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All issues Volume 2 (2019) 4open, 2 (2019) 23 Full HTML
Open Access
Review
Issue
4open
Volume 2, 2019
Article Number 23
Number of page(s) 10
Section Life Sciences - Medicine
DOI https://doi.org/10.1051/fopen/2019016
Published online 03 July 2019

© M. Pakharukova et al., Published by EDP Sciences, 2019

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

Opisthorchis felineus (O. felineus) is a foodborne liver fluke, a member of the genus Opisthorchis, family Opisthorchiidae, order Digenea, class Trematoda, phylum Platyhelminthes, and kingdom Animalia. This liver fluke is a causative agent of opisthorchiasis felinea, a helminthiasis affecting mainly the hepatobiliary system and pancreas. Infection occurs after consumption of raw or undercooked freshwater fish infested with helminth larvae. Characteristics of the human disease are: long duration, frequent exacerbations, and possible induction of primary liver cancer [1–6].

Liver flukes O. viverrini and Clonorchis sinensis, also members of the family Opisthorchiidae, cause opisthorchiasis viverrini and clonorchiasis, the diseases that are very similar to opisthorchiasis felinea in symptomatology and pathophysiology [7–10]. Opisthorchiasis and clonorchiasis are trematodiases whose natural hot spots cover a considerable part of Europe and Asia. Nonetheless, currently, these diseases might be arbitrarily attributed to natural focal infections. Many migrants from Asia live in the non-endemic areas of opisthorchiasis and clonorchiasis, and the tourist traffic among various countries is steadily increasing. Consequently, patients with liver fluke infection can be registered far from the corresponding endemic regions [6].

The International Agency for Research on Cancer (IARC) has classified liver flukes O. viverrini and C. sinensis as Group 1 agents, i.e., the agents carcinogenic to humans [7] and as the major causative factors of cholangiocarcinoma (CCC) in endemic regions [7–9]. CCC with features of cholangiocyte differentiation is one of the main histological types of malignant tumors of biliary-tract epithelia and is a relatively rare type of liver cancer [10]. Nevertheless, over the last 15 years, its incidence has steadily increased worldwide, and nowadays, it represents the second most common type of primary liver cancer (15–20% of cases) after hepatocellular carcinoma [11]. The only available therapy for CCC is surgical resection or a liver transplant. Usually, CCC is diagnosed at advanced stages and is regarded as an incurable and lethal cancer with a poor survival rate of <24 months [12]. Both experimental and epidemiological evidence strongly implicate liver fluke infection in the etiology of CCC [13].

Opisthorchis felineus is still officially classified as a Group 3 carcinogen; this group includes factors not classified as carcinogenic to humans [7]. Meanwhile, data have been accumulating that show the carcinogenic potential of O. felineus and support its classification as a human biological carcinogen. This review summarizes the data indicating that O. felineus is an underestimated parasite, and that there is a need to revisit and revise the status of this liver fluke.

Biology

The complex life cycle of O. felineus includes the first and second intermediate hosts and one final host (Fig. 1) [14, 15]. By getting into water containing the feces of humans and animals, eggs can be eaten by aquatic, gastropod snail of the genus Bithynia. In their intestines, mobile larvae (miracidia) hatch from the eggs, penetrate through the intestinal wall into the body cavity of the mollusk, and turn into sporocysts. The latter give birth to rediae, which can then produce cercariae: free-living motile larvae that enter water, where they actively swim. The parthenogenetic phase in the life cycle of the helminth (from the stage of sporocysts to the release of cercaria) lasts ~2 months. Development is hampered by the diapause of the host during the winter period (freezing of rivers) in Western Siberia. The first cercariae appear in May of the following year. Mature cercariae are motile and begin to emerge from mollusks in bright sunny weather at a rate of up to several hundred a day [15].

thumbnail Figure 1

The life cycle of O. felineus [15]. The eggs are shed in the biliary tree, enter the intestine, and are passed with feces. They need to be ingested by freshwater gastropod Bithynia snails, the first intermediate host, to develop into sporocysts, rediae, and free-swimming cercariae: the stage infective for the second intermediate host, cyprinid fish. Humans and other fish-eating mammals and birds may serve as a definitive host after ingesting infected fish. Upon entering the host body, metacercariae infect the biliary tract of mammals, where they mature into adult worms. Pictures of cercariae and eggs are adapted from [15]; Bithynia snail, metacercaria, and adult O. felineus are original pictures.

Freshwater fish susceptible to opisthorchiid infestation are Cyprinidae species: ide Leuciscus idus, dace L. leuciscus, roach Rutilus rutilus, and sunbleak Leucaspius delineatus [14, 15]. When fish and cercariae encounter each other, cercariae attach to them, discard the tail and penetrate through the skin into the muscles, where they form the inner membrane, then the outer connective tissue capsule, and turn into the next stage, the metacercariae. After 3–4 weeks, metacercariae become invasive and can infect definitive hosts: domestic fish-eating animals (cats, dogs, and pigs), wild carnivores (muskrats, water voles, foxes, bears, and wolves), and humans [14–23]. In the acidic content of the definitive host’s stomach, the membrane of the metacercaria is destroyed, and the juveniles migrate along the bile ducts to the liver and gall bladder, where after 25–30 days, the helminth reaches maturation [14, 15].

The human infection is most likely due to the consumption of undercooked fish, because sun-dried, lightly salted, and lightly pickled fish are traditional beer snacks (Fig. 2). Furthermore, in the Northern regions of Western Siberia, eating of frozen ribbons of fresh-water whitefish served with spices, so-called stroganina, is a popular tradition [1, 23].

thumbnail Figure 2

The Maloe lake tributary of the Ob River (Novosibirsk city) and intermediate host for the liver fluke Opisthorchis felineus. (A) Maloe lake. (B) Backwater of Maloe lake, a habitat of Bithynia snails. (C) Fresh ides (L. idus) on ice at a market.

Many authors have demonstrated the presence of metacercariae and adult O. felineus worms in the wild. The complete life cycle of O. felineus, however, has been demonstrated only by Fedorov, and he has also provided the data about the structure and timing of the development of larval forms [15]. It has been reported that red foxes Vulpes vulpes L. play a certain role in keeping up the natural hot spots of opisthorchiasis in Europe, caused by the trematode O. felineus [16–21]. The natural host for O. felineus in Russia is thought to be the muskrat Ondatra zibethicus [15], which was introduced in early 1920s. In Western Siberia, the role of muskrats is the primary contribution to the natural causes of the diseases induced by many opisthorchiids like O. felineus, O. longissimus, and Metorchis bilis [15]. The muskrat leads a semiaquatic lifestyle and settles along the banks of rivers, lakes, and freshwater marshes. It prefers shallow (1–2 m deep), ponds that do not freeze, with banks that are covered with dense grass [15].

Epidemiology

The trematode O. felineus is an epidemiologically important liver fluke. This causative agent of opisthorchiasis has been detected for some 150 years in cats, dogs, foxes, wild bears, and other animals (the definitive hosts) as well as mollusks and carps (intermediate hosts) in Western and Eastern Europe (Russia, Ukraine, Belorussia, Spain, Portugal, Germany, and Italy) [14, 24, 25]. All these data indicate the breadth of the geographical range of opisthorchiasis and the undoubted participation of animals in the circulation of the pathogen within this area, whereas the human opisthorchiasis has a disjointed local (focal) character. The greatest importance of humans in the circulation of infection is seen in Western Siberia, namely in the Ob–Irtysh basin, as evidenced by the high prevalence of infection in this population (up to 60% in some rural regions). Thus, most likely, in this region, the participation of humans in the maintenance of the infection is almost certain. Toward the periphery of the basin up to the Arctic Ocean, the percentage of the population living in the area drops to less than one person per square kilometer. Nevertheless, prevalence of the infection among sensitive fish species in this region is almost maximal when compared with other territories and can be up to 100% (ide). Consequently, the infection circulation becomes more zoonotic in the wild (mainly with participation of domestic and wild animals).

In accordance with the Russian clinical standards, diagnosis of opisthorchiasis is based on the microscopic detection of eggs in stool and/or eggs and adult helminths in bile samples after duodenal intubation [26]. The average opisthorchiasis incidence in Russia between 1991 and 1993 and 2011–2013 was relatively constant (26.5–24.7 cases per 100 000 people per year). The incidence of opisthorchiasis in Russia is unevenly distributed across regions. Accordingly, there are hyper-endemic areas (with prevalence rates > 100 per 100 000 people), regions with high prevalence (53–100), regions with average prevalence (22–52), and those with low frequency of the disease (<22). The Ob–Irtysh basin in Western Siberia is regarded as a hyper-endemic area. In this region, opisthorchiasis prevalence rates exceed 100 per 100 000 people [1]: Khanty-Mansiiskiy Autonomous Region (600 per 100 000 people), Tyumen Region (201 per 100 000 people), Tomsk Region (189 per 100 000 people), and Novosibirsk Region (127 per 100 000 people). In most regions of Russia, Eastern Siberia, and the Far East, only low prevalence is reported (2.5 per 100 000 population; reviewed in [1]).

On the other hand, short-term screening programs in some rural regions in this area have revealed that the actual frequency of O. felineus infection is much higher [5, 27]. In particular, the prevalence rate in the Tomsk Region has been found to be 18–20% [27]; Tyumen oblast, 37%; and Chelyabinsk oblast, 18.6%. According to autopsy data, 18.3–45.0% of individuals have been found to be infected with opisthorchiasis [5, 28, 29].

The carcinogenic potential of O. felineus

1. Experimental evidence

Today, carcinogenesis is thought to be triggered by chronic inflammation and changes in the cellular microenvironment that result in a precancerous state and mutations, which lead to the cell proliferation and malignancy [30]. In subsequent sections of this paper, we present experimental data on the histopathology of opisthorchiasis felinea in hamster liver and O. felineus metabolites that can cause mutations in the chromosomal deoxyribonucleic acid (DNA) of host cells. A comparative study of opisthorchiasis felinea and viverrini in a hamster model suggests that the histopathology of O. felineus infection involves bile duct dysplasia, periductal fibrosis, and inflammatory infiltration and could be considered to be more severe than that of O. viverrini infection [31].

The main histopathological features of O. felineus infection in rodents are extensive periductal fibrosis, chronic inflammation, proliferation of the bile duct, bile duct dysplasia, egg granulomas, and biliary intraepithelial neoplasia (BilIN), with grades of 1–3. BilIN is a precursor lesion of invasive adenocarcinoma in the biliary tract [32–34], and represents a multistep process in carcinogenesis. Biliary intraepithelial neoplasia with grade 1 (BilIN-1) and biliary intraepithelial neoplasia with grade 2 (BilIN-2) lesions have been demonstrated in O. felineus-infected hamsters. The totality of biochemical and histopathological changes indicates that O. felineus infection in this rodent model induces precancerous lesions conducive to the development of a malignant tumor.

Opisthorchis felineus infection results in CCC in experimental animals if it is accompanied by a chemical carcinogen (e.g., diethylnitrosamine or dimethylnitrosamine). It has been shown that histopathological features of CCC appear in the liver of the hamsters at 18 weeks post-infection [35]. In one study, after 26 weeks, in three of six hamsters, a mass-forming CCC was found, and after 30 weeks postinfection, CCC was detected in all the hamsters [35].

The accumulated data on histopathology in mammals suggest that the carcinogenic potential of O. felineus in an experimental model is very similar to the carcinogenicity of O. viverrini and C. sinensis [31, 35]. The three species of epidemiologically important opisthorchiids are closely related to one another in terms of the phenotype of adults, the habitats of different life stages, and the genetics. The liver fluke infections have similar characteristics of the pathogenesis (i.e., mechanism). In addition, the ability to secrete proteins and oxysterol metabolites is also characteristic for liver flukes including O. felineus.

The pathogenesis of CCC resulting from the infection with liver flukes is unknown [13, 36]. Nevertheless, it can be assumed that several important factors are involved. In particular, one of the most important factors is mechanical damage to the wall of the bile duct from suckers of the helminths. When the tissue is damaged, a cascade of immunological reactions is launched both against the destroyed cells and against the helminth antigens and eggs.

Another important factor determining the parasite–host interaction, which probably makes a significant contribution to epithelial neoplasia, is helminth secretory products, consisting of a large number of proteins that induce cell proliferation and inhibit apoptosis [36–38]. Such an effect on the proliferation of epithelial cells of the bile ducts has been demonstrated for O. viverrini granulin-1 [36]. The results of CRISPR/Cas9 genome editing of O. viverrini granulin-1 proved the suggestion about its role in the hepatobiliary morbidity of liver fluke infection [37]. Moreover, for another O. viverrini protein, thioredoxin peroxidase (TpX), an immunomodulatory effect has been demonstrated [36]. Particularly, thioredoxin peroxidase can inhibit T helper 1 (Th1)-type of immune response and activate the Th2 type. A remarkable influence on the host–parasite interplay has also been demonstrated for a defense molecule of Fasciola hepatica helminth. This protein inhibits antigen presentation by macrophages due to its affinity for the membrane of host macrophages [39].

The liver fluke excretory-secretory products (ESPs) stimulate chronic inflammation and proliferation of the bile duct epithelium. Proteomic mass spectrometry of the proteins in O. felineus ESPs has identified 37 proteins [40]. Some of O. felineus ESPs are highly immunogenic [41, 42], homologs of host defense molecule (HDM), TpX, and glutathione-S-transferase (GST) have been found in O. felineus ESPs [40]. Moreover, O. felineus ESPs may interact with the epithelium and may accumulate inside the cells because they are found in the gallbladder of the hamsters with experimental opisthorchiasis and patients with the infection [41, 42].

In addition, it can be assumed that the specific low-molecular-weight cholesterol metabolites, which are also found in the helminth secretory product, apparently have oxidative and genotoxic properties, i.e., can damage the DNA of host cells [13, 32]. Such low-molecular-weight metabolites (catechol estrogens and oxysterols) in other species of helminths have been demonstrated, some of which are associated with cancer initiation and are recognized as biological carcinogens. In particular, the trematodes O. viverrini, O. felineus, and S. haematobium produce specific oxysterols and catechol estrogens. Oxysterol-like metabolites in the egg and adult worms, and in bile, serum, and urine of O. felineus-infected hamsters have been detected by liquid chromatography with mass spectroscopy [32]. Related DNA adducts suggest that infection-associated oxysterols induce chromosomal lesions in host cells [13]. Associations between oxysterols and the initiation and progression of cancer of the colon, lungs, breast, and bile ducts have been proposed [43, 44].

The origin of these metabolites is unknown. It can be assumed that there are two pathways for their synthesis: enzymatic and nonenzymatic. The nonenzymatic pathway is the reaction with the free oxygen and nitrogen species [45]. The enzymatic pathway is the result of the liver fluke xenobiotic metabolism network activity [46, 47].

