https://orcid.org/0000-0002-1195-3806
Figures
Abstract
Mosquitoes are hematophagous insects that transmit parasites and pathogens with devastating effects on humans, particularly in subtropical regions. Different mosquito species display various behaviors, breeding sites, and geographic distribution; however, they can be difficult to distinguish in the field due to morphological similarities between species and damage caused during trapping and transportation. Vector control methods for controlling mosquito-borne disease epidemics require an understanding of which vector species are present in the area as well as the epidemiological patterns of disease transmission. Although molecular techniques can accurately distinguish between mosquito species, they are costly and laborious, making them unsuitable for extensive use in the field. Thus, alternative techniques are required. Geometric morphometrics (GM) is a rapid and inexpensive technique that can be used to analyze the size, shape, and shape variation of individuals based on a range of traits. Here, we used GM to analyze the wings of 1,040 female mosquitoes from 12 different species in Thailand. The right wing of each specimen was removed, imaged microscopically, and digitized using 17 landmarks. Wing shape variation among genera and species was analyzed using canonical variate analysis (CVA), while discriminant function analysis was used to cross-validate classification reliability based on Mahalanobis distances. Phenetic relationships were constructed to illustrate the discrimination patterns for genera and species. CVA of the morphological variation among Aedes, Anopheles, Armigeres, Culex, and Mansonia mosquito genera revealed five clusters. In particular, we demonstrated a high percentage of correctly-distinguished samples among Aedes (97.48%), Armigeres (96.15%), Culex (90.07%), and Mansonia (91.67%), but not Anopheles (64.54%). Together, these findings suggest that wing landmark-based GM analysis is an efficient method for identifying mosquito species, particularly among the Aedes, Armigeres, Culex, and Mansonia genera.
Citation: Champakaew D, Junkum A, Sontigun N, Sanit S, Limsopatham K, Saeung A, et al. (2021) Geometric morphometric wing analysis as a tool to discriminate female mosquitoes from different suburban areas of Chiang Mai province, Thailand. PLoS ONE 16(11): e0260333. https://doi.org/10.1371/journal.pone.0260333
Editor: Shawky M. Aboelhadid, Beni Suef University Faculty of Veterinary Medicine, EGYPT
Received: May 12, 2021; Accepted: November 8, 2021; Published: November 29, 2021
Copyright: © 2021 Champakaew et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: This research was supported financially by the Walailak University Research Fund (WU grant: WU-IRG-63-023), Thailand and the Faculty of Medicine (Grant no. PAR-2563–07268) and the Office of Research Administration, Chiang Mai University, Thailand. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Mosquitoes are hematophagous insects that are considered to be one of the most dangerous vectors in the world due to their potential to transmit parasites and pathogens responsible for serious diseases, including malaria, filariasis, yellow fever, dengue, and Japanese encephalitis [1]. Indeed, over 1 billion cases and 1 million deaths due to mosquito-borne diseases are reported annually [2], with mosquitoes becoming an increasing problem in tropical and subtropical regions [3]. Although more than 3,000 species of mosquito exist worldwide, the main vectors of clinical importance are Anopheles spp. (malaria, lymphatic filariasis, and Japanese encephalitis), Culex spp. (lymphatic filariasis, Japanese encephalitis), Aedes spp. (dengue/dengue hemorrhagic fever, yellow fever, lymphatic filariasis), and Mansonia spp. (lymphatic filariasis) [4, 5]. In Thailand, there are over 400 species of mosquito and the major vectors of mosquito-borne diseases are Anopheles spp. (An. dirus and An. minimus), Mansonia spp. (Mn. annulata and Mn. annulifera), Culex spp. (Cx. tritaeniorhynchus), and Aedes spp. (Ae. aegypti and Ae. albopictus) [6].
