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Erschienen in: BMC Public Health 1/2018

Open Access 01.12.2018 | Review article

A systematic review of human pathogens carried by the housefly (Musca domestica L.)

verfasst von: Faham Khamesipour, Kamran Bagheri Lankarani, Behnam Honarvar, Tebit Emmanuel Kwenti

Erschienen in: BMC Public Health | Ausgabe 1/2018

Abstract

Background

The synanthropic house fly, Musca domestica (Diptera: Muscidae), is a mechanical vector of pathogens (bacteria, fungi, viruses, and parasites), some of which cause serious diseases in humans and domestic animals. In the present study, a systematic review was done on the types and prevalence of human pathogens carried by the house fly.

Methods

Major health-related electronic databases including PubMed, PubMed Central, Google Scholar, and Science Direct were searched (Last update 31/11/2017) for relevant literature on pathogens that have been isolated from the house fly.

Results

Of the 1718 titles produced by bibliographic search, 99 were included in the review. Among the titles included, 69, 15, 3, 4, 1 and 7 described bacterial, fungi, bacteria+fungi, parasites, parasite+bacteria, and viral pathogens, respectively. Most of the house flies were captured in/around human habitation and animal farms. Pathogens were frequently isolated from body surfaces of the flies. Over 130 pathogens, predominantly bacteria (including some serious and life-threatening species) were identified from the house flies. Numerous publications also reported antimicrobial resistant bacteria and fungi isolated from house flies.

Conclusions

This review showed that house flies carry a large number of pathogens which can cause serious infections in humans and animals. More studies are needed to identify new pathogens carried by the house fly.
Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1186/​s12889-018-5934-3) contains supplementary material, which is available to authorized users.
Abkürzungen
EAEC
Enteroaggregative Escherichia coli
EHEC
Enterohaemorhagic Escherichia coli
EPEC
Enteropathogenic Escherichia coli
ETEC
Enterotoxigenic Escherichia coli
PCR
Polymerase chain reaction
PRRS
Porcine reproductive and respiratory syndrome

Background

The house fly, Musca domestica L. (Diptera: Muscidae), is the most common and widespread species of fly in the world. It is said to have originated from the savannahs of Central Asia and spread throughout the world, and can be found in both rural and urban areas of tropical and temperate climates [1, 2]. The house fly belongs to a group of flies often referred to as “filth flies”; the other members belong to the families Calliphoridae and Fanniidae [3]. The house fly has been in existence since the origin of human life [4] and well adapted to life in human habitations [5]. M. domestica is an eusynanthropic, endophilic species, i.e. it lives closely in association with humans and is able to complete its entire lifecycle within habitations of humans and domestic animals [6]. House flies are often found in abundance in areas of human activities such as hospitals, food markets, slaughter houses, food centers or restaurants, poultry and livestock farms where they constitute a nuisance to humans, poultry, livestock and other farm animals, and also act as potential vector of diseases [7].
The house fly is known to carry pathogens that can cause serious and life-threatening diseases in humans and animals. Over 100 pathogens including bacteria, viruses, fungi and parasites (protozoans and metazoans) have been associated with the insect [8, 9]. Molecular analysis revealed that house flies carry very diverse groups of microorganisms [10]. Evidence supporting the role of the house fly in transmission of diseases are mostly circumstantial, with the strongest evidence pointing to the correlation between the rise in incidence of diarrhoea and an increase in the fly population [1114].
The characteristics of the pathogens carried by house flies depend on the area where the insect is collected; house flies captured from the hospital environment or animal farms (where there is extensive use of antibiotics as growth promoters) commonly carry antimicrobial resistant bacteria and fungi [9, 1520]. More so, house flies presenting in the hospital environment may also be associated with the transmission of nosocomial infections [9, 21].
House fly causes mechanical transmission of pathogens, which is the most widely recognised mechanism [2224]. This occurs when pathogens are transmitted from one vertebrate hosts to another without amplification or development of the organism within the vector [22]. House flies usually feed and reproduce in feces, animal manure, carrion and other decaying organic substances, and thus live in intimate association with various microorganisms including human pathogens, which may stick to body surfaces of the fly. The constant back and forth movement of house flies between their breeding sites and human dwellings can lead to the transmission of pathogens to humans and animals.
Currently, there is no systematic review on the pathogens carried by the house fly. The aim of this systematic review was to identify the types and prevalence of human pathogens carried by the house fly.

Methods

For this systematic review, we did a literature search to identify scientific articles reporting pathogens (bacteria, viruses, fungi and parasites) that has been isolated from the house fly (Musca domestica). The current study conforms to the Preferred Reporting Items for Systematic reviews and Meta-analyses (PRISMA) guidelines [25] (Additional file 1).

