Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Antennal-Expressed Ammonium Transporters in the Malaria Vector Mosquito Anopheles gambiae

  • R. Jason Pitts ,

    Contributed equally to this work with: R. Jason Pitts, Stephen L. Derryberry Jr.

    Affiliations Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee, United States of America, Vanderbilt Institute for Global Health, Nashville, Tennessee, United States of America

  • Stephen L. Derryberry Jr. ,

    Contributed equally to this work with: R. Jason Pitts, Stephen L. Derryberry Jr.

    Affiliation Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee, United States of America

  • Fadi E. Pulous,

    Affiliation Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee, United States of America

  • Laurence J. Zwiebel

    l.zwiebel@vanderbilt.edu

    Affiliations Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee, United States of America, Vanderbilt Institute for Global Health, Nashville, Tennessee, United States of America, Department of Pharmacology, Vanderbilt Brain Institute, Program in Developmental Biology and Institute of Chemical Biology, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America

Antennal-Expressed Ammonium Transporters in the Malaria Vector Mosquito Anopheles gambiae

  • R. Jason Pitts, 
  • Stephen L. Derryberry Jr., 
  • Fadi E. Pulous, 
  • Laurence J. Zwiebel
PLOS
x

Abstract

The principal Afrotropical malaria vector mosquito, Anopheles gambiae remains a significant threat to human health. In this anthropophagic species, females detect and respond to a range of human-derived volatile kairomones such as ammonia, lactic acid, and other carboxylic acids in their quest for blood meals. While the molecular underpinnings of mosquito olfaction and host seeking are becoming better understood, many questions remain unanswered. In this study, we have identified and characterized two candidate ammonium transporter genes, AgAmt and AgRh50 that are expressed in the mosquito antenna and may contribute to physiological and behavioral responses to ammonia, which is an important host kairomone for vector mosquitoes. AgAmt transcripts are highly enhanced in female antennae while a splice variant of AgRh50 appears to be antennal-specific. Functional expression of AgAmt in Xenopus laevis oocytes facilitates inward currents in response to both ammonium and methylammonium, while AgRh50 is able to partially complement a yeast ammonium transporter mutant strain, validating their conserved roles as ammonium transporters. We present evidence to suggest that both AgAmt and AgRh50 are in vivo ammonium transporters that are important for ammonia sensitivity in An. gambiae antennae, either by clearing ammonia from the sensillar lymph or by facilitating sensory neuron responses to environmental exposure. Accordingly, AgAmt and AgRh50 represent new and potentially important targets for the development of novel vector control strategies.

Introduction

Gaseous ammonia and its protonated ionic form, ammonium, (collectively referred to as ammonium) are important molecules for life on earth. For many organisms, ammonium is a critical precursor for a wide range of biologically active macromolecules. For example, plants cannot utilize atmospheric nitrogen gas and must fix nitrogen from the soil via symbiotic bacteria and fungi [1], [2]. While some organisms do not uptake ammonium directly, they import other nitrogen sources and convert them into ammonium for use in biosynthetic pathways [3]. Paradoxically, while ammonium uptake is crucial for biological systems, it is also produced as a waste product of nucleic acid and amino acid metabolism and is toxic at high concentrations [4]. It is therefore not surprising that regulation of ammonium levels at cellular, organ, tissue, and organismal levels is paramount to viability of virtually all forms of life. Cells have devised a number of mechanisms to deal with excess ammonia, including conjugation of amines to larger non-toxic compounds and secretion of ammonium in various forms [4][6]. The latter process requires the action of transmembrane proteins that increase the permeability of ammonium across cell membranes, and are accordingly classified as ammonium transporters [6], [7]. Diverse mechanisms have evolved for the transport of ammonium and ammonium derivatives in cells. These include the ammonium transporters (Amt) in bacteria and plants, the methylammonium/ammonium permeases (MEPs) in yeast, and the Rhesus (Rh) proteins in mammals [6], [8], [9]. In microbes, a role for ammonium transporters in sensing environmental levels of ammonia has been described [10][13].

Canonically, ammonium transporter proteins have been thought to facilitate the movement of ammonium ions across cell membranes [6], [9]. After ammonium is accumulated inside, it is used for metabolic purposes such as in the synthesis of biological macromolecules. However, there has been support from various studies involving fungi and bacteria that indicate that ammonium transporters may additionally function as ammonium sensors [14]. In Saccharomyces cerevisiae, mep2 null mutants do not exhibit wild-type levels of pseudohyphal growth upon nitrogen starvation that is thought to occur as the cell is searching for a source of nutrients [10]. Researchers later concluded that MEP2 was necessary but not sufficient for the production of these filamentous growths under nitrogen-limiting conditions [10]. In a similar manner, AmtB from Escherichia coli is regulated by GlnK, a PII class signal transduction protein [15]. When ammonium is sparse, GlnK is in its fully-uridylylated state and is not membrane associated; however, in conditions when ammonium concentrations are high, GlnK is deuridylylated and associates tightly with AmtB causing ammonium flux to stop [12]. An intriguing possibility is that as a result of their ability to facilitate ammonium flux across cell membranes eukaryotic ammonium transporters also act as either direct, or indirect chemosensors. While ammonium transporters have been described in numerous species, little is known about the specifics of their expression and functionality in insects.

In An. gambiae and other insects, three families of ligand-gated receptors are known to participate in various aspects of chemosensation: the odorant receptors (AgOrs), the variant ionotropic glutamate receptors (AgIrs), and the gustatory receptors (AgGrs) [16][18]. The Ors are primarily expressed in the olfactory receptor neurons (ORNs) that are housed within sensilla extending from the surfaces of the adult head appendage: antennae, maxillary palps, and proboscises [17], [19], [20]. They function primarily as ionotropic receptors that mediate sensitivities to volatile environmental odors that are carried by air currents in the near, or even distant, vicinity of the mosquito [21][24]. The well-conserved coreceptor, Orco, plays a vital role in mediating Or localization and function in a broad array of insect taxa [25]. The Grs are sensors of soluble compounds that include sugars, bitter tastants, and contact pheromones and are broadly expressed in the proboscises and leg tarsi of insects [26][31]. In adult An. gambiae, the major components of human sweat, such as ammonia, lactic acid, and carboxylic acids activate ORNs found in trichoid and basiconic (grooved peg) sensilla [32], the latter of which lack AgOrs [19]. While AgOrs are likely to account for a significant component of the molecular basis of trichoid sensitivities, the broad gaps in AgOr-based odor coding [33], [34] suggest an alternative molecular foundation for grooved peg sensitivities. Studies in Drosophila melanogaster [35][38] and Schistocerca gregaria [39] indicate that Irs are expressed in grooved peg sensilla and mediate their responses to chemical odors. By inference, the AgIRs are the most likely candidates to mediate grooved peg physiological responses in An. gambiae [18], [40]. Considering the importance of ammonia and amine compounds as human-derived kairomones affecting An. gambiae host-seeking behavior, identifying sensory receptors as well as salient ancillary proteins that are involved in the perception of these compounds would both improve our understanding of An. gambiae chemosensory mechanisms and provide additional targets for intervention strategies that could lower the incidence of human malaria transmission.

