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  • Research Article
  • Open Access

Identification and characterization of the causative triatomine bugs of anaphylactic shock in Zhanjiang, China

  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 2Email author and
  • 1Email author
Infectious Diseases of Poverty20187:127

https://doi.org/10.1186/s40249-018-0509-1

  • Received: 19 April 2018
  • Accepted: 23 November 2018
  • Published:

Abstract

Background

Two health concerns primarily related to triatomine bugs are transmission of Trypanosoma cruzi through infective feces, and allergic reactions induced by triatomine bites. In the Southwestern United States, reduviid bugs bites commonly cause insect allergy. In South China, four cases of anaphylactic shock have been reported after this bite exposure. To further classify the species of these bugs and confirm the sensitization of the triatomine saliva, we caught triatomine bugs from the region where the bites occurred and performed phylogenetic and immunohistochemical (IHC) analysis.

Methods

Triatomine bugs were collected in Donghai Island of Zhanjiang City in South China. The genomic DNA was extracted from three legs of the bugs. The fragments of mitochondrial 16S rRNA, cytochrome c oxidase subunit I (COI) gene and nuclear ribosomal 18S and 28S rRNA genes were obtained by PCR and sequenced. A phylogenetic tree was constructed based on the sequence of 16S rRNA gene using a maximum likelihood method with MEGA 7.0 software. Trypanosomal specific fragments and vertebrate COI genes were amplified from the fecal DNA to detect the infection of trypanosomes and analyze the blood feeding patterns, respectively. Paraffin-embedded sections were then prepared from adult triatomines and sent for IHC staining.

Results

We collected two adult triatomine bugs in Donghai Island. Morphological and molecular analyses indicated that the triatomines were Triatoma rubrofasciata. No fragments of T. cruzi or other trypanosomes were detected from the fecal DNA. Mitochondrial gene segments of Homo sapiens and Mus musculus were successfully amplified. The allergens which induced specific IgE antibodies in human serum were localized in the triatomine saliva by IHC assay.

Conclusions

The two triatomine bugs from Donghai Island were T. rubrofasciata. They had bitten humans and mice. Their saliva should contain the allergens related to the allergic symptoms and even anaphylactic shock of exposed residents. Great consideration should be given to this triatomine bugs due to their considerable distribution and potential threat to public health in South China.

Keywords

  • Triatoma rubrofasciata
  • Chagas disease
  • Trypanosoma cruzi
  • Anaphylactic shock

Background

According to the World Health Organization (WHO), vector borne diseases account for more than 17% of all infectious disease and cause more than 700 000 deaths annually [1]. Most of them are transmitted by bloodsucking insects such as mosquitoes, sandflies, ticks, flies and triatomine bugs. The reduviid subfamily Triatominae (triatomine bugs) is a group of medically important insects characterized by obligate hematophagy and transmitting Trypanosoma cruzi [2]. These parasites can invade the human body after the individual contacts with the feces of an infected triatomine bug, causing a potentially life-threatening illness called Chagas disease [3].

As one of 21 subfamilies in the large family Reduviidae, Triatominae consists of 5 tribes, 15 genera and 151 species at present [4]. Most triatomine species are reported to be distributed in the Americas roughly from 46°N to 46°S, except for the aberrant Indian genus Linshcoteus and the tropicoplitan Triatoma rubrofasciata [5, 6]. Triatomines inhabited in Asia contained six species in the genus Linshcoteus and eight species in the genus Triatoma [7, 8]. In China, two species of triatomines have been recorded: T. sinica Hsaio collected in Nanjing in 1965, and T. rubrofasciata, with a wider distribution in South China including Guangdong, Guangxi, Hainan and Taiwan [8, 9].