Search strategy and selection criteria

Relevant studies were searched in health-related electronic databases including PubMed, PubMed Central, Google Scholar and Science Direct using the keywords: House fly OR Musca domestica OR Pathogens OR bacteria OR fungi OR parasites OR viruses.
The search was limited to the studies published in English or containing at least an English abstract until November 2017. Subsequently, the titles and abstracts of the selected articles were examined by 2 reviewers, independently (parallel method) to identify articles reporting pathogens isolated from the house fly. When there was any discrepancy in their report, a third reviewer was invited to resolve the issue. Relevant papers were also manually cross checked in order to identify further references. In the selected articles, the following data were extracted by the first reviewer and checked by the second reviewer. The data included type and species of pathogen isolated, stage of house fly from which pathogen was isolated, frequency of occurrence of pathogen, method used in isolation of pathogen, type of study (field or experimental), site of the house fly from where the pathogen was isolated, nature of pathogen isolated (whether the pathogen was carrying genes that were resistant to antimicrobials or not), and location of capture of the house fly (human residents, animal farms, markets/shops, hospitals etc.). Excluded articles were those reporting pathogens isolated from flies in general without specifying the fly species. The selection process is detailed in Fig.1.

Risk of bias in individual studies

Level of risk of bias for the study was likely to be high mainly because of differences in study and the methods used to isolate pathogens from the house fly. Most of the studies were not designed to isolate all the types of pathogens. Moreover, studies using molecular methods (PCR and/or sequences) yielded more pathogens compared to studies using standard cultural methods.

Results

Figure 1 (PRISMA flowchart) provides a four-phase study selection process in the present systematic review study. A total of 1718 studies were identified in the initial search. After the title and abstract screening, 131 full- text articles were retrieved. Of these, a final 99 articles were identified for this review [224, 2693]
Seventy-three 73 (73.73%) of the works described bacterial pathogens (Table 1), 18 (18.18%) fungi (Table 2), 5 (5.05%) parasites (Table 3) and 7 (7.07%) described viruses. The selected studies were done in 21 countries and the study period covered the years 1970–2017. Sixty-eight of the studies were field studies (performed on house flies caught in the wild) (68.69%) while 31 were experimental studies (performed in the laboratory) (31.31%). Of the 68 field studies, 12 described pathogens isolated from house flies caught in the wild in Europe, 16 in the Middle East, 15 in Africa, 13 in USA, 10 in Asia, and 2 in South America. Twenty studies (28.88%) reported on house flies that were caught from within human habitation, 28 (28.28%) from animal farms (including poultry, dairy and piggery farms), 10 (10.10%) from the surroundings, 10 (10.10%) from food centers (including cafeteria, restaurants), 7 (7.07%) from markets or shops, 14 (14.14) from hospitals, 7 (7.07%) from dump sites or sanitary landfills while 4 (4.04%) were from gardens or farms.
Table 1
Bacteria species that have been isolated from house flies, including the site of isolation, the frequencies and their distribution
Bacteria genera
Species
Medical and/or veterinary importance
Geographical occurrence
Site of specimen collection
Host stage infected
Prevalence
Lab or field study
Site of isolation
References
Helicobacter
H. pylori
Medical
Worldwide
Laboratory reared
Adult
Lab
External surfaces/internal organs
[7072]
Campylobacter
C. jejuni
Medical and veterinary
Worldwide
Poultry, piggery
Adult/larvae
6.2%
Field/ Lab
External surfaces/internal organs
[73, 74, 87, 90]
C. coli
Medical and veterinary
Worldwide
Poultry, piggery
Adult
90.1%
Field
External surfaces/internal organs
[74]
Others
Medical and veterinary
Worldwide
Restaurant, refuse dumps, barbecue shops, fruits and food vendors, markets, poultries (broiler farms)
Adult
Field
External surfaces/internal organs
[38, 75]
Salmonella
S. typhimurium
Medical
Worldwide
Laboratory experiment
Adult
Lab
 
