Zoonotic Helminthiases in Rodents (Bandicota indica, Bandicota savilei, and Leopoldamys edwardsi) from Vientiane Capital, Lao PDR

Phaviny Sithay Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand;

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Thaksaporn Thongseesuksai Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand;

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Somphonephet Chanthavong Department of Medical Laboratory, Faculty of Medical Technology, University of Health Sciences, Vientiane, Lao PDR;

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Onekham Savongsy Department of Medical Laboratory, Faculty of Medical Technology, University of Health Sciences, Vientiane, Lao PDR;

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Naly Khaminsou Department of Medical Laboratory, Faculty of Medical Technology, University of Health Sciences, Vientiane, Lao PDR;

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Thidarut Boonmars Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand;
Neglected, Zoonosis and Vector-Borne Disease Research Group, Khon Kaen University, Khon Kaen, Thailand

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Porntip Laummaunwai Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand;
Neglected, Zoonosis and Vector-Borne Disease Research Group, Khon Kaen University, Khon Kaen, Thailand

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ABSTRACT

Zoonotic helminths of three rodent species, Bandicota indiaca, Bandicota savilei, and Leopoldamys edwardsi, were investigated in Vientiane capital, Lao PDR. A total of 310 rodents were infected with 11 species of helminth parasites. There were 168 (54.2%) of 310 rodents infected with zoonotic helminths. From our results, there are six recorded zoonotic helminth species, and the highest prevalence was exhibited by Raillietina sp. (30.7%), followed by Hymenolepis diminuta (17.7%), Hymenolepis nana (2.6%), Echinostoma ilocanum (1.9%), Echinostoma malayanum (1.3%), and Angiostrongylus cantonensis (1%). This is the first study of zoonotic helminths in L. edwardsi and the first report of H. diminuta, H. nana, E. ilocanum, and E. malayanum in Bandicota indica and B. savilei, and the first demonstration of A. cantonenensis in B. indica in Lao PDR. From our results, these three rodents are potentially important reservoir hosts of zoonotic helminths. Thus, effective control programs should be considered for implementation to prevent the transmission of these zoonoses in this area.

INTRODUCTION

Zoonotic helminth parasites are considered as neglected diseases by the WHO.1 Although most helminths cause mild symptoms in healthy people, however, the level of severity can increase in cases of immunocompromised and immunosuppressive individuals.2,3 In addition, schoolchildren harbor some of the most intense helminthic infections that significantly impair physical, nutritional, cognitive, and intellectual development.1 Rodents are known as the important reservoir hosts of zoonosis parasites, including helminths.4,5 Helminths in rodents that have been reported to cause human infections in Southeast Asia and the Pacific region include echinostome, Hymenolepis nana, Trichinella spiralis, Hymenolepis diminuta, Raillietina sp., and Angiostrongylus cantonensis.6,7 There are more than 200 species of murid rodents that have been reported in Southeast Asia.7–10 Although there have been several reports of helminth infections in rodents from other parts in Southeast Asia,11–18 studies from Lao PDR are limited. To our knowledge, only one publication has been reported on the helminth fauna of rodents in Lao PDR, Luang Prabang, and Champasak Province.19 They reported four zoonotic helminths (Raillietina sp., H. diminuta, H. nana, and Echinostoma malayanum) in 12 rodent species, and only small number of Bandicota indica (3) and Bandicota savilei (17) were investigated. They found only Raillietina sp., in these two species, whereas the previous studies had reported more than one zoonotic helminth species.20,21 In addition, they have no study about zoonotic helminths in Leopaldamys edwardsi. This rodent was also reported to be the reservoir host of zoonotic helminths.20,21 These three rodent species are commonly hunted for food in Southeast Asia, including in Lao PDR.22,23

Thus, the aim of this study was to investigate the zoonotic helminths in three rodent species, B. indica, B. savilei, and L. edwardsi, from Vientiane Capital in Lao PDR, where there have not been studied until now. As we mentioned earlier, these three rodents are commonly hunted for food. Therefore, we can increase the number of the target rodents by collecting them from the local markets in Vientiane Capital, Lao PDR. The results in this study can fill the gap in the knowledge of the role of these rodents as reservoirs of zoonotic helminthiases in Lao PDR, and might help for the development of control program.

MATERIALS AND METHODS

Rodents’ collection and examination for helminths.

In mid-February to mid-April 2020, rodents were collected from three markets (Koudsambath, Nagna, and Dongmarkkhay markets) in Vientiane Capital, Lao PDR (Figure 1). They were hunted and sold for food. Rodent species were identified using morphological criteria.24 Rodents were examined following international standards (the American Veterinary Medical Association Council on Research). The study was approved by the Ministry of Health National Ethics Committee for Health Research, Lao PDR (No. 05/NECHR). The collected helminths were preserved in 70% alcohol, and the recovered helminths were identified using the general helminth identification keys and the specific literature on each helminth.25–28 The parasitological descriptors such as prevalence, mean intensity, and mean abundance were reported as quantitative parameters. The relationship between rodent species and helminth infection was analyzed by chi-squared test. For the potential zoonotic species, we searched from previous human case reports and relevant research publications.

Figure 1.
Figure 1.

Study area is Vientiane capital, Lao PDR.

Citation: The American Journal of Tropical Medicine and Hygiene 103, 6; 10.4269/ajtmh.20-0778

RESULTS

A total of 310 rodents belonging to Bandicota indiaca (97), B. savilei (32), and L. edwardsi (181) were examined for helminth infections. Among them, 233 were infected by 11 helminth species, giving an overall prevalence of 75.2%. The highest prevalence of helminth infection was exhibited by L. edwardsi (85.1%), followed by B. indiaca (68%) and B. savilei (40.6%). The rodent of L. edwardsi showed statistically significant helminth infection compared with the two other investigated rodent species (P < 0.05). In the present study, we have focus only on zoonotic helminth. Therefore, not all helminths were identified to the species level, and the total prevalence for zoonotic helminths was 54.2% (168 parasitized rodents). From our results, there were six zoonotic helminths found, H. nana, H. diminuta, Raillietina sp., A. cantonensis, E. malayanum, and Echinostoma ilocanum. The highest number of zoonotic helminths was found in B. indica (six species of zoonotic helminths). The highest prevalence of zoonotic helminths was exhibited by Raillietina sp. (30.6%) followed by H. diminuta (17.7%), H. nana (2.6%), E. ilocanum (1.9%), E. malayanum (1.3%), and A. cantonensis (1%). Apart from zoonotic helminths, the other non-zoonotic helminths are Trichostrongylