #AI099919) and the National Institutes of General Medical Sciences (award #P20GM103476). Gary Crispell is the recipient of the Mississippi-INBRE summer undergraduate research fellowship. These funding bodies played no role in the study design, data collection, analysis, decision to publish, or manuscript preparation.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Biological Sciences, University of Southern Mississippi

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© Crispell et al. 2016

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