Much work has been done in recent years to determine the vector competence of Aedes albopictus (Skuse) for Zika virus (ZIKV). If competent, Ae. albopictus could become an important vector in the spread of ZIKV to areas which until now have been considered safe from the virus. Despite much speculation about Ae. albopictus’ competence for ZIKV, there have been, to date, no quantitative syntheses of Ae. albopictus’ competence, nor have the potentially confounding differences between studies been addressed.
Methodology/ principle findings
This study represents a quantitative meta-analysis of the literature surrounding this topic by examining infection rates (IR) and transmission rates (TR) among sample populations of Ae. albopictus at 7 and 14 days post infection (dpi) across 15 journal articles comprising 23 studies. Our analyses examined potentially confounding variables in the studies contained therein, including: geographic origin of viral strain or mosquito population tested, whether sympatry of the tested viral strain and mosquito population was important, and freshness of blood meal. Our results suggest 1) Ae albopictus is a competent vector for ZIKV and 2) that origin of Ae. albopictus population and origin of viral strain had significant effects on the competence of Ae. albopictus to transmit ZIKV.
These results indicate a need to further explore the effects of methodology on vector competence studies and to examine in more detail the geographic variation in the competence of Ae. albopictus for ZIKV as well as the underlying causes of said variation. The ability of Ae. albopictus to carry and transmit ZIKV also points to a need to create new vector control strategies in case of a ZIKV outbreak in an area where Ae. albopictus is prominent. Finally, this study represents a potential template for future meta-analyses in the field of vector competence, where this type of study has been under-utilized despite the abundance of relevant studies.
Citation: McKenzie BA, Wilson AE, Zohdy S (2019) Aedes albopictus is a competent vector of Zika virus: A meta-analysis. PLoS ONE 14(5): e0216794. https://doi.org/10.1371/journal.pone.0216794
Editor: Luciano Andrade Moreira, Centro de Pesquisas René Rachou, BRAZIL
Received: November 20, 2018; Accepted: April 29, 2019; Published: May 21, 2019
Copyright: © 2019 McKenzie 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 as a supplementary data table and cited references.
Funding: Funding was provided by the United States Department of Agriculture to AW and SZ. 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.
Zika virus (ZIKV) is a mosquito-borne virus from the family Flavaviridae, genus Flavivirus, a genus which also contains dengue fever (DENV), West Nile (WNV), Japanese encephalitis (JEV), and yellow fever (YFV) viruses . ZIKV was first isolated in 1947 from a sentinel rhesus monkey (Macaca mulatta) in the Zika forest of Uganda . Over the next 60 years, ZIKV was detected several times in serological studies and routine arthropod-borne viruses (or arboviruses) surveillance across Africa and Southeast Asia [3–6]. In 2007, the first large ZIKV outbreak among humans occurred on Yap Island, in the Federated States of Micronesia [7,8]. Nearly 73% of the population op the island was infected during this outbreak . Another outbreak which began French Polynesia in 2013 and spread across the pacific region further raised concerns because of the number of people infected and because ZIKV infection was linked in several cases to an autoimmune disease known as Guillaine-Barré Syndrome (GBS), which causes acute or subacute flaccid paralysis [9–11]. This outbreak of the Asian lineage of ZIKV spread to the Americas in 2015, infecting around a million citizens in Brazil alone, and spread to a total of 50 countries and territories by 2017 . Along with GBS, this recent outbreak has also been linked to microcephaly in infants [13–15] and has shown potential for sexual transmission [16–19] making ZIKV an emerging infectious disease of high concern.
Many mosquito species have been implicated as potential vectors of ZIKV. The sylvatic vector of ZIKV is thought to be Aedes africanus , while Aedes henselli was implicated in the Yap Island outbreak [7,8,20], but the primary vector of the outbreak in the Americas, the Pacific region and Asia is thought to be Aedes aegypti [10,21], which has demonstrated competence for ZIKV in multiple laboratory tests . Vector competence, in this case, meaning the ability to be infected by and to transmit a pathogen [23–25]. In contrast, most other Aedes species have shown potential for infection by ZIKV, but low potential for transmission [26,27]. Ae. aegypti is a medically important vector as it has a broad distribution, lives largely in urban areas, and has anthropophilic feeding tendencies [28,29]. Along with ZIKV, Ae. aegypti is considered the primary vector of DENV, urban YFV, and chikungunya fever virus (CHIKV) in most parts of the world . A few studies have suggested Culex quinquefasciatus, a known vector of WNV, as a potential vector of ZIKV [31,32]. However, Cx. quinquefasciatus has largely been discounted as a vector of ZIKV through experimentation and critical review[26,33]. Currently, much of the debate in the field surrounds the species Aedes albopictus, which has long been considered the secondary vector of ZIKV even before its competence was experimentally assessed [34–36]. In the past decade or so, Ae. albopictus’ role as a vector for arboviruses has become more widely recognized . Ae. albopictus is already widely considered a competent vector for 26 arboviruses, including viruses from the families Flaviviridae (e.g. DENV, YFV, etc.), Togaviridae (e.g. CHIKV, etc.) and Bunyaviridae (e.g. La Crosse virus, or LCV, etc.) [37–40]. In some parts of the world Ae. albopictus is even considered to be the primary vector of DENV and CHIKV [41–45].
If competent to carry and transmit ZIKV, Ae. albopictus represents a major new threat in the global transmission of the disease [34,35]. From the 1980s-2000s, Ae. albopictus spread from its native Asian range to occupy a nearly global distribution , making it one of the most invasive mosquito species in the world. Ae. albopictus’ current range stretches across every continent but Antarctica, and it is continuing to spread further into North America and Europe [29,46]. Thus, if Ae. albopictus mosquitoes prove to be a competent vector for ZIKV world-wide, it may expand the ZIKV threat in more temperate countries once considered safe due to the absence of Ae. aegypti [34,35]. This means control strategies designed to limit the spread of ZIKV must be broader than if Ae. aegypti is the sole vector . It must also be considered that vector competence may vary by mosquito population and viral strain, and that not all strains of ZIKV are thought to have the same epidemic potential [48–50]. Understanding the connections between vector competence and virus/ vector phylogeny may help to further focus control strategies and public health efforts.