Vector control methods are an important strategy for controlling mosquito-borne disease epidemics [7]; however, their success relies on a good understanding of the biology and geographic distribution of mosquito vectors [8]. Since different mosquito species have different characteristics, such as behavior, breeding site, and geographic distribution, their accurate identification is of great importance for medical entomology [9]. The most common method of species identification relies on morphological taxonomic keys and is a laborious process that requires intensive training. Unfortunately, it can be difficult to identify mosquito vectors in the field based on morphological features due to the prevalence of cryptic, sibling, or isomorphic species with similar genetics and morphologies. Although some mosquito species are easily distinguished when in good condition, morphological identification is often hampered by damage to the external characteristics of field specimens during trapping and transportation [10] or through their preservation in ethanol [11, 12]. Consequently, several molecular or phenotypic tools have been developed for the identification of problematic species. Although molecular techniques can accurately distinguish mosquito species, they are very costly and labor intensive, making them unsuitable for routine use in the field where many samples are collected. Therefore, novel alternatives to classical morphology or DNA identification are required to identify mosquito vectors in the field.
Morphometric methods, such as geometric morphometrics (GM), are a rapid, inexpensive, and valuable tool for analyzing the biological size, shape, and shape variation of individuals based on various traits [13]. GM has been applied extensively in a number of fields, including entomology, where it has been used to analyze blow flies, mosquitoes, bees, and Triatominae eggs [14]. In addition, several recent studies have used GM to classify species and examine variation among clinically important mosquitoes that are morphologically similar or are sibling species [15–17]. Currently, GM based on the geometry of wing features (landmark-based) is largely used in medical entomology to reliably distinguish between closely related species [18, 24]. In particular, wing landmark-based GM has been successfully used to identify three Stomoxys fly species that are difficult to separate using external morphological characteristics, with a correct classification rate of 76–100% [19]. Wing landmark-based GM has also been used to distinguish 12 medically and forensically important blow fly species in Thailand at both the genus and species levels [18]. Moreover, GM analysis has been used to identify clinically important mosquito species, sibling species, or cryptic species based on adult female wing morphometry alone [15, 20–24]. In this study, we aimed to determine whether the wing landmark-based GM analysis can be used as an identification tool for clinically important mosquito genera/species in Thailand.
Materials and methods
Mosquito samples and identification
A total of 1,040 female mosquitoes were collected from field and laboratory colonies for use in this study (Table 1). Free-mating laboratory colonies of mosquito vectors from the Aedes, Anopheles, and Culex genera were reared and maintained continually in the insectary of the Department of Parasitology, Faculty of Medicine, Chiang Mai University, Chiang Mai province, Thailand. The colonies were housed without exposure to any pathogens or insecticides at a constant temperature of 27±2°C and 70–80% relative humidity under a 12:12 h light/dark photoperiod. Laboratory colonies of Ae. aegypti, An. cracens (formerly An. dirus B), An. dirus, An. minimus sensu stricto (formerly An. minimus A), and Cx. quinquefasciatus were reared and maintained in an insectary for several generations. Ae. aegypti (Muang Chiang Mai-susceptible: MCM-S), An. cracens, An. dirus, An. minimus, and Cx. quinquefasciatus (National Institute of Health of Thailand: NIH strain) originated from field larvae collected originally in Chiang Mai province, Muang Chiang Mai district in 1995, the Armed Forces Research Institute of Medical Sciences (AFRIMS, Bangkok, Thailand), the Vector Borne Disease Section, Office of Disease Prevention and Control No. 10 (Chiang Mai, Thailand), and the National Institute of Health, Ministry of Public Health (Nonthaburi province, Thailand), respectively. Mass rearing was conducted according to previously described procedures [25], with slight modifications. Rearing trays containing aquatic stage mosquitoes were covered tightly at all times with a nylon screen in order to ensure that all colonies were strictly isolated from each other. Adults were fed continually with 10% sucrose and 10% v/v multivitamin syrup using soaked cotton pads. Female mosquitoes were collected using a mount aspirator, frozen at -20°C for 10 min, and stored in 80% ethanol.
