An odorant receptor from Anopheles sinensis in China is sensitive to oviposition attractants
Anopheles sinensis is an important vector for the spread of malaria in China. Olfactory-related behaviours, particularly oviposition site seeking, offer opportunities for disrupting the disease-transmission process.
This is the first report of the identification and characterization of AsinOrco and AsinOR10 in An. sinensis. AsinOrco and AsinOR10 share 97.49% and 90.37% amino acid sequence identity, respectively, with related sequences in Anopheles gambiae. A functional analysis demonstrated that AsinOrco- and AsinOR10-coexpressing HEK293 cells were highly sensitive to 3-methylindole, but showed no significant differences in response to other test odorants when compared to DMSO.
AsinOrco was characterized as a new member of the Orco ortholog subfamily. AsinOR10, which appears to be a member of the OR2-10 subfamily, is directly involved in identification of oviposition sites. This finding will help to elucidate the molecular mechanisms underlying olfactory signaling in An. sinensis and provide many more molecular targets for eco-friendly pest control.
KeywordsAnopheles sinensis AsinOrco AsinOR10 3-Methylindole
Malaria is one of the most important infectious diseases seriously endangering human health and safety. The World Health Organization (WHO) lists malaria with AIDS and tuberculosis as the top three public health problems globally. Malaria is also one of the most important mosquito-borne diseases in China. To respond proactively to the global action to eliminate malaria, China launched the Malaria Action Plan  in 2010, which clearly states that “by 2015, the country except for some border areas of Yunnan and other areas have no local malaria cases”; “by 2020, the national malaria elimination.” Currently, most counties (districts) in China have completed an assessment of malaria elimination. However, conditions are still favourable for the spread of malaria in some regions; even if the source of infection can be discovered and cleared in a timely, there is still a risk of local transmission and epidemic rebound. With rapid globalization and implementation of the national “Belt and Road” initiative, the number of people visiting areas of high malaria transmission, such as Africa and Southeast Asia, for business, employment and tourism purposes has increased significantly. As a result, the proportion of overseas imported cases, which reached 99.9% (3317/3321) in 2016, shows an increasing trend . Such an increase poses a potential risk to relatively stable malaria-endemic areas. For example, a short-term and large-scale clustered imported outbreak occurred in Guangxi Province in 2013 . In addition, malaria-nonendemic areas lack diagnostic awareness of imported malaria cases, and severe illness and death can occur.
Anopheles sinensis, with a wide distribution and a large population, is an important vector for the spread of malaria in China. The main strategy for the elimination of malaria by the WHO is the timely and effective removal of infection sources and preventing spread among epidemic sites. Given the resistance of An. sinensis populations to commonly used insecticides, alternative control methods are crucially needed. Researchers have combined Bacillus thuringiensis var. israelensis with oviposition attractants in “attract-and-kill” strategies  to collect more gravid females  and  eggs than with control traps. As mosquitoes use their olfactory system to search for oviposition sites, research on these systems is of key importance.
The olfactory system of insects mainly includes olfactory receptors (ORs), odorant-binding proteins (OBPs) and olfactory receptor neurons (ORNs). Previous studies have demonstrated that ORs can convert odour-stimulating chemical signals into electrical signals and transmit nerve impulses to the dendrites of olfactory neurons . Accordingly, ORs are involved in mating, blood sucking, oviposition site searching and other important life activities of mosquitoes.
ORs in insect olfactory sensory neurons (OSNs) include a coreceptor designated Orco (OR7) and conventional ligand-binding odorant receptors (ORXs). Orco genes from different species are highly conserved [8, 9]. Other highly divergent ORs are conventional odorant receptors, correlating with some olfactory-mediated behavioural functions , and these ORs have been associated with certain biological information about odorants . Consistently, AgamOR2, AgamOR5, AgamOR8 and AgamOR65  are narrowly tuned to indole, 2,3-butanedione, 1-octen-3-ol, and 2-ethylphenol, respectively. In addition, some ORs respond strongly to specific odorants; for example, CquiOR10  has been shown to respond strongly to 3-methylindole , an oviposition site volatile attractant, whereas AgamOR10 [12, 15] is highly sensitive to 3-methylindole and indole. Indole [12, 16] is a volatile attractant component of both human sweat and oviposition sites. In the previous research, AablOR10 was linked to host- and oviposition-seeking behaviours, prompting us to examine the odorant response profile of AsinOR10. This study identified AsinOrco and AsinOR10 of An. sinensis and examined the odorant response profile of AsinOR10.
Mosquito rearing and blood feeding
Anopheles sinensis (laboratory-susceptible strain) larvae and pupae were reared on yeast powder, and adults were maintained on a 10% sugar solution at 25–27 °C and 70–80% relative humidity with a photoperiod of 12:12 h. Three-day-old adult females were blood-fed on a human volunteer arm using standard protocols .
