Skip to main content
Download PDF

The global prevalence of parasites in non-biting flies as vectors: a systematic review and meta-analysis

Parasites & Vectors volume 16, Article number: 25 (2023) Cite this article

Abstract

Background

Non-biting flies such as the house fly (Musca domestica), the Australian sheep blowfly (Lucilia cuprina) and the oriental latrine fly (Chrysomya megacephala) may carry many parasites. In the present study, we performed a systematic overview of the different species of parasites carried by non-biting flies, as well as of isolation methods, different geographical distribution, seasonality and risk assessment.

Methods

A meta-analysis was carried out with the aim to review the global prevalence of parasite transmission in non-biting flies. A total sample size of 28,718 non-biting flies reported in studies worldwide satisfied the predetermined selection criteria and was included in the quantitative analysis.

Results

The global prevalence of parasites in non-biting flies was 42.5% (95% confidence interval [CI] 31.9–53.2%; n = 15,888/28,718), with the highest prevalence found for non-biting flies in Africa (58.3%; 95% CI 47.4–69.3%; n = 9144/13,366). A total of 43% (95% CI 32.1–54.4%; n = 7234/15,282) of house flies (M. domestica), the fly species considered to be the most closely associated with humans and animals, were found with parasites. The prevalence of parasites in the intestine of non-biting flies was 37.1% (95% CI 22.7–51.5%; n = 1045/3817), which was significantly higher than the prevalence of parasites isolated from the body surface (35.1%; 95% CI 20.8–49.4%; n = 1199/3649; P < 0.01). Of the 27 reported parasites, a total of 20 known zoonotic parasites were identified, with an infection rate of 38.1% (95% CI 28.2–48.0%; n = 13,572/28,494).

Conclusions

This study provides a theoretical basis for the public health and ecological significance of parasites transmitted by non-biting flies.

Graphical Abstract

Background

Many species of flies (Diptera) are closely associated with humans and can complete their entire life-cycle in the close proximity of human habitations and areas with domestic animals [1]. At least 305 fly species belonging to the Muscidae, Calliphoridae and Sarcophagidae families are known to transmit diseases [2]. Flies can be divided into non-biting flies and biting flies. Non-biting flies are often commonly found in areas of human and animal activities, such as food markets, restaurants and poultry and livestock farms where they have the potential to be vectors of diseases [3, 4].

Non-biting flies can have sponging mouthparts, which are mainly used to lick and suck food, and can be either mechanical or biological vectors of food-borne pathogens [5, 6]. Biting flies have piercing-sucking mouthparts and suck blood through punctures made by piercing human and animal skin [7, 8]. Non-biting flies are mechanical carriers of pathogens that adhere to their body, mouthparts and body hair. These flies transmit pathogens mainly by contact, and they can contaminate their surrounding environment as they move about [9]. Food-borne pathogens can reproduce in the intestines of non-biting flies and infect food through fly excretion and regurgitation [10]. After exposure to food-borne pathogens, humans and animals can experience diarrhea and other symptoms that sometimes lead to death [11]. As such, non-biting flies can carry many pathogens, and these pathogens have detrimental effects on public health.

Non-biting flies can carry more than 100 kinds of pathogens, including parasites, bacteria, fungi and viruses [12]. Among these, parasite eggs/cysts (such as those of Cryptosporidium spp., Giardia spp., Taenia spp.) have been isolated from the body surface and intestines of non-biting flies, with most being zoonotic parasites. Such parasites harm humans and animals by depriving the host of nutrients and damaging host tissues and organs [13, 14].

No systematic investigation has been conducted on the parasites carried by non-biting flies. This study provides a systematic overview of the different species, isolation methods, different geographical distribution, seasonality and risk assessment of parasites carried by non-biting flies.

Methods

Search strategy

To determine the prevalence of parasites transmitted by non-biting flies worldwide, we performed a systematic search of the PubMed, PubMed Central, GeenMedical, Web of Science and Science Direct electronic databases, with the aim to identify relevant literature (Fig. 1). The search was performed according to the Preferred Reporting Items of Systematic Reviews and Meta-Analyses (PRISMA) guidelines [15]. The keywords used were: “house fly (Musca domestica),” “Lucilia sericata,” “Chrysomya megacephala,” “Ascaris lumbricoides,” “Trichuris trichiura,” “Taenia solium,” “Entamoeba coli,” “Enterobius vermicularis,” “Hookworm,” “Strongyloides stercoralis,” “Hymenolepis nana,” “Entamoeba histolytica,” “Cryptosporidium parvum,” “Giardia lamblia” and “Enterocytozoon bieneusi”, using “AND” and/or “OR” Boolean operators [16]. The search formula used was (host 1) OR (host 2) AND (parasite 1) OR (parasite 2). . Literature data were obtained based on different non-biting fly species, different parasite species, different national geographic distribution, seasonality, sample size, positive number and identification method [17].

Fig. 1
figure 1

PRISMA flow diagram on the different stages of the literature search process

Full size image

Selection criteria

We searched all English articles on the epidemiology of parasites carried by non-biting flies without a publishing time limit. According to the PRISMA guidelines (Additional file 1: Table S1), titles were screened first for eligibility based on full and legible citations and journal article titles only [18]. Then, in groups of two reviewers at a time, the titles and abstracts were assessed. Articles meeting the selection criteria include the following points: (i) detailed and comprehensive sample information; (ii) details on sample size and number of positive specimens provided; (iii) peer-reviewed journal articles; and (iv) clear description of detection methods provided.

Study selection

Articles that did not meet the selection criteria were removed, and articles from which reference data could be extracted were filtered out. Exclusion criteria were: (i) duplicate articles in the five databases; (ii) incomplete information on the sample; (iii) review article; (iv) only the prevalence was provided, without information on sample size and positivity; (v) no details on the sample, and the data is not easy to distinguish; and (vi) experimental studies, letters and articles published in a language other than English (Additional file 1).