Based on previous research [26–28], adult mosquitoes were collected from natural populations between 18:00 and 22:00 h using a modified human bait trap at suburban sites in three locations in Muang district, Chiang Mai province: Sunpesua, Maehia, and Sri Phum subdistrict. Field trials were conducted after receiving permission from the possessor of the private land. Each human volunteer was covered with a long-sleeved jacket with hood, shoes with socks, gloves, and long pants rolled up to the knee (exposed area: the lower leg). Mosquitoes landing on the exposed area of volunteers were mouth aspirated by proficient collectors before the natural mosquitoes could imbibe any blood. The captured insects were kept in paper cups for counting and identification. A total of 787 adult female mosquitoes from five genera, (Aedes, Anopheles, Armigeres, Culex, and Mansonia) were counted under a stereomicroscope and their species were identified using previously reported taxonomic keys [29] before they were stored in 80% ethanol (Table 1, Fig 1). This project was approved and conducted according to protocol PAR-2556-01588 of the Research Ethics Committee, Faculty of Medicine, Chiang Mai University.
Mosquitoes were collected from three subdistricts (Maehia, Sri Phum, and Sunpesua) in the Muang district of Chiang Mai province, northern Thailand.
GM sample preparation
The right wing was dissected from the thorax of each female mosquito using an insect needle under a stereomicroscope (Olympus SZX7, Germany). The wings were then mixed with normal saline solution (NSS) in an Eppendorf tube using a vortexer (VORTEX-GENIE2, Scientific Industries, Inc., New York, United States) at shake level 3 for 3–5 min to remove the wing scales. Next, each wing was placed on a glass slide in one drop of distilled water and the remaining scales were removed using a small round paintbrush (No. 0).
Image manipulation and data acquisition
The wing was placed onto a glass microscope slide and photographed using a digital camera (Olympus DP22) connected to a light microscope under 4× magnification. A 500-μm scale bar was embedded into each image and kept in the same folder. Tps files were built from the images using TpsUtil32 v.1.78 software [30] to reduce liable marking (LM) bias when digitizing landmark locations. Seventeen selected landmarks [31–33] (Fig 2) were digitized using TpsDig2 v.2.31 software [34]. The LM of the venation pattern of each wing was digitized in duplicate to reduce measurement error by the same handler [35].
Right wing of female Ae. aegypti showing the 17 plotted landmarks based on Dujardin et al. (2017).
GM analysis
The duplicate.tps files produced by digitizing wing landmark locations were used to measure the isometric estimator known as centroid size (CS), which is defined as the square root of the sum of the squared distances between the center of the LM or centroid configuration [36]. All samples were analyzed using MorphoJ software v.1.07a [37] and aligned and superimposed using the “Procrustes Fit” function to remove variation due to differences in scale, position, and orientation of the coordinates. The CS and Procrustes coordinates obtained from the landmark data were averaged for each specimen prior to further statistical analysis.
Wing shape variation
To assess the effect of wing size on wing shape (allometry), the regression of the Procrustes coordinates (dependent variable) against CS (independent variable) was analyzed using a permutation test with 10,000 randomizations. The variations in wing shape between five genera/12 species of mosquitoes were determined using CVA, and the reliability of classification within each genus/species was confirmed using discriminant function analysis (DFA), a cross-validation test based on Mahalanobis distances. Additionally, each sample was reclassified according to the similarity of its wings to the average wing shape of all species using a pairwise cross-validated reclassification test based on Mahalanobis distances. All the analyses were conducted in MorphoJ software v.1.07, and a permutation test with 10,000 replications was used.
Phenetic wing morphology relationships
A Neighbor-Joining (NJ) analysis was constructed with 1,000 bootstrap replicates based on Mahalanobis distances obtained through pairwise comparison of analyzed species via CVA using PAST software v.4.03 (https://past.en.lo4d.com/windows) to illustrate the phenetic relationships between the wing data of 12 mosquito species.
Results
Wing shape variation
The regression of Procrustes coordinates against CS revealed the allometry effect of wing size on wing shape (permutation test with 10,000 rounds in MorphoJ: 5.92%, p < 0.0001). Although small, the allometry effect was not removed from the analysis as we considered the allometric size variation of the species identification process [15]. CVA of wing shape among genera revealed five different clusters with morphological variation that were classified by color, including the mosquito genera Aedes (red), Anopheles (yellow), Armigeres (green), Culex (light blue), and Mansonia (purple; Fig 3). At the genus level, CVA revealed five canonical variates, among which the first two (Fig 3) explained 85.0% of the total variation (CV1 = 57.9%, CV2 = 27.1%). The scatter plot of CV1 and CV2 showed that Aedes and Armigeres specimens were separated into distinct groups, while Mansonia and Culexs specimens overlapped considerably with Anopheles specimens (Fig 3). At the species level (Fig 4), CVA explained 67.6% of the total variation (CV1 = 49.4%, CV2 = 18.2%), with the scatter plot revealing a morphometric difference between the Anophelinae and Culicinae subfamilies. In addition, overlapping was observed between all 12 mosquito species except Ar. subalbatus, which was clearly distinct.