In addition, triatomine bites can cause allergic reactions in humans, which pose another great threat to public health in the endemic regions [10]. Anaphylaxis is a rapidly developing and life-threatening hypersensitive reaction caused by repeated exposure to a specific allergen such as drugs, foods, or insect stings [11]. Although anaphylaxis caused by triatomine bites was reported early in 1894, it is still an unrecognized problem easily ignored by patients and medical staffs because this painless sting usually happens in the evening [10]. The manifestations of allergic reactions to triatomine bites vary from localized allergies to more systematic reactions such as anaphylactic shock and even death [12]. Anaphylactic reactions to triatomines were mainly reported in the endemic areas such as Western and Southwestern United States [13]. Several species (T. protracta, T. gerstaeckeri, T. sanguisuga, T. rubida, T. recurve, Paratriatoma hirsuta and T. rubrofasciata, etc) of Triatoma genera have been suggested to be associated with allergic reactions in the United States [10].

In China, few studies have been performed on triatomine bugs except for sporadic case reports. Dermatitis caused by T. rubrofasciata bites was recorded in Hainan in 1986 [9]. From 2000 to 2003, four local residents developed anaphylactic shock after triatomine bites on Donghai Island of Zhanjiang City in South China [14]. They displayed insect bite wounds and developed typical allergic symptoms, such as skin rashes, chest tightness, dyspnea and circulatory compromises. Anti-shock treatment achieved good responses and reversed the life-threatening conditions. In this study, to identify the classification of the involved triatomines and investigate the sensitization of the triatomine saliva, as well as to determine the infection of T. cruzi and characterize the blood feeding pattern, we searched the beds, walls and roof cracks of the houses and caught two triatomines from Donghai Island and collected their feces for further analysis.

Materials and methods

Triatomine and human serum collection

The triatomine bugs were caught from Hewujing Village, Min’an Town of Donghai Island in July, 2017 (Fig. 1). In this region, four local residents have been reported to be bitten by the triatomine bugs and showed anaphylactic shock. The beds, wall and roof cracks of villagers’ houses were the primary collection sites. The housekeeper who was bitten by triatomines and developed allergic reactions was also included in the research. We collected the serum of the allergic person for immunohistochemistry (IHC) analysis. Serum of the healthy donor in Shenzhen City who never contacted with triatomine bugs was also collected.
Fig. 1
Fig. 1

The location of Hewujing Village on Donghai Island of South China

Genomic DNA extraction, sequencing and phylogenetic analysis

Total DNA was extracted from three legs of two bugs with QIAamp DNA Mini Kit (Qiagen 51 304, Germany) combined with the TissueLyser LT (Qiagen 85 600, Germany) according to the manufacturer’s instructions. The primers that were used to amplify mitochondrial 16S rRNA, cytochrome c oxidase subunit I (COI) gene and nuclear ribosomal 18S and 28S rRNA gene are listed in Table 1 [1517]. PCR reactions were conducted with an AccuPrime™ Taq DNA Polymerase System (Invitrogen 12 339 016, USA). The PCR products were examined with 1% agarose gel electrophoresis, purified with a QIAquick PCR Purification Kit (Qiagen 28 104, Germany) and sequenced with Sanger sequencing technology (BGI, Shenzhen, China). The obtained sequences were assembled using SeqMan Lasergene v. 7.0 software (DNAStar, Inc., Wisconsin, USA) and submitted to GenBank (https://www.ncbi.nlm.nih.gov/genbank/) under the accession numbers MG674717, MG923959, MG674716 and MG675575. A phylogenetic tree was constructed based on the sequence of 16 s rRNA genes using the maximum likelihood method with MEGA 7.0 software (https://www.megasoftware.net/download_form). Evolutionary distances were calculated using the Tamura-Nei substitution model and the bootstrap consensus tree inferred from 1000 replicates.
Table 1

Primers used to amplify the mitochondrial 16S rRNA, cytochrome c oxidase subunit I (COI) gene and nuclear ribosomal 18S and 28S rRNA genes

Gene target

Forward primer (5’→3’)

Reverse primer (5’→3’)

Expected length (bp)

16S rRNA

CGCCTGTTTATCAAAAACAT [15]

CTCCGGTTTGAACTCAGATCA [15]

552

28S rRNA

GCGAGTCGTGTTGCTTGATAGTGCAG [16]