Quality assessment

The Grading of Recommendations Assessment, Development and Evaluation (GRADE) system was used to grade article quality. Article quality was assessed according to current standards, and scores were determined [19]. Each criterion was graded with a score of 1 point. The scoring criteria included whether the study subjects were clearly defined; whether there was ≥ 3 types of grouping analysis; whether the identification method was clearly described; whether the sampling time was reported in sufficient detail; and whether the sample size was > 200. Score grades were divided into 3 grades, with 0–1 indicating low quality, 2–3 indicating medium quality and 4–5 indicating high quality [20].

Data extraction

All titles, abstracts and full texts were separately screened by two authors (YFL and YCC), and the data were independently extracted. Disagreements were resolved by discussion with a third author (NHW). The data included species of non-biting flies, different parasite species, country, seasonality, total sample sizes, positive sample sizes, identification method, publication year, first author’s name, sampling time and external surface/internal organs of non-biting flies (Table 1).

Table 1 Study quality assessment and score grading of the 28 studies included in the meta-analysis
Full size table

Statistical analysis

All statistical analyses were performed using Stata version 14.0 (StataCorp, College Station, TX, USA). Because there was heterogeneity in the data, heterogeneity of the study was determined as low heterogeneity (I2 < 25%), moderate heterogeneity (I2 = 25–75%) and high heterogeneity (I2 > 75%), and P-value < 0.05 was considered to be statistically significant [20]. Random effects models were used for the meta-analysis, including the sensitivity analysis, subgroup analysis and univariate regression analysis, to identify factors affecting heterogeneity. To evaluate the reliability of the data, we performed sensitivity analyses by removing individual studies one by one and combining other studies to assess the effect of selected studies on the pooled prevalence [47]. Forest plots were used to estimate differences across groups, and funnel plots and Egger’s tests were used to indicate possible publication bias in the study [48]. Potential sources of heterogeneity were assessed, including region (5 comparisons of continents), non-biting fly species (Musca domestica compared to other fly species), identification methods (morphology, molecular biology and immunofluorescence techniques), risk assessment (zoonotic and non-zoonotic parasites), non-biting fly body surface and gut (body surface only, gut and both combined prevalence), seasonality (four-season comparison) and parasite classification (protozoa compared to helminth) (Table 2).

Table 2 Analysis of the different groups based on the role of non-biting flies in the transmission of parasites
Full size table

Results

Literature selection and research data extraction

Using the search strategy described above, 2193 studies were initially retrieved from the five databases (PubMed, 117 studies; PubMed Central, 841 studies; GeenMedical, 109 studies; Web of Science, 1113 studies; Science Direct, 13 studies). A total of 632 studies met the first round of screening criteria after deletion of duplicate articles in the databases. A total of 120 studies passed the second round of screening, with 512 studies whose titles and abstracts did not meet the selection criteria being excluded. Finally, 28 studies were identified for inclusion in the meta-analysis following review of the full text, with 92 studies excluded due to incomplete sample information (n = 20), incomplete data (n = 45) and review articles (n = 27) (Fig. 1).

To date, 28 studies on the prevalence of parasites carried by non-biting flies cover 16 countries on five continents.(Fig. 2; Table 1). Among these, the highest number of studies were carried out in Africa, including Nigeria (n = 4), Ethiopia (n = 3) and Egypt (n = 1), followed by Asian countries, with seven studies, including China (n = 2), Philippines (n = 1), Iran (n = 1), Mongolia (n = 1), Malaysia (n = 1) and Thailand (n = 1). Seven studies were carried out in European countries, including Spain (n = 2), England (n = 2), Ukraine (n = 1), Germany (n = 1) and Sweden (n = 1). Those studies carried out in South America are mainly concentrated in Brazil (n = 2), and those carried out in North America are concentrated in the USA (n = 4) (Table 1). The prevalence and geographical distribution of parasites carried by non-biting flies are shown in Fig. 2. .

Fig. 2
figure 2

Prevalence and geographical distribution of non-biting flies carrying parasites. (This figure was originally designed using ArcGIS 10.4 software. The original vector diagram, imported in ArcGIS, was then adapted from Natural Earth (http://www.naturalearthdata.com). CI, Confidence interval

Full size image

Quality assessment

Evaluation of article quality showed that 21 of the 28 studies scored 4–5, indicating high quality, and seven studies scored 2–3, indicating moderate quality due to unclear sampling time and insufficient data on group analysis (Table 1).

Sensitivity analysis and publication bias

The sensitivity analysis showed that the data were stable and the analysis was reliable (Fig. 3). Funnel plots were constructed to observe whether there was publication bias in the meta-analysis results. The plots showed that the effect points presented a basically symmetrical pattern and showed no publication bias (Fig. 4). Egger’s test (Table 3) was used to give P > 0.05, indicating that there was no publication bias in the data.