Identification of putative AsinOrco sequences
Predicted amino acid sequences of An. sinensis (ASIS023681-RA) , Anopheles funestus (KF819859), Anopheles gambiae (AGAP002560-RA) and Culex pipiens quinquefasciatus (DQ231246) Orco orthologs were obtained from VectorBase. Primers (Additional file 1: Table S1) used for two-step RT-PCR were first designed based on these sequences using primer 5.0 to amplify partial gene sequences of AsinOrco and AsinOR10. Total RNA extraction from female adult mosquitoes (3–7 days old) and cDNA synthesis were performed using an RNeasy Mini Kit (QIAGEN, Hilden, Germany), the TURBO DNA-free™ Kit (Ambion, Carlsbad, CA, USA) and TaKaRa PrimeScript™ RT-PCR Kit (Takara, Otsu, Shiga, Japan) following the manufacturers’ instructions. Gene-specific primers (Additional file 1: Table S1) were then designed for 5′- or 3′-end rapid amplification of cDNA ends (RACE) to amplify full-length coding sequences using a SMARTer™ RACE cDNA amplification kit (Clontech, Mountain View, CA, USA).
Identification of putative AsinOR10 sequences
Nested RT-PCR primers (Additional file 1: Table S1) were designed based on the predicted amino acid sequences of An. sinensis (ASIC007209-RA) , Culex pipiens (FJ008065), Culex quinquefasciatus (GU945397), Anopheles quadriannulatus (FJ008069), An. gambiae (AGAP009520-RA) and Anopheles stephensi (FJ008074) OR10 orthologs. PCR was carried out using TaKaRa Tks Gflex DNA Polymerase (Takara, Otsu, Shiga, Japan). PCR amplification products were examined by 1.5% agarose gel electrophoresis and verified by DNA sequencing (Invitrogen, Shanghai, China). The obtained sequences were compared with predicted AsinORs and AgamORs using DNAMAN.
Amino acid sequences of ORs were aligned using the program ClustalW, and the neighbor-joining tree was built using the MEGA 5.0 program . The membrane topology of the OR sequences was predicted using the HMMTOP (version 2.0) and TMHMM (version 2.0)  servers.
Expression of AsinORs in HEK293 cells
The full-length coding sequences (CDSs) of AsinORs were cloned into the pME18s mammalian expression plasmid  using specific primers (Additional file 1: Table S1). The DsRed coding sequence was amplified from pIRES2-DsRed plasmids (Clontech, Mountain View, CA, USA) using primers containing the appropriate restriction sites. AsinORs were cloned into the pME18s plasmid in-frame with the DsRed coding sequence . HEK293 (human embryo kidney 293) cells (purchased from the Chinese Academy of Sciences) were cultured in an incubator at a constant temperature of 37 °C with 5% CO2 and transiently transfected with AsinORs using Lipofectamine® 2000 Reagent (Invitrogen, Carlsbad, CA) . Expression of ORs was confirmed by RT-PCR after 24 h; subcellular location analysis and western blotting were performed after 48 h. The two-step RT-PCR primers and nested RT-PCR primers are provided in Additional file 1: Table S1. Cells were lysed with RIPA buffer (50 mM Tris, pH 7.5, 150 mM NaCl, 1 mM EDTA, 0.25% sodium deoxycholate, 0.1% Triton X-100, 1% Nonidet P-40). The lysates were mixed with in SDS–PAGE buffer (62.5 mM Tris, pH 6.8, 2% SDS, 5% 2-mercaptoethanol, 10% glycerol, 0.02% bromophenol blue), heated at 95 °C for 5 min, separated by 10% SDS-PAGE gel electrophoresis and transferred to a PVDF membrane (ImmobilonTM-P, Millipore). The blot was washed with TBST, incubated with 5% skim milk for 60 min, and incubated overnight with an anti-RFP antibody (Abcam, Cambridge, US) raised in mice at a dilution ratio of 1:1000 in 1 × PBS or anti-GAPDH antibody (Abcam, Cambridge, US) at 1:3000 dilution at 4 °C. The blot was then incubated with a horseradish peroxidase (HRP)-conjugated anti-mouse IgG secondary antibody (1:4000) (Bethyl Laboratories, Montgomery, TX, USA) at room temperature for 90 min.
Forty-eight hours after transfection, AsinOR-expressing cells were rinsed three times with HBSS. Fluo4-AM (Dojindo Laboratories, Tokyo, Japan) at a concentration of 2 μM was added, and the cells were incubated for 30 min at 37 °C in the dark. The cells were rinsed three times with HBSS before the addition of fresh HBSS (containing Ca2+)  and tested using a panel of odorants, including indole, 1-octen-3-ol, 1-methylindole, 3-methylindole, 2-methylphenol, 2,3-butanedione, 2-ethylphenol, and dimethyl sulfoxide (Sigma). All odorants (≥ 98% pure) were dissolved in DMSO and added to a final concentration of 10−6 M.
Fluorescence images were acquired using a laser scanning confocal microscope (Olympus, Japan). The Ca2+ level is represented as relative fluorescence change (ΔF/F0), where ΔF is the difference in peak fluorescence caused by stimulation and F0 is the baseline fluorescence [22, 23]. Baseline fluorescence was measured 100 s prior to adding the chemicals. Responses were quantified by the mean values of the maximal elevations (ΔF/F0) . Each odorant was assayed in triplicate per dish, and at least seven cells per dish were selected randomly. All assays were performed in triplicate.
