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Molecular and physiological characterization of the chitin synthase B gene isolated from Culex pipiens pallens (Diptera: Culicidae)



The growth and development of insects is strictly dependent on the precise regulation of chitin synthase (CHS), which is absent in vertebrates and plants. Therefore, CHS represents an attractive target for insecticides. At present, the research on the CHS gene in mosquitoes, especially its biological functions, remains limited.


The full-length cDNA of the chitin synthase B gene in Culex pipiens pallens (CpCHSB) was prepared and consists of 5158 nucleotides with an open reading frame (ORF) of 4722 nucleotides encoding a protein of 1573 amino acid residues. Among different tissues, CpCHSB gene is mainly expressed in the midgut tissue with the highest expression in adult mosquitoes. Knockdown of CpCHSB in the larval stage significantly lowered the chitin content (16.5%) decreased body size (reduced by 25.6% in the larval stage and by 25.6% in the adult stage), and diminished reproduction (20%). Injecting siCHSB into adult mosquito mainly decreased reproduction (27%).


CpCHSB plays essential roles in growth and development, by severely reducing larval chitin content, midgut permeability, and reducing the number of female mosquito offspring. These results indicate that CHSB may serve as a potential novel target for exploring biosafe insecticides.


Mosquitoes are among the most dangerous vectors for many severe diseases including malaria, dengue fever, Zika fever, yellow fever and chikungunya [1,2,3]. These mosquito-borne diseases cause serious public health problems and large economic losses in tropical and subtropical areas. At present, mosquito control programmes mainly rely on the application of chemical insecticides, but their widespread and improper use leads to the development of resistance in vectors. Of the 80 countries in which malaria is endemic that provided data for 2010–2017, 68 have reported resistance to at least one class of insecticide, and 57 of those reported resistance to two or more classes [1]. In addition, since chemical insecticides accumulate in the environment, they may have adverse effects on non-target organisms, including humans [4]. New and more accurately targeted tools are indeed needed [5,6,7].

Chitin, a linear polymer of β-(1,4)-N-acetyl-d-glucosamine (GlcNAc), is the second most abundant natural polysaccharide after cellulose [8]. It is widely distributed in arthropods, nematodes and fungi, but is absent in vertebrates and plants. In insects, chitin is the key structural component of the cuticular exoskeleton, trachea, head capsule, cuticular lining of the foregut, hindgut, and peritrophic membrane (PM) that lines the lumen of the midgut [9]. Chitin functions as a scaffold material and plays an important role in protecting insects against external invasion and the abrasion of food [10]. Therefore, chitin may be a potential selective target for novel insect control strategies.

Chitin synthase (CHS), an enzyme that transfers NDP-acetylglucosamine (NAP-GlcNAc) to polymerise chitin [10], catalyses the last step of chitin synthesis. During development and metamorphosis, the chitin content in insects fluctuates as a complex function of the activities of CHS. In general, insect CHS fall into two different classes; CHSA and CHSB. Although both share some conserved motifs (DXD [hD(S/A)DT], EDR[E(D562E)R], and QRRRW[(Q601N)RR(R604L)(W605Y)]) [6, 11] and have some basic properties in common, they are believed to have different functions during insect growth and development. CHSA is responsible for chitin synthesis in cuticle and trachea in Anopheles gambiae [12], Tribolium castaneum [13] and Locusta migratoria [14], whereas CHSB is mainly located in the midgut and is presumably responsible for synthesising chitin in the PM during the feeding stage in Anopheles gambiae [12], Ostrinia nubilalis [10] and L. migratoria [14]. Moreover, a recent study showed that both CHSA and CHSB proteins were present in the newly formed compound eyes of Anopheles gambiae pupae according to immunohistochemical analysis [12].

Previous functional analyses of the CHSB gene using RNA interference (RNAi) in several different insect species demonstrated its requirement for various physiological processes. In Bactrocera dorsalis, CHSB regulates the chitin content of the midgut, and thereby affects growth and development. CHSB in Bombyx mori can affect the chitin synthesis-dependent form of the PM and is related to food intake and the molting process. Silencing of the CHSB gene in Leptinotarsa decemlineata significantly reduces food consumption, decreases chitin content and retards larval growth. Although the CHSB gene has been characterised in several mosquito species [12, 15], physiological functional information is rather limited. In Aedes aegypti, mature and immature larvae treated with dsRNA targeting CHSB gene catalytic sites displayed decreased viability, and a few larval and adult survivors displayed altered morphology, including a reduction in chitinous bristles located on the abdominal segments and thorax [4]. In addition, relatively high CHSB gene expression occurs in the A. gambiae pupal stage compared with larval stages [12]. This finding suggests that although CHSB may not be useful for PM-associated chitin development in pupae these enzymes may have other physiological roles, suggesting that further study is needed to understand the functions of the enzyme encoded by CHSB.