[37]
S. enterica serovar Enteritidis
Medical
Worldwide
Poultry, dumpsters
Adult/larvae
6–70%
Lab/field
External surfaces/internal organs
[23, 28, 39]
Others
Medical
Worldwide
Restaurant, refuse dumps, barbecue shops, fruits and food vendors, markets, fish vendors, human habitation
Adult
11.8–66.67%
Field
External surfaces/internal organs
[25, 27, 29, 7072, 91]
Escherichia
E. coli
Medical
Worldwide
Human habitation, cafeteria and food centers, hospitals, open fields, poultry farms, slaughter houses, cattle farms, animal hospitals
Adult/larvae
10.5–76.3%
Field/lab
External surfaces/internal organs
[224, 2938, 40, 4346, 48, 89, 92]
Bacillus
B. anthrax
Medical and veterinary
Worldwide
Laboratory reared
Adult
Lab
External surfaces/Internal organs
[76]
B. megatarium
non
Worldwide
Cafeteria and food centers
Adult
50%
Field
External surfaces/Internal organs
[7]
B. sphaericus
Medical
Worldwide
Cafeteria and food centers
Adult
50%
Field
External surfaces/Internal organs
[7]
B. cereus
Medical
Worldwide
Fresh fish
Larvae
Field
External surfaces/Internal organs
[46, 53]
B. alvei
Medical
Worldwide
Cafeteria and food centers
Adult
50%
Field
External surfaces/Internal organs
[7]
B. pumilus
Medical
Worldwide
 
Adult
Field
External surfaces/Internal organs
[46]
B. thuringiensis
non
Worldwide
 
Adult
Field
External surfaces/Internal organs
[46]
Others
Medical
Worldwide
Dairy farms, hospitals, slaughter houses, fruit and food centers
Adult
31.1%
Field
External surfaces
[10, 20, 44, 61, 89]
Staphylococcus
S. aureus
Medical
Worldwide
Human habitation, fresh fish
Adult/ larvae
26.9%
Field
External surfaces/Internal organs
[40, 45, 53, 77, 92]
S. epidermidis
Medical
Worldwide
Human habitation
Adult
Field
External surfaces/Internal organs
[40]
S. sciuri
Medical/veterinary
Worldwide
Dumpsters of restaurants
Adult
Field
External surfaces
[46]
S. saprophyticus
Medical
Worldwide
Dumpsters of restaurants
Adult
Field
External surfaces
[46]
S. xylosus
Medical
Worldwide
Dumpsters of restaurants
Adult
Field
External surfaces
[46]
Others
Medical/veterinary
Worldwide
Poutry, animal farms, garden, garbage/dump areas, restaurants/cafeteria, markets, human habitation, hospitals
Adult
22.9–28.2%
Field
External surfaces/Internal organs
[10, 20, 48, 78, 79, 89, 91]
Enterococcus
E. faecalis
Medical
Worldwide
Restaurants, piggery farms
Adult
55.5–88.2%
Field/lab
External surfaces/Internal organs
[21, 49, 50]
E. faecium
Medical
Worldwide
Restaurants, piggery farms
Adult
6.8–12.8%
Field/lab
External surfaces/Internal organs
[49, 50]
E. casseliflavus
Medical
Worldwide
Restaurants, piggery farms
Adult
4.9–6.7%
Field/lab
External surfaces/Internal organs
[49, 50]
E. hirae
Medical/veterinary
Worldwide
piggery farms
Adult
12.8%
Field/lab
External surfaces/Internal organs
[50]
Aeromonas
A. caviae
Medical
Worldwide
Hospitals, streets, slaughter houses (abattoir)
Adult
39–78%
Field
Internal organs
[48, 80, 81]
A hydrophila
Medical
Worldwide
Open field
Adult
Field
Internal organs
[82]
Others
Medical
Worldwide
Poutry, animal farms, garden, garbage/dump areas, restaurants/cafeteria, markets, human habitation, hospitals
Adult
Field
Internal organs
[79]
Shigella
S. sonnei
Medical
Worldwide
Hospitals, streets, slaughter houses
Adult
Field
Internal organs
[48]
S. dysenteriae
Medical
Worldwide
Dumpsters of restaurants
Adult
Field
Internal organs
[46]
Others
Medical
Worldwide
Poultry, animal farms, garden, garbage/dump areas, restaurants/cafeteria, markets, human habitation, hospitals
Adult
4.8–66.67%
field
External surfaces/ internal organs
[11, 13, 29, 38, 40, 43, 79, 91]
Klebsiella
K. pneumoniae
Medical
Worldwide
Hospitals, human habitation, slaughter houses
Adult
11.3–82%
field
External surfaces/ internal organs
[15, 47, 82]
K. oxytoca
Medical
 
Open field
Adult
Field
External surfaces
[83]
Others
Medical
 
Poutry, animal farms,garden, garbage/dump areas, restaurants/cafeteria, markets, human habitation, hospitals, slaughter houses, open field
Adult
Field
External surfaces
[40, 44, 48, 61, 79, 89]
Pseudomonas
P. aeruginosa
Medical
Worldwide
Dump sites, slaughter houses, open field, human habitation, fresh fish, hospitals
Adult/larvae
37%
field
External surfaces/internal organs
[15, 19, 53, 61, 84]
Others
Medical
Worldwide
Hospitals, streets, slaughter houses,
Adult
21.8%
Field
External surfaces/internal organs
[44, 48, 92]
Proteus
P. mirabilis
Medical
Worldwide
Slaughter houses, hospitals
Adult
29.1%
field
External surfaces/internal organs
[15]
P. vulgaris
Medical
Worldwide
Human habitation
Adult
Field
External surfaces/internal organs
[40]
Proteus sp.
Medical
Worldwide
Slaughter houses, dump sites, open fields, human habitations
Adult
14.8%
Field
External surfaces/internal organs
[61, 89, 92]
Citrobacter
C. freundi
Medical
Worldwide
Cafeteria and food centers, Slaughter houses, hospitals
Adult
28.4%
field
External surfaces/internal organs
[7, 15]
Chronobacter
C. turicensis,
Medical
Worldwide
Poultry, dumpsters
Adult/larvae
14%
Field/lab
External surfaces/internal organs
[23, 28]
C. universalis
Medical
Worldwide
Poultry, dumpsters
Adult/larvae
Field/lab
External surfaces/internal organs
[23, 28]
C. sakazakii
Medical
Worldwide
Poultry, dumpsters
Adult/larvae
Field/lab
External surfaces/internal organs
[23, 28, 46]
Listeria
L. monocytogenes
Medical
Worldwide
Poultry, dumpsters
Adult/larvae
3–49.4%
Field/lab
External surfaces/internal organs
[23, 28, 54]
Others
Medical/veterinary
Worldwide
Animal farms
Adult
Field
External surfaces/internal organs
[78]
Streptococcus
S. pyogenes
medical
Worldwide
Fresh fish, human habitation
Adult/larvae
Field
External surfaces/internal organs
[40, 53]
S. faecalis
Medical
Worldwide
Fresh fish
Larvae
Field
External surfaces/internal organs
[53]
Others
Medical
Worldwide
Hospitals, slaughter houses, streets, dump sites, open fields, human habitation
Adult
66.67%
Field
External surfaces/internal organs
[48, 61, 89, 91]
Alternaria
Alternaria spp.
Medical
Worldwide
Fresh fish, Human habitation
Larvae
1.4–6%
Field
 