Fig. 3
figure 3

Sensitivity analysis of global prevalence of non-biting flies that have been found to transmit parasites

Full size image
Fig. 4
figure 4

Funnel plot for the determination of publication bias of the global prevalence estimates of non-biting flies found to transmit parasites

Full size image
Table 3 Egger’s test for publication bias
Full size table

Different geographical distribution of parasites carried by non-biting flies

The overall infection rate of parasites carried by non-biting flies worldwide is about 42.5% (95% confidence interval [CI] 31.9–53.2%;; n = 15,888/28,718) with heterogeneity (I2 = 99.8%, P < 0.001) (Table 2). Of the five continents reported in the literature, the highest number of studies were carried out in Africa, which also had the highest infection rate (58.3%; 95% CI 47.4–69.3%;; n = 9144/13,366) with heterogeneity (I2 = 99.2%, P < 0.001), followed by South America (48.6%; 95% CI 31.8–65.3%; n = 1413/4619) with heterogeneity (I2 = 98.9%, P < 0.001), North America (39.9%; 95% CI 6.4–73.5%;; n = 2989/4982) with heterogeneity (I2 = 99.6%, P < 0.001), Asia (36.9%; 95% CI 24.0–49.9%;; n = 1616/3184) with heterogeneity (I2 = 99.0%, P < 0.001) and Europe (29.5%; 95% CI 13.2–45.8%;; n = 726/2567) with heterogeneity (I2 = 99.4%, P < 0.001) (Table 2; Fig. 5). Among the 16 countries reported, Thailand had the highest infection rate (80.0%; 95% CI 69.6–90.4%; n = 48/60), and Ukraine has the lowest infection rate (1.9%; 95% CI 0.4–3.5%; n = 6/312) (Fig. 2).

Fig. 5
figure 5

Forest plot of the global prevalence estimates of non-biting flies found to transmit parasites

Full size image

Pooled prevalence based on parasites carried by different non-biting flies

Among the 28 studies, 23 reported that the house fly (M. domestica) carried parasites, which accounted for > 90% of all reported parasite species (Table 2). According to the statistics, the infection rate of parasites carried by the house fly (M. domestica) was 43.3% (95% CI 32.1–54.4%; n = 7234/15,282) with heterogeneity (I2 = 99.6%, P < 0.001), while the infection rate of parasites carried by the other 16 non-biting flies was 44.1% (95% CI 23.9–64.3%; n = 8654/13,436) with heterogeneity (I2 = 99.9%, P < 0.001) (Table 2; Fig. 6). These results showed that the house fly (M. domestica) was the most common fly species and its potential risk to human health could not be ignored. However, although other non-biting fly species are uncommon, their safety risks also cannot be ignored.

Fig. 6
figure 6

Forest plot of the prevalence estimates of parasites carried by different non-biting flies

Full size image

Pooled prevalence based on different identification methods, risk assessment and seasonality

Of the different identification methods listed in the studies, morphological identification is the most commonly used method for parasite identification; 17 of the 28 studies identified parasite species by microscopy, with an infection rate of 47.4% (95% CI 33.0–61.7%; n = 12,188/20,351) with heterogeneity (I2 = 99.8%, P < 0.001). The prevalence rates according to routine PCR molecular identification and immunofluorescence identification methods were 34.8% (95% CI 24.6–45.1%; n = 761/3469) with heterogeneity (I2 = 98.2%, P < 0.001) and 33.5% (95% CI 7.1–74.1%; n = 2939/4898) with heterogeneity (I 2 = 99.7%, P < 0.001), respectively (Table 2; Fig. 7). Non-biting flies are mechanical carriers of many parasitic species, most of which are zoonotic parasites. Among the 27 parasites reported, a total of 20 known zoonotic parasites were identified. The infection rate was 38.1% (95% CI 28.2–48.0%; n = 13,572/28,494) with heterogeneity (I2 = 99.7%, P < 0.001), and the prevalence rate of non-zoonotic parasitic diseases was 13.3% (95% CI 9.4–17.3%; n = 2316/17,626) with heterogeneity (I2 = 98.3%, P < 0.001) (Table 2; Fig. 8). The species of parasites carried by non-biting flies can differ seasonally. The highest infection rate was 70.0% (95% CI 69.1–70.9%; n = 6685/9550) and occurred in the spring, followed by the autumn, winter and summer, with infection rates of 44.6% (95% CI 31.7–57.5%; n = 1253/3003) with heterogeneity (I2 = 98.0%, P < 0.001), 42.0% (95% CI 4.9–88.9%; n = 121/522) with heterogeneity (I2 = 99.4%, P < 0.001) and 29.7% (95% CI 13.7–45.6%; n = 4331/9809) with heterogeneity (I 2 = 99.7%, P < 0.001), respectively (Table 2; Fig. 9).

Fig. 7
figure 7

Forest plot of prevalence estimates for the different identification methods

Full size image
Fig. 8
figure 8

Forest plot of prevalence estimates for risk assessment of parasite transmission by non-biting flies

Full size image
Fig. 9
figure 9

Forest plot of seasonal prevalence estimates of non-biting flies found to transmit parasites

Full size image

Pooled prevalence based on parasites carried on the body surface and guts of non-biting flies

Non-biting flies can infect humans and animals by contacting and adhering to parasite eggs/cysts through mouthparts and body hair covering their entire body. They can also indirectly infect humans and animals through intestinal excretion of contaminated water and body waste. Several studies have shown that parasites can be isolated from both the body surface and gut of non-biting flies, with a prevalence of 51.1% (95% CI 41.5–60.7%; n = 13,644/21,252) with heterogeneity (I2 = 99.5%, P < 0.001). The prevalence of parasites isolated from the intestine of the non-biting flies investigated only was 37.1% (95% CI 22.7–51.5%; 1045/3817) with heterogeneity (I2 = 99.2%, P < 0.001), which was significantly higher than the prevalence of parasites isolated from the body surface (35.1%; 95% CI 20.8–49.4%; n = 1199/3649) with heterogeneity (I2 = 99.3%, P < 0.001) (Table 2; Fig. 10).

Fig.10
figure 10

Forest plot for estimation of prevalence of parasites carried on the body surface and gut of non-biting flies

Full size image

Pooled prevalence based on protozoa cysts and helminths eggs carried by non-biting flies

According to the subgroup analysis (protozoa compared with helminths), the prevalence of helminth eggs carried by non-biting flies was 42.6% (95% CI 33.5–51.8%; n = 7791/20,084) with heterogeneity (I2 = 99.5%, P < 0.001) was significantly higher than that of protozoa cysts (32.1%; 95% CI 22.9–41.3%; n = 8097/21,789) with heterogeneity (I2 = 99.5%, P < 0.001) (Table 2; Fig. 11).