Even with the current advances in medical and other technologies, malaria remains a significant threat to global health [41]. Anopheles gambiae, the sub-Saharan human malaria vector mosquito, has been responsible for millions of deaths worldwide as a consequence of its anautogenous lifestyle. Human host odors, including those found in analyses of human sweat (ammonium, lactic acid, various carboxylic acids), are able to elicit electrophysiological responses in the adult female mosquito antennae [32], [40], [42][44]. Despite understanding which sensilla are responsive to ammonium, the molecular basis for An. gambiae's sensitivity to ammonia remains unknown [32].

We have previously utilized next generation RNA sequencing to examine the transcriptome profile from chemosensory tissues of An. gambiae [45], [46]. In addition to numerous other transcripts with similar expression profiles, we have identified 2 candidate ammonium transporters, AgAmt and AgRh50, whose transcripts are highly abundant in the antennae of An. gambiae. We postulate that enhanced antennal expression indicates that AgAmt and AgRh50 play important roles in the peripheral chemosensory signal transduction pathways that detect environmental ammonia in An. gambiae. AgAmt and AgRh50 transcripts were also found in whole bodies of both females and males, consistent with their roles in ammonia clearance in Malpighian tubules and other body tissues. We have employed heterologous expression systems to confirm that AgAmt and AgRh50 are indeed functional ammonium transporters. The successful functional characterization of An. gambiae ammonium transporters strengthens our basic understanding of chemosensory processes in mosquitoes, and accordingly, may have profound implications for global health.

Materials and Methods

Ethics Statement

This study adhered to the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The use of Xenopus laevis for oocyte harvesting was approved by the Vanderbilt University Institutional Animal Care and Use Committee (Protocol M/10/174). Surgeries were performed under Tricaine methanesulfonate (MS-222) and cold anesthesia using aseptic technique. Every effort was made to minimize pain and suffering.

Gene Identification and Phylogeny

Ammonium transporter sequences (AGAPs 003989 and 002011) in the An. gambiae genome annotation v3.7 were queried in tBLASTn and BLASTp searches using default parameters (http://www.vectorbase.org) to identify other homologous sequences, but no other significantly similar hits were found. Conceptual exons and intron were identified using the Softberry HMM gene search software (http://www.softberry.com). Protein sequences were aligned with Clustal X software [57]. Neighbor-Joining trees [58] were constructed from peptide alignments with 100 bootstrap replicates. Transmembrane plots were generated using the Protter protein display software [59].

Reverse Transcription/Polymerase Chain Reaction

AgAmt and AgRh50 transcript levels were determined by means of quantitative RT-PCR. Each sample was comprised of 10 heads, 50 antennae, 50 palps or 10 carcasses that were hand-dissected from batches of control and experimental 5–7 d.o. An. gambiae adult females. RNA was extracted using the trizol method as described [45] and cDNA synthesis were performed using the Transcriptor First Strand cDNA Synthesis Kit (Roche, Inc.). All primers in the assay were designed to span predicted introns in order to distinguish well between genomic DNA and cDNA templates. An. gambiae ribosomal protein lysosomal aspartic protease (AGAP003277; AgLap), which is constitutively expressed at high levels in all tissues, was chosen as control gene to measure the levels of AgAmt and AgRh50 mRNA in vivo. Primer sequences are as follows: AgLap forward 5′-CCAACTATCTCGATGCTCAAT-3′; AgLap reverse 5′-ATTCTTCTCGAACGAGGACG-3′ (product size: 188 bp); AgAmt forward 5′-GGAAGTTTCAGCATCATCTATT-3′ and reverse 5′-CCGACGGCTAGCACACCCCA-3′ (product size: 266 bp); AgRh50a forward 5′-GCGTCGAAACATACGGCACC-3′ and AgRh50a reverse 5′-GAGGGTGATTTGAGTATCAATCCGG-3′ (product size: 233 bp); AgRh50b forward 5′-GGCGGGCTGATAACCGGAGTGA-3′ and AgRh50b reverse 5′-GAGGGTGATTTGAGTATCAATCCTT-3′ (product size: 213 bp). PCR amplicons were cloned and sequenced to confirm their identities. qRT-PCR was carried out using an Applied Biosystems 7300 Real-time PCR system and SYBR green as fluorescent dye. Three experimental repetitions were analyzed for each biological sample and the data processed using System 7300 Sequence Detection Software (version 1.3.1). Primer efficiency was determined using a standard curve for all the primers used. In the amplification of AgAmt and Rps7, 8 µl and 2 µl cDNA, respectively, from each group were used as templates. In each trial, AgAmt or AgRh50 cDNA levels were quantified relative to AgLap levels using the method of Pfaffl [60].

RNA Sequencing

Illumina RNA-seq read files from a previous study [45] were derived from An. gambiae tissues and are freely available at the National Center for Biotechnology Information Sequence Read Archive (http://trace.ncbi.nlm.nih.gov/Traces/sra/; SRA study accession: SRP028873). Total weighted reads and transcript lengths for AgAmt, AgRh50a, and AgRh50b were used to calculate normalized transcript abundance levels in units Reads Per Kilobase per Million reads mapped (RPKM) [61].

cDNA Vector Construction and cRNA synthesis

The full-length coding sequences of AgAmt and AgRh50 were amplified by polymerase chain reaction from a cDNA library derived from An. gambiae antennae using primers specific for their coding sequences: AgAmt forward 5′-CACCATGGCCAACGGCACAACGATGG-3′; AgAmt reverse 5′-TTATCAATCCACGCAAAGTT-3′; AgRh50a/b forward 5′-CACCATGCACACACCAGGATCCTC-3′ AgRh50a/b reverse 5′-CTAGTTGGATGATTCGTTGGT3′. Once amplified, AgAmt, AgRh50a and AgRh50b were cloned into pSP64T-Oligo expression plasmid using the Gateway SystemR (Invitrogen). cRNA for was synthesized from linearized plasmid (XbaI digest) using the mMessage mMachineR SP6 RNA polymerase kit (Life Technologies, Inc.).