[15, 53, 55]
Serratia
Serratia spp.
Medical
worldwide
Human habitation
Adult
Field
Internal organs
[40]
Enterobacter
Enterobacter spp.
Medical
Worldwide
Human habitation
Adult
Field
Internal organs
[40, 89]
Edwardsiella
Edwardsiella spp.
Medical
Worldwide
Poultry
Adult
field
External surfaces/internal organs
[43]
Providencia
Providencia spp.
Medical
Worldwide
Poultry, animal farms, garden, garbage/dump areas, restaurants/cafeteria, markets, human habitation, hospitals, slaughter houses, open field
Adult
Field
External surfaces/ internal organs
[43, 79]
Vibrio
Vibrio cholera non O1
Medical
Worldwide
Human habitation
Adult
45.7%
Field
Internal organs
[29]
Others
Medical / veterinary
Worldwide
Animal farms
Adult
Field
External surfaces/ internal organs
[78]
Morganella
M. morgana
Medical
Worldwide
Poutry, animal farms,garden, garbage/dump areas, restaurants/cafeteria, markets, human habitation, hospitals, slaughter houses, open field
Adult
16.67%
Field
External surfaces/Internal organs
[7, 79]
Clostridium
Clostridium spp.
Medical
Worldwide
Dairy farms
Adult
Field
Internal organs
[10]
Corynebacterium
Corynebacterium spp.
Medical
Worldwide
Dairy farms
Adult
Field
Internal organs
[10]
Lactobacillus
Lactobacillus spp.
Medical
Worldwide
Dairy farms
Adult
Field
Internal organs
[10]
Yersinia
Y. enterocolitica
Medical
Worldwide
Hospitals, streets, slaughter houses
Adult
Field
Internal organs
[48]
Burkholderia
B. pseudomallei
Medical
Worldwide
Open field
Adult
Field
Internal organs
[83]
Acinetobacter
A. baumanni
Medical
worldwide
Poultry, dumpsters
Adult
Field
Internal organs
[46, 89]
Methylobacterium
M. persicinum
Medical
Worldwide
Poultry, dumpsters
Adult
Field
Internal organs
[46]
Micrococcus
Micrococcus sp.
Medical
Worldwide
Garbage/dump areas, poultry, restaurants
Adult
Field
External surfaces/Internal organs
[89]
Table 2
Fungi species that have been isolated from house flies, including the site of isolation, the frequencies and their distribution
Fungi genera
Species
Medical, veterinary or agricultural importance
Geographical occurrence
Site of specimen collection
Host stage infected
Prevalence
Lab or field study
Site of isolation
References
Cladosporum
C. cladosporoides
Medical
Worldwide
Cattles diagnosed with bovine ringworm, animal pens, dump sites
Adult/larvae
4.7–85%
Field/lab
External surfaces
[56, 57]
Others
Medical
Worldwide
Human habitation
Larvae
0.2
Field
External surfaces
[53, 55]
Penicillium
P. axalicum
Medical
Worldwide
Fresh fish
Larvae
Field
External surfaces
[53]
P. corylophilum
Medical
Worldwide
Animal pens, dump sites
Larvae
Field
External surfaces
[57]
P. fellutanum
Medical
Worldwide
Animal pens, dump sites
Larvae
11.9%
Field
External surfaces
[57]
P. verrucosum
Medical
Worldwide
Human habitation
Adult
Field
External surfaces
[60]
P. aurantiogriseum
Medical
Worldwide
Human habitation
Adult
Field
External surfaces
[60]
Others
Medical
Worldwide
Human habitation, Cattles diagnosed with bovine ringworm, hospitals, slaughter houses
adult
3.4–21%
Field/lab
External surfaces
[55, 56, 58, 59]
Aspergillus
A. flavus
Medical
Worldwide
Animal pens, dump sites, poultry farms, dairy, piggery, slaughter houses, open field
Adult/larvae
23.8%
Field
External surfaces
[52, 57, 60]
A niger
Medical
Worldwide
Animal pens, dump sites
Adult/larvae
14.4–85.71%
Field
External surfaces
[7, 57]
A fumigatus
Medical
Worldwide
Cafeteria and food centers
Adult
85.71
Field
External surfaces
[7]
A tamari
Medical
Worldwide
Fresh fish
Larvae
Field
External surfaces
[53]
A parasiticus
Medical
Worldwide
Human habitation
Adult
Field
External surfaces
[60]
Others
Medical
Worldwide
Human habitation, Cattles diagnosed with bovine ringworm, hospitals, slaughter houses
Adult
2.8–67.4%
Field/lab
External surfaces
[55, 56, 58, 59]
Beauveria
B. bassiana
Medical
Worldwide
Poultry farms, dairy, piggery, open field, slaughter houses
Adult
Field
External surfaces
[52]
Mucor
M. cirinelloides
Medical
Worldwide
Cafeteria and food centers
Adult
Field
External surfaces
[7]
Others
Medical
Worldwide
Human habitation
Adult
2%
Field
External surfaces
[55]
Alternaria
A. alternata
Medical
Worldwide
Animal pens, dump sites
Adult/larvae
1.4–11.9%
Field
External surfaces
[53, 55, 57, 58]
Fusarium
F. oxysporum
Medical
Worldwide
Fresh fish
Larvae
Field
External surfaces
[53]
F. verticilliodes
Medical
Worldwide
Human habitation
Adult
Field
External surfaces
[60]
F. proliferatum
Medical
Worldwide
Human habitation
Adult
Field
External surfaces
[60]
Others
Medical
Worldwide
Animal pens, dump sites, Human habitation, hospitals, slaughter houses
Larvae
4.7–17%
Field
External surfaces
[55, 57, 58]
Curvularia
C. brachyspora
Medical
Worldwide
Animal pens, dump sites
Adult
2.4%
Field
External surfaces
[57]
Mycelia
M. sterilia
Medical
Worldwide
Animal pens, dump sites
Adult
2.4%
Field
External surfaces
[57]
Candida
C. albicans
Medical
Worldwide
Pig pen, Human habitation
Adult
44.6%
Field
External surfaces
[51, 54]
C. glabrata
Medical
Worldwide
Human habitation
Adult
23%
Field
External surfaces
[51]
C. krusei
Medical
Worldwide
Human habitation
Adult
19.6%
Field
External surfaces
[51]
C. tropicalis
Medical
Worldwide
Pig pen, Human habitation
Adult
7.4%
Field
External surfaces
[51, 54]
C. dubliniensis
Medical
Worldwide
Human habitation
Adult
3.6%
Field
External surfaces
[51]
C. parapsilisis
Medical
Worldwide
Human habitation
Adult
1.8%
Field
External surfaces
[51]
Others
Medical
Worldwide
Human habitation
Adult
10.5%
Field
External surfaces
[59]
Microsporum
M. canis
Veterinary
Worldwide
Laboratory experiment
Adult/larvae
Field
External surfaces/internal organs
[85]
M. gypseum
Medical
Worldwide
Hospitals, slaughter houses
Adult
Field
External surfaces
[58]
Chrysosporium
Chrysosporium spp.
Medical
Worldwide
Human habitation
Adult
2%