Fig. 11
figure 11

Forest plot of global estimated prevalence of protozoa and helminths carried by non-biting flies

Full size image

Sources of heterogeneity by meta-regression analysis

All studies included in this meta-analysis had significant heterogeneity, and the source of heterogeneity was further determined by univariate regression analysis. The results showed whether or not zoonotic parasites (P < 0.05) were the key factors of heterogeneity (Table 2).

Discussion

Non-biting flies are common on farms and in residential areas and have a close relationship with humans and animals [41]. Feces, garbage and sewage attract non-biting flies and are often the most suitable locations for reproduction [33, 43]. Non-biting flies mainly pollute water sources, fruits and vegetables and animal feed through body surface contact and intestinal excretions [28, 32]. Humans and animals are indirectly infected by eating food and water containing parasitic eggs or cysts. In addition to transmission through water and food, non-biting flies can also spread parasitic eggs/cysts through contact with human and animal skin, which increases the risk of human and animal infection [33, 31].

This systematic review included 28 studies covering 16 countries across five continents. The reliability of estimated prevalence of parasites carried by non-biting flies worldwide was derived by meta-analysis. The highest prevalence was found in Afric (58.3%; 95% CI 47.4–69.3%; n = 9144/13,366); two studies, one each in South America and North America were reported, but these were not representative [38]. Prevalence is reported to be generally high in African and Asian countries, such as Ethiopia (69.9%; 95% CI 69.0–70.7%; n = 7885/11,286) [29], Nigeria (66.6%;(95% CI 64.3–68.9%; n = 1047/1572) [30], Iran (60.0%; 95% CI 53.3–66.7%; n = 126/210) [40] and Thailand (80.0%; 95% CI 69.6–90.4%; n = 48/60) [42]. In contrast, the prevalence ranged from 1.9% to 65.7% in European countries [24, 25, 27], from 41.7% to 69.9% in African countries and from 14.8% to 80.0% in Asian countries, mainly due to environmental factors affecting health [26]. According to the literature, most feces and garbage in Africa are handled improperly, and open-air defecation is prevalent in children and a small number of adults [29].

Different non-biting fly species are likely to carry various kinds of parasites [49]. Individual non-biting flies can carry ≥ 2 parasites, and eggs of the same parasites, such as hookworm, Ascaris lumbricoides and Trichuris trichiura can be isolated from different species of flies [39]. The house fly (M. domestica) are common in areas of human habitation and are closely associated with human activities [17]; as such, they are most likely involved in parasite transmission. In general, studies have focused on the house fly (M. domestica), including some laboratory studies and surveys of the prevalence of transmitted parasites. However, although other fly species are not as abundant in human habitations and animal environments as the house fly (M. domestica), the prevalence of parasites carried by these fly species has shown a linear increase in some countries with poor sanitary conditions, such as Africa and Asia [45].

Methods are available for the isolation and identification of parasites carried on the body surface and intestine of non-biting flies. The parasite species can be identified by morphological observation of eggs/cysts under magnification by optical microscopy. They can also be identified by molecular methods and immunofluorescence techniques [50]. Morphological identification is the most commonly used method for parasite identification, with prevalence statistics reaching 47.4% (95% CI 33.0–61.7%; n = 12,188/20,351) [51, 52]. However, most parasite eggs/cysts share similar morphological characteristics, and in most cases species cannot be identified using light microscopy [53]. In addition, microscopy may overestimate the prevalence due to the long publication time of multiple studies, mostly concentrated in Africa, in some countries with limited experimental conditions. To address this problem, molecular techniques are a viable alternative for identifying parasite species [54, 55]. Molecular identification is mainly based on conventional PCR, which has the advantages of strong specificity, high sensitivity, easy operation and low cost [56]. The identification of parasites using genetic characteristics is now widely applied, and species identified in this way include Cryptosporidium spp. and Giardia lamblia [35, 23, 46]. Cryptosporidium spp. can be accurately identified based on its small subunit ribosomal RNA (SSU rRNA) gene [57]. The 60-kDa glycoprotein gene (gp60) is the most commonly used gene locus in Cryptosporidium spp. genotyping [58]. Commonly used gene loci for genotyping G. lamblia are SSU rRNA [59], β-giardin (bg), glutamate dehydrogenase (gdh) and triose-phosphate isomerase (tpi) [60, 61, 44]. Immunofluorescence technology combines a fluorescent-labeled antibody or antigen with the corresponding antigen or antibody in the test sample and detects fluorescence under a microscope. It is a reliable, rapid, sensitive and widely applicable application and can detect Cryptosporidium parvum oocysts [21].

Non-biting flies are mechanical carriers of many parasitic species, most of which are zoonotic parasites [40, 37, 62]. In addition to farms, the environments used for sample collection included residential areas, restaurants and fruit and vegetable stores [1]. The sequences of the SSU rRNA gene and the gp60 locus of C. parvum in non-biting flies were 100% homologous with the sequences of C. parvum from humans, indicating that non-biting flies were likely vectors of C. parvum [63]. The IIdA19G1 subtype identified in non-biting flies was the same as that of found in cattle from the same dairy farm studied [43, 34]. Non-biting flies will therefore increase the risk of Cryptosporidium infection in humans. The present study provided evidence for assessing the role of non-biting flies as transport hosts of parasites in the transmission of parasitic diseases.