It is generally accepted that CCC tumors in this hamster model occur as a result of a combined action of infection with the liver flukes, O. felineus, O. viverrini, or C. sinensis and exposure to N-nitrosodimethylamine [35]. In contrast, a series of studies on the pathogenesis of opisthorchiasis felinea has revealed enhanced expression of p53, and the presence of intraepithelial bile duct neoplasia [32, 35]. Recent studies have also shown that epithelial-to-mesenchymal transition (EMT) is involved in chronic opisthorchiasis in rodents. At 22 weeks of chronic opisthorchiasis in hamsters, processes of EMT intensify in the liver [48]. The increased expression of markers of the SMAD signaling pathway and enhanced accumulation of α-smooth muscle actin (α-SMA) protein have been shown by immunohistochemistry. The elevated messenger ribonucleic acid (mRNA) expression of transforming growth factor beta 1 (Tgfb1), annexin A1 (Anxa1), exostosin glycosyltransferase 1 (Ext1), and keratin 7 (Krt7) genes has been demonstrated in the liver of O. felineus-infected hamsters [48]. Taken together, these data indicate that precancerous changes can occur in hamsters without exposure to an exogenous carcinogen such as N-nitrosodimethylamine (NDMA). These processes cause damage to genetic material, with the mutations being fixed during DNA replication. Eventually, accumulation of mutations might lead to malignant transformation of cholangiocytes and progression to CCC [13].

1. The link between O. felineus infection and CCC in humans

The most important step in the validation of results obtained in a study on the carcinogenic potential of O. felineus in an experimental model is analysis of the association of opisthorchiasis felinea and CCC in humans. Given that there are no systemic epidemiological and clinical programs for the control of opisthorchiasis in Russia, the solution to this problem remains difficult. Undoubtedly, the similarity in clinical manifestations, the disorders caused by O. felineus and O. viverrini [28, 29], and the data on the pathogenesis of these two helminthiases acquired in experimental opisthorchiasis models [1, 31, 32, 34] are suggestive of a rather high probability of O. felineus involvement in the induction of these tumors. Here, we briefly discuss the data published in the Russian medical literature on the complications associated with opisthorchiasis as well as the data from hospitals and morgues on autopsy results over a long period. Unfortunately, the data on liver cancer prevalence have certain drawbacks, in particular, the performed examinations and criteria for selection of control groups are insufficiently detailed. Nonetheless, in the absence of other epidemiological data, the number of cases recorded in hospitals during a given period is also valuable information, of course, with a disclaimer that this is simple recording of the number of cases rather than full-fledged epidemiological studies.

In general, it is reported that the incidence of malignant tumors, in particular, primary liver cancer is significantly higher in regions with high prevalence of opisthorchiasis. In a number of regions of Western Siberia in the period 1962–1971, the prevalence of primary liver cancer was 9.4 cases per 100 000 people [49, 50] (reviewed in [7]). In the period 1990–2001, liver cancer ranked seventh among the most common cancers registered in the Tomsk region (3.9%). The prevalence of this type of cancer in men in this period was 11.2 cases per 100 000 people [51]. This is almost 2.5-fold more than the average prevalence rate of liver cancer in the Russian Federation in 2012, according to the official statistics [51, 52]. For comparison, in Moscow and Moscow region (non-endemic areas of opisthorchiasis) the prevalence of primary liver cancer was 1.77 and 2.3 cases per 100 000 people, respectively [53]. The incidence of primary liver cancer in these regions is not correlated with alcohol consumption, in particular Moscow region was in the top three for the consumption of strong alcoholic drinks (2016–2017), whereas Tomsk and Tyumen regions (hyper-endemic) were with low or moderate scores [54].

In the Russian medical literature, there is information indicating a link between O. felineus infection and liver cancer in the population of Western Siberia. Thus, during analysis of the results of more than 2250 autopsies conducted during 37 years in the city morgue of Tobolsk, it was found that in 45% of the cases, infection with opisthorchiasis was present. Primary liver cancer has been diagnosed in 8.7% of the infected patients [55]. According to the Tomsk City Morgue, among persons with a confirmed diagnosis of chronic opisthorchiasis [~350 autopsies], CCC cases have been registered in 5% of the group [28, 29]. Furthermore, according to the information from the Tomsk Hepatology Center, ~3% of patients with chronic opisthorchiasis have been operated on for biliary tract cancer and pancreatic cancer [29].