Culex pipiens pallens is widely distributed in China [16]. This species is the major vector of the Japanese encephalitis virus as well as Wuchereria bancrofti, the causative agent of filariasis [17]. In the present study, we performed molecular characterization and expression profiling of the CHSB gene in Cx. pipiens pallens (CpCHSB) and explored the biological functions by gene silencing via microinjection experiments.



Culex pipiens pallens larvae were reared at 28 ± 1 °C in water supplemented with rat chow. Adult mosquitoes were reared at 27 °C and 60–70% relative humidity with unlimited access to water and 7% (w/v) sucrose solution under a 16:8 h light:dark photoperiod. To allow females to lay eggs, 3-day-old females were fed fresh mouse blood [18, 19].

CpCHSB cDNA cloning and sequencing

Total RNA was isolated from 3-day-old female mosquitoes, 10 mosquitoes as a biological replicate using RNAiso Plus reagent (TaKaRa, Tokyo, Japan) according to the manufacturer’s instructions. The CpCHSB cDNA sequence was determined by sequencing six overlapping PCR fragments (Additional file 1: Table S1), and primers were designed based on the ORF of Culex quinquefasciatus (GenBank: XM_001846240.1). The 5′- and 3′-RACE ends were amplified using a SMARTer RACE 5′/3′ Kit following the instructions of the manufacturer (TaKaRa). PCR was carried out with rTaq polymerase (TaKaRa) in a 50 μl reaction mixture containing 2.5 μl cDNA templates, 1 μl GSP (10 μM), 25 μl 2× SeqAmp buffer, 1.0 μl SeqAmp DNA Polymerase, 5 μl 10× UPM and 15.5 μl ddH2O. Thermal cycling involved 20 cycles of denaturation at 95 °C for 30 s, annealing at 55–65 °C (based on the primer annealing temperature) for 30 s, and extension at 72 °C for 2–3 min (based on the size of the expected fragment). Amplified PCR products were analyzed on a 1% agarose gel and purified using a Gel Extraction Mini Kit (Tiangen, Beijing, China). The product was placed at −20 °C. Purified DNA was ligated into the pMD18-T vector and sequenced completely from both directions.

Nucleotide and amino acid sequence analysis

The amino acid sequence of CpCHSB was translated using the ExPASy website ( Similar sequences were searched using the non-redundant protein sequence (nr) database of the National Center for Biotechnology Information (NCBI) website ( Prediction of molecular weight, isoelectric point and transmembrane helices was conducted using (, and N-glycosylation sites were also analyzed ( [20, 21].

Analysis of developmental stage and tissue-specific expression of CpCHSB by real-time quantitative PCR (RT-qPCR)

To assess developmental expression of CpCHSB, total RNA was extracted from eggs (0 and 24 h), fourth-instar larvae, pupae (0 and 24 h) and adult females (0, 24, 48 and 72 h post-eclosion and 24, and 48 h post-blood meal). Total RNA was isolated from 5 adult female mosquitoes for each biological replicate using RNAiso Plus reagent (TaKaRa). For tissue-specific expression analysis of CpCHSB, RNA was extracted from six different tissues (head, foregut, midgut, hindgut, Malpighian tubules and carcass) from fourth-instar larvae [8, 10]. Total RNA was isolated from 10 fourth-instar larvae for each biological replicate using RNAiso Plus reagent (TaKaRa). RT-qPCR was performed using a LightCycler® 96 Instrument (Roche, Switzerland, Germany) with Power SYBR Green PCR Master Mix (Applied Biosystems, Vancouver, USA), according to the manufacturer’s protocol. The reaction volume (10 μl) contained Power SYBR Green PCR Master Mix, specific forward and reverse primers (Additional file 2: Table S2), and diluted cDNA. The relative expression levels were normalized β-actin as an internal control [22] using the 2−ΔΔCq method [23]. The quality of RNA was assessed by gel electrophoresis and spectrophotometry. The integrity of RNA was by analysed by visualising bands for 28S and 18S ribosomal RNA [24]. All experiments were performed in triplicate and included three biological replicates and at least four technical replicates. Data are presented as the mean transcription ratio ± standard error of the mean (SE).