While it is thought that Ae. albopictus may be a vector of ZIKV, at least in some parts of the world [22,51], there have been no meta-analyses of Ae. albopictus’ competence for ZIKV. It is especially important to understand how competence varies across studies, as this may give us insight into potential geographical differences in Ae. albopictus ability to carry and transmit ZIKV, which is thought to be variable [22,51–54], as well as giving us a chance to examine other potential variables in the literature. Studies to date of Ae. albopictus’ competence for ZIKV vary in methods, mosquito strains, and viral strains among other things. All of these variables are known to impact mosquitoes’ vector competence for DENV, CHIKV and other flaviviruses, and it seems likely that they would affect competence for ZIKV as well [22,43,44]. The variation in vector competence among different mosquito populations/viral strains may be due to micro-adaptations in the host-pathogen genome, which could mean co-occurrence of mosquito population and ZIKV strain could affect competence of populations for arboviruses . Laboratory-based infection methods can also cause variation in vector competence results. Richards et al., 2007  and Ciota et al., 2017  suggest that freezing viral blood meals before allowing mosquitoes to feed on them can cause dramatic underestimates of vector competence. Meanwhile, Roundy et al., 2017  suggests that mosquitoes fed on live mice demonstrate higher vector competence than those fed on artificial blood meals. It is important to understand how different methods affect the findings of Ae. albopictus’ competence for ZIKV.
The objectives of this study were to: 1) determine the overall vector competence of Ae. albopictus for ZIKV and 2) examine the variation in the literature and the effects of geography and methodology on Ae. albopictus’ competence for ZIKV. Specifically, whether geographic origin of viral strain, geographic origin of mosquito test population, sympatric co-occurrence of mosquito population and viral strain, freshness of blood-meal, viral titer (or dose) of blood-meal, and whether the blood-meal was artificial or taken from a live, murine source, have significant effects on Ae. albopictus vector competence for ZIKV.
Meta-analysis for vector competence
Despite the widespread use of meta-analyses as a tool in both the medical and ecological fields [57,58], surprisingly, and with a few notable exceptions [59,60], it has not been widely used in synthesizing vector competence research. Here, a meta-analysis of the literature surrounding Ae. albopictus’ competence for ZIKV was used to address objectives associated with determining vector competence, infection rate (IR), and transmission rate (TR) among Ae. albopictus’ groups subjected to infection by ZIKV. For our purposes, IR is defined as the proportion of the test population of Ae. albopictus with positive titers of ZIKV in their midguts and TR is defined as the proportion of infected Ae. albopictus individuals with positive titers of ZIKV in their salivary glands or saliva. Since these rates vary throughout the incubation time of a virus, IR and TR were used at both 7 and 14 dpi, the most common windows of time at which these metrics are examined.
Identification of studies and inclusion criteria.
This study was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) 2018 Guidelines . Relevant studies were identified using searches of keywords through Clarivate Analytics’ Web of Science (http://webofknowledge.com/WOS_GeneralSearch) and PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) search engines. The search was refined to include only papers published in English between January 2014 and March 2018. The key terms used were as follows: Aedes albopictus, vector, competenc*, transmiss*, dissem*, infect*, zik*. Results were screened initially excluding all studies that did not include Ae. albopictus as a study organism. With the study objective to quantify Ae. albopictus’ competence for ZIKV, results were further refined to include only primary, experimental vector competence studies and exclude field studies. Furthermore, only studies that assessed both IR and TR were included. Since vector competence varies a great deal over the infection period, all papers that did not examine competence at 7 and/or 14 dpi (the most commonly reported sampling times) were excluded. Studies in which mosquitoes were infected with a viral titer of 1 x 107 ffu/pfu/TCID50 or lower were also excluded because they were significantly below the ID50 of Ae. albopictus for ZIKV as found by Ciota et al., 2017 . A few papers (Azar et al. 2017, in particular) reported multiple IRs and TRs from separate experiments that used different methods, therefore these effect sizes (i.e. standardized numbers to measure the relationship between two variables) were listed as separate studies in our analyses.
Of the 34 results originally identified by the search criteria, 13 were removed as duplicates. Two additional papers [62,63] were identified through a search of the literature. Two more papers [64,65], were identified in October of 2018, following the original analysis, using the same keyword search in Google Scholar and refining the search to papers published in 2018. Of the remaining 26 studies screened for eligibility, 10 were excluded, either because they did not include Aedes albopictus as a study species or because they did not study competence for ZIKV (Fig 1). Ciota et al., 2017  was excluded because it only reported IR and TR after 21 dpi. This left a total of 14 papers for the analysis [23,62–74]. Two papers, Heitmann et al., 2017  and Azar et al., 2017  assessed multiple populations in their papers using different methods, so data from these papers were split into separate “studies” (experiments using different methodologies, such as viral dosage, or different viral strain/ vector population combinations, and thus useful for understanding the effects of methodological moderators) and tested separately. A full list of studies long with their characteristics, and the models in which they were included can be found in S1 Table. Ten studies from Azar et al., 2017  were excluded because they studied mosquitoes infected with viral titers lower than 1 x 107 ffu/pfu/TCID50. This left a total of 23 studies. A list of which studies were used in which models can be found in the S1 Table.
This meta-analysis was carried out and reported according to PRISMA guidelines . Search of the databases returned 34 records, while 2 additional records were identified through a search of the literature and 3 more through later search of the literature. After all duplicates were removed 26 records remained, of which 10 were excluded because they were not relevant to this study. 1 article was excluded because they did not meet the criteria for inclusion. The remaining 15 articles were divided into multiple studies based on the number of separate effect sizes reported and included in different parts of the meta-analysis, depending on which metrics they reported (IR at 7 dpi, IR at 14 dpi, TR at 7 dpi, TR at 14 dpi).
The following study characteristics from the research articles matching inclusion criteria were extracted by a single reviewer and entered into a database: IR at 7 dpi, IR at 14 dpi, TR at 7 dpi, TR at 14 dpi, origin of viral strain, origin of Ae. albopictus test population strain, whether infected blood-meal was given to mosquitoes fresh or after having been frozen, log transformed viral titer of blood-meal, and whether the blood-meal was given artificially or taken from a live, murine source. IR and TR were taken directly from tables or extracted from figures using the R package “metaDigitise” . Variation exists between studies in reporting transmission rates, with some reporting TR as the proportion of transmitting mosquitoes in the whole test population instead of the infected population. All data not conforming to our definitions were transformed using information on sample size found in the papers.