The species of parasites carried by non-biting flies can differ seasonally. The seasonal growth and decline of non-biting flies show a three-peak curve. The highest peak, sub-peak and minimum peak appear in late May, early March and early September, respectively [11]. Non-biting flies pass through egg, larva, pupa and adult stages, and the developmental rates of these stages depend on temperature [10, 36]. Under favorable conditions in the summer and autumn, the development from egg to adult fly can be completed in 7 days. This rapid generation time explains why the fly populations sometimes grow explosively under warm conditions [31]. An increase in the number of flies can increase parasite prevalence in humans and animals [32, 33]. Although the prevalence rate was found to be highest in the spring, only one study reported this result, and there is no reference value: despite a large sample size, the detection method was by microscopic observation, and mistakes are likely when this method is used to identify protozoal parasites [31]. The second-higest prevalence was found in the autumn, as reported by five studies; this conclusion was reliable according to the seasonal fluctuation law [30, 28]. Finally, although the infection rate was lowest in the summer, nine studies reported this result; however, this conclusion was not credible according to the law of seasonal waxing and waning, and most of these nine studies focused on European countries with better sanitary conditions compared with the studies in the spring and autumn studies which were carried out in African countries [30, 21, 11].

Several studies combined the prevalence of parasites carried on the body surface and gut of non-biting flies (51.1%; 95% CI 41.5–60.7%; n = 13,644/21,252), and combined prevalence was selected for the statistical analysis in the present meta-analysis because data could not be subdivided [22, 64]. In addition, it has been shown that the prevalence of parasites isolated from the gut of non-biting flies alone is 37.1% (95% CI 22.7–51.5%; n = 1045/3817), which is significantly higher than the prevalence of parasites isolated from the body surface (35.1%; 95% CI 20.8–49.4%; n = 1199/3649). These results indicate that parasites were more easily transmitted by intestinal excretion. The results of this study are consistent with previous findings in Nigeria on the potential risk of transmission of human intestinal helminths eggs by non-biting flies [30] and with previous studies in Ethiopia that investigated the transmission of intestinal helminths eggs by non-biting flies in residential areas [31].

The most common methods used to identify helminths eggs are mostly morphological ones, and egg morphology is observed using a microscope. Identification can be directly made because some eggs have specific characteristics, with a prevalence of 42.6% (95% CI 33.5–51.8%). However, for the detection of protozoa, morphological identification alone cannot be used to make an accurate judgment, and even fungal spores can be mistaken for protozoa, with a prevalence of 32.1% (95% CI 22.9–41.3%). In some publications, only Cryptosporidium spp. and Giardia spp. were observed by microscopy, and no specific species could be identified; therefore, the best way to distinguish parasite species is by molecular tools [31, 29]. Most studies identified Entamoeba histolytica and Escherichia coli by morphological observation and did not apply molecular tools to distinguish them; consequently, the prevalence of E. histolytica has likely been overestimated [30, 28].

Although this systematic review covers studies reporting on non-biting flies that transmit parasites in multiple countries, there are a number of limitations. First, some of the studies/publications identified during the search could not be downloaded and were therefore not included in the analysis [65]. Second, the publication of relevant articles spans many years, there are only a few such published studies and there is a lack of understanding of the prevalence of parasites carried by non-biting flies. Third, the identification methods for detecting parasites are limited, and published studies mostly use conventional microscopic identification, with the likelihood that some prevalence rates may be overestimated. However, even with these limitations, the purpose of using meta-analysis in this study was to increase the sample size and power of the meta-analysis, so that the study results were close to the true prevalence.

Conclusion

Available studies have shown that the prevalence of parasites transmitted by non-biting flies worldwide is relatively high at 42.5%, and associated risk factors, such as zoonotic risk, should be considered so that people can implement effective management plans according to local conditions that may differ between geographical regions and environments, and prevent zoonotic transmission. Non-biting flies are mechanical vectors of a variety of parasites, most of which are zoonotic parasites, which can circulate between humans and humans, and between humans and animals as vectors. Thus, fly vectors should be controlled, especially in human residential areas and farms. This study provides a theoretical basis for the public health and ecological significance of parasites transmitted by non-biting flies. Future studies should mostly use molecular diagnostic tools because it not only improves detection rates, but also accurately distinguishes parasite species and reduces errors.

Availability of data and materials

All data used and analyzed in this study are represented in Tables 1, 2, 3.

Abbreviations

bg :

β-Giardin gene

gdh :

Glutamate dehydrogenase gene

PRISMA:

Preferred Reporting Items for Systematic Reviews and Meta-Analyses

SSU rRNA:

Small subunit ribosomal RNA

tpi :

Triose-phosphate isomerase gene

References

  1. Patel A, Jenkins M, Rhoden K, Barnes AN. A systematic review of zoonotic enteric parasites carried by flies, cockroaches, and dung beetles. Pathogens. 2022;11:90.

    Article  Google Scholar 

  2. Ranjbar R, Izadi M, Hafshejani TT, Khamesipour F. Molecular detection and antimicrobial resistance of Klebsiella pneumoniae from house flies (Musca domestica) in kitchens, farms, hospitals and slaughterhouses. J Infect Public Health. 2016;9:499–505.

    Article  Google Scholar 

  3. Park R, Dzialo MC, Spaepen S, Nsabimana D, Gielens K, Devriese H, et al. Microbial communities of the house fly Musca domestica vary with geographical location and habitat. Microbiome. 2019;7:147.

    Article  Google Scholar 

  4. Adenusi AA, Akinyemi MI, Akinsanya D. Domiciliary cockroaches as carriers of human intestinal parasites in Lagos Metropolis, Southwest Nigeria: implications for public health. J Arthropod Borne Dis. 2018;12:141–51.

    Article  Google Scholar 

  5. Pava-Ripoll M, Pearson RE, Miller AK, Ziobro GC. Detection of foodborne bacterial pathogens from individual filth flies. J Vis Exp. 2015;96:e52372–e52372.