Analysis of morphological characteristics

Small interfering RNA for silencing the CpCHSB gene (siCHSB) and negative control (NC) RNA was purchased from Gene Pharma (Shanghai, China; Additional file 2: Table S2). Approximately 0.30 μg of siCHSB or NC was injected into the abdomen of third-instar larvae [25] and the thorax of 1-day-old adult female mosquitoes [19], and the same volume of wild type (WT) and negative control (NC) were injected as controls. After 72 h of recovery, knockdown levels of the CpCHSB transcript were measured by RT-qPCR.

After injecting siCHSB, NC into third-instar larvae, the body length of 4-day-old final-instar larvae was measured between the initial vertex of the head capsule and terminal vertex of abdominal segments. Adult body length was estimated from wing length, measured from the apical notch to the axillary margin [23]. Lengths were measured using Fiji Image J software [26]. To minimise measurement errors, all appendage measurements were determined by a single researcher, and data from at least four replicate experiments were combined for statistical comparisons. All experiments included three biological replicates and at least four technical replicates. Significant differences were analyzed using Student’s t-tests.

Chitin analysis

The chitin content of larvae and adult mosquito was quantified as described previously by Arakane et al. [27]. After injection of siRNA, extract from control and siRNA larvae or adults of a similar weight were subjected to absorbance measurement at 585 nm using a microplate reader. Standard curves were prepared from stocks of 0.05 to 2.25 mM GlcNAc. The same weight of mosquito was used for normalisation of chitin content across different samples [28, 29].

This method can quickly assess whether the larval midgut is defective. Larvae were dissected after 72 h injected with siCHSB, NC and midgut tissue was transferred to a glass vial. Samples were incubated with Rhodamine B (final concentration 1 mM in water; Solarbio, Beijing, China) on a shaker for 1 min, rinsed thoroughly with water, and stained midgut was photographed using a Coolpix 4300 (Nikon, Tokyo, Japan) [30].

Third-instar larvae were injected with siRNA, and after 72 h samples were collected for section staining. The head and tail were removed, and the body including the middle part of the intestine was incubated in fixing solution (4% paraformaldehyde) overnight. After paraffin embedding, samples were dewaxed and stained with Fluorescent Brightener 28 (Sigma-Aldrich, Shanghai, China) for 10 s, washed three times with water for 1 min each time, counterstained with propidium iodide for 10 s, washed three times with water for 1 min each time, and excess water was removed from the air-dried slide. Anti-fluorescent stain was added dropwise for sealing and samples were observed under a fluorescence microscope [31].

Statistical analysis

SPSS 23.0 and GraphPad Prism 6.0 software [31] was used for statistical analysis. Differences in efficiency, length, and chitin content between treatments (WT, NC, siCHSB) were compared using Student’s t-tests [31]. To compare more than two sets, we used one-way analysis of variance analysis (ANOVA) followed by Tukey’s post-hoc tests. All statistical values are presented as the mean ± standard error of the mean (SE). All experiments were performed using at least three independent cohorts, and P-values of < 0.05 were considered statistically significant.


CpCHSB cDNA and deduced amino acid sequences

The full-length CpCHSB cDNA was amplified by multiplex PCR using a cDNA template from mosquitoes, and RACE-PCR was used to amplify the 5′ and 3′ regions. The full-length cDNA of CpCHSB (GenBank: MK303758) spans 5158 nucleotides and includes an open reading frame (ORF) of 4722 nucleotides encoding a protein of 1573 amino acid residues. The CpCHSB cDNA includes a 5′-untranslated region (UTR) 335 nucleotides upstream of the initiation codon (ATG) and a 101 nucleotide 3′ UTR, ending with a poly(A) tail. The putative CpCHSB protein contains three domains; an N-terminal domain with seven transmembrane helices, a highly conserved central domain, and a C-terminal domain with an additional seven transmembrane helices. Sequences characteristic of chitin synthase (QRRRW and EDR) were identified in CpCHSB.

We also derived amino acid sequences of CHSA and CHSB, both containing seven highly conserved motifs (M1–M7; Fig. 1). Since these motifs are present in all chitin synthases, they are considered characteristic sequences [6].

Fig. 1
figure 1

Alignment of the conserved catalytic domain of chitin synthases from three mosquito species Seven characteristic motifs (M1–M7) in insect chitin synthases are highlighted. Dashes are used to denote gaps introduced to maximise alignment. Abbreviations: Ae, Aedes aegypti; Ag, Anopheles gambiae; Cp, Culex pipiens pallens

Tissue-specific expression of CpCHSB

Our results showed that CpCHSB was expressed in the head, foregut, midgut, hindgut, Malpighian tubules and carcass of fourth-instar larvae (Fig. 2), with highest levels in the midgut and lowest levels in Malpighian tubules.