Field
External surfaces
[55]
Curvalaria
Curvalaria spp.
Agricultural
Worldwide
Human habitation
Adult
0.4%
Field
External surfaces
[55]
Epicoccum
Epicoccum spp.
Medical
Worldwide
Human habitation
Adult
1%
Field
External surfaces
[55]
Eupenicillium
Eupenicillium spp.
Medical
Worldwide
Human habitation
Adult
1%
Field
External surfaces
[55]
Moniliella
Moniliella spp.
Medical and veterinary
Worldwide
Human habitation
Adult
9%
Field
External surfaces
[55]
Nigrospora
Nigrospora spp.
Agricultural
Worldwide
Human habitation
Adult
1%
Field
External surfaces
[55]
Rhizopus
Rhizopus spp.
Veterinary
Worldwide
Human habitation
Adult
2%
Field
External surfaces
[55]
Scopulariopsis
Scopulariopsis spp.
Veterinary
Worldwide
Human habitation
Adult
2%
Field
External surfaces
[55]
Mucorales
Mucorales spp.
Medical
Worldwide
Hospitals
Adult
11%
Field
External surfaces
[59]
Rhodotorula
Rhodotorula spp.
Medical/veterinary
Worldwide
Hospitals
Adult
8.4%
Field
External surfaces
[59]
Moniliella
M. suaveolans
Medical
Worldwide
Human habitation
Adult
Field
External surfaces
[60]
Table 3
Parasites that have been isolated from house flies, including the site of isolation, the frequencies and their distribution
Parasite genera
Species
Medical or veterinary importance
Geographical occurrence
Site of specimen collection
Host stage infected
Prevalence
Lab or field study
Site of isolation
References
Ascaris
A. lumbricoides
Medical
Worldwide
Slaughter houses, dump sites, human habitation, open fields
Adult
12.6–14.29%
Field
External surfaces
[6163, 98, 99]
A. suum
Veterinary
Worldwide
piggery
Adult
62%
Field/lab
External surfaces/internal organs
[54]
Entamoeba
E. histolytica
Medical
Worldwide
Slaughter houses, dump sites, human habitation, open fields
Adult
35.43–53.57%
Field
External surfaces
[6163]
Hookworm
Ancylostoma duodenale/Necator americanus
Medical
Worldwide
Slaughter houses, dump sites, human habitation, open fields
Adult
8.93%
Field
External surfaces
[61, 62, 64]
Trichuris
T. trichiura
Medical
Worldwide
Slaughter houses, dump sites, human habitation, open fields, piggery
Adult
12.5–74.0%
Field
External surfaces
[6164]
T. suis
Medical/veterinary
Worldwide
Piggery
Adult
Field/lab
External surfaces/internal organs
[54]
Strongyloides
S. stercoralis
Medical
Developing countries
Slaughter houses, dump sites, human habitation, open fields
Adult
10.7%
Field
External surfaces/internal organs
[61]
S. ransomi
Veterinary
Tropical regions
Piggery
Adult
21%
Field
External surfaces
[54]
Metastrongylus
M. spp
Veterinary
Worldwide
Piggery
Adult
Field
External surfaces/internal organs
[54]
Haematopinus
H. suis
Veterinary
Worldwide
Piggery
Adult
Field
External surfaces/internal organs
[54]
Crytosporidium
C. parvum
Medical/ Veterinary
Worldwide
Laboratory experiment
Adult/larvae
Lab
Internal organs
[65]
Giardia
G. lamblia
Medical
Developing countries
Human habitation, refuse dumps, tomato/vegetable and soft drink shops
Adult
23.62%
Field
External surfaces
[3, 63]
Enterobius
E. vermicularis
Medical
Worldwide but more prevalent in developed world
Poultry
Adult
Field
External surfaces
[3]
Taenia
T. spp.
Medical/veterinary
Worldwide
Human habitation, refuse dumps, tomato/vegetable and soft drink shops
Adult
15.75%
Field
External surfaces
[63, 64]
Hymenolepis
H. nana
Medical
Worldwide
Human habitation, refuse dumps, tomato/vegetable and soft drink shops
Adult
5.51%
Field
Internal organs
[63]
Pathogens were isolated more frequently from the body surfaces of the flies as reflected from 44 studies (44.44%), followed by 33 studies (33.33%) reporting isolation from both the body surfaces and the gut, while 22 studies (22.22%) indicated isolation from the gut. Most studies reported isolation of pathogens from adult flies 91 (91.92%), followed by larvae 5 (5.05%) and from both the adults and the larvae 3 (3.03%).
The most frequent method used in the isolation of pathogens was standard cultural methods 77 (77.78%), followed by molecular methods (such as polymerase chain reaction [PCR] or sequencing) 14 (14.14%) and other parasitological techniques 8 (8.08%).
Among the bacterial pathogens isolated, 7 studies reported virulent bacteria (8.97%), 14 reported bacteria carrying genes which confer resistance to multiple antibiotics (17.95%), and the enteric bacteria were the most frequently isolated bacteria as shown in 55 studies (70.51%) (Table 1). Among the parasites, Ascaris spp. Entamoeba spp., hookworms and Trichiuris spp. were most frequently reported (Table 2). Among the fungi, Penicillum spp., Aspergillus spp., and Candida spp. were the most frequently reported (Table 3). Very few studies reported on viruses isolated from the house fly, most of which were experimental studies (Table 4).
Table 4
Viruses that have been isolated from house flies, including the site of isolation, the frequencies and their distribution
Virus family
Common name
Medical or veterinary importance
Geographical occurrence
Site of specimen collection
Host stage infected
Prevalence
Lab or field study
Site of isolation
References
Picornavirus
Senecavirus A
Medical/veterinary
Worldwide
Laboratory experiment
Adult
Lab
Internal organs
[65]
Filoviridae
Ebola virus
Medical
West and Central Africa
Laboratory experiment
Adult
Lab
Internal organs
[68]
Arteriviridae
Porcine reproductive and respirator syndrome virus
Veterinary
Worldwide
Piggery
Adult
Lab
Internal organs
[86]
Orthomyxoviridae
Avian Influenza virus H5N1
Veterinary
Worldwide
Laboratory experiment
Adult
Lab
Internal organs
[66]
Hytrosaviridae
Musca domestica salivary gland hypertrophy virus (MdSGHV)
Veterinary
Worldwide
Laboratory experiment
Adult
3–24%
Lab
Internal organs
[88]
Paramyxoviridae
Newcastle disease virus
Medical/veterinary
Worldwide
Laboratory experiment
Adult
Lab
Internal organs
[67]