Because IR and TR are easily comparable between vector competence studies and are inherently meaningful measurements, these raw proportions were used as effect sizes in this study. Data were compiled into a spreadsheet and analyzed using the R package “metafor” . A mixed-effects restricted maximum likelihood (REML) model was used to determine pooled estimates of IR and TR at both 7 and 14 dpi, using sample size to weight estimates. Since not all studies examined IR and TR at both 7 dpi and 14 dpi, not every study was included in every model. Heterogeneity of IR and TR across studies were assessed using a Cochran Q test (P < 0.05 is considered to indicate statistically significant heterogeneity). Because they are easy to analyze and widely understood and utilized, funnel plots were used to look for publication bias, while Egger’s method was used to test for asymmetry. Results of tests for asymmetry can be found in the S1 Fig. Models were rerun using study characteristics thought to affect outcome (i.e., geographic origin of viral strain, geographic origin of mosquito test population, geographic co-occurrence of mosquito population and viral strain, freshness of blood-meal, viral titer (or dose) of blood-meal, and whether the blood-meal was artificial or taken from a live, murine source) as moderators. We also tested for collinearity among our moderators using linear regression, finding a strong collinearity between artificial or live blood meal and freshness of bloodmeal. We determined these to be confounding moderators, as models with one moderator removed artificially inflated the effect of the other. The R code for models can be found in the S1 Table.
The pooled estimated IR of Ae. albopictus was 0.79 (95% CI 0.69–0.89) at 7 dpi and 0.81 (95% CI 0.72–0.90) at 14 dpi (Fig 2). Significant heterogeneity in IR estimates at both 7 and 14 dpi were observed with an I2 (Cochran’s Q test) of 93.6% (P < 0.0001) and 95.1% (P < 0.0001), respectively. For TR, significantly heterogeneous pooled estimates at 7 dpi of 0.15 (Fig 2; 95% CI 0.05–0.24; I2 = 90.3%; P < 0.0001) and at 14 dpi of 0.29 (Fig 2; 95% CI 0.16–0.42; I2 = 94.9%; P < 0.0001) were detected.
Ae. albopictus shows high infection rates at both 7 dpi (IR = 0.79, 95% CI = 0.69–0.81) and 14 dpi (IR = 0.81, 95% CI = 0.72–0.90). Transmission rates were considerably lower at both 7 dpi (TR = 0.15, 95% CI = 0.05–0.24), and 14 dpi (TR = 0.29, 95% CI = 0.16–0.42).
Tests of all moderators showed significant effects only on TR at 14 dpi (Q = 260.1, P < 0.0001). No significant moderator effects were found on IR at 7 dpi (Q = 13.1, P = 0.22) and 14 dpi (Q = 15.6, P = 0.11) or TR at 7 dpi (Q = 10.0, P = 0.44). Among moderators, geographic origin of Ae. albopictus test populations had significant TR at 14 dpi (Fig 3), as did origin of viral strain (Fig 4). Using mosquitoes from East Asia/Oceania as a reference group, models show that European, North American and South American mosquitoes displayed significantly lower TRs 14 dpi (P = 0.0025, P = 0.0002, P = 0.0013). Origin of viral strain also had significant effects on TR at 14 dpi (Fig 4), with East Asian/Oceanic, North American and South American viral strains showing significantly lower TRs than the reference African strains (P = 0.0079, P < 0.0017, P < 0.0001). Finally, freshness of blood meal, artificial or murine source of blood-meal, log viral dosage, and co-occurrence of mosquito population and viral strain had no significant effects on IR or TR at any stage.
Scatter plot showing mean IR and TR for ZIKV (± 95% CI) of geographically separated populations of Ae. albopictus at 7 (A) and 14 (B) dpi. East Asian/ Oceanic and North American Ae. albopictus demonstrated higher IRs than other Ae. albopictus populations at both 7 dpi (IRs: East Asian/ Oceanic = 0.71, 95% CI = 0.50–0.92; European = 0.50, 95% CI = 0.28–0.72; North American = 0.90, 95% CI = 0.80–1.00; South American = 0.65, 95% CI = 0.37–0.93) and 14 dpi (IRs: East Asian/ Oceanic = 0.87, 95% CI = 0.70–1.04; European = 0.57, 95% CI = 0.41–0.74; North American = 0.91, 95% CI = 0.81–1.01; South American = 0.65, 95% CI = 0.37–0.93) though these results were not statistically significant. East Asian/ Oceanic and European Ae. albopictus showed the highest TRs at 7dpi (TRs: East Asian/ Oceanic = 0.31, 95% CI = 0.01–0.60; European = 0.33, 95% CI = 0.05–0.62; North American = 0.11, 95% CI = -0.03–0.24; South American = 0.05, 95% CI = -0.23–0.34) while East Asian/ Oceanic Ae. albopictus showed significantly higher TRs than other strains at 14dpi (TRs: East Asian/ Oceanic = 0.82, 95% CI = 0.61–1.03; European = 0.17, 95% CI = -0.01–0.35; North American = 0.21, 95% CI = 0.10–0.31; South American = 0.05, 95% CI = -0.19–0.28).
Scatter plot showing mean IR and TR (± 95% CI) of Ae. albopictus infected with geographically separated strains of ZIKV at 7 (A) and 14 (B) dpi. African and South American strains of ZIKV demonstrated significantly higher IRs than other ZIKV strains at both 7 dpi (IRs: African = 0.95, 95% CI = 0.74–1.17; East Asian/ Oceanic = 0.61, 95% CI = 0.46–0.76; North American = 0.84, 95% CI = 0.67–1.01; South American = 0.90, 95% CI = 0.71–1.10) and 14 dpi (IRs: African = 0.97, 95% CI = 0.73–1.2; East Asian/ Oceanic = 0.69, 95% CI = 0.54–0.84; North American = 0.81, 95% CI = 0.66–0.97; South American = 0.92, 95% CI = 0.72–1.13). African strains of ZIKV also demonstrated the highest TRs at 7 dpi (TRs: African = 0.42, 95% CI = 0.26–0.57; East Asian/ Oceanic = 0.06, 95% CI = -0.01–0.13; North American = 0.08, 95% CI = 0.01–0.14; South American = 0.06, 95% CI = -0.02–0.13) while African and East Asian/ Oceanic strains of ZIKV demonstrated the highest TRs at 14 dpi (TRs: African = 0.79, 95% CI = 0.56–1.03; East Asian/ Oceanic = 0.36, 95% CI = 0.20–0.52; North American = 0.15, 95% CI = 0.01–0.30; South American = 0.06, 95% CI = -0.13–0.25).