Fig. 2
figure 2

Expression profiles of CpCHSB in different tissues of fourth-instar C. pipiens pallens larvae. Tissues include head (HE), foregut (FG), midgut (MG), hindgut (HG), Malpighian tubules (MT) and carcass (CA). Relative expression levels were calculated based on the lowest expression value, which was ascribed an arbitrary value of 1. Results are shown as the mean ± SE

Expression of CpCHSB during different developmental stages

Expression of CpCHSB during different developmental stages from eggs to adults was examined by RT-qPCR (Fig. 3). The results showed that CpCHSB was expressed at all stages, and expression gradually increased from larvae and peaked in adults after 72 h of eclosion. Relative CpCHSB expression levels in eggs, larvae and pupae were significantly lower than in adults.

Fig. 3
figure 3

Expression profiles of CpCHSB during different developmental stages. Stages include egg (EG), fourth-instar larvae (L4), pupae (PU), post-eclosion (PE), and post-blood meal (PBM). Relative expression levels were calculated based on the lowest expression value, which was ascribed an arbitrary value of 1. Results are shown as the mean ± SE

RNAi silencing of CpCHSB affects growth

To evaluate the function of CpCHSB in mosquitoes, we injected siCHSB into 200 third-instar larvae to knock down expression of CpCHSB, and 30% died during the course of growth due to the injection, while 10% died before the fourth-instar stage, 7% were unable to enter the pupal stage and died before pupation, and 13% pupae not forming in mosquitoes and died before eclosion. Levels of CpCHSB transcription were decreased (by 65%, Student’s t-tests: t(4)= 5.429, P = 0.003) at 72 h after injection with siCHSB (Fig. 4a). Compared with the NC group, the siCHSB group displayed smaller larval body size (reduced by 25.6%, t(18) = 10.925, P < 0.0001) [23] (Fig. 4b), smaller midgut size (reduced by 40%, t(18) = 11.414, P < 0.0001) (Fig. 4c), and delayed and reduced pupation (Fig. 4d). Wing length is considered a feature associated with and used to assess body size in mosquitoes [32]. Using this estimate, adult mosquitoes in the siCHSB group also displayed smaller body size (reduced by 25%, t(18) = 11.566, P < 0.0001) (Fig. 4e). Continued observation showed that the ovarian volume at 72 h post-blood meal (PBM) was smaller in the siCHSB group, there were fewer follicles present (reduced by 24.5%, t(18) = 5.132, P < 0.0001) (Fig. 4f), and after deposition the number of eggs was also decreased compared with the control group (reduced by 25.6%, t(18) = 4.534, P < 0.0001) (Fig. 4g, Additional file 3: Figure S1).

Fig. 4
figure 4

RNA interference (RNAi) of CpCHSB in third-instar larvae (n = 200). a Expression levels of CpCHSB at 72 h after injecting siCHSB assessed by RT-qPCR. b siCHSB injection into third-instar reduces body length in fourth-instar larvae, as well as midgut length (c). d Percentage of pupation (x-axis) after egg-hatching. e Comparison of wing length in wild type (WT), negative control (NC) and siCHSB adults. f Number of follicles per ovary and the number of eggs per female mosquito (g) after injecting (n = 50) siCHSB. All surviving individuals were used for measurements, and results are shown as the mean ± SE (Student’s t-tests: **P < 0.01, ***P < 0.001)

RNAi silencing of CpCHSB affects reproduction in adult females

A total of 200 1-day-old female mosquitoes were injected with siCHSB, and the RNAi efficiency was confirmed by RT-qPCR. CpCHSB transcription levels were decreased (by 58%, Student’s t-tests: t(4)= 5.424, P = 0.006) after siCHSB injection (Fig. 5a), but knockdown of CpCHSB expression did not alter the body size, length of the midgut, or chitin content. However, we evaluated ovarian development in female mosquitoes at 72 h PBM, and found that the ovary was reduced in volume, the number of follicles had declined (by 26.4%, t(18) = 5.414, P < 0.0001) (Fig. 5d), and fewer eggs were deposited (reduced by 27%, t(18) = 4.482, P < 0.0001) in the siCHSB group compared with the NC group (Fig. 5e, Additional file 4: Figure S2).