An interesting study has been conducted in another region of Western Siberia: the Tyumen region. There, the prevalence rates of various types of liver cancer in opisthorchiasis-positive (target group) and negative individuals (control group) were determined. It was established that CCC is most common in opisthorchiasis: according to the results of histological analysis in the target group, this diagnosis was made in 77% of the cases. Hepatocellular carcinoma (HCC) in the same group of patients was detected in 19% of cases, and 4% of patients had other types of malignant liver tumors. In the control group, CCC occurred in 34% of patients, hepatocellular carcinoma in 56% of cases, and other liver tumors in 10% [49].

In agreement with these results, the data obtained in the Tyumen region – after autopsies of 44 individuals with confirmed primary liver cancer – have revealed that CCC was present in almost 80% of cases. It is important to note that O. felineus infection was confirmed in 42 of 44 cases in that study (reviewed in [7, 56]). Thus, in endemic regions, malignant tumors of the biliary tract are some of the most common types of liver cancer. It is noteworthy that in the presence of O. felineus infection, the prevalence of CCC exceeds that of other types of liver cancer by the factor of four (or by 400%). Recently, two cases of CCC associated with chronic opisthorchiasis were reported. Both cases presented with nonspecific symptoms and severe pathological complications. Both patients were living in endemic areas [26].

In non-endemic areas of opisthorchiasis in Russia, the proportion of CCC does not exceed 15% of all cases of liver cancer. For example, according to generalized data accumulated at the Blokhin Russian Cancer Research Center (Moscow), CCC is responsible for 14.9%, and hepatocellular cancer for 85.1% of liver cancer cases [57]. In general, data on the prevalence of CCC in the endemic and non-endemic regions well match the general epidemiology of this type of cancer in other endemic and non-endemic regions of the world [9, 58].

Prevention

Prevention of opisthorchiasis is based primarily on the inactivation of O. felineus larvae in the fish by proper cooking, the disease diagnostics, and effective treatment of the patients. Preventive measures include (i) protection of reservoirs from eggs of the parasite, (ii) the inactivation of metacercariae in relevant species of fish, and (iii) sanitation/educational programs for the population.

In Russia, where the rate of infection with opisthorchiids among fish is high, standards have been developed to combat the contamination of fish by larvae of epidemiologically important liver flukes including O. felineus, M. bilis, and C. sinensis [59]. These standards stipulate first and foremost salting, freezing, and heat treatment. Salting should be done by means of sufficient amounts of salt at a temperature of 1–20 °C, when the mass fraction of salt in fish is 14%. Duration of salting should be 10 days for bleak Alburnus alburnus, gudgeon Gobio gobio, minnow Phoxinus percnurus, and sunbleak Leucaspius delineatus; 21 days for roach R. rutilus, dace L. leuciscus, common rudd Scardinius erythrophthalmus, small common bream Abramis brama, and ide Leuciscus idus; and 40 days for large common bream and ide [60].

Standards provide for the resistance of the metacercariae to low temperatures. Fish should be frozen under the following conditions: −40 °C for 7 h; −35 °C for 14 h; −28 °C for 32 h [58]. Hot and cold smoking, dry curing, and drying performed properly according to the official standards disinfect all kinds of fish except ide. Unfortunately, metacercariae inactivation measures are difficult to use when fish is processed at home. Thus, it is almost impossible to provide the necessary conditions for freezing in home refrigerators [61]. Traditional drying of fish and cold smoking do not inactivate parasite larvae [62]. Modern methods have been developed to inactivate the larvae, for example, the high efficiency of the use of microwave ovens in the disinfection of large fish has been demonstrated as compared with other methods [63].