This meta-analysis assessed 14 papers that accounted for 23 studies to determine the suitability of an invasive Asian mosquito species, Ae. albopictus, that is found on all continents except Antarctica, as a competent vector to both carry and transmit ZIKV. Across the studies analyzed, Ae. albopictus is a competent vector to both carry and transmit ZIKV in laboratory settings. Infection rates of ZIKV in Ae. albopictus at both 7 dpi (IR = 0.80; 95% CI 0.70–0.92) and 14 dpi (IR = 0.83; 95% CI 0.72–0.92) are high, on par with those found in similar studies of Ae. aegypti . Transmission rates for ZIKV in this mosquito at 7 dpi (TR = 0.15; 95% CI 0.05–0.26) and 14 dpi (TR = 0.3; 95% CI 0.16–0.45) are low compared to Ae. albopictus’ competence for other RNA viruses [40,77], but are still similar to numbers reported in many studies that examined the competence of Ae. aegypti for ZIKV .
Studies have suggested that geographically disparate populations of Ae. aegypti vary in their competence for ZIKV [24,67]. This meta-analysis suggests that Ae. albopictus’ competence for ZIKV varies geographically as well. The reason for geographic variation in vector competence of Ae. aegypti and Ae. albopictus for ZIKV has been hypothesized to be a barrier that prevents infection of epithelial cells in the midgut [52,56,67,68] and/ or prevent transmission of ZIKV from the salivary gland to a host [53,64]. These barriers may be related to mosquitoes’ microbiome [78,79] or to interactionsbetween viral and mosquito genomes, which may also drive mosquito competence for a multitude of arboviruses, including ZIKV [48,80]. Since vector competence is thought to be influenced by regional micro-adaptions in the genome [48,80], a significantly positive effect of co-occurrence of ZIKV viral strain and Ae. albopictus population on the competence of Ae. albopictus for ZIKV was expected, however, none of the models in this meta-analysis support this. The lack of correlation may reflect a lack of coevolution between ZIKV and Ae. albopictus due to ZIKV’s relatively recent emergence, or it may be due to the broadness of our geographic characterizations (continent scale) or to a small sample size.
Analyses of both IR and TR at 7 and 14 dpi suggest that East Asian/Oceanic populations of Ae. albopictus have the greatest capacity to carry and transmit ZIKV (Fig 2). This may be because East Asian/Oceanic Ae. albopictus populations would have been the first to be infected by ZIKV as the virus spread from Africa eastward, thus giving the virus more time to adapt to its host in this part of the world . However, as of yet, no field studies exist that examine the role of Ae. albopictus in ZIKV transmission in Asia . The greater capacity of East Asian Ae. albopictus to carry and transmit ZIKV may have direct public health ramifications, as there is evidence that Ae. albopictus may already be the primary vector of DENV and CHIKV in some parts of Asia . In these areas it seems likely that in the event of an outbreak, Ae. albopictus will also act as the primary vector for ZIKV, and thus vector control strategies should include Ae. albopictus. Furthermore, Ae. albopictus’ ability to carry and transmit ZIKV highlights the need to understand its distribution, making vector surveillance of the species a high priority everywhere the species does or may occur.
Test of moderators for TR at 14 dpi also suggests that African strains of ZIKV have the highest potential to infect Ae. albopictus (Fig 3), which is in line with similar studies carried out on Aedes aegypti . This study indicates a need to determine the potential of these strains to spread to areas with large populations of Ae. albopictus, such as Europe, North America, and Asia.
We expected to see a significant positive effect of fresh blood meals (vs. previously frozen blood meals) on Ae. albopictus TR, as described in previous papers [51,52], which we did not observe. Nor did we observe a significant difference between mosquitoes infected by feeding from live, murine blood meals and mosquitoes infected with artificial blood meals. This may be because of collinearity between fresh vs. frozen blood meal categories and the artificial vs. live blood meal categories in this study, or because of small sample size. The lack of effect of viral titer on IRs suggests that likelihood of infection for Ae. albopictus is not increased above a certain threshold, possibly around 1 x 107 pfu/ffu/TCID50. These results demonstrate the necessity of evaluating the methods by which vector competence studies are carried out and creating a consensus regarding best practices for evaluating vector competence. This standardization could help to increase the speed with which the scientific community identifies vectors of emerging diseases and thus allow us to create effective vector control strategies in a timely manner.
There are also possible ecological barriers to Ae. albopictus’ potential as a critical vector for ZIKV. Unlike the primary vector of ZIKV, Ae. aegypti, Ae. albopictus tends to take one large bloodmeal as opposed to several smaller ones, which limits Ae. albopictus’ ability to transfer viruses from one organism to another . Ae. albopictus has also been shown to be opportunistic in its feeding behaviors, taking blood meals from a wider variety of animals than the largely anthropophilic Ae. aegypti, though Ae. albopictus’ blood meal preference seems to somewhat vary geographically [84–88]. More variable blood meal preference may make Ae. albopictus a less efficient vector than Ae. aegypti for ZIKV and other viruses, since Ae. albopictus are less likely to feed on humans than are Ae. aegypti. However, opportunistic feeding may also make Ae. albopictus a better bridge vector, carrying diseases such as ZIKV between humans and wildlife reservoirs, thus increasing its potential importance as a vector .