TTGGTCCGTGTTTCAAGACGGG [16]

710

COI

CCTGCAGGAGGAGGAGAYCC [17]

TAAGCGTCTGGGTAGTCTGARTAKCG [17]

650

18S rRNA-1a

TGGTTGATCCTGCCAGTAGTC

TCGACACTCGTTTAAGAGCACC

822

18S rRNA-2a

TGTTGCGGTTAAAAAGCTCG

TCGGAATTAACCAGACAAATCG

803

18S rRNA-3a

AGGTTCGAAGGCGATCAGATAC

TCCTTCCGCAGGTTCACCTA

829

adesigned for this study

Fecal DNA extraction and blood feeding patterns of the two triatomine bugs

The feces of adult bugs before laboratory rearing were collected for DNA extraction with QIAamp®DNA Stool Mini Kit (Cat. No. 51504, QIAGEN, Hilden, Germany). To investigate whether the triatomine bugs had sucked blood of vertebrates in natural environment, the vertebrate cytochrome c oxidase I subunit gene (vCOI) was amplified with a set of the primers (vCOI_F:5’-AAGAATCAGAATARGTGTTG-3′; vCOI_R: 5’-AACCACAAAGACATTGGCAC-3′) from fecal DNA samples according to previous study [18]. The purified PCR fragments were inserted into pGEM-T Easy cloning vectors (Promega A1360, USA) and sent to be sequenced (BGI, Shenzhen, China). The sequenced gene fragments were compared with those from GenBank to identify the blood meal sources.

Identification of trypanosomes by nest-PCR and q-PCR

Five microliters of fecal DNA was used for PCR amplification in a 50 μl reaction with an AccuPrime™ Taq DNA Polymerase System (Cat. No. 12339016, Invitrogen, Carlsbad, CA, USA), as follows: 94 °C for 2 min; 35 cycles at 94 °C for 30 s, 55 °C for 30 s, 68 °C for 1 min. Primers were designed as described previously, targeting the 24S alpha subunit rRNA gene of trypanosomatids and a nested-PCR was subsequently conducted to amplify the T. cruzi-specific region of the same gene using primers D71 and D72 [19, 20]. PCR products were examined with 2% agarose gel electrophoresis. Additionally, the qPCR reactions were used to detect T. cruzi satellite DNA gene fragments with 2 × Premix Ex Taq™ (Code No. RR390A, Takara Bio Inc., Japan) as described previously [21]. Primers and probes were synthesized by Sangon Biotech (Shanghai, China).

Immunolocalization of salivary allergens in the triatomine bugs

The bodies of adult bugs were fixed with 4% paraformaldehyde. The fixed tissues were embedded in paraffin wax, and processed to obtain 5-μm-pore-size sections. After deparaffinization and rehydration, the slides were steamed in 0.01 mol/L sodium citrate buffer (pH 6.0) for 10 min with the microwave antigen retrieval method. The endogenous peroxidase was quenched with 3% H2O2 in 80% methanol for 20 min, and then nonspecific absorption was minimized by incubating the sections in 5% normal goat serum in PBS for 30 min at room temperature. The sections were then incubated overnight with a 1:20 dilution of the serum from the allergic patient or with control serum of healthy people. Specific labeling was detected with a horseradish peroxidase (HRP) labeled goat anti-human IgE antibody (ab73901, Abcam, USA) and the DAB Immunohistochemistry Color Development Kit (E670033, Sangon Biotech, Shanghai, China).