It should be noted that in terms of control of opisthorchiasis, educational programs for the population of Western Siberia are not being actively pursued [64]. Thus, a significant part of the population of the north Tyumen region thinks that raw fish is healthy food (32% of the surveyed population) and less than a half of the population know about liver fluke infections (45.9% of the population). The infection prevalence of the population in this region is ~40%. It is noteworthy that newcomers also get rapidly infected: in the first year after arrival: 2%, within five years: 10%, and within 10 years, 25% of newcomers become infected. During the first year after arrival, only 8% of newcomers consider raw fish a healthy food, but after 5–10 years, their number significantly increases and constitutes 17%. These data point to successful adaptation of the settlers to the peculiarities of local nutrition and their eating habits in the aboriginal style.

Only 39% of healthcare professionals in the region know how to use the technology of pickling, which guarantees disinfection of fish. It should be noted that drying in this region is one of the most common ways of processing of fish. Only 9% of physicians, 27% of epidemiologists, and 11.5% of other medical professionals in the region have mastery of the proper fish drying technology that guarantees decontamination [64]. Accordingly, the level of knowledge about the invasion of fish by opisthorchiids and about the dangers of contamination is low even among people with medical education in this region. Apparently, all these factors in combination lead to the high prevalence of infection with opisthorchiids in this region.

Conclusion

The carcinogenic potential of the trematode O. felineus appears to be poorly studied as compared to that of closely related liver flukes O. viverrini and C. sinensis. Nevertheless, O. felineus habitat covers vast areas in Europe and Asia, and opisthorchiasis outbreaks caused by this helminth are expectable in many countries. Thus, the opisthorchiasis caused by O. felineus becomes a large-scale problem, outside the scope of health care and public health measures in individual regions.

Opisthorchiasis is a common human helminthiasis in Russia. In Thailand and Korea, the consumption of raw fish is traditionally widespread; in Russia, the tradition of eating raw fish is not as popular as eating sun-dried and lightly salted fish, which are apparently infected with metacercaria of the parasite. In contrast to Thailand (the endemic area for O. viverrini), where CCC is a predominant type of cancer, primary liver cancer is not the leading cancer type in Russia. There are probably some additional factors that lead to carcinogenesis in humans. Apparently, one of the key factors, as shown by experiments on model animals, is the presence of weak carcinogens in food, such as nitrosamines, which act as initiators of carcinogenesis. Hence, this chronic infection is expected to promote the initiation of biliary cancers. There are some other factors that are relative risks and cofactors for CCC formation. In Thailand and the Republic of Korea, the highest relative risk has been adjusted for alcohol consumption, smoking, and physiological characteristics such as sex and age [7]. These factors should be taken into consideration in the areas endemic for opisthorchiasis felinea as well.

To date, the IARC has classified O. felineus infection as a Group 3 carcinogen, i.e. there is insufficient evidence yet for its classification as carcinogenic, unlike the situation with the closely related liver flukes O. viverrini and C. sinensis, and the blood fluke S. haematobium which are group 1 carcinogens: definitely carcinogenic to humans. For IARC approval O. felineus as Group 1 carcinogen, carcinogenic activity should be demonstrated in animal and human studies.

The accumulated data on the histopathology in animal models show that the carcinogenic activity of O. felineus in an experimental model is very similar to the carcinogenicity of O. viverrini and C. sinensis. All species of epidemiologically important opisthorchiids are similar to one another in terms of the phenotype of adults, the habitats of different life stages, and the genetics. The liver fluke infections share nearly the same pathogenesis and host liver histopathology. In addition, the ability to secrete proteins and oxysterol metabolites is characteristic of liver flukes including O. felineus.

Large-scale studies on the association of opisthorchiasis felinea with CCC in humans have not been conducted, but such information might be found at least partly in the published literature and in hospital records. The consolidated data show that the prevalence of primary liver cancer in Western Siberian regions, the world’s largest endemic area of opisthorchiasis felinea, is considerably higher as compared with the non-endemic regions. Nevertheless, the presented data were obtained by separate groups of researchers and cannot present a comprehensive picture of the association of opisthorchiasis and liver cancer. This task requires large-scale epidemiological studies that take advantage of the expertise gained in similar studies in other countries [9].

thumbnail Figure 3

Biliary histological features in the liver biopsies from hamsters with the experimental opisthorchiasis felinea. (A) Intact animal. (B) High-grade biliary neoplasia caused by O. felineus three months p.i. (C) Cholangiocarcinoma in the liver of hamster as a result of a combined action of O. felineus and dimethylnitrosoamine, three months p.i. BD, bile duct; OF, O. felineus; CCC, cholangiocarcinoma. High-grade biliary neoplasia is indicated with arrows. Pictures 3A and 3C were kindly provided by Maksimova GA.