Wing shape variation in Aedes, Anopheles, Armigeres, Culex, and Mansonia mosquitoes is shown along the first two canonical variate (CV1 and CV2) axes with 90% confidence ellipses.
Wing shape variation is shown along the first CV1 and CV2 axes with 90% confidence ellipses.
The Mahalanobis distances obtained from pairwise comparisons between the 12 mosquito species ranged from 2.1351 (An. dirus and An. cracens) to 9.6419 (Mn. indiana and Ae. aegypti), with statistical analysis revealing significant differences (permutation test in MorphoJ: p< 0.0001; p< 0.01; and p< 0.05; S1 Table). Cross-validation (permutation test in MorphoJ) further showed that the percentage of specimens correctly classified by genus in the majority of comparisons ranged from 90.07% (Culex) to 97.48% (Aedes), with the exception of Anopheles, which had correct classification rates of less than 70.00% (Table 2).
The Procrustes coordinate distances of 12 mosquito species ranged from 0.0369 (Mn. uniformis and Mn. indiana) to 0.7542 (Mn. indiana and Ae. albopictus), with statistical analysis (permutation test in MorphoJ) indicating highly significant differences between most of these species (p< 0.0001; p< 0.01; and p< 0.05; S2 Table). The pairwise cross-validated reclassification test between mosquito species yielded a high percentage of correctly classified specimens in majority of the comparisons (80%-100%), except six pairwise comparisons, Ae. albopictus and Ae. aegypti (70%), Ae. vexans and Ae. albopictus (67%-76%), An. minimus and An. cracens (78%), An. minimus and An. dirus (71%), An. minimus and Cx. gelidus (78%), An. minimus and Cx. quinquefasciatus (67%), which had percentages of correct classification below 80%. When Mn. indiana was compared with Mn. uniformis, the lowest reclassification score was 0% in all 12 comparisons of the species (Table 3).
Phenetic wing morphology relationships among species
The Neighbor-Joining tree showing the phenetic wing morphology relationships among the 12 mosquito species based on the Mahalanobis distances revealed two main clusters comprising the Culicinae and Anophelinae subfamilies. Three species from the genus Culex grouped together, with the highest levels of similarity between Cx. gelidus and Cx. quinquefasciatus. An identical pattern was observed for the genera Mansonia and Aedes; all the species clustered together in each genus branch. Regarding Anopheles species, they were placed into two distinct clusters (An. minimus and two sibling species; An. cracens and An. dirus) (Fig 5).
The tree was constructed based on the Mahalanobis distances between species.
Discussion
Morphological analysis using taxonomic keys is currently the standard method for identifying mosquito species; however, wing GM analysis also represents a reliable and inexpensive alternative that yields satisfactory results when discriminating between morphologically analogous species. In this study, we evaluated the ability of GM to correctly identify undamaged wing samples from 12 different mosquito species.