Strengths and limitations
ZIKV was not commonly considered a major threat to public health before the 2015–2017 epidemic in the Americas. Therefore at the time of this study, relatively few studies of vector competence have been carried out on the disease, and most of them were done within a short time frame (Summer 2016 –Winter 2017). With an increasing number of studies, higher resolution analysis can be conducted that may provide insight into how ZIKV is evolving and adapting to new hosts and new environments. The high level of unexplained heterogeneity, as well as collinearity between variables in studies currently available may be due to small sample size (especially for TR at 7 dpi), exclusion criteria (for instance, exclusion of studies using viral titers below 1 x 107 pfu/ffu/TCID50), or the influence of variables we did not consider in our models. Furthermore, considering the potential significance of a salivary gland barrier to transmission, this study’s inclusion of studies that measured TRs by the salivary glands instead of expectorated saliva may contribute to inflated estimates of TR, as there is potentially a salivary gland barrier that prevents viral expectoration in some mosquitoes [53,64]. Hopefully, future studies will allow re-examination the moderators in this meta-analysis in more detail and to evaluate their significance more robustly. Additionally, future field studies and virus/ vector population level studies will be important to validating the results of laboratory tests and to understand how outbreaks occur on a local level.
The results of our study indicate that Ae. albopictus has the potential and competence to be a vector of ZIKV across the globe. The identification of Ae. albopictus as a competent vector for ZIKV raises multiple other points of concern, such as the continuation of Ae. albopictus’ spread across North America and Europe [29,46], the high densities in which Ae. albopictus establishes itself [37,39], and the increasing realization that Ae. albopictus may either be growing more anthropophilic or may have always been more anthropophilic than previously thought [37,44]. Questions of vector competence are typically difficult to resolve given differing laboratory conditions and pathogen and vector sources. Here, we highlight the underutilized method of meta-analyses to clarify issues of vector competence studies, such as variable methodology which complicates comparison, given that this method has the potential to synthesize findings from existing studies, and unlike any individual study, allows researchers to incorporate a wide range of moderators to allow for better comparison between studies. Efforts to understand the ecology of both ZIKV and Ae. albopictus must be strengthened to understand what other, non-physiological, factors may still prevent Ae. albopictus from acting as a major vector for the disease. Finally, efforts at rural and sylvatic surveillance for ZIKV should increase. If Ae. albopictus can be infected by, and transmit ZIKV, there is more potential for the disease to become established in areas where monitoring systems are not looking for it.
S1 Fig. Funnel plots tended to have an asymmetrical shape, with the exception of the funnel for TR at 14 dpi (S1 Fig).
Egger’s tests likewise suggested significant asymmetry for all funnel plots except for TR at 14 dpi (for IR at 7 dpi, P < 0.0012; for IR at 14 dpi, P <0.0001; for TR at 7 dpi, P < 0.0001; for TR at 14 dpi, P = 0.23).
S1 Table. Data used in the meta-analysis presented here.
We would like to thank the Auburn University School of Forestry and Wildlife Sciences, the Office of the Vice President for Research and Economic Development, the Alabama Agricultural Experiment Station, the Hatch Program of the National Institute of Food and Agriculture, and U.S. Department of Agriculture for supporting this work. We’d also like to thank Todd Steury of Auburn University for his help and input on the meta-analyses used in this study.
- 1. Kuno G, Chang G-JJ, Tsuchiya KR, Karabatsos N, Cropp CB. Phylogeny of the Genus Flavivirus. J Virol. 1998;72: 73–83. pmid:9420202
- 2. Dick GWA, Kitchen SF, Haddow AJ. Zika Virus (I). Isolations and serological specificity. T Roy Soc Trop Med H. 1952;46: 509–520.
- 3. Marchette NJ, Garcia R, Rudnick A. Isolation of Zika Virus from Aedes Aegypti Mosquitoes in Malaysia. Am J Trop Med Hyg. 1969;18: 411–415. pmid:4976739
- 4. Moore DL, Causey OR, Carey DE, Reddy S, Cooke AR, Akinkugbe FM, et al. Arthropod-borne viral infections of man in Nigeria, 1964–1970. Ann Trop Med Parasit. 1975;69: 49–64. pmid:1124969
- 5. Simpson DIH. Zika virus infection in man. T Roy Soc Trop Med H. 1964;58: 335–338.
- 6. Weinbren MP, Williams MC. Zika virus: Further isolations in the Zika area, and some studies on the strains isolated. T Roy Soc Trop Med H. 1958;52: 263–268.
- 7. Duffy MR, Chen T-H, Hancock WT, Powers AM, Kool JL, Lanciotti RS, et al. Zika Virus Outbreak on Yap Island, Federated States of Micronesia. New Engl J Med. 2009;360: 2536–2543. pmid:19516034
- 8. Lanciotti RS, Kosoy OL, Laven JJ, Velez JO, Lambert AJ, Johnson AJ, et al. Genetic and Serologic Properties of Zika Virus Associated with an Epidemic, Yap State, Micronesia, 2007. Emerg Infect Dis. 2008;14: 1232–1239. pmid:18680646
- 9. Cao-Lormeau V-M, Roche C, Teissier A, Robin E, Berry A-L, Mallet H-P, et al. Zika Virus, French Polynesia, South Pacific, 2013. Emerg Infect Dis. 2014;20: 1085–1086. pmid:24856001
- 10. Musso D, Nilles EJ, Cao-Lormeau V-M. Rapid spread of emerging Zika virus in the Pacific area. Clin Microbiol Infec. 2014;20: O595–O596. pmid:24909208
- 11. Oehler E, Watrin L, Larre P, Leparc-Goffart I, Lastère S, Valour F, et al. Zika virus infection complicated by Guillain-Barré syndrome–case report, French Polynesia, December 2013. Euro Surveill. 2014;19.