Fig. 5
figure 5

CpCHSB gene suppression by RNAi at 1 day after injection (n = 200) in adult mosquitoes. a Expression levels of CpCHSB at 72 h after injecting siCHSB assessed by RT-qPCR. The group injected with siCHSB show a reduction in CpCHSB expression of 53% compared with the control group. b Relative chitin content at 72 h after siCHSB injection. c Midgut length at 72 h after siCHSB injection. d Number of follicles per ovary and number of eggs per female mosquito (e) after injecting siCHSB. Results are shown as the mean ± SE (Student’s t-tests; **P < 0.01, ***P < 0.001, ns, not significant)

RNAi silencing of CpCHSB affects chitin content in the midgut

At 72 h after siCHSB injection into 200 third-instar larvae, the chitin content of fourth-instar larvae were decreased (by 28%, Student’s t-tests: t(18) = 2.7317, P = 0.021) (Fig. 6a). To determine whether knockdown of CpCHSB affects the permeability of the larval midgut, we employed the chemical marker Rhodamine B to stain the midgut, and the midgut was more translucent in the siCHSB group (Fig. 6b). We also performed eosin staining and chitin staining in the midgut by injecting at 48 h and 72 h, respectively, and observed a significant decrease in chitin content in the midgut of the siCHSB group (Fig. 6c) [33].

Fig. 6
figure 6

Effect of CpCHSB silencing in third instar larvae on chitin content. a Relative chitin content in fourth-instar larvae at 72 h after siCHSB injection (n = 10). b Rhodamine B staining of the midgut of fourth-instar larvae isolated after 72 h after siCHSB injection. c Chitin staining in the midgut at 48 and 72 h after siCHSB injection (n = 10). Results are shown as the mean ± SE (Student’s t-tests; *P < 0.05, **P < 0.01). Scale-bar: 50 μm


In the present study, we report the first full-length cDNA encoding CHSB from C. pipiens pallens. We conducted bioinformatics, catalytic domain and phylogenetic analyses, and all confirmed its status as a CHSB gene. Isolation of the CHSB cDNA allowed us to study the physiological functions of this gene in vivo.

CHSB is mainly responsible for synthesis of chitin in the midgut. The primary functions of the midgut include digestive enzyme production and nutrient absorption of digestion products [34]. Herein, CpCHSB was mainly expressed in the midgut, and knockdown during the larval stage resulted in shorter midgut size. Moreover, the chitin content of the midgut was lower in the siCHSB group, which likely had a weakened epidermis structure. These results indicate an impaired midgut function after knockdown of CpCHSB. It is well known that energy available during larval growth has a strong influence on the growth and development of mosquitoes [23]. In our experiment, both larval and adult body size were significantly smaller in siCHSB groups than in the NC group. Also, pupation was delayed in the siCHSB group. Therefore, we hypothesized that knocking out CpCHSB may reduce the length of the midgut and the accumulation of chitin in the midgut, which affects the intake of nutrients by mosquitoes, leading to the failure of normal growth and development. Mosquitoes must ingest a blood meal to obtain the nutrients required for oogenesis [35]. We therefore evaluated ovarian development in siCHSB-injected females at 72 h PBM and the ovary volume was smaller, the number of follicles was decreased, and egg deposition was diminished. Our results suggest that knocking down the expression of CpCHSB during the larval stage not only affects the growth and development of mosquitoes, but also has a serious impact on offspring.

We discovered that knockdown of CpCHSB in 1-day-old adults did not cause any changes in body size, the length of the midgut, or the chitin content. However, in the siCHSB group the volume of the ovary was decreased, there were fewer follicles, and egg deposition was diminished. Therefore, although the external morphology of mosquitoes was not altered significantly, knockdown had a serious impact on reproduction, indicating that CpCHSB plays an important role in reproduction in adult mosquitoes.

We also found that knocking down the expression of CpCHSB during the larval stage resulted in a lower rate of egg deposition compared with knockdown in adults, indicating that silencing of CpCHSB had a less pronounced effect in adult mosquitoes. The above results indicate that even though CHSB could be used as a target gene for insecticides in future, the duration of application may have a pronounced influence on the effects. Our results suggest that controlling the expression of CHSB in larvae may be more effective for mosquito vector control.

CpCHSB was found to be expressed during all developmental stages, indicating a role throughout the life-cycle. CpCHSB expression was highest in adults, consistent with results in B. dorsalis [11] and A. gambiae [12]. Highest expression was observed in the midgut, but CpCHSB was also expressed in many other tissues, suggesting that targeting of this gene may be more extensive than first thought. We suspect that CHSB is not only functional in the midgut, and this warrants further exploration.

Chitin is an attractive target for insecticides because the chitin synthesis pathway does not exist in vertebrates and plants. However, resistance and non-target toxicity affected their use in vector control [36]. Recently, a large number of benzoylurea derivatives have been synthesised, and 15 benzoylurea chitin synthesis inhibitors have been commercialized [37]. However, benzoylurea derivatives have detrimental effects on some beneficial species, such as bees, aquatic organisms and natural predators, when administered by dispersion, which led to a ban on flufenoxuron in the European Union in 2011 [38]. Our present results indicate that CHSB could be a new target for chitin synthesis inhibitors. Whether CHSB could be applied to the field mosquito control remains to be further investigated.