Xenopus laevis Oocyte Retrieval, Microinjection, and Incubation

Expression and functional characterization of AgAmt was carried out essentially as described for AgOR proteins [17], [34], [62]. X. laevis ovarian lobes were extracted from fully mature females via laparotomy. An incision less than 1 cm was made ventrally, lateral of the midline, in the organism's skin, and then the ovarian wall. The ovarian lobes were then extracted and placed in a washing buffer (96 mM NaCl, 2 mM KCl, 5 mM MgCl2, and 5 mM Hepes, pH 7.6) supplemented with gentamycin. The ovarian lobes were gently separated via forceps and subsequently treated with 2 mg/mL collagenase S-1 in washing buffer for 45 minutes to an hour at room temperature while on a laboratory shaker. Oocytes were then washed twice with washing buffer and incubated in ND96 buffer (96 mM NaCl, 2 mM KCl, 1 mM MgCl2, 1 mM CaCl2, and 5 mM Hepes, pH 7.5) supplemented with 5% dialyzed, heat-inactivated horse serum, 50 µg/mL tetracycline, 100 µg/mL streptomycin, and 550 µg/mL sodium pyruvate at 18°C until microinjection.

Each oocyte was selected for injection based on health (appearance) and developmental stage (stage V or VI). Each oocyte was injected with approximately 30 ng AgAmt cRNA. After injection, oocytes were incubated separately at 18°C in supplemented ND96 buffer. Oocytes were allowed to incubate for 2 to 5 days until assayed by two-electrode voltage clamp electrophysiology.

Solutions

Salts of the highest commercial grade available were obtained from Fisher Scientific, Alfa Aesar, or Sigma Aldrich. 1M chloride salts, originally diluted in ND96, were diluted further in ND96 to reach the tested concentrations. During the TEVC and voltage-step assay, ND96 was continuously perfused over each oocyte. Different stimuli were introduced using the ValveLink 8.2 stimulus controller (AutoMate Scientific).

It is known that ammonium (NH4+) will induce endogenous currents in X. laevis oocytes when the concentration of the species is equal to or greater than 1 mM [47], [48]. Most solutions used in these experiments did not exceed a concentration of 200 µM ammonium to monitor the effects that ammonium has on AgAmt and not endogenous proteins found in the oocyte; however, to observe whether the contribution of AgAmt was greater than the endogenous currents elicited by ammonium concentrations greater than 1 mM, the magnitude of the currents resulting in water-injected oocytes were compared to those resulting in AgAmt-injected oocytes.

Two-Electrode Voltage Clamp Electrophysiology

Whole-cell currents were recorded from injected oocytes using the OC-725C feedback amplifier (Warner Instruments). The amplifier was connected to a computer interface through the Axon Digidata 1440A Digitizer; data acquisition and analysis were carried out using pCLAMP 10 software (Axon Instruments). The current-injecting and voltage-sensing electrodes were made of Ag/AgCl wires housed in pulled borosilicate glass capillaries each containing 0.2 µM filtered 3M KCl. A salt bridge (3M KCl and 4% w/v agarose) connected the bath solution and the sense electrode. Each oocyte was clamped at a holding potential of −80 mV, excluding current-voltage analysis. Stimuli were delivered to oocytes until steady state currents developed. The resulting magnitude of the change in current before the stimulus and steady state was calculated using pCLAMP 10 software and was subsequently used for data analysis.

Voltage-Step Assay

Current versus voltage plots were generated using the following protocol. Stimuli were continuously applied to an oocyte voltage-clamped at −100 mV. After approximately 30 seconds (the time required to reach steady state), a voltage-step protocol was executed in which the voltage increased by 10 mV with each run, starting at −100 mV and ending with +40 mV. Each run lasted 200 milliseconds in order to minimize the effect of rectifying currents. Current magnitudes were calculated by calculating the absolute difference of the currents measured for a stimulus at a given voltage (either ammonium chloride or methylammonium chloride) from the currents resulting from the perfusion of ND96 at those same voltages.

Yeast Transformation and Complementation

S. cerevisiae yeast strains were obtained from the laboratory of Dr. Anna Maria Marini (Université Libre de Bruxelles). Strain 31019b is a triple mutant of the methyl ammonium permeases mep1, mep2 and mep3 (mep1-3Δ) and strain 23344c is the wild type background ura3 deletion strain [63]. An. gambiae ammonium transporter coding sequences were cloned into yeast expression plasmid, pAG426GAL-ccdB (www.Addgene.org; plasmid 14155) using the LR Clonase system (Invitrogen) and verified by PCR, restriction digest analysis and Sanger sequencing. Yeast transformations were carried out using the polyethylene glycol and lithium chloride method as previously described [64]. Selection for transformed yeast was performed on solid medium without uracil, plus 0.17% yeast nitrogen base (YNB) lacking amino acids and ammonium sulfate (Difco #Y1251), supplemented with 2% galactose and 1 mM Arginine as the sole nitrogen source. Transformants were verified by PCR using gene specific primers as described above.

Yeast strains were cultured in liquid medium containing 1 mM Arginine as the sole nitrogen source until optical density at 600 nm (OD600) reached 0.6–0.8. Cells were pelleted by centrifugation, washed in sterile water, and resuspended in fresh medium to an initial OD600 of 0.05 in liquid culture or 10 ul droplets of 1000–2000 cells per spot on solid media. Growth at 30°C was then monitored every 24 hours in 1 mM ammonium sulfate or Arginine for each transformant and compared with controls; wild type or mep1-3Δ transformed with the empty pAG426GAL-ccdB plasmid. Growth assays were repeated 4 times for liquid and solid media. Mann-Whitney U tests were conducted as a non-parametric test of means comparing average OD600 at 4–7 days post-inoculation for liquid cultures of wild type and An. gambiae ammonium transporter transformants against mep1-3Δ. Colonies growing on solid media at 2–4 days post-inoculation were photographed with the aid of a dissecting microscope and digital camera. Individual colonies located within 10 ul circular spots were analyzed using ImageJ software [65] to determine average area in square millimeters.