    Google Scholar 

  6. Förster M, Klimpel S, Mehlhorn H, Sievert K, Messler S, Pfeffer K. Pilot study on synanthropic flies (e.g. Musca, Sarcophaga, Calliphora, Fannia, Lucilia, Stomoxys) as vectors of pathogenic microorganisms. Parasitol Res. 2007;101:243–6.

    Article  Google Scholar 

  7. Baldacchino F, Muenworn V, Desquesnes M, Desoli F, Charoenviriyaphap T, Duvallet G. Transmission of pathogens by Stomoxys flies (Diptera, Muscidae): a review. Parasite. 2013;20:26.

    Article  Google Scholar 

  8. Mohd AK. A review on respiratory allergy caused by insects. Bioinformation. 2018;14:540–53.

    Article  Google Scholar 

  9. Stoffolano JG. Fly foregut and transmission of microbes. Adv In Insect Phys. 2019;57:27–95.

    Article  Google Scholar 

  10. Graczyk TK, Cranfield MR, Fayer R, Bixler H. House flies (Musca domestica) as transport hosts of Cryptosporidium parvum. Am J Trop Med Hyg. 1999;61:500–4.

    Article  CAS  Google Scholar 

  11. Conn DB, Weaver J, Tamang L, Graczyk TK. Synanthropic flies as vectors of Cryptosporidium and Giardia among livestock and wildlife in a multispecies agricultural complex. Vector Borne Zoonotic Dis. 2007;7:643–51.

    Article  Google Scholar 

  12. Khamesipour F, Lankarani KB, Honarvar B, Tebit KE. A systematic review of human pathogens carried by the housefly (Musca domestica L.). BMC Public Health. 2018;18:1049.

    Article  Google Scholar 

  13. Matthews K. Controlling and coordinating development in vector-transmitted parasites. Science. 2011;331:1149–53.

    Article  CAS  Google Scholar 

  14. Tatfeng YM, Usuanlele MU, Orukpe A, Digban AK, Okodua M, Oviasogie F, et al. Mechanical transmission of pathogenic organisms: the role of cockroaches. J Vector Borne Dis. 2005;42:129–34.

    CAS  Google Scholar 

  15. Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6:e1000097.

    Article  Google Scholar 

  16. Patramool S, Choumet V, Surasombatpattana P, Sabatier L, Thomas F, Thongrungkiat S, et al. Update on the proteomics of major arthropod vectors of human and animal pathogens. Proteomics. 2012;12:3510–23.

    Article  CAS  Google Scholar 

  17. Barreiro C, Albano H, Silva J, Teixeira P. Role of flies as vectors of foodborne pathogens in rural areas. ISRN Microbiol. 2013;2013:718780.

    Article  Google Scholar 

  18. Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:n71.

    Article  Google Scholar 

  19. Guyatt GH, Oxman AD, Vist GE, Kunz R, Falck-Ytter Y, Alonso-Coello P, et al. GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ. 2008;336:924–6.

    Article  Google Scholar 

  20. Badri M, Olfatifar M, Wandra T, Budke CM, Mahmoudi R, Abdoli A, et al. The prevalence of human trichuriasis in Asia: a systematic review and meta-analysis. Parasitol Res. 2022;121:1–10.

    Article  Google Scholar 

  21. Clavel A, Doiz O, Morales S, Varea M, Gómez-Lus R. House fly (Musca domestica) as a transport vector of Cryptosporidium parvum. Folia Parasitol. 2002;49:163–4.

    Article  Google Scholar 

  22. Förster M, Klimpel S, Sievert K. The house fly (Musca domestica) as a potential vector of metazoan parasites caught in a pig-pen in Germany. Vet Parasitol. 2009;160:163–7.

    Article  Google Scholar 

  23. Doiz O, Clavel A, Morales S, Varea M, Castillo FJ, Rubio C, et al. House fly (Musca domestica) as a transport vector of Giardia lamblia. Folia Parasitol. 2000;47:330–1.

    Article  CAS  Google Scholar 

  24. Roberts EW. The part played by the faeces and vomit-drop in the transmission of Entamoeba histolytica by Musca domestica. Ann Trop Med Parasitol. 1947;41:129–42.

    Article  CAS  Google Scholar 

  25. Pegg EJ. Infection of dogs by Toxocara canis carried by flies. Parasitology. 1971;62:409–14.

    Article  CAS  Google Scholar 

  26. Paliy A, Sumakova N, Mashkey A, Petrov R, Ishchenko K. Contamination of animal-keeping premises with eggs of parasitic worms. Biosyst Divers. 2018;26:327–33.

    Article  Google Scholar 

  27. Lalander C, Diener S, Magri ME, Zurbrügg C, Lindström A, Vinnerås B. Faecal sludge management with the larvae of the black soldier fly (Hermetia illucens)—from a hygiene aspect. Sci Total Environ. 2013;458–460:312–8.

    Article  Google Scholar 

  28. Ahmadu YM, Goselle ON, Ejimadu LC, James Rugu NN. Microhabitats and pathogens of houseflies (Musca domestica). J Biol. 2016;12:378–80.

    Google Scholar 

  29. Fetene T, Worku N. Public health importance of non-biting cyclorrhaphan flies. Trans R Soc Trop Med Hyg. 2009;103:187–91.

    Article  Google Scholar 

  30. Adenusi AA, Adewoga TO. Human intestinal parasites in non-biting synanthropic flies in Ogun State. Nigeria Travel Med Infect Dis. 2013;11:181–9.

    Article  Google Scholar 

  31. Getachew S, Gebre-Michael T, Erko B, Balkew M, Medhin G. Non-biting cyclorrhaphan flies (Diptera) as carriers of intestinal human parasites in slum areas of Addis Ababa, Ethiopia. Acta Trop. 2007;103:186–94.