Abbreviations used in the text and figures

α-SMA: α-smooth muscle actin

Anxa1: Annexin A1

BD: Bile duct

BilIN-1: Biliary intraepithelial neoplasia with grade 1

BilIN-2: Biliary intraepithelial neoplasia with grade 2

CCC: Cholangiocarcinoma

DNA: Deoxyribonucleic acid

EMT: Epithelial-to-mesenchymal transition

ESPs: Excretory-secretory products

Ext1: Exostosin glycosyltransferase 1

GST: Glutathione-S-transferase

HCC: Hepatocellular carcinoma

HDM: Host defense molecule

IARC: International Agency for Research on Cancer

Krt7: Keratin 7

mRNA: Messenger ribonucleic acid

NDMA: N-nitrosodimethylamine

OF: O. felineus

p.i.: Postinfection

Tgfb1: Transforming growth factor beta 1

TpX: Thioredoxin peroxidase

Acknowledgments

Figure 3A and BC were kindly provided by Galina A Maksimova (ICG SB RAS, Novosibirsk, Russia). Authors acknowledge the support of members of the TOPIC [Tomsk OPIsthorchiasis Consortium]. The English language was corrected and certified by shevchuk-editing.com.

Funding

This work was supported financially by the Russian Foundation for Basic Research, https://www.rfbr.ru/rffi/eng [No. 18-04-00417A [VAM] and the state project of the Institute of Cytology and Genetics, the Siberian Branch of the Russian Academy of Sciences [project No. 0324-2019-0041] (MYP, VAM). The sponsor had no role in this study such as study design, data collection, or decision to publish.

Conflict of interest

The authors declare that they have no competing interests.

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Cite this article as: Pakharukova MY, Correia da Costa JM & Mordvinov VA, 2019. The liver fluke Opisthorchis felineus as a group III or group I carcinogen. 4open, 2, 23.

All Figures

thumbnail Figure 1

The life cycle of O. felineus [15]. The eggs are shed in the biliary tree, enter the intestine, and are passed with feces. They need to be ingested by freshwater gastropod Bithynia snails, the first intermediate host, to develop into sporocysts, rediae, and free-swimming cercariae: the stage infective for the second intermediate host, cyprinid fish. Humans and other fish-eating mammals and birds may serve as a definitive host after ingesting infected fish. Upon entering the host body, metacercariae infect the biliary tract of mammals, where they mature into adult worms. Pictures of cercariae and eggs are adapted from [15]; Bithynia snail, metacercaria, and adult O. felineus are original pictures.
In the text
thumbnail Figure 2

The Maloe lake tributary of the Ob River (Novosibirsk city) and intermediate host for the liver fluke Opisthorchis felineus. (A) Maloe lake. (B) Backwater of Maloe lake, a habitat of Bithynia snails. (C) Fresh ides (L. idus) on ice at a market.
In the text
thumbnail Figure 3

Biliary histological features in the liver biopsies from hamsters with the experimental opisthorchiasis felinea. (A) Intact animal. (B) High-grade biliary neoplasia caused by O. felineus three months p.i. (C) Cholangiocarcinoma in the liver of hamster as a result of a combined action of O. felineus and dimethylnitrosoamine, three months p.i. BD, bile duct; OF, O. felineus; CCC, cholangiocarcinoma. High-grade biliary neoplasia is indicated with arrows. Pictures 3A and 3C were kindly provided by Maksimova GA.
In the text

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