Results

An. gambiae Ammonium Transporter Genes

The An. gambiae genome encodes two candidate ammonium transporter genes, AGAP003989 and AGAP002011, one representative from each of the Amt and Rhesus subfamilies, which we have named AgAmt and AgRh50, respectively (Figure 1). AgAmt appears to encode a single transcript (Figure 1) and a conceptual peptide of 591 amino acids (Figure 2A). AgRh50 appears to encode 2 alternatively spliced transcripts, AgRh50a and AgRh50b (Figure 1), the latter containing a novel 175 bp exon near the 3′ end of the transcript that was not predicted in the An. gambiae genome annotation (Figure 1). The transcripts for AgRh50a and AgRh50b encode conceptual peptides of 470 and 497 amino acids, respectively (Figure 2B). In addition, both peptides are predicted to form 11 transmembrane helices with an extracellular N-terminus and intracellular C-terminus (Figure 2), similar to other known ammonium transporters [47]. AgAmt and AgRh50 are clearly distinguishable as members of the two major ammonium transporter subfamilies (Figure 3) and share significant homologies with proteins encoded in several other insect genomes that are also putative ammonium transporters (Figure 3, Table S1).

thumbnail
Figure 1. An. gambiae ammonium transporter gene structures.

Schematic representation of the exon (boxes) and intron (lines) structure of AgAmt and AgRh50 genomic loci. Alternative splicing at 3′ end of AgRh50 indicated by white boxes (AgRh50a) and black box and shaded region of final exon (AgRh50b) and TAG and TGA stop codons, respectively. Scale bar is for exons only; introns lengths in base pairs are indicated above or below splice sites.

https://doi.org/10.1371/journal.pone.0111858.g001

thumbnail
Figure 2. Amino acid plots of AgAmt (A) and AgRh50 (B) depicting the 11 transmembrane domains.

AgRh50a and AgRh50b differ only in their C-terminal regions.

https://doi.org/10.1371/journal.pone.0111858.g002

thumbnail
Figure 3. Phylogenetic tree of ammonium transporter families.

Neighbor-joining tree comparing relationships among ammonium transporter proteins from prokaryotes and eukaryotes. Rhesus (blue shaded region) and Amt (green shaded region) proteins segregate into distinct families, with insects having representatives in both groups. Bootstrap support for branches is indicated. Scale bar is 1% corrected distance. Sequences and species names are found in Table S1.

https://doi.org/10.1371/journal.pone.0111858.g003

AgAmt and AgRh50 Transcript Abundances

RNA sequencing and RT-PCR confirmed the presence of AgAmt and AgRh50 transcripts in several adult tissues including antennae, maxillary palps, heads and whole bodies of An. gambiae (Table 1, Figure 4). Strikingly, transcripts for AgAmt and the AgRh50b splice variant were highly enriched in antennae compared with other tissues, while the AgRh50a transcript was much more evenly distributed in abundance (Table 1, Figure 4). Quantitative PCRs (qPCRs) confirmed the enhanced antennal specificity of AgAmt and AgRh50b, which were >100 fold overabundant in antennae relative to bodies (Figure 4). This analysis also revealed an enhancement (>4.5–24 fold) of AgRh50a transcripts in heads devoid of chemosensory appendages relative to bodies (Figure 4). While AgAmt and AgRh50b protein levels have yet to be determined in these tissues, enhanced levels of AgAmt and AgRh50 transcripts in antennae are consistent with important roles for ammonium transporters in antennae function.

thumbnail
Figure 4. An. gambiae ammonium transporter expression in adult tissues.

Left panels: RT-PCR amplification of AgAmt, AgRh50a, AgRh50b using cDNAs derived from adult female bodies, heads, antennae, and maxillary palps. +/− indicates presence or absence of reverse transcriptase in cDNA synthesis reactions. 100 bp marker shown for each gel image. Amplicons are of the expected sizes for each transcript: AgAmt (266 bp), AgRh50a (223 bp), AgRh50b (213 bp). Right panels: qRT-PCR amplification of AgAmt, AgRh50a, and AgRh50b relative to body (x:body) expression using AgLap as a normalizing transcript in each of 3 biological replicates (Samples 1–3). AgAmt (black bars) and AgRh50b (white bars) transcripts are dramatically enhanced in antennae (a), while AgRh50a (gray bars) transcript is enhanced in heads (h), minus antennae (a) and palps (p).

https://doi.org/10.1371/journal.pone.0111858.g004

thumbnail
Table 1. Transcript abundance values for An. gambiae ammonium transporters in adult tissues (adapted from [45]).

https://doi.org/10.1371/journal.pone.0111858.t001

TEVC Analysis of AgAmt-Injected Oocytes

In order to determine whether AgAmt and AgRh50 can form functional ammonium transporters, we used the Xenopus laevis heterologous expression system and two-electrode voltage clamp electrophysiology (TEVC). Oocytes injected with AgAmt cRNAs consistently evoked inward currents when voltage clamped at −80 mV in response to perfusions of ammonium chloride concentrations ranging from 200 nM to 200 µM (Figure 5A). As a negative control, buffer-injected oocytes were perfused with the same concentrations of ammonium chloride, yet no currents were observed (Figure 5A). A similar characterization of both splice forms of AgRh50 was attempted using the oocyte system; however, currents were not observed when AgRh50a or AgRh50b cRNA-injected oocytes were perfused with ammonium and methylammonium (data not shown). While we can reasonably conclude the observed inward currents from AgAmt-injected oocytes are likely due to the functional presence of AgAmt in the oocyte plasmid membrane, we cannot exclude the possibility that the observed currents are due to the interaction of the exogenously expressed transporter with endogenous proteins (Figure 5A). Previous studies have demonstrated that X. laevis oocytes produce endogenous inward currents in response to concentrations of ammonium at or above 1 mM [48], [49]. AgAmt-injected oocytes showed increasing responses to ammonium chloride at concentrations up to 500 mM that were always much larger in amplitude than endogenous currents recorded from water-injected controls (Figure 5B). These results suggest that the total whole cell current in AgAmt-injected oocytes is the summation of currents produced by the endogenously expressed ammonium transporters and the AgAmt transporter, which is responsible for the larger amplitudes compared to controls (Figure 5B).

thumbnail
Figure 5. Function of AgAmt in Xenopus oocytes.