Although the number of laboratory strains was greater than the minimum number of samples per species required for precise genus and species differentiation using GM analysis, the number of some field strain mosquito species was beneath this threshold for clear species identification using GM. However, we found that the four important genera, Aedes, Armigeres, Culex, and Mansonia, could be correctly classified at the genus level using wing shape (90.07%-97.48%). In particular, the wing shape of Aedes and Armigeres species was clearly distinct from that of Anopheles, Culex, and Mansonia species. Conversely, the wing shape of Anopheles highly overlapped with that of Culex species (64.54% correctly classified). The broad overlapping indicated that these two sibling species members have a similar wing shape, which is morphologically identical (isomorphic) and has minimal morphological distinction. Therefore, correct identification among cryptic species based on morphological characteristics is difficult, which is consistent with previously reported findings [38, 39]. When cryptic diversity occurs in Anopheles and Culex (e.g., sibling, isomorphic, or cryptic species), molecular identification assays can help distinguish between samples [40–47]. In some studies, male and female genitalia have been used for reliable identification or for confirming identification of Culex species within the subgenus [48]. Our results revealed that the score of Culex species reclassification was higher than 80%, proving that these species can be identified through GM wing analysis. The reclassification score in the comparison of some pairs of species, including Ae. albopictus and Ae. aegypti, Ae. vexans and Ae. albopictus, An. minimus and An. cracens, An. minimus and An. dirus, An. minimus and Cx. gelidus, An. minimus and Cx. quinquefasciatus, and Mn. uniformis and Mn. indiana indicated low percentage of correct classification (0%-78%). Hence, it is recommended that GM be used in addition with traditional taxonomic identification keys or molecular tools for precise species identification. Species from the Mansonia genus were incorrectly identified with the lowest reclassification scores, which may explain that these two mosquitoes (Mn. uniformis and Mn. indiana) are members of the same subgenus Mansonioides, with similarities in wing shape structures. Therefore, the landmark-based analysis of wings can partially help to identify the genus level of Mansonia used in this study. However, morphological taxonomic keys needed for precise identification of Mansonia species require specific training and non-damaged wings for analysis [49].
We also produced a NJ tree showing the phenetic relationships in right-wing morphology based on the Mahalanobis distances between the 12 mosquito species examined in this study, which initially revealed two main clusters. The Anophelinae subfamilies were categorized into two clusters containing An. minimus complex (An. minimus) and An. dirus complex (An. cracens and An. dirus), which are the primary malaria vectors in Thailand. The Anopheles complex groups remain problematic because of overlapping morphological characters between sibling species. Therefore, wing GM analysis should be performed in combination with traditional morphological methods and molecular assays for accurate species identification within Anophelinae and Culicinae morphometric groups [44–48, 50].
Together, the results of this study demonstrate that landmark-based wing morphometry analysis could be an alternative tool for identifying mosquito species in Thailand, consistent with the findings of previous studies on three epidemiologically important genera (Anopheles, Aedes, and Culex) [15, 17, 23] and Mansonia [49]. However, this study utilized a limited number of Ae. vexans, Mn. indiana, and Mn. uniformis samples (30≤ N >10); therefore, further studies should be performed using more specimens from natural populations of these species to improve the reliability of wing shape analysis for species discrimination. Although landmark-based GM analysis can be time-consuming as a result of right-wing preparation and marking all the landmarks in duplicate samples, this method is less expensive and simpler than genetic sequencing, whilst still being reliable. The reliability of wing morphometric analysis depends on several factors: 1) consistent wing preparation to provide the most precise wing measurements; 2) using the same conditions and photographic equipment; and 3) wing landmark location by the same person and duplicate digitization to reduce data measurement errors. Thus, wing morphometric analysis requires less proficiency for an inexperienced person compared to standard taxonomic key identification. Moreover, the majority of female mosquitoes can be correctly identified even when using wing samples preserved in ethanol.
In conclusion, the findings of this study demonstrate that wing landmark-based GM analysis can be used to discriminate female mosquitoes at the genus and species levels. In particular, we found that this method is highly reliable when used for classification of Aedes, Armigeres, Culex, and Mansonia genera, but less reliable when used for discriminating Anopheles species, resulting in high percentage of correct classification for most mosquito species comparisons, except Mansonia species. However, the use of GM analysis could be an alternative technique, as it is easy to use, does not require proficient entomological skills, is a quick, practical, and simple technique, and has become particularly attractive for use in the field to facilitate the control of abundant vector species that are present in the area.
Supporting information
S1 Table. Wing shape variation among mosquito genera analyzed using CVA.
https://doi.org/10.1371/journal.pone.0260333.s001
(DOCX)
S2 Table. CVA of wing shape variation among the 12 mosquito species analyzed.
https://doi.org/10.1371/journal.pone.0260333.s002
(DOCX)
Acknowledgments
The authors would like to thank the staff at the Department of Parasitology, Faculty of Medicine, Chiang Mai University for their support.
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