- 12. Silva GS, Richards GA, Baker T, Hidalgo J, Jiménez JIS, Amin P. Zika virus: Report from the task force on tropical diseases by the world Federation of Societies of intensive and critical care medicine. J Crit Care. 2018; pmid:29779827
- 13. Calvet G, Aguiar RS, Melo ASO, Sampaio SA, de Filippis I, Fabri A, et al. Detection and sequencing of Zika virus from amniotic fluid of fetuses with microcephaly in Brazil: a case study. Lancet Infect Dis. 2016;16: 653–660. pmid:26897108
- 14. Cauchemez S, Besnard M, Bompard P, Dub T, Guillemette-Artur P, Eyrolle-Guignot D, et al. Association between Zika virus and microcephaly in French Polynesia, 2013–15: a retrospective study. Lancet. 2016;387: 2125–2132. pmid:26993883
- 15. Mlakar J, Korva M, Tul N, Popović M, Poljšak-Prijatelj M, Mraz J, et al. Zika Virus Associated with Microcephaly. New Engl J Med. 2016;374: 951–958. pmid:26862926
- 16. Duggal NK, Ritter JM, Pestorius SE, Zaki SR, Davis BS, Chang G-JJ, et al. Frequent Zika Virus Sexual Transmission and Prolonged Viral RNA Shedding in an Immunodeficient Mouse Model. Cell Rep. 2017;18: 1751–1760. pmid:28199846
- 17. Gaskell KM, Houlihan C, Nastouli E, Checkley AM. Persistent Zika Virus Detection in Semen in a Traveler Returning to the United Kingdom from Brazil, 2016. Emerg Infect Dis. 2017;23: 137–139. pmid:27748650
- 18. Musso D, Roche C, Robin E, Nhan T, Teissier A, Cao-Lormeau V-M. Potential Sexual Transmission of Zika Virus. Emerg Infect Dis. 2015;21: 359–361. pmid:25625872
- 19. Foy BD, Kobylinski KC, Foy JLC, Blitvich BJ, Travassos da Rosa A, Haddow AD, et al. Probable Non–Vector-borne Transmission of Zika Virus, Colorado, USA. Emerg Infect Dis. 2011;17: 880–882. pmid:21529401
- 20. Ledermann JP, Guillaumot L, Yug L, Saweyog SC, Tided M, Machieng P, et al. Aedes hensilli as a potential vector of Chikungunya and Zika viruses. PLoS Negl Trop Dis. 2014;8: e3188–e3188. pmid:25299181
- 21. Guerbois M, Fernandez-Salas I, Azar SR, Danis-Lozano R, Alpuche-Aranda CM, Leal G, et al. Outbreak of Zika Virus Infection, Chiapas State, Mexico, 2015, and First Confirmed Transmission by Aedes aegypti Mosquitoes in the Americas. J Infect Dis. 2016;214: 1349–1356. pmid:27436433
- 22. Boyer S, Calvez E, Chouin-Carneiro T, Diallo D, Failloux A-B. An overview of mosquito vectors of Zika virus. Microbes Infect. 2018; pmid:29481868
- 23. Liu Z, Zhou T, Lai Z, Zhang Z, Jia Z, Zhou G, et al. Competence of Aedes aegypti, Ae. albopictus, and Culex quinquefasciatus Mosquitoes as Zika Virus Vectors, China. Emerg Infect Dis. 2017;23: 1085–1091. pmid:28430562
- 24. Roundy CM, Azar SR, Rossi SL, Huang JH, Leal G, Yun R, et al. Variation in Aedes aegypti Mosquito Competence for Zika Virus Transmission. Emerg Infect Dis. 2017;23: 625–632. pmid:28287375
- 25. Richard V, Paoaafaite T, Cao-Lormeau V-M. Vector Competence of French Polynesian Aedes aegypti and Aedes polynesiensis for Zika Virus. PLoS Negl Trop Dis. 2016;10: e0005024. pmid:27654962
- 26. Diagne CT, Diallo D, Faye O, Ba Y, Faye O, Gaye A, et al. Potential of selected Senegalese Aedes spp. mosquitoes (Diptera: Culicidae) to transmit Zika virus. BMC Infect Dis. 2015;15: 492. pmid:26527535
- 27. O’Donnell KL, Bixby MA, Morin KJ, Bradley DS, Vaughan JA. Potential of a Northern Population of Aedes vexans (Diptera: Culicidae) to Transmit Zika Virus. J Med Entomol. 2017;54: 1354–1359. pmid:28499036
- 28. Christophers S. Aëdes aegypti (L.) the Yellow Fever Mosquito: its Life History, Bionomics and Structure. Aëdes aegypti (L) the Yellow Fever Mosquito: its Life History, Bionomics and Structure. 1960; Available: https://www.cabdirect.org/cabdirect/abstract/19602901825
- 29. Kraemer MU, Sinka ME, Duda KA, Mylne AQ, Shearer FM, Barker CM, et al. The global distribution of the arbovirus vectors Aedes aegypti and Ae. albopictus. eLife Sci. 2015;4: e08347. pmid:26126267
- 30. WHO | Vector-borne diseases. In: WHO [Internet]. [cited 17 Apr 2018]. Available: http://www.who.int/mediacentre/factsheets/fs387/en/
- 31. Guedes DR, Paiva MH, Donato MM, Barbosa PP, Krokovsky L, Rocha SW dos S, et al. Zika virus replication in the mosquito Culex quinquefasciatus in Brazil. Emerg Microbes Infec. 2017;6: e69. pmid:28790458
- 32. Guo X, Li C, Deng Y, Xing D, Liu Q, Wu Q, et al. Culex pipiens quinquefasciatus: a potential vector to transmit Zika virus. Emerging Microbes & Infections. 2016;5: e102. pmid:27599470
- 33. Amraoui F, Atyame-Nten C, Vega-Rúa A, Lourenço-de-Oliveira R, Vazeille M, Failloux AB. Culex mosquitoes are experimentally unable to transmit Zika virus. Euro Surveill. 2016;21. pmid:27605159
- 34. Gardner LM, Chen N, Sarkar S. Global risk of Zika virus depends critically on vector status of Aedes albopictus. Lancet Infect Dis. 2016;16: 522–523. pmid:26997578
- 35. Gardner L, Chen N, Sarkar S. Vector status of Aedes species determines geographical risk of autochthonous Zika virus establishment. PLoS Negl Trop Dis. 2017;11: e0005487. pmid:28339472
- 36. Vasilakis N, Weaver SC. Flavivirus transmission focusing on Zika. Curr Opin Virol. 2017;22: 30–35. pmid:27936448