Results

Morphological characteristics of the triatomine bugs

One pair of adult bugs was caught under the bed in a farmer’s house in Hewujing Village, Min’an Town of Donghai Island. The house was crowded and heaped with sundry, clothes and living supplies (Fig. 2). The housekeeper complaint that he had been bitten by this kind of bugs several times and experienced symptoms such as skin rashes, pruritus, sudden increase of heart rate and dyspnea.
Fig. 2
Fig. 2

The house where we collected the two adult triatomine bugs

The two bugs were identified to be heterosexual and showed morphological characteristics of T. rubrofasciata (Fig. 3). The female and male were approximately 25 mm and 20 mm in length. The genital region of the female adult bug was strongly projecting posteriad (Fig. 3a and b). Adults exhibited orange-red margin along the side of the pronotum and the outer edge of the abdomen which extended horizontally between segments (Fig. 3a, b, c and d). The eyes were very prominent at the sides of a long and cone-shaped head (Fig. 3e). The ocelli were behind and above the eyes (Fig. 3e). The antennae had four segments and the first segment surpassed the apex of its head (Fig. 3e). The pronotum was black and sulcated, with two anterior angles produced into short spines of a reddish yellow color (Fig. 3e). The scutellum was dark and broad, triangular to tip (Fig. 3e). The proboscis was stout and hinged beneath the head, and covered with short hairs which were progressively longer towards tip (Fig. 3f).
Fig. 3
Fig. 3

a and b Dorsal and ventral views of the female T. rubrofasciata; c and d Dorsal and ventral views of the male T. rubrofasciata. I: Orange-red margin along the outer edge of the abdomen which extended horizontally between segments; II: Orange-red margin along the side of the pronotum; III: The genital region of the female adult bug was strongly projecting posteriad; IV: The first segment surpassed the apex of its head; V: Eyes at the sides of a long and cone-shaped head; VI: Ocelli; VII: Anterior angles produced into short spines of a reddish yellow color; VIII: The stout proboscis hinged beneath the thorax, covered with short hairs which were progressively longer towards tip

Molecular characteristics of the triatomine bugs

In addition to the morphological classification method, molecular and phylogenic analyses were also performed to identify their species. The partial sequences of mitochondrial 16S rRNA (546 bp), COI gene (651 bp), nuclear ribosomal 18S rRNA (1880 bp) and 28S rRNA (693 bp) genes were sequenced and submitted to the GenBank under the accession numbers of MG674717, MG923959, MG674716 and MG675575, respectively. The nucleotide sequences of these DNA markers from the female and male triatomine bugs were absolutely the same. These fragments showed more than 98% identity with the genes of T. rubrofasciata identified and sequenced in other areas such as Taiwan of China, Vietnam and Brazil.

A phylogenetic tree was established based on the triatomine 16S rRNA gene of Zhanjiang bugs and other reference sequences in GenBank (Fig. 4). According to the phylogenetic tree, the Triatomini tribe was divided into three main clades: (1) Northern American Triatoma (dimidiata subcomplex + protracta complex + lecticularia subcomplex + phyllosoma subcomplex) + T. rubrofasciata complex +Linshcosteus; (2) Panstrongylus + flavida complex; (3) Southern American Triatoma (including infestans, brasiliensis, rubrovaria and matogrossensis subcomplex as well as Mepraia and Eratyrus). The 16S rRNA sequence of the Zhanjiang triatomine was identical to that of Taiwan and Foshan. This Chinese group was closest to the Vietnam strain (HQ337018). The Chinese triatomines and Vietnam strain were classified in the rubrofasciata complex of the Northern American Triatoma clade.
Fig. 4
Fig. 4

Phylogenetic tree inferred by mitochondrial 16S rRNA genes. The Maximum Likelihood method with the Tamura-Nei mode was used

Identification of blood feeding patterns and detection of trypanosomes in feces of bugs

The mitochondrial COI genes of both Homo sapiens and Mus musculus were detected in the feces samples of the field caught triatomines, suggesting that these triatomines had bitten humans and mice.

The gene fragments of trypanosomatids and T. cruzi could not be amplified from the fecal DNA samples of the field-caught triatomines. It suggested that the two T. rubrofasciata from Donghai Island did not host the trypanosome parasites.

Immunolocalization of salivary allergens in the triatomine bugs

IHC was performed to identify whether the patient could produce specific IgE antibodies in the serum after the stimulation of the triatomine saliva proteins. The goat anti-human IgE antibody was used as the secondary antibody. We found that the salivary glands of the field-caught triatomines that were incubated with the serum of allergic patient showed brown yellow color. The positive staining was localized in the cytoplasm of epithelium and the luminal contents of the salivary glands (Fig. 5b). However, the salivary glands that were incubated with the serum of healthy people as primary antibody showed negative staining (Fig. 5a). The results suggested that there were IgE antibodies specific to the triatomine saliva in the serum of the allergic patient.
Fig. 5
Fig. 5

Immunolocalization of salivary allergens of the triatomine bug. The bugs were fixed, embedded, and sectioned as described in Materials and Methods. a The serum (1:20) of healthy people as control antibody; b The serum (1:20) of the allergic patient as primary antibody. HRP labeled secondary antibody (goat anti-human IgE antibody) localizes allergens in the luminal contents of the salivary glands (I and II) and the cytoplasm of epithelium (III and IV) (original magnification, × 400)

Discussion

T. rubrofasciata is the most widespread species in Asia and distributed throughout the Indo-Pacific region including Andaman Islands, Borneo, Burma, Cambodia, Carolina Islands, China, Comoros Islands, India, Indonesia, Japan, Madagascar, Mauritius, Philippines, Reunion, Rodriguez Islands, Sri Lanka, Singapore, Seychelles, Thailand, Tonga, Vietnam [79, 22, 23]. We caught two triatomine bugs from Donghai Island of Zhanjiang in South China from a farmer’s house who had been bitten by the bugs for several times and developed allergic symptoms. The morphological and phylogenetic analyses confirmed that these two bugs were T. rubrofasciata. The fecal examination suggested that the bugs had sucked blood from humans and mice. Therefore, the local residents would be under the threat of infectious disease and bite related complications caused by T. rubrofasciata.

Donghai Island (E 110°11′–110°31′, N 20°55′–21°05′) is located in the south of the equator and near Pacific Ocean and Southeast Asian countries. It has a tropical monsoon climate and abundant rainfall suitable for the breeding of a variety of hematophagous insects. The tropical agriculture is well developed and vegetation is rich which can provide appropriate peri-domestic shelters for triatomines. The house where we found the triatomine bugs was cluttered with living supplies, which provided the bugs good domestic shelters. Klotz et al. thought after the entry of the triatomine bugs into houses they may commonly feed on house owners and pets for months or until discovered [24]. Thus, it is very important to launch a health education about the triatomine habitats to the local residents to reduce the risk of exposure to these dangerous bugs.

All species of triatomines need the blood of a vertebrate for their complete development [25]. All triatomines defecate shortly after their blood meals [25]. The vertebrate blood genes in the triatomine feces are concordant with its food sources. We detected specific mitochondrial COI gene of both Homo sapiens and Mus musculus from their feces samples, which hinted that these two bugs had bitten both humans and mice.

All species of triatomines are considered capable of transmitting T. cruzi including T. rubrofasciata through their infective feces [6]. In addition, T. rubrofasciata can transmit another species of trypanosome-T. conorhini, which was found to infect Rattus rattus and Macaca cyclopis [7, 22, 26]. T. conorhini infections in humans have not been reported, but it may still be a threat to the immunocompromised patients [7]. According to our results, no trypanosomes including T. cruzi and T. conorhini were detected in the feces of the wild T. rubrofasciata. There is also no record of Chagas disease in China so far [27]. Chagas disease was once distributed only in the Americas, principally Latin America, but later began to spread to other continents [3]. The migration of insect vectors might increase the risk of disease spreading. As a result, it is very necessary to monitor this important insect and prevent imported Chagas disease.