Representative traces showing an AgAmt cRNA injected oocyte and water injected oocyte to concentrations of ammonium chloride. Black bars indicate stimulus length. Histogram showing normalized magnitude of inward current measured at steady state for AgAmt injected oocytes (green) and water injected oocytes (blue) to concentrations of ammonium chloride. Currents were normalized with respect to the average steady state current that resulted from AgAmt oocytes when stimulated with 200 µM ammonium chloride. Higher Concentrations: Representative traces showing an AgAmt cRNA injected oocyte and water injected oocyte to concentrations of ammonium chloride. Black bars indicate stimulus length. Histogram showing normalized magnitude of inward current measured at steady state for AgAmt injected oocytes (green) and water injected oocytes (blue) to concentrations of ammonium chloride. Currents were normalized with respect to the average steady state current that resulted from AgAmt oocytes when stimulated with 500 mM ammonium chloride. Different Compounds: Representative traces showing an AgAmt cRNA injected oocyte and water injected oocyte to different chloride salts at 200 µM. Black bars indicate stimulus length. Histogram showing normalized magnitude of inward current measured at steady state for AgAmt injected oocytes (green) and water injected oocytes (blue) to 200 µM chloride salt. Currents were normalized with respect to the average steady state current that resulted from AgAmt oocytes when stimulated with 200 µM ammonium chloride.

https://doi.org/10.1371/journal.pone.0111858.g005

Previously characterized ammonium transporters have the ability to transport a slightly larger derivative of ammonium, methylammonium [50][53]. To examine whether AgAmt is similarly able to transport this ion, 200 µM methylammonium chloride was perfused over voltage clamped AgAmt-injected oocytes. Inward currents in response to 200 µM methylammonium were approximately 55% of the magnitude of the inward currents recorded from the same oocytes perfused with 200 µM ammonium chloride (Figure 5C). In addition, other chloride salts were also perfused over AgAmt-injected oocytes to ascertain whether the observed inward currents were due to the presence of chloride anions. In these studies no inward currents were evoked in response to Na+, K+, or Ca2+ chloride salts at 200 µM (Figure 5C). As before, inward currents were not observed from water-injected controls to any of the tested chloride salts at 200 µM (Figure 5C). On the whole, these results are consistent with previous studies in that AgAmt-injected oocytes display inward currents in response to perfusions of ammonium and to a lesser magnitude with methylammonium, but fail to elicit inward currents with other ions [51], [54].

A current-voltage plot was generated by measuring ion-induced currents at several different membrane holding potentials in order to further examine the relationship between AgAmt-dependent ammonium and methylammonium conductances (Figure 6). The slope of current/voltage (I/V = conductance) in response to 200 µM ammonium chloride was much greater than the corresponding slope in response to 200 µM methylammonium chloride (Figure 6). This result clearly shows that ammonium elicits a larger whole-cell conductance than methylammonium at the same concentrations. In addition, the reversal potential of each ion, defined as the voltage at which the recorded current is zero, was approximately 20 mV for ammonium and >40 mV for methylammonium under these conditions.

thumbnail
Figure 6. I–V Plot of whole cell conductances in oocytes expressing AgAmt.

Current-voltage relationship for AgAmt cRNA injected oocytes to ammonium chloride (orange) and methylammonium chloride (purple). The x-axis shows voltage measured in millivolts and the y-axis shows current measured in microamps.

https://doi.org/10.1371/journal.pone.0111858.g006

Yeast Ammonium Transporter Complementation

Given the lack of function of AgRh50 transcripts in Xenopus oocytes, we attempted to complement a S. cerevisiae ammonium transporter triple mutant with plasmids expressing the An. gambiae ammonium transporters, AgAmt, AgRh50a and AgRh50b under the control of the galactose promoter. In these studies the mep1-3Δ mutant lacks all 3 endogenous ammonium transporters and accordingly grows very poorly in media where ammonium salts are the only source of free nitrogen (Figure 7). When the An. gambiae ammonium transporters were expressed in the mutant background, partial complementation of the mep1-3Δ mutant was observed for AgRh50a and AgRh50b both in liquid and solid media (Figure 7). Although not restored to wild-type levels, clear improvement in growth of the mutant strain was consistently observed after 4–6 days of growth in liquid culture (Figure 7 B,C) and after 2–4 days on solid plates (Figure 7D). In addition to improved growth based on optical density measurements of liquid cultures, colony size was similarly increased on solid media, being approximately 2–3 times larger for AgRh50b and AhRh50a, respectively (Figure 7D). The average optical density of AgRh50a-expressing strains compared with the triple mutant was significant (p = 0.08) at a reduced constraint P<0.1 in a Mann-Whitney U test (Figure 7C). We did not observed complementation of the mutant phenotype in AgAmt transformants.

thumbnail
Figure 7. AgRh50 Complements a Yeast Ammonium Transporter Mutant.

Representative growth curve of wild type yeast and mep1-3Δ triple mutant transformants in minimal medium supplemented with 1 mM Arginine (A) or 1 mM ammonium sulfate (B) as the sole nitrogen source. (C) Histogram plot of mean optical densities for yeast transformants grown in minimal medium supplemented with 1 mM Arginine (white bards) or 1 mM ammonium sulfate (black bars). Error bars are SEM; n = 4. (D) Growth of yeast transformants spotted onto solid minimal medium with indicated supplements as above. Circles are 10 ul spots of ∼1000–2000 cells each, showing confluent growth on 1 mM Arginine (top panels) and reduced growth on 1 mM ammonium sulfate (bottom panels). Mean colony area (mm2) indicated in lower corner of bottom panes.

https://doi.org/10.1371/journal.pone.0111858.g007

Discussion

We have used molecular approaches to identify AgAmt and AgRh50 as ammonium transporter homologs with discrete transcripts (Figures 13) that are expressed in the antennae of host-seeking female An. gambiae mosquitoes. Interestingly, both the AgAmt and AgRh50b transcripts were highly enhanced in female antennae compared to bodies, palps or heads (devoid of antennae and palps), in multiple independent analyses (Table 1, Figure 4). Conversely, the AgRh50a transcript was more uniformly expressed with a lesser enhancement in heads (Table 1, Figure 4). These findings suggests partitioning of function between different isoforms of the resulting peptides, perhaps reflecting a more critical role for AgRh50a in ammonia clearance in the head and body and more specialized sensory roles for AgAmt and AgRh50b in the antennae. One possibility is that AgAmt and AgRh50b are expressed in the support cells surrounding ORNs and are involved in the clearance of ammonia from the aqueous lymph of antennal sensilla. This would serve to effectively reduce the noise associated with low constant exposure to environmental ammonia and would consequently allow the mosquito to maintain a high threshold of sensitivity to changes in ammonia concentration. Another possibility is that one or both ammonia transporters are localized within dendritic membranes of ORNs and directly facilitate rapid and highly effective transport of ammonia/ammonium into the cells, thereby evoking membrane potential changes that may lead to action potential firing via an unknown signaling mechanism(s). In either case, these models represent important and perhaps essential roles for this class of transporters in maintaining mosquito sensitivity to ammonia. Further studies will be required to resolve the exact functions of AgAmt and AgRh50 in physiological and behavioral responses of An. gambiae females to ammonia.

We have also used heterologous expression and TEVC analysis in oocytes to examine the ammonium transporter functionality of AgAmt and the two AgRh50 isoforms. While previous studies have found that uninjected, clamped oocytes display inward currents in response to ammonium concentrations greater than or equal to 1 mM [48], [49], we demonstrated that AgAmt cRNAs are sufficient to evoke dose dependent inward currents to ammonium at concentrations well below 1 mM (Figure 5A). In our studies, injection of AgAmt cRNAs into oocytes subsequently assayed with TEVC yielded dose dependent inward currents to ammonium chloride concentrations ranging from 200 nM to 200 µM when voltage clamped at −80 mV (Figure 5A). We interpret these dose-dependent currents as evidence of functional AgAmt complexes in oocytes, as currents were not observed in buffer-injected control oocytes when the same concentrations of ammonium chloride were presented (Figure 5A).

We also confirmed that AgAmt-injected oocytes display inward currents larger in magnitude than buffer-injected controls in response to higher concentrations of ammonium >1 mM (Figure 5B). Assuming that only these two ammonium-induced currents are present in AgAmt-injected oocytes, subtracting the control inward currents from the currents recorded from AgAmt-injected oocytes would yield the net contribution of AgAmt complexes to each ammonium chloride concentration tested. Pharmacological analysis aimed towards inhibiting the individual currents will be necessary to further support this conclusion.

Other functionally characterized Amts have the ability to transport methylammonium, a slightly larger derivative of ammonium, although with less efficacy and/or potency [53], [55], [56]. We also observed inward currents in AgAmt-injected oocytes in response to methylammonium chloride (Figure 5C). 200 µM methylammonium chloride evoked inward currents in voltage clamped AgAmt-injected oocytes that were approximately 55% of the magnitude of ammonium at the same concentration (Figure 5C). In addition to testing ammonium chloride and methylammonium chloride, Na+, K+, and Ca2+ chloride salts were tested at 200 µM to determine if chloride was eliciting the observed currents (Figure 5C). Neither AgAmt-injected oocytes, nor control oocytes elicited currents when perfused with Na+, K+, and Ca2+ chloride salts at 200 µM (Figure 5C). These findings strongly suggest that AgAmt is capable of transporting both ammonium and the larger derivative, methylammonium, across biological membranes, thus increasing our confidence that AgAmt can function as an ammonium transporter in vivo, although the exact mechanisms and consequences of its transport activity in An. gambiae tissues remains unresolved.

When oocytes were injected with either AgRh50a or AgRh50b cRNAs, the TEVC response profiles were not different from buffer-injected controls in response to varying concentrations of ammonium chloride and methylammonium chloride (data not shown). The lack of inward currents observed from AgRh50-injected oocytes could be the result of missing protein co-factors required for the formation of functional AgRh50 complexes. Alternatively, functional AgRh50 complexes may not be electrogenic, like some mammalian Rh50 transporters, such that their activity cannot be detected within the TEVC assay [8].

In yeast growth assays, we observed at least partial complementation of a triple mutant yeast strain when expressing AgRh50a and a trend toward improved growth when expressing AgRh50b (Figure 7). These results support the conclusion that both AgRh50 proteins are able to function as ammonium transporters in yeast cells, albeit at a reduced efficiency compared to the endogenous yeast proteins. Incomplete complementation by An. gambiae ammonium transporters could simply reflect the inability of a single subunit to compensate for the loss of all 3 endogenous genes. In addition, we could not control for expression levels, transport/membrane localization or differences in efficiencies of ammonium transporters that may be a consequence of divergences in their primary sequences.

Taken together, these data provide compelling evidence that AgAmt and AhRh50 are functional ammonium transporters. The abundance and antennal localization of both AgAmt and AgRh50 suggest they may have specialized functions in sensory physiology of An. gambiae antennae where they mediate responses to ammonia, arguably one of the most important odor cues utilized by host seeking female mosquitoes. Given the eroding efficacy of current mosquito control methods, which rely heavily on the use of insecticides for mosquito control, the identification of novel sensory mechanisms may ultimately lead to the development of new tools for individual personal protection or surveillance that can help reduce disease transmission.

Supporting Information

Table S1.

Ammonium transporters sampled from a broad range of species. Peptide sequences were used in the construction of the phylogenetic tree in Figure 3.

https://doi.org/10.1371/journal.pone.0111858.s001

(CSV)

Acknowledgments

We thank Ms. Zhen Li for mosquito rearing and assistance with Xenopus laevis oocyte harvesting and injections. We also thank David Menger, Drs. Willem Takken and Joop van Loon (Wagenigen University, Netherlands) for gene silencing efforts and members of the Zwiebel lab for critical reading of the manuscript. S. cerevisiae strains were the kind gift of Dr. Anna Maria Marini (Université Libre de Bruxelles). Plasmid pAG426GAL-ccdB was obtained via the Addgene plasmid repository (submitted by Dr. Susan Lindquist, Whitehead Institute for Biomedical Research).

Author Contributions

Conceived and designed the experiments: RJP SLD LJZ. Performed the experiments: RJP SLD FEP. Analyzed the data: RJP SLD. Contributed reagents/materials/analysis tools: RJP SLD. Wrote the paper: RJP SLD LJZ.