    Article  Google Scholar 

  32. Oyeyemi OT, Agbaje MO, Okelue UB. Food-borne human parasitic pathogens associated with household cockroaches and houseies in Nigeria. Parasite Epidemiol Control. 2016;1:10–3.

    Article  Google Scholar 

  33. Adenusi AA, Adewoga TO. Studies on the potential and public health importance of non-biting synanthropic flies in the mechanical transmission of human enterohelminths. Trans R Soc Trop Med Hyg. 2013;107:812–8.

    Article  Google Scholar 

  34. El-Sherbini GT, Gneidy MR. Cockroaches and flies in mechanical transmission of medical important parasites in Khaldyia Village, El-Fayoum, Governorate, Egypt. J Egypt Soc Parasitol. 2012;42:165–74.

    Article  Google Scholar 

  35. Fetene T, Worku N, Huruy K, Kebede N. Cryptosporidium recovered from Musca domestica, Musca sorbens and mango juice accessed by synanthropic flies in Bahirdar, Ethiopia. Zoonoses Public Health. 2011;58:69–75.

    Article  CAS  Google Scholar 

  36. Graczyk TK, Fayer R, Knight R, Mhangami-Ruwende B, Trout JM, Da Silva AJ, et al. Mechanical transport and transmission of Cryptosporidium parvum oocysts by wild filth flies. Am J Trop Med Hyg. 2000;63:178–83.

    Article  CAS  Google Scholar 

  37. Szostakowska B, Kruminis-Lozowska W, Racewicz M, Knight R, Tamang L, Myjak P, et al. Cryptosporidium parvum and Giardia lamblia recovered from flies on a cattle farm and in a landfill. Appl Environ Microbiol. 2004;70:3742–4.

    Article  CAS  Google Scholar 

  38. Lima MSCS, Soares MRA, Pederassi J, Aguiar BCG, Pereira CAS. The housefly Musca domestica L. (Diptera: Muscidae) as a potential paratenic host in the city of Bom Jesus-Piauí, Brazil. Comun Sci. 2014;5:349–55.

    Google Scholar 

  39. De Oliveira VC, de Mello RP, d’Almeida JM, et al. Muscoid dipterans as helminth eggs mechanical vectors at the zoological garden, Brazil. Rev Saude Publica. 2002;36:614–20.

    Article  Google Scholar 

  40. Hemmati S, Afshar AA, Mohammadi MA, Afgar A, Nasibi S, Harandi MF. Experimental and field investigation of non-biting flies as potential mechanical vectors of Echinococcus granulosus eggs. Exp Parasitol. 2018;189:43–8.

    Article  Google Scholar 

  41. Yu F, Qi M, Zhao Z, Lv C, Wang Y, Wang R. The potential role of synanthropic rodents and flies in the transmission of Enterocytozoon bieneusi on a dairy cattle farm in China. J Eukaryot Microbiol. 2018;66:435–41.

    Article  Google Scholar 

  42. Pornruseetriratn S, Maipanich W, Sa-nguankiat S, Pubampen S, Poodeepiyasawat A, Thaenkham U. A simple and effective multiplex PCR technique for detecting human pathogenic taenia eggs in houseflies. Southeast Asian J Trop Med Public Health. 2017;48:9–17.

    Google Scholar 

  43. Zhao Z, Dong H, Wang R, Zhao W, Chen G, Li S, et al. Genotyping and subtyping Cryptosporidium parvum and Giardia duodenalis carried by flies on dairy farms in Henan, China. Parasit Vectors. 2014;7:190.

    Article  Google Scholar 

  44. Sulaiman IM, Fayer R, Bern C, Gilman RH, Trout JM, Schantz PM, et al. Triosephosphate isomerase gene characterization and potential zoonotic transmission of Giardia duodenalis. Emerg Infect Dis. 2003;9:1444–52.

    Article  CAS  Google Scholar 

  45. Monzon RB, Sanchez AR, Tadiaman BM, Najos OA, Valencia EG, De Rueda RR, et al. A comparison of the role of Musca domestica (Linnaeus) and Chrysomya megacephala (Fabricius) as mechanical vectors of helminthic parasites in a typical slum area of Metropolitan Manila. Southeast Asian J Trop Med Public Health. 1991;22:222–8.

    CAS  Google Scholar 

  46. Barnes AN, Davaasuren A, Baasandavga U, Lantos PM, Gonchigoo B, Gray GC. Zoonotic enteric parasites in Mongolian people, animals, and the environment: using one health to address shared pathogens. PLoS Negl Trop Dis. 2021;15:e0009543.

    Article  Google Scholar 

  47. Wang ZD, Liu Q, Liu HH, Li S, Zhang L, Zhao YK, et al. Prevalence of Cryptosporidium, Microsporidia and Isospora infection in HIV-infected people: a global systematic review and meta-analysis. Parasit Vectors. 2018;11:28.

    Article  Google Scholar 

  48. Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315:629–34.

    Article  CAS  Google Scholar 

  49. Graczyk TK, Knight R, Tamang L. Mechanical transmission of human protozoan parasites by insects. Clin Microbiol Rev. 2005;18:128–32.

    Article  Google Scholar 

  50. Graczyk TK, Grimes BH, Knight R, Da Silva AJ, Pieniazek NJ, Veal DA. Detection of Cryptosporidium parvum and Giardia lamblia carried by synanthropic flies by combined fluorescent in situ hybridization and a monoclonal antibody. Am J Trop Med Hyg. 2003;68:228–32.

    Article  Google Scholar 

  51. Atiokeng Tatang RJ, Tsila HG, Wabo PJ. Medically important parasites carried by cockroaches in Melong subdivision, Littoral, Cameroon. J Parasitol Res. 2017;2017:7967325.