Apart from the important infectious Chagas disease, the allergic reaction is another health issue caused by the triatomine bites in sensitized individuals [812]. In the United States, anaphylaxis is the most serious complication of a triatomine bug bite [12]. A case review indicated that there were at least 110 persons who had allergic reactions to triatomine bites in Mariposa County of California alone [28]. In Southeast Asia, the bite reaction is also the main nuisance posed by triatomine bugs [8]. Cases of allergic reactions to the bites of T. rubrofasciata have been reported in Singapore, Philippines, Vietnam and China [8, 9, 14, 23, 29]. But up to now, the pathogenesis of this allergy has not received systematical studies in the whole Asia area. In the Americas, the researchers mainly focused on the allergies to T. protracta [3033]. We firstly collected the serum of allergic patient and investigated the sensitization of the T. rubrofasciata saliva.

During the triatomine’s blood suckling, the triatomine saliva will travel through the salivary ducts to the proboscis and be injected into the bite victims [30]. The allergens responsible for sensitization of T. protracta were found in the saliva [30]. It has been proven that the saliva induced IgE-mediated hypersensitivity is the cause of the triatomine bite related anaphylaxis [31, 32]. We found that the IgE antibodies specific to T. rubrofasciata saliva were present in the serum of the allergic patient who had been bitten for many times through the IHC analysis. Similarly, Rohr et al. also measured that the IgE levels specific to T. protracta salivary extracts in the sera of five patients with life threatening allergic reactions were 200 to 400% greater than that of the control sera by the radioimmunoassay method [33]. But the particular components in the saliva responsible for the allergies are remained to be determined. Previous studies indicate that major allergic proteins of T. protracta are of low molecular weight (18000–20 000 Daltons) such as procalin [12, 30]. In addition, a study demonstrates that the salivary allergens do not cross react between different triatomine species [30]. There were no reports and literature of relevant studies on the specific allergen proteins of T. rubrofasciata to date. With specific IgE antibodies in the serum of the allergic patient, we can identify and construct the allergens in salivary proteins of T. rubrofasciata once collected enough bugs. This study was conducted to determine the presence of trypanosome infections in local triatomine bugs and the sensitization of the T. rubrofasciata. Due to the limited sample size and sampling area, it could not cover all the conditions of Chinese triatomines. With the established methods, we would expand the study area and deepen the research on mechanisms of anaphylaxis.

Conclusions

T. rubrofasciata was the causative triatomine responsible for the anaphylactic shock experienced by the residents in Donghai Island of Zhanjiang City in South China. The wild caught bugs had sucked blood from humans and mice. No evidence was found for the infections of trypanosomes in these triatomine bugs. Our findings revealed the basic characteristics of the T. rubrofasciata in South China and their ability to cause anaphylaxis, which may help you to have a better understanding of this dangerous bug and benefit for its control. Further identification of the specific allergens in the saliva is warranted.

Abbreviations

COI: 

Cytochrome c oxidase subunit I

HRP: 

Horseradish peroxidase

IHC: 

Immunohistochemistry

WHO: 

World Health Organization

Declarations

Acknowledgements

The authors wound like to thank Dr. Liu Qin, Dr. Chen Mu-Xin in National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, and Dr. Yang Yi-Chao, Dr. Shi Yun-Liang in Guangxi Center for Disease Control and Prevention for kindly providing the instructions of laboratory rearing and identification of the triatomine bugs.

Funding

This work was supported by National Key Research and Development Program of China (No. 2016YFC1202000, 2016YFC1202001, and 2016YFC1200500), and Shenzhen San-Ming Project for prevention and research on vector-borne diseases (SZSM201611064).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding authors on reasonable request.

Authors’ contributions

HYL raised the triatomine bugs, extracted the DNA and performed the PCR and IHC analysis, and wrote the manuscript. ZRL and PLF convinced the idea and designed the research, supervised the study, revised the manuscript. HDN, WWH, TYJ and ZQ collected and identified the triatomine bugs. YF, ZXM and WM revised the article. All the authors reviewed and approved the final version of the manuscript submitted to the journal.