References

  1. 1. Santi C, Bogusz D, Franche C (2013) Biological nitrogen fixation in non-legume plants. Annals of Botany 111: 743–767.
  2. 2. Day DA, Poole PS, Tyerman SD, Rosendahl L (2001) Ammonia and amino acid transport across symbiotic membranes in nitrogen-fixing legume nodules. Cell Mol Life Sci 58: 61–71.
  3. 3. Wirén NV, Merrick M (2004) Regulation and function of ammonium carriers in bacteria, fungi, and plants. Topics in Current Genetics. Topics in Current Genetics. Berlin, Heidelberg: Springer Berlin Heidelberg, Vol. 9. pp. 95–120.
  4. 4. Campbell R, Reece JB (2002) Biology. Benjamin Cummings, Publ. San Francisco. Chapter 44, pp 925–954.
  5. 5. Weiner ID, Verlander JW (2013) Renal ammonia metabolism and transport. Compr Physiol 3: 201–220.
  6. 6. Andrade SLA, Einsle O (2007) The Amt/Mep/Rh family of ammonium transport proteins. Mol Membr Biol 24: 357–365.
  7. 7. Ludewig U, Neuhäuser B, Dynowski M (2007) Molecular mechanisms of ammonium transport and accumulation in plants. FEBS Lett 581: 2301–2308.
  8. 8. Nakhoul NL, Hamm LL (2013) Characteristics of mammalian Rh glycoproteins (SLC42 transporters) and their role in acid-base transport. Molecular Aspects of Medicine 34: 629–637.
  9. 9. Huang C-H, Ye M (2009) The Rh protein family: gene evolution, membrane biology, and disease association. Cell Mol Life Sci 67: 1203–1218.
  10. 10. Lorenz MC, Heitman J (1998) The MEP2 ammonium permease regulates pseudohyphal differentiation in Saccharomyces cerevisiae. EMBO J 17: 1236–1247.
  11. 11. Yakunin AF, Hallenbeck PC (2002) AmtB Is Necessary for NH4+-Induced Nitrogenase Switch-Off and ADP-Ribosylation in Rhodobacter capsulatus. J Bacteriol 184: 4081–4088.
  12. 12. Coutts G, Thomas G, Blakey D (2002) Membrane sequestration of the signal transduction protein GlnK by the ammonium transporter AmtB. EMBO J
  13. 13. Tremblay PL, Hallenbeck PC (2008) Ammonia-Induced Formation of an AmtB-GlnK Complex Is Not Sufficient for Nitrogenase Regulation in the Photosynthetic Bacterium Rhodobacter capsulatus. J Bacteriol 190: 1588–1594.
  14. 14. Tremblay P-L, Hallenbeck PC (2009) Of blood, brains and bacteria, the Amt/Rh transporter family: emerging role of Amt as a unique microbial sensor. Molecular Microbiology 71: 12–22.
  15. 15. Merrick M, Javelle A, Durand A, Severi E, Thornton J, et al. (2006) The Escherichia coli AmtB protein as a model system for understanding ammonium transport by Amt and Rh proteins. Transfus Clin Biol 13: 97–102.
  16. 16. Hill CH, Fox AN, Pitts RJ, Hunt LH, Collins FC, et al. (2002) G Protein-Coupled Receptors in Anopheles gambiae. Science 298: 176–8.
  17. 17. Lu Qiu, Wang G, Kwon Rutzler, et al. (2007) Odor Coding in the Maxillary Palp of the Malaria Vector Mosquito Anopheles gambiae. Curr Biol 17: 1533–1544.
  18. 18. Liu C, Pitts RJ, Bohbot JD, Jones PL, Wang G, et al. (2010) Distinct Olfactory Signaling Mechanisms in the Malaria Vector Mosquito Anopheles gambiae. PLoS Biol 8.
  19. 19. Pitts RJ, Fox AN, Zwiebel LJ (2004) A highly conserved candidate chemoreceptor expressed in both olfactory and gustatory tissues in the malaria vector Anopheles gambiae. Proc Natl Acad Sci USA 101: 5058–5063.
  20. 20. Schymura D, Forstner M, Schultze A, Kröber T, Swevers L, et al. (2010) Antennal expression pattern of two olfactory receptors and an odorant binding protein implicated in host odor detection by the malaria vector Anopheles gambiae. Int J Biol Sci 6: 614–626.
  21. 21. Wicher D, fer RS, Bauernfeind R, Stensmyr MC, Heller R, et al. (2008) Drosophila odorant receptors are both ligand-gated and cyclic-nucleotide-activated cation channels. Nature 452: 1007–11.
  22. 22. Sato K, Pellegrino M, Nakagawa T, Nakagawa T, Touhara LBVK (2008) Insect olfactory receptors are heteromeric ligand-gated ion channels. Nature 452: 1002–6.
  23. 23. Smart R, Kiely A, Beale M, Vargas E, Carraher C, et al. (2008) Drosophila odorant receptors are novel seven transmembrane domain proteins that can signal independently of heterotrimeric G proteins. Insect Biochem Mol Biol 38: 770–780.
  24. 24. Jones PL, Pask GM, Rinker DC, Zwiebel LJ (2011) Functional agonism of insect odorant receptor ion channels. Proceedings of the National Academy of Sciences 108: 8821–8825.
  25. 25. Vosshall LB, Hansson BS (2011) A unified nomenclature system for the insect olfactory coreceptor. Chem Senses 36: 497–8.
  26. 26. Kent , Walden , Robertson (2008) The Gr Family of Candidate Gustatory and Olfactory Receptors in the Yellow-Fever Mosquito Aeded aegypti. Chem Senses 33: 79–93.
  27. 27. Scott K, Brady R, Cravchik A, Morozov P, Rzhetsky A, et al. (2001) A chemosensory gene family encoding candidate gustatory and olfactory receptors in Drosophila. Cell 104: 661–673.
  28. 28. Kent L, Robertson H (2009) Evolution of the sugar receptors in insects. BMC Evolutionary Biology 9: 41–50.
  29. 29. Robertson HM, Warr CG, Carlson JR (2003) Molecular evolution of the insect chemoreceptor gene superfamily in Drosophila melanogaster. Proc Natl Acad Sci USA 100 Suppl 2: 14537–14542.
  30. 30. Montell C (2009) A taste of the Drosophila gustatory receptors. Curr Opin Neurobiol 19: 345–353.
  31. 31. Sparks JT, Vinyard BT, Dickens JC (2013) Gustatory receptor expression in the labella and tarsi of Aeded aegypti. Insect Biochem Mol Biol 43: 1161–1171.
  32. 32. Qiu YT, van Loon JJA, Takken W, Meijerink J, Smid HM (2006) Olfactory Coding in Antennal Neurons of the Malaria Mosquito, Anopheles gambiae. Chem Senses 31: 845–863.
  33. 33. Carey AF, Wang G, Su C-Y, Zwiebel LJ, Carlson JR (2010) Odorant reception in the malaria mosquito Anopheles gambiae. Nature 1–38.