We obtained the full-length cDNA encoding CpCHSB from C. pipiens pallens, which was mainly expressed in the midgut, and was more highly expressed in adult mosquitoes than in larvae. We found that knockdown of CpCHSB at different stages produced different effects. Knockdown in the larval stage resulted in shorter body length, shorter midgut length, decreased chitin content, delayed pupation, decreased survival rare, and shorter adult body length in the siCHSB group compared with the NC group. Knockdown in the adult stage did not alter body length, midgut length, or chitin content in the siCHSB group, but reduced the number of ovarian follicles, and decreased egg production. Our results revealed that CpCHSB was essential for growth and development, which sheds new light on the characteristics and functions of CHSB in C. pipiens pallens. This finding could lead to the development of future vector control applications.

Availability of data and materials

Data supporting the conclusions of this article are included within the article and its additional files. Raw data are available from the corresponding author upon request. The sequence was submitted to the GenBank database under the accession number XM_001846240.1.



chitin synthase


rapid amplification of cDNA ends


gene-specific primers


universal primer mix


National Center for Biotechnology Information


chitin synthase A


chitin synthase B


chitin synthase B gene in Culex pipiens pallens


small interfering RNA for silencing the CpCHSB gene


open reading frame




peritrophic membrane




post-blood meal


negative control


standard error of the mean


wild type


untranslated region


  1. Chiodini J. Apps from the World Health Organization—the world malaria report and more. Travel Med Infect Dis. 2018;22:82–4.

    Article  Google Scholar 

  2. Guedes DR, Paiva MH, Donato MM, Barbosa PP, Krokovsky L, Rocha S, Saraiva K, Crespo MM, Rezende TM, Wallau GL, et al. Zika virus replication in the mosquito Culex quinquefasciatus in Brazil. Emerg Microbes Infect. 2017;6:e69.

    Article  Google Scholar 

  3. Kraemer MUG, Reiner RC Jr, Brady OJ, Messina JP, Gilbert M, Pigott DM, Yi D, Johnson K, Earl L, Marczak LB, et al. Past and future spread of the arbovirus vectors Aedes aegypti and Aedes albopictus. Nat Microbiol. 2019;4:854–63.

    Article  CAS  Google Scholar 

  4. Lopez SBG, Guimaraes-Ribeiro V, Rodriguez JVG, Dorand F, Salles TS, Sa-Guimaraes TE, et al. RNAi-based bioinsecticide for Aedes mosquito control. Sci Rep. 2019;9:4038.

    Article  Google Scholar 

  5. Barreaux P, Barreaux AMG, Sternberg ED, Suh E, Waite JL, Whitehead SA, et al. Priorities for broadening the malaria vector control tool kit. Trends Parasitol. 2017;33:763–74.

    Article  Google Scholar 

  6. Merzendorfer H. Insect chitin synthases: a review. J Comp Physiol B. 2006;176:1–15.

    Article  CAS  Google Scholar 

  7. Williams YA, Tusting LS, Hocini S, Graves PM, Killeen GF, Kleinschmidt I, et al. Expanding the vector control toolbox for malaria elimination: a systematic review of the evidence. Adv Parasitol. 2018;99:345.

    Article  Google Scholar 

  8. Zhang J, Liu X, Zhang J, Li D, Sun Y, Guo Y, et al. Silencing of two alternative splicing-derived mRNA variants of chitin synthase 1 gene by RNAi is lethal to the oriental migratory locust, Locusta migratoria manilensis (Meyen). Insect Biochem Mol Biol. 2010;40:824–33.

    Article  CAS  Google Scholar 

  9. Moussian B. Recent advances in understanding mechanisms of insect cuticle differentiation. Insect Biochem Mol Biol. 2010;40:363–75.

    Article  CAS  Google Scholar 

  10. Khajuria C, Buschman LL, Chen MS, Muthukrishnan S, Zhu KY. A gut-specific chitinase gene essential for regulation of chitin content of peritrophic matrix and growth of Ostrinia nubilalis larvae. Insect Biochem Mol Biol. 2010;40:621–9.

    Article  CAS  Google Scholar 

  11. Chen L, Yang WJ, Cong L, Xu KK, Wang JJ. Molecular cloning, characterization and mRNA expression of a chitin synthase 2 gene from the oriental fruit fly, Bactrocera dorsalis (Diptera: Tephritidae). Int J Mol Sci. 2013;14:17055–72.

    Article  Google Scholar 

  12. Zhang X, Zhang J, Park Y, Zhu KY. Identification and characterization of two chitin synthase genes in African malaria mosquito, Anopheles gambiae. Insect Biochem Mol Biol. 2012;42:674–82.

    Article  CAS  Google Scholar 

  13. Arakane Y, Specht CA, Kramer KJ, Muthukrishnan S, Beeman RW. Chitin synthases are required for survival, fecundity and egg hatch in the red flour beetle, Tribolium castaneum. Insect Biochem Mol Biol. 2008;38:959–62.

    Article  CAS  Google Scholar 

  14. Liu X, Zhang H, Li S, Zhu KY, Ma E, Zhang J. Characterization of a midgut-specific chitin synthase gene (LmCHS2) responsible for biosynthesis of chitin of peritrophic matrix in Locusta migratoria. Insect Biochem Mol Biol. 2012;42:902–10.

    Article  CAS  Google Scholar 

  15. Zhang J, Zhu KY. Characterization of a chitin synthase cDNA and its increased mRNA level associated with decreased chitin synthesis in Anopheles quadrimaculatus exposed to diflubenzuron. Insect Biochem Mol Biol. 2006;36:712–25.

    Article  CAS  Google Scholar 

  16. Liu H, Xie L, Cheng P, Xu J, Huang X, Wang H, Song X, Liu L, Wang H, Kou J, et al. Trends in insecticide resistance in Culex pipiens pallens over 20 years in Shandong, China. Parasit Vectors. 2019;12:167.

    Article  Google Scholar 

  17. Luo QC, Hao YJ, Meng F, Li TJ, Ding YR, Hua YQ, et al. The mitochondrial genomes of Culex tritaeniorhynchus and Culex pipiens pallens (Diptera: Culicidae) and comparison analysis with two other Culex species. Parasit Vectors. 2016;9:406.

    Article  Google Scholar 

  18. Guo J, Ye W, Liu X, Sun X, Guo Q, Huang Y, Ma L, et al. piRNA-3312: a putative role for pyrethroid resistance in Culex pipiens pallens (Diptera: Culicidae). J Med Entomol. 2017;54:1013–8.

    Article  CAS  Google Scholar 

  19. Sun X, Guo J, Ye W, Guo Q, Huang Y, Ma L, et al. Cuticle genes CpCPR63 and CpCPR47 may confer resistance to deltamethrin in Culex pipiens pallens. Parasitol Res. 2017;116:2175–9.

    Article  Google Scholar 

  20. Kumar NS, Tang B, Chen X, Tian H, Zhang W. Molecular cloning, expression pattern and comparative analysis of chitin synthase gene B in Spodoptera exigua. Comp Biochem Physiol B Biochem Mol Biol. 2008;149:447–53.

    Article  Google Scholar 

  21. Yang WJ, Xu KK, Cong L, Wang J. Identification, mRNA expression, and functional analysis of chitin synthase 1 gene and its two alternative splicing variants in oriental fruit fly, Bactrocera dorsalis. Int J Biol Sci. 2013;9:331–42.

    Article  Google Scholar 

  22. Hansen IA, Attardo GM, Park JH, Peng Q, Raikhel AS. Target of rapamycin-mediated amino acid signalling in mosquito anautogeny. Proc Natl Acad Sci USA. 2004;101:10626–31.

    Article  CAS  Google Scholar 

  23. Ling L, Raikhel AS. Serotonin signalling regulates insulin-like peptides for growth, reproduction, and metabolism in the disease vector Aedes aegypti. Proc Natl Acad Sci USA. 2018;115:E9822–31.

    Article  CAS  Google Scholar 

  24. Muyal JP, Muyal V, Kaistha BP, Seifart C, Fehrenbach H. Systematic comparison of RNA extraction techniques from frozen and fresh lung tissues: checkpoint towards gene expression studies. Diagn Pathol. 2009;4:9.

    Article  Google Scholar 

  25. Potter P. Improvised microinjection technique for mosquito vectors. Emerg Microbes Infect. 2012;18:2098–9.

    Article  Google Scholar 

  26. Mysore K, Sun L, Tomchaney M, Sullivan G, Adams H, Piscoya AS, et al. siRNA-mediated silencing of doublesex during female development of the dengue vector mosquito Aedes aegypti. PLoS Negl Trop Dis. 2015;9:e0004213.

    Article  Google Scholar 

  27. Bolognesi R, Arakane Y, Muthukrishnan S, Kramer KJ, Terra WR, Ferreira C. Sequences of cDNAs and expression of genes encoding chitin synthase and chitinase in the midgut of Spodoptera frugiperda. Insect Biochem Mol Biol. 2005;35:1249–59.