Ethics approval and consent to participate

All experiments were approved by the Ethics Committee of Shenzhen Center for Disease Control and Prevention (Permission number: 2016012, Shenzhen, China). All the participants were fully explained the research content and signed the informed consent.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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

Authors’ Affiliations

(1)
Shenzhen Center for Disease Control and Prevention, Shenzhen, 518055, China
(2)
Department of Parasitology, Guangdong Medical University, Zhanjiang, 524005, China

References

  1. World Health Organization: Vector-borne diseases. http://www.who.int/mediacentre/factsheets/fs387/en/. Accessed 31 Oct 2017.
  2. Gorla DE, Dujardin JP, Schofield CJ. Biosystematics of Old World Triatominae. Acta Trop. 1997;63:127–40.View ArticleGoogle Scholar
  3. World Health Organization: Chagas disease (American trypanosomiasis). http://www.who.int/mediacentre/factsheets/fs340/en/. Accessed 1 Feb 2018.
  4. Justi SA, Galvão C. The evolutionary origin of diversity in Chagas disease vectors. Trends Parasitol. 2017;33:42–52.View ArticleGoogle Scholar
  5. Schofield C. Trypanosoma cruzi - the vector-parasite paradox. Mem Inst Oswaldo Cruz. 2000;95:535–44.View ArticleGoogle Scholar
  6. Schofield CJ, Galvão C. Classification, evolution, and species groups within the Triatominae. Acta Trop. 2009;110:88–100.View ArticleGoogle Scholar
  7. Dujardin JP, Lam TX, Khoa PT, Schofield CJ. The rising importance of Triatoma rubrofasciata. Mem Inst Oswaldo Cruz. 2015;110:319–23.View ArticleGoogle Scholar
  8. Dujardin JP, Pham Thi K, Truong Xuan L, Panzera F, Pita S, Schofield CJ. Epidemiological status of kissing-bugs in South East Asia: a preliminary assessment. Acta Trop. 2015;151:142–9.View ArticleGoogle Scholar
  9. Chen M. The prevention and treatment of the dermatitis caused by triatomine bites. Hainan Med J. 1986;14:35 (in Chinese).Google Scholar
  10. Moffitt JE, Venarske D, Goddard J, Yates AB, deShazo RD. Allergic reactions to Triatoma bites. Ann Allergy Asthma Immunol. 2003;91:122–8.View ArticleGoogle Scholar
  11. Finkelman FD, Khodoun MV, Strait R. Human IgE-independent systemic anaphylaxis. J Allergy Clin Immunol. 2016;137:1674–80.View ArticleGoogle Scholar
  12. Klotz JH, Dorn PL, Logan JL, Stevens L, Pinnas JL, Schmidt JO, et al. “Kissing bugs”: potential disease vectors and cause of anaphylaxis. Clin Infect Dis. 2010;50:1629–34.View ArticleGoogle Scholar
  13. Paddock CD, McKerrow JH, Hansell E, Foreman KW, Hsieh I, Marshall N. Identification, cloning, and recombinant expression of procalin, a major triatomine allergen. J Immunol. 2001;167:2694–9.View ArticleGoogle Scholar
  14. Wang LY, Peng LF. Four cases of anaphylactic shock caused by triatomine bugs. Clin Focus. 2006;21:1059–61 (in Chinese).Google Scholar
  15. Weirauch C, Munro JB. Molecular phylogeny of the assassin bugs (Hemiptera: Reduviidae), based on mitochondrial and nuclear ribosomal genes. Mol Phylogenet Evol. 2009;53:287–99.View ArticleGoogle Scholar
  16. Dietrich CH, Rakitov RA, Holmes JL, Black WC 4th. Phylogeny of the major lineages of Membracoidea (Insecta: Hemiptera: Cicadomorpha) based on 28S rDNA sequences. Mol Phylogenet Evol. 2001;18:293–305.View ArticleGoogle Scholar
  17. Palumbi SR, Benzie J. Large mitochondrial DNA differences between morphologically similar Penaeid shrimp. Mol Mar Biol Biotechnol. 1991;1:27–34.PubMedGoogle Scholar