  34. 34. Wang G, Carey AF, Carlson JR, Zwiebel LJ (2010) Molecular basis of odor coding in the malaria vector mosquito Anopheles gambiae. Proceedings of the National Academy of Sciences 107: 4418–4423.
  35. 35. Benton R, Vannice K, Gomezdiaz C, Vosshall L (2009) Variant Ionotropic Glutamate Receptors as Chemosensory Receptors in Drosophila. Cell 136: 149–162.
  36. 36. Croset V, Rytz R, Cummins S, Budd A, Brawand D, et al. (2010) Ancient Protostome Origin of Chemosensory Ionotropic Glutamate Receptors and the Evolution of Insect Taste and Olfaction. PLoS Genet 6(8): e1001064.
  37. 37. Abuin L, Bargeton B, Ulbrich MH, Isacoff EY, Kellenberger S, et al. (2011) Functional architecture of olfactory ionotropic glutamate receptors. Neuron 69: 44–60.
  38. 38. Ai M, Min S, Grosjean Y, Leblanc C, Bell R, et al. (2010) Acid sensing by the Drosophila olfactory system. Nature 468: 691–695.
  39. 39. Guo M, Krieger J, Grosse-Wilde E, Mißbach C, Zhang L, et al. (2014) Variant Ionotropic Receptors Are Expressed in Olfactory Sensory Neurons of Coeloconic Sensilla on the Antenna of the Desert Locust (Schistocerca gregaria). Int J Biol Sci 10: 1.
  40. 40. Cork A, Park KC (1996) Identification of electrophysiologically-active compounds for the malaria mosquito, Anopheles gambiae, in human sweat extracts. Med Vet Entomol 10: 269–276.
  41. 41. World Health Organization (2011) World Malaria Report 2011. World Health Organization: 1–389.
  42. 42. Bernier UR, Kline DL, Barnard DR, Schreck CE, Yost RA (2000) Analysis of Human Skin Emanations by Gas Chromatography/Mass Spectrometry. 2. Identification of Volatile Compounds That Are Candidate Attractants for the Yellow Fever Mosquito (Aedes aegypti). Anal Chem 72: 747–756.
  43. 43. Meijerink J, van Loon J (1999) Sensitivities of antennal olfactory neurons of the malaria mosquito, Anopheles gambiae, to carboxylic acids. J Insect Physiol 45: 365–373.
  44. 44. Meijerink J, Braks MA, Van Loon JJ (2001) Olfactory receptors on the antennae of the malaria mosquito Anopheles gambiae are sensitive to ammonia and other sweat-borne components. J Insect Physiol 47: 455–464.
  45. 45. Pitts RJ, Rinker DC, Jones PL, Rokas A, Zwiebel LJ (2011) Transcriptome profiling of chemosensory appendages in the malaria vector Anopheles gambiae reveals tissue- and sex-specific signatures of odor coding. BMC Genomics 12: 271.
  46. 46. Rinker DC, Zhou X, Pitts RJ (2013) AGC Consortium (2013) Rokas A, et al. (2013) Antennal transcriptome profiles of anopheline mosquitoes reveal human host olfactory specialization in Anopheles gambiae. BMC Genomics 14: 749.
  47. 47. Khademi S, Stroud RM (2006) The Amt/MEP/Rh Family: Structure of AmtB and the Mechanism of Ammonia Gas Conduction. Physiology 21: 419–429.
  48. 48. Burckhardt BC, Burckhardt G (1997) NH4+ conductance in Xenopus laevis oocytes. I. Basic observations. Pflugers Arch 434: 306–312.
  49. 49. Cougnon M, Bouyer P, Hulin P, Anagnostopoulos T, Planelles G (1996) Further investigation of ionic diffusive properties and of NH 4+ pathways in Xenopus laevis oocyte cell membrane. Pflugers Arch 431: 658–667.
  50. 50. Meier-Wagner J, Nolden L, Jakoby M, Siewe R, Krämer R, et al. (2001) Multiplicity of ammonium uptake systems in Corynebacterium glutamicum: role of Amt and AmtB. Microbiology (Reading, Engl) 147: 135–143.
  51. 51. Ninnemann O, Jauniaux JC, Frommer WB (1994) Identification of a high affinity NH4+ transporter from plants. EMBO J 13: 3464–3471.
  52. 52. Siewe RM, Weil B, Burkovski A, Eikmanns BJ, Eikmanns M, et al. (1996) Functional and genetic characterization of the (methyl)ammonium uptake carrier of Corynebacterium glutamicum. J Biol Chem 271: 5398–5403.
  53. 53. Ludewig U (2002) Uniport of NH4+ by the Root Hair Plasma Membrane Ammonium Transporter LeAMT1;1. Journal of Biological Chemistry 277: 13548–13555.
  54. 54. Nakhoul NL, Dejong H, Abdulnour-Nakhoul SM, Boulpaep EL, Hering-Smith K, et al. (2005) Characteristics of renal Rhbg as an NH4(+) transporter. Am J Physiol Renal Physiol 288: F170–81.
  55. 55. Neuhäuser B, Dynowski M, Ludewig U (2009) Channel-like NH3 flux by ammonium transporter AtAMT2. FEBS Lett 583: 2833–2838.
  56. 56. Neuhauser B, Ludewig U (2014) Uncoupling of Ionic Currents from Substrate Transport in the Plant Ammonium Transporter AtAMT1;2. Journal of Biological Chemistry 289: 11650–11655.
  57. 57. Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25: 4876–4882.
  58. 58. Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4: 406.
  59. 59. Omasits U, Ahrens CH, Müller S, Wollscheid B (2013) Protter: interactive protein feature visualization and integration with experimental proteomic data. Bioinformatics
  60. 60. Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29: e45.
  61. 61. Mortazavi A, Williams BA, Mccue K, Schaeffer L, Wold B (2008) Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nat Meth 5: 621–628.
  62. 62. Xia Y, Wang G, Buscariollo D, Pitts RJ, Wenger H, et al. (2008) The molecular and cellular basis of olfactory-driven behavior in Anopheles gambiae larvae. Proc Natl Acad Sci USA 105: 6433–8.
  63. 63. Marini A-M, Matassi G, Raynal V, André B, Cartron J-P, Chérif-Zahar B (2000) The human Rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast. Nature Genetics 26: 341–4.
  64. 64. Gietz RD, Schiestl RH (2007) Quick and easy yeast transformation using the LiAc/SS carrier DNA/PEG method. Nat Protoc 2: 35–7.
  65. 65. Schneider CA, Rasband WS, Eliceiri KW (2012) NIH Image to ImageJ: 25 years of image analysis. Nature Methods 9: 671–5.