    Article  CAS  Google Scholar 

  52. Erol U, Danyer E, Sarimehmetoglu HO, Utuk AE. First parasitological data on a wild grey wolf in Turkey with morphological and molecular confirmation of the parasites. Acta Parasitol. 2021;66:687–92.

    Article  CAS  Google Scholar 

  53. Rondón S, Cavallero S, Renzi E, Link A, González C, D’Amelio S. Parasites of free-ranging and captive American primates: a systematic review. Microorganisms. 2021;9:2546.

    Article  Google Scholar 

  54. Ahmed M, Singh MN, Bera AK, Bandyopadhyay S, Bhattacharya D. Molecular basis for identification of species/isolates of gastrointestinal nematode parasites. Asian Pac J Trop Med. 2011;4:589–93.

    Article  CAS  Google Scholar 

  55. Lymbery AJ, Thompson RC. The molecular epidemiology of parasite infections: tools and applications. Mol Biochem Parasitol. 2012;181:102–16.

    Article  CAS  Google Scholar 

  56. Duflot M, Setbon T, Midelet G, Brauge T, Gay M. A review of molecular identification tools for the Opisthorchioidea. J Microbiol Methods. 2021;187:106258.

    Article  CAS  Google Scholar 

  57. Xiao L, Escalante L, Yang C, Sulaiman I, Escalante AA, Montali RJ. Phylogenetic analysis of Cryptosporidium parasites based on the small-subunit rRNA gene locus. Appl Environ Microbiol. 1999;65:1578–83.

    Article  CAS  Google Scholar 

  58. Essid R, Chelbi H, Siala E, Bensghair I, Menotti J, Bouratbine A. Polymorphism study of Cryptosporidium hominis gp60 subtypes circulating in Tunisia. Microb Pathog. 2017;110:298–303.

    Article  CAS  Google Scholar 

  59. Appelbee AJ, Frederick LM, Heitman TL, Olson ME. Prevalence and genotyping of Giardia duodenalis from beef calves in Alberta, Canada. Vet Parasitol. 2003;112:289–94.

    Article  CAS  Google Scholar 

  60. Lalle M, Pozio E, Capelli G, Bruschi F, Crotti D, Cacciò SM. Genetic heterogeneity at the beta-giardin locus among human and animal isolates of Giardia duodenalis and identification of potentially zoonotic subgenotypes. Int J Parasitol. 2005;35:207–13.

    Article  CAS  Google Scholar 

  61. Cacciò SM, Beck R, Lalle M, Marinculic A, Pozio E. Multilocus genotyping of Giardia duodenalis reveals striking differences between assemblages A and B. Int J Parasitol. 2008;38:1523–31.

    Article  Google Scholar 

  62. Knols B, Smallegange RC. Book review: public health significance of urban pests. Lancet Infect Dis. 2009;9:535–6.

    Article  Google Scholar 

  63. Collinet-Adler S, Babji S, Francis M, Kattula D, Premkumar PS, Sarkar R, et al. Environmental factors associated with high fly densities and diarrhea in Vellore. India Appl Environ Microbiol. 2015;81:6053–8.

    Article  CAS  Google Scholar 

  64. Pava-Ripoll M, Pearson RE, Miller AK, Ziobro GC. Prevalence and relative risk of Cronobacter spp., Salmonella spp., and Listeria monocytogenes associated with the body surfaces and guts of individual filth flies. Appl Environ Microbiol. 2012;78:7891–902.

    Article  CAS  Google Scholar 

  65. Chen Y, Qin H, Huang J, Li J, Zhang L. The global prevalence of Cryptosporidium in sheep: a systematic review and meta-analysis. Parasitology. 2022;24:1–14.

    Google Scholar 

Download references

Funding

This study was supported in part by the National Natural Science Foundation of China (U1904203) and the Leading talents of the Thousand Talents Program of Central China (19CZ0122). The sponsors played no role in the study design or in the collection, analysis or interpretation of the data, in writing the report or in the decision to submit the report for publication.

Author information

Authors and Affiliations

  1. College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, 450046, People’s Republic of China

    Yufeng Liu, Yuancai Chen, Nanhao Wang, Huikai Qin, Longxian Zhang & Sumei Zhang

  2. International Joint Research Center for Animal Immunology of China, Zhengzhou, Henan, People’s Republic of China

    Yufeng Liu, Yuancai Chen, Nanhao Wang, Huikai Qin, Longxian Zhang & Sumei Zhang

  3. Key Laboratory of Quality and Safety Control of Poultry Products (Zhengzhou), Ministry of Agriculture and Rural Affairs, Zhengzhou, People’s Republic of China

    Yufeng Liu, Yuancai Chen, Nanhao Wang, Huikai Qin, Longxian Zhang & Sumei Zhang

Authors
  1. Yufeng Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Yuancai Chen
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Nanhao Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Huikai Qin
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Longxian Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Sumei Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

SZ conceived and designed the review. YL, YC, NW and HQ analyzed the data and wrote the original draft of the manuscript. LZ, SZ and YL revised the final manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Sumei Zhang.

Ethics declarations

Ethics approval and consent to participate

The present study was approved by the Independent Ethics Committee of Henan Agricultural University (Approval No. IEC-HENAU-20180323-06).

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Liu, Y., Chen, Y., Wang, N. et al. The global prevalence of parasites in non-biting flies as vectors: a systematic review and meta-analysis. Parasites Vectors 16, 25 (2023). https://doi.org/10.1186/s13071-023-05650-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13071-023-05650-2

Keywords

  • Non-biting flies
  • Vectors
  • Parasites
  • Meta-analysis

Parasites & Vectors

ISSN: 1756-3305

Contact us