  18. Niare S, Berenger JM, Dieme C, Doumbo O, Raoult D, Parola P, et al. Identification of blood meal sources in the main African malaria mosquito vector by MALDI-TOF MS. Malar J. 2016;15:87.View ArticleGoogle Scholar
  19. Souto RP, Vargas N, Zingales B. Trypanosoma rangeli: discrimination from Trypanosoma cruzi based on a variable domain from the large subunit ribosomal RNA gene. Exp Parasitol. 1999;91:306–14.View ArticleGoogle Scholar
  20. Morales EA, Mayor P, Bowler M, Aysanoa E, Pérez-Velez ES, Pérez J, et al. Prevalence of Trypanosoma cruzi and other Trypanosomatids in frequently-hunted wild mammals from the Peruvian Amazon. Am J Trop Med Hyg. 2017;97:1482–5.View ArticleGoogle Scholar
  21. Moreira OC, Verly T, Finamore-Araujo P, Gomes SAO, Lopes CM, de Sousa DM, et al. Development of conventional and real-time multiplex PCR-based assays for estimation of natural infection rates and Trypanosoma cruziload in triatomine vectors. Parasit Vectors. 2017;10:404.View ArticleGoogle Scholar
  22. Cross JH, Hsu MY, Hung CK. Studies on trypanosomes in the Taiwan monkey. Southeast Asian J Trop Med Public Health. 1983;14:536–42.PubMedGoogle Scholar
  23. Africa CM. Three cases of poisonous insect bite involving Triatoma rubrofasciata. Philipp J Sci. 1934;53:169–78.Google Scholar
  24. Klotz SA, Schmidt JO, Dorn PL, Ivanyi C, Sullivan KR, Stevens L. Free-roaming kissing bugs, vectors of Chagas disease, feed often on humans in the southwest. Am J Med. 2014;127:421–6.View ArticleGoogle Scholar
  25. Lent H, Wygodzinsky P. Revision of the Triatominae (Hemiptera: Reduviidae) and their significance as vectors of Chagas disease. Bull Am Mus Nat Hist. 1979;163:125–520.Google Scholar
  26. Espinosa-Álvarez O, Ortiz PA, Lima L, Costa-Martins AG, Serrano MG, Herder S, et al. Trypanosoma rangeli is phylogenetically closer to Old World trypanosomes than to Trypanosoma cruzi. Int J Parasitol. 2018;48:569–84.View ArticleGoogle Scholar
  27. Liu Q, Guo YH, Zhang Y, Zhou ZB, Zhang LL, Zhu D, et al. First records of Triatoma rubrofasciata (De Geer, 1773) (Hemiptera, Reduviidae) in Foshan, Guangdong Province, southern China. Infect Dis Poverty. 2017;6:129.View ArticleGoogle Scholar
  28. Nichols N, Green TW. Allergic reactions to “kissing bug” bites. Calif Med. 1963;98:267–8.PubMedPubMed CentralGoogle Scholar
  29. Teo SK, Cheah JS. Severe reaction to the bite of the triatomid bug (Triatoma rubrofasciata) in Singapore. J Trop Med Hyg. 1973;76:161–2.PubMedGoogle Scholar
  30. Pinnas JL, Lindberg RE, Chen TM, Meinke GC. Studies of kissing bug-sensitive patients: evidence for the lack of cross-reactivity between Triatoma Protracta and Triatoma Rubida salivary gland extracts. J Allergy Clin Immunol. 1986;77:364–70.View ArticleGoogle Scholar
  31. Marshall NA, Street DH. Allergy to Triatoma protracta (Heteroptera; Reduviidae). I. Etiology, antigen preparation, diagnosis and immunotherapy. J Med Entomol. 1982;19:248–52.View ArticleGoogle Scholar
  32. Klotz JH, Klotz SA, Pinnas JL. Animal bites and stings with anaphylactic potential. J Emerg Med. 2009;36:148–56.View ArticleGoogle Scholar
  33. Rohr AS, Marshall NA, Saxon A. Successful immunotherapy for Triatoma protracta-induced anaphylaxis. J Allergy Clin Immunol. 1984;73:369–75.View ArticleGoogle Scholar

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