Statistical analyses of differences in the cellular experimental results were conducted with one-way ANOVA followed by post hoc Tukey HSD tests (homogeneity of variance: P > 0.05).
Identification of putative AsinOR genes
Heterologous expression of AsinOR10 in HEK293 cells
This study is the first report of the identification and characterization of AsinOrco and AsinOR10. Although ORs typically display a high level of divergence , AsinOrco and AsinOR10 share 97.49% and 90.37% amino acid sequence identity with the coreceptor and OR2-10 subfamilies, respectively. This study utilized the nomenclature for Orco  and found that AsinOrco exhibits at least 50% sequence identity with orthologs from other insect species, and the predicted protein size is larger than that of conventional ORs. Membrane topology predictions show that AsinOrco and AsinOR10 belong to the TM7 protein family and have an intracellular amino-terminus. In addition, AsinOrco has the putative CaM-binding site (328SAIKYWVER336) identified in DmelOrco (336SAIKYWVER344) and in AalbOrco (329SAIKYWVER337) . This conservation of structure may also account for functional similarity. Overall, identification and functional validation of Orco orthologs are hot research topics. In the previous study, AalbOrco was demonstrated to transmit olfactory signaling, but did not recognize odorants . In fact, Orco forms a complex with conventional odorant receptors and is essential for odour signal transduction . Indeed, silencing or mutation of Orco [8, 28, 29] damages normal odorant responses. Notably, the function of Orco is so similar that some researchers  have even used Drosophila melanogaster Orco as a heterodimerization partner to examine the function of AalbORs. In this study, AsinOrco was characterized as a new member of the Orco ortholog subfamily. Furthermore, HEK293 cells coexpressing AsinOrco and AsinOR10 responded to odorants.
Conventional OR sequence homology has often been associated with odorant specificity [21, 30, 31], and the narrow OR response to odorants may be highly relevant to mosquito ecology . In previous studies, OR2-10 orthologs [12, 13, 21, 30] were found to be more likely to be highly sensitive to indole and 3-methylindole, attractants of oviposition sites, therefore, this study focused on the ability of AsinOR10 to perceive oviposition attractants. AsinOrco- and AsinOR10-coexpressing cells were exposed to seven odorants, including indole, 1-methylindole, 3-methylindole, 1-octen-3-ol, 2-methylphenol, 2,3-butanedione, and 2-ethylphenol. Indole [12, 16] is a volatile attractant of oviposition sites and human sweat. 3-Methylindole [14, 32, 33], also known as skatole, is a ubiquitous oviposition site volatile attractant and an egg raft pheromone; 1-methylindole is another methylindole compound. 1-Octen-3-ol , a volatile attractant from large herbivores and humans, is known to attract some anophelines [33, 34], and 2-methylphenol , identified as the best ligand among phenols, elicits a strong electrophysiological response from CquiOR2. 2,3-Butanedione  is a metabolic byproduct of human skin microflora, which excites narrowly tuned AgamOR5 , and 2-ethylphenol  is found in the urine of animals and evokes a strong electrophysiological response from AgamOR65 .
In contrast to DMSO, 3-methylindole elicits a fluorescence reaction (measured as relative fluorescence change, ΔF/F0). This finding is similar to previous results showing that CquiOR10 [13, 30], AalbOR10  and AgamOR10  orthologs respond sensitively to 3-methylindole and thus further confirm the functional conservation of OR10 orthologs. Regardless, CquiOR10 [13, 30], AalbOR10  and AgamOR10  responded to a set of aromatic compounds, including each of the methylindoles, 1-octen-3-ol and indole, using the Xenopus Oocyte System or the Drosophila melanogaster “empty neuron” system, whereas AsinOR10 showed no significant differences in responses to indole, 1-octen-3-ol and 1-methylindole compared to DMSO in HEK293 cells. These results might be due to differences in the intracellular epitope tags of these systems, which may influence the selectivity of the receptor, or this OR might not be responsive to the chemicals tested. Despite the use of a heterogeneous expression system, the results indicate that AsinOR10 is directly involved in oviposition site-seeking behaviour.
In summary, AsinOrco was characterized as a new member of the Orco ortholog subfamily, and AsinOR10 was found to be a member of the OR2-10 subfamily. AsinOR10 is directly involved in oviposition site identification. These results will help in exploration of the molecular mechanism underlying the olfactory signal transduction pathway in An. sinensis and provide more molecular targets for eco-friendly pest control.
HML, LHL and PC provided the experimental data and wrote the paper. XDH participated the revision of the paper. MQG reviewed and edited the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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This work was supported by grants from the National Natural Science Foundation of China [81702034 (HML),81471985 (MQG),81672059 (MQG)], China Postdoctoral Science Foundation funded project [2017M622733 (HML)], medical and health science and technology development project of Shandong Province [2016WS0393 (HML)] and the Innovation Project of Shandong Academy of Medical Sciences.
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