Discussion

This systematic review revealed a total of at least 130 pathogens that have been isolated from the house fly. Bacterial pathogens were by far the most frequently reported, suggesting the house fly may play an important role as vector of bacterial diseases. Fungi were the second most frequently isolated pathogens followed by parasites, and viruses were the least frequent. The differences in the rate of isolation of these pathogens could be attributed to individual biases at the level of the study, pertaining to the method used in the isolation of the pathogens. Most of the articles reviewed used standard cultural methods for the isolation of pathogens, which may have skewed the outcome towards bacterial pathogens; more advanced methods including cell culture and PCR, which are required for the detection of viruses, are expensive and not readily available. This may explain the low number of reports on isolation of viruses from house flies.
Pathogens were more frequently isolated from the body surfaces of house flies, especially from those captured from within human habitations and animal farms. House flies habitually feed on feces, animal manure, carrion and other decaying organic matter. In the process of feeding, pathogens stick on their mouth parts, wings, legs and other body surfaces, which they carry back to human habitations and animal farms, where they live and complete their lifecycle [6]. The constant movement of the house fly back and forth from feces (or other animal waste) to food and drinking water therefore places humans and animals at risk of infection. The frequent isolation of pathogens from the body surfaces of the flies makes it plausible that when house flies transmit pathogens, they only act as mechanical vectors [2224, 26]. Unlike in biological transmission, there is no multiplication (amplification) of the pathogen in the host in mechanical transmission. However, the fly has been demonstrated to carry sufficient quantity of pathogens on its body surface, enough to cause an infection [27]. The quantity of pathogens present in the gut is usually higher than the quantity present on the body surfaces, suggesting that feces and vomitus may also serve as a major route of transmission of pathogens [28, 94].
Enteric bacteria were the most frequently isolated bacteria [224, 27, 2935, 3739]. This could be due to the fact that house flies feed mainly on feces and other animal waste, which is a rich source of enteric bacteria. Some of the bacteria isolated from house flies were highly virulent species including enteropathogenic strains such as enteroaggregative E. coli (EAEC), enterohaemorhagic E. coli (EHEC), enterotoxigenic E. coli (ETEC), and enteropathogenic E. coli (EPEC) [18, 2934], Vibrio cholera and Bacillus anthracis that cause enteric diseases, cholera and anthrax respectively. Others including Klebsiella spp., Pseudomonas, Staphylococci, Streptococci, Clostridium spp. and Enterococci to name just a few, are also important causes of diseases in humans (including nosocomial infection). Furthermore, several studies reported bacteria that were resistant to multiple antibiotics including E. coli (20,35,36), Klebsiella pneumoniae [15, 47] and Pseudomonas aeruginosa [15, 19, 48]. Most of the antibiotic resistant bacteria were isolated from flies caught in and around hospital environments and animal farms (where there is an extensive use of antibiotics as growth promoters) [15, 1720, 49, 50], suggesting that house flies may also play a role in the dissemination of antibiotic resistant bacteria to different environments [17].
Fungi species frequently isolated from the house fly belonged to the genera: Candida, Aspergillus, and Penicillium [7, 5160]. Some of these genera (including Candida and Aspergillus) contain fungi species that are important human pathogens, but most others contain fungi species that are of veterinary (e.g. Microsporum, Rhizopus, Scopularipsis and Rhodotorula) and agricultural importance (e.g. Curvalaria and Nigrospora). Furthermore, genera Epicoccum contain fungi species which are important allergens. Some species of fungi that have been isolated from the house fly were resistant to multiple antifungals, example of which includes Candida [51]. Most of the fungi that have been isolated from the house fly were reportedly isolated from the outer cuticle of the insect and rarely from internal organs, feces or vomitus.
Very few studies reported the isolation of parasites from the house fly. Among these studies, almost all the parasites described were isolated from the body surfaces of the flies. The parasites species frequently reported belonged to the genera: Ascaris, Entamoeba, Trichiuris, and the hookworms [6164]. These parasites commonly cause enteric diseases in humans and their frequent occurrence on the house fly could also be attributed to the food source of the house fly. Parasites of the genera Metastrongylus and Heamatopinus, which are known to be strict pathogens of domestic animals including pigs were also reported [54].
Reports of the isolation of viruses from wild-caught flies are very rare. However, house flies were reported to be capable of carrying a number of viruses in laboratory experiments. The majority of these viruses were of veterinary importance including the Senecavirus A whose natural hosts are pigs and cows [65]; the porcine reproductive and respiratory syndrome virus which causes a disease of pigs called porcine reproductive and respiratory syndrome (PRRS), also referred to as the blue-ear pig disease; Avian influenza virus and Newcastle disease virus which cause diseases in birds including poultry [66, 67]. In addition, one study demonstrates the ability of the house fly to carry the Ebola virus in laboratory experiments [68]. However, its role in the transmission of the virus is still to be confirmed.