- 37. Paupy C, Delatte H, Bagny L, Corbel V, Fontenille D. Aedes albopictus, an arbovirus vector: From the darkness to the light. Microbes Infect. 2009;11: 1177–1185. pmid:19450706
- 38. Mitchell CJ. Vector competence of North and South American strains of Aedes albopictus for certain arboviruses: a review. J Am Mosq Control Assoc. 1991;7: 446–451. pmid:1791455
- 39. Gratz NG. Critical review of the vector status of Aedes albopictus. Med Vet Entomol. 2004;18: 215–227. pmid:15347388
- 40. Sardelis MR, Turell MJ, O’Guinn ML, Andre RG, Roberts DR. Vector competence of three North American strains of Aedes albopictus for West Nile virus. J Am Mosq Control Assoc. 2002;18: 284–289. pmid:12542184
- 41. Vazeille M, Moutailler S, Coudrier D, Rousseaux C, Khun H, Huerre M, et al. Two Chikungunya Isolates from the Outbreak of La Reunion (Indian Ocean) Exhibit Different Patterns of Infection in the Mosquito, Aedes albopictus. PLoS One. 2007;2: e1168. pmid:18000540
- 42. Zhao H, Zhang F-C, Zhu Q, Wang J, Hong W-X, Zhao L-Z, et al. Epidemiological and Virological Characterizations of the 2014 Dengue Outbreak in Guangzhou, China. PLoS One. 2016;11. pmid:27257804
- 43. Paupy C, Ollomo B, Kamgang B, Moutailler S, Rousset D, Demanou M, et al. Comparative Role of Aedes albopictus and Aedes aegypti in the Emergence of Dengue and Chikungunya in Central Africa. Vector-Borne Zoonot. 2010;10: 259–266. pmid:19725769
- 44. Pagès F, Peyrefitte CN, Mve MT, Jarjaval F, Brisse S, Iteman I, et al. Aedes albopictus Mosquito: The Main Vector of the 2007 Chikungunya Outbreak in Gabon. PLoS One. 2009;4: e4691. pmid:19259263
- 45. Charrel RN, de Lamballerie X, Raoult D. Chikungunya Outbreaks—The Globalization of Vectorborne Diseases. New Engl J Med. 2007;356: 769–771. pmid:17314335
- 46. Benedict MQ, Levine RS, Hawley WA, Lounibos LP. Spread of The Tiger: Global Risk of Invasion by The Mosquito Aedes albopictus. Vector-Borne Zoonot. 2007;7: 76–85. pmid:17417960
- 47. Ayres CFJ. Identification of Zika virus vectors and implications for control. Lancet Infect Dis. 2016;16: 278–279. pmid:26852727
- 48. Lambrechts L, Chevillon C, Albright RG, Thaisomboonsuk B, Richardson JH, Jarman RG, et al. Genetic specificity and potential for local adaptation between dengue viruses and mosquito vectors. BMC Evol Bio. 2009;9: 160. pmid:19589156
- 49. Dupont-Rouzeyrol M, Diancourt L, Calvez E, Vandenbogaert M, O’Connor O, Teissier A, et al. Zika virus evolution on the edges of the Pacific ocean. Emerg Microbes Infec. 2017;6: e111. pmid:29235552
- 50. Pettersson JH-O, Eldholm V, Seligman SJ, Lundkvist Å, Falconar AK, Gaunt MW, et al. How Did Zika Virus Emerge in the Pacific Islands and Latin America? mBio. 2016;7. pmid:27729507
- 51. Zika Virus. In: CDC [Internet]. 5 Nov 2014 [cited 29 Apr 2018]. Available: https://www.cdc.gov/zika/vector/range.html
- 52. Uraki R, Hastings AK, Gloria-Soria A, Powell JR, Fikrig E. Altered vector competence in an experimental mosquito-mouse transmission model of Zika infection. PLoS Negl Trop Dis. 2018;12: e0006350. pmid:29505571
- 53. Calvez E, O’Connor O, Pol M, Rousset D, Faye O, Richard V, et al. Differential transmission of Asian and African Zika virus lineages by Aedes aegypti from New Caledonia. Emerg Microbes Infec. 2018;7: 159. pmid:30254274
- 54. Calvez E, Mousson L, Vazeille M, O’Connor O, Cao-Lormeau V-M, Mathieu-Daudé F, et al. Zika virus outbreak in the Pacific: Vector competence of regional vectors. PLoS Negl Trop Dis. 2018;12: e0006637. pmid:30016372
- 55. Richards SL, Pesko K, Alto BW, Mores CN. Reduced infection in mosquitoes exposed to blood meals containing previously frozen flaviviruses. Virus Res. 2007;129: 224–227. pmid:17686541
- 56. Ciota AT, Bialosuknia SM, Zink SD, Brecher M, Ehrbar DJ, Morrissette MN, et al. Effects of Zika Virus Strain and Aedes Mosquito Species on Vector Competence. Emerg Infect Dis. 2017;23: 1110–1117. pmid:28430564
- 57. Egger M, Smith GD. Principles of and Procedures for Systematic Reviews. System Review H Care. Wiley-Blackwell; 2008. pp. 23–42. https://doi.org/10.1002/9780470693926.ch2
- 58. Stewart G. Meta-analysis in applied ecology. Biol Lett. 2010;6: 78–81. pmid:19776064
- 59. Lambrechts L, Scott TW, Gubler DJ. Consequences of the Expanding Global Distribution of Aedes albopictus for Dengue Virus Transmission. PLoS Negl Trop Dis. 2010;4: e646. pmid:20520794
- 60. Oliveira ARS, Cohnstaedt LW, Strathe E, Etcheverry L, McVey DS, Piaggio J, et al. Meta-Analyses of Japanese Encephalitis Virus Infection, Dissemination, and Transmission Rates in Vectors. Am J Trop Med H. 2018;98: 883–890. pmid:29363456
- 61. McInnes MDF, Moher D, Thombs BD, McGrath TA, Bossuyt PM, Clifford T, et al. Preferred Reporting Items for a Systematic Review and Meta-analysis of Diagnostic Test Accuracy Studies: The PRISMA-DTA Statement. JAMA. 2018;319: 388–396. pmid:29362800
- 62. Vazeille M, Dehecq J-S, Failloux A-B. Vectorial status of the Asian tiger mosquito Aedes albopictus of La Réunion Island for Zika virus. Med Vet Entomol. 32: 251–254. pmid:29194706