    Article  CAS  Google Scholar 

  28. Arakane Y, Muthukrishnan S, Kramer KJ, Specht CA, Tomoyasu Y, Lorenzen MD, et al. The Tribolium chitin synthase genes TcCHS1 and TcCHS2 are specialized for synthesis of epidermal cuticle and midgut peritrophic matrix. Insect Mol Biol. 2005;14:453–63.

    Article  CAS  Google Scholar 

  29. Guo J, Xu Y, Yang X, Sun X, Sun Y, Zhou D, et al. TRE1 and CHS1 contribute to deltamethrin resistance in Culex pipiens pallens. Arch Insect Biochem Physiol. 2019;100:e21538.

    Article  Google Scholar 

  30. Isoe J, Koch LE, Isoe YE, Rascon AA Jr, Brown HE, et al. Identification and characterization of a mosquito-specific eggshell organizing factor in Aedes aegypti mosquitoes. PLoS Biol. 2019;17:e3000068.

    Article  Google Scholar 

  31. Yang M, Wang Y, Jiang F, Song T, Wang H, Liu Q, et al. miR-71 and miR-263 jointly regulate target genes chitin synthase and chitinase to control locust molting. PLoS Genet. 2016;12:e1006257.

    Article  Google Scholar 

  32. Zhu L, Fulcher A, Hossain T, Davidson C, Beier JC, Xue RD. Body size, blood feeding activity, and fecundity of Psorophora howardii, Psorophora ciliata, and Psorophora ferox (Diptera: Culicidae). J Med Entomol. 2014;51:382–6.

    Article  Google Scholar 

  33. Konno K, Shimura S, Ueno C, Arakawa T, Nakamura M. Abnormal swelling of the peritrophic membrane in Eri silkworm gut caused by MLX56 family defense proteins with chitin-binding and extensin domains. Phytochemistry. 2018;147:211–9.

    Article  CAS  Google Scholar 

  34. Alves SN, Serrão JE, Melo AL. Alterations in the fat body and midgut of Culex quinquefasciatus larvae following exposure to different insecticides. Micron. 2010;41:592–7.

    Article  CAS  Google Scholar 

  35. Nepomuceno DB, Santos VC, Araujo RN, Pereira MH, Sant’Anna MR, Moreira LA, et al. pH control in the midgut of Aedes aegypti under different nutritional conditions. J Exp Biol. 2017;220:3355–62.

    Article  Google Scholar 

  36. Mohammed AMA, Diab MR, Abdelsattar M, Khalil SMS. Characterization and RNAi-mediated knockdown of chitin synthase A in the potato tuber moth, Phthorimaea operculella. Sci Rep. 2017;7:9502.

    Article  Google Scholar 

  37. Sun R, Liu C, Zhang H, Wang Q. Benzoylurea chitin synthesis inhibitors. J Agric Food Chem. 2015;63:6847–65.

    Article  CAS  Google Scholar 

  38. Tian X, Zhang C, Xu Q, Li Z, Shao X. Azobenzene-benzoylphenylureas as photoswitchable chitin synthesis inhibitors. Org Biomol Chem. 2017;15:3320–3.

    Article  CAS  Google Scholar 

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This study was supported by the National Natural Science Foundation of China (Grant Nos. 81772227, 81672056 and 81672058) and the National S & T Major Programme (Grant No. 2017ZX10303404-002-006).

Author information

Authors and Affiliations



DZ and BS designed the study. XSY, QY, XXL and YX performed the research. XSY, DZ and BS analyzed the data and wrote the manuscript. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Dan Zhou or Bo Shen.

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Ethics approval and consent to participate

All animal procedures were approved by the Institutional Animal Care and Use Committee (IACUC) of Nanjing Medical University for the Use of Laboratory Animals (Protocol No. 582/2017).

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Not applicable.

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The authors declare that they have no competing interests.

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Supplementary information

Additional file 1: Table S1.

PCR primers used to amplify the full-length CpCHSB cDNA from Culex pipiens pallens.

Additional file 2: Table S2.

Primers used for RT-qPCR analysis and siRNA silencing of CpCHSB.

Additional file 3: Figure S1.

Morphological variations in WT, NC and siCHSB with RNA interference (RNAi) in third-instar larvae.

Additional file 4: Figure S2.

Morphological variations in WT, NC and siCHSB by RNAi at day 1 after injection in adult mosquitoes.

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Yang, X., Yin, Q., Xu, Y. et al. Molecular and physiological characterization of the chitin synthase B gene isolated from Culex pipiens pallens (Diptera: Culicidae). Parasites Vectors 12, 614 (2019).

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