Study limitations

Although this systematic review addresses a key gap in the evidence base by identifying the types and prevalence of pathogens carried by the house fly, there are some key limitations in the evidence collected. Firstly, the survival of these pathogens on the house fly and the house fly’s role in the transmission of these pathogens to humans and animals remains largely undefined. Secondly, it is unclear how representative these pathogens reported are of the wider population of pathogens that are carried by the house fly.

Future perspectives

Mechanical transmission of pathogens by arthropods including house flies is often overlooked because too much importance is given to biologically transmitted diseases such as malaria, yellow fever etc. [26]. Nevertheless, there is enough evidence to show that house flies can carry pathogens capable of causing serious diseases in humans and domestic animals, and should therefore be controlled. The control of the house fly can be achieved by physical (such as composting manure [95, 96]), chemical and biological methods. The use of chemical pesticides, which is the most common method today, is fast losing grounds due to the growing resistance by the house fly and other pests, couple to the effects they may have on non-target organisms [9799], have led to the consideration of other methods, including biological control. Biological control agents including fungi of the genera Metarhizium and Beauveria, and bacteria including Bacillus thuringiensis can be used to control the housefly [93, 97]. Furthermore, the sequencing of the genome of the house fly presents new opportunities for the identification of novel targets for controlling the housefly and also for understanding the mechanism of resistance to insecticides as well as the genetic adaptation of the house fly to high pathogen loads [69].

Conclusion

This review showed that the common house fly is a mechanical vector of a diverse range of pathogens including bacteria, fungi, viruses and parasites. However, more studies on identifying new pathogens and the survival of these pathogens are needed.

Acknowledgements

We would like to thank Health Policy Research Center (HPRC) of Shiraz University of Medical Sciences. Acknowledgments also go to Dr. Natasha Potgieter and Dr. Farhat Afrin for the kind comments.

Funding

No funding was received.

Availability of data and materials

The original research articles included in this systematic review are publicly available.
Not applicable.
Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
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Metadaten
Titel
A systematic review of human pathogens carried by the housefly (Musca domestica L.)
verfasst von
Faham Khamesipour
Kamran Bagheri Lankarani
Behnam Honarvar
Tebit Emmanuel Kwenti
Publikationsdatum
01.12.2018
Verlag
BioMed Central
Erschienen in
BMC Public Health / Ausgabe 1/2018
Elektronische ISSN: 1471-2458
DOI
https://doi.org/10.1186/s12889-018-5934-3

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