- 63. Lozano-Fuentes S, Kenney JL, Varnado W, Byrd BD, Burkhalter KL, Savage HM. Susceptibility and Vectorial Capacity of American Aedes albopictus and Aedes aegypti (Diptera: Culicidae) to American Zika Virus Strains. J Med Entomol. 2018; pmid:30102327
- 64. Garcia-Luna SM, Weger-Lucarelli J, Rückert C, Murrieta RA, Young MC, Byas AD, et al. Variation in competence for ZIKV transmission by Aedes aegypti and Aedes albopictus in Mexico. Armstrong PM, editor. PLoS Negl Trop Dis. 2018;12: e0006599. pmid:29965958
- 65. Knecht H, Richards S, Balanay J, White A, Knecht H, Richards SL, et al. Impact of Mosquito Age and Insecticide Exposure on Susceptibility of Aedes albopictus (Diptera: Culicidae) to Infection with Zika Virus. Pathogens. 2018;7: 67. pmid:30103526
- 66. Heitmann A, Jansen S, Lühken R, Leggewie M, Badusche M, Pluskota B, et al. Experimental transmission of Zika virus by mosquitoes from central Europe. Euro Surveill. 2017;22: 30437. pmid:28106528
- 67. Chouin-Carneiro T, Vega-Rua A, Vazeille M, Yebakima A, Girod R, Goindin D, et al. Differential Susceptibilities of Aedes aegypti and Aedes albopictus from the Americas to Zika Virus. PLoS Negl Trop Dis. 2016;10: e0004543. pmid:26938868
- 68. Azar SR, Roundy CM, Rossi SL, Huang JH, Leal G, Yun R, et al. Differential Vector Competency of Aedes albopictus Populations from the Americas for Zika Virus. Am J Trop Med H. 2017;97: 330–339. pmid:28829735
- 69. Luca MD, Severini F, Toma L, Boccolini D, Romi R, Remoli ME, et al. Experimental studies of susceptibility of Italian Aedes albopictus to Zika virus. Euro Surveill. 2016;21: 30223. pmid:27171034
- 70. Duchemin J-B, Mee PT, Lynch SE, Vedururu R, Trinidad L, Paradkar P. Zika vector transmission risk in temperate Australia: a vector competence study. Virol J. 2017;14: 108. pmid:28599659
- 71. Jupille H, Seixas G, Mousson L, Sousa CA, Failloux A-B. Zika Virus, a New Threat for Europe? PLoS Negl Trop Dis. 2016;10: e0004901. pmid:27505002
- 72. Ryckebusch F, Berthet M, Missé D, Choumet V. Infection of a French Population of Aedes albopictus and of Aedes aegypti (Paea Strain) with Zika Virus Reveals Low Transmission Rates to These Vectors’ Saliva. Int J Mol Sci. 2017;18: 2384. pmid:29125545
- 73. Wong P-SJ, Li MI, Chong C-S, Ng L-C, Tan C-H. Aedes (Stegomyia) albopictus (Skuse): A Potential Vector of Zika Virus in Singapore. Turell MJ, editor. PLoS Negl Trop Dis. 2013;7: e2348. pmid:23936579
- 74. Richards SL, White AV, Balanay JAG. Potential for sublethal insecticide exposure to impact vector competence of Aedes albopictus (Diptera: Culicidae) for dengue and Zika viruses. In: Res Rep Trop Med. 29 May 2017 [cited 26 Feb 2018]. pmid:30050345
- 75. Pick JL, Nakagawa S, Noble DW. Reproducible, flexible and high throughput data extraction from primary literature: The metaDigitise R package. 2018;
- 76. Viechtbauer W. Conducting Meta-Analyses in R with the metafor Package. J Stat Softw. 2010;36.
- 77. Vega-Rúa A, Zouache K, Girod R, Failloux A-B, Lourenço-de-Oliveira R. High Level of Vector Competence of Aedes aegypti and Aedes albopictus from Ten American Countries as a Crucial Factor in the Spread of Chikungunya Virus. J Virol. 2014;88: 6294–6306. pmid:24672026
- 78. Jupatanakul N, Sim S, Dimopoulos G. The Insect Microbiome Modulates Vector Competence for Arboviruses. Viruses. 2014;6: 4294–4313. pmid:25393895
- 79. Weiss B, Aksoy S. Microbiome influences on insect host vector competence. Trends Parasitol. 2011;27: 514–522. pmid:21697014
- 80. Rico-Hesse R. Microevolution and virulence of dengue viruses., Microevolution and Virulence of Dengue Viruses. Adv Virus Res. 2003;59, 59: 315, 315–341. pmid:14696333
- 81. Weaver SC, Costa F, Garcia-Blanco MA, Ko AI, Ribeiro GS, Saade G, et al. Zika Virus: History, Emergence, Biology, and Prospects for Control. Antiviral Res. 2016;130: 69–80. pmid:26996139
- 82. de Lamballerie X, Leroy E, Charrel RN, Ttsetsarkin K, Higgs S, Gould EA. Chikungunya virus adapts to tiger mosquito via evolutionary convergence: a sign of things to come? Virol J. 2008;5: 33. pmid:18304328
- 83. Hawley WA. The biology of Aedes albopictus. J Am Mosq Control Assoc Suppl. 1988;1: 1–39. pmid:3068349
- 84. Haddad N, Mousson L, Vazeille M, Chamat S, Tayeh J, Osta MA, et al. Aedes albopictus in Lebanon, a potential risk of arboviruses outbreak. BMC Infect Dis. 2012;12. pmid:23151056
- 85. Kamgang B, Nchoutpouen E, Simard F, Paupy C. Notes on the blood-feeding behavior of Aedes albopictus (Diptera: Culicidae) in Cameroon. Parasite Vector. 2012;5: 57. pmid:22433236
- 86. Kim KS, Tsuda Y, Yamada A. Bloodmeal Identification and Detection of Avian Malaria Parasite From Mosquitoes (Diptera: Culicidae) Inhabiting Coastal Areas of Tokyo Bay, Japan. J Med Entomol. 2009;46: 1230–1234. pmid:19769059
- 87. Ponlawat A, Harrington LC. Blood Feeding Patterns of Aedes aegypti and Aedes albopictus in Thailand. J Med Entomol. 2005;42: 844–849. pmid:16363170
- 88. Richards SL, Ponnusamy L, Unnasch TR, Hassan HK, Apperson CS. Host-Feeding Patterns of Aedes albopictus (Diptera: Culicidae) in Relation to Availability of Human and Domestic Animals in Suburban Landscapes of Central North Carolina. J Med Entomol. 2006;43: 543–551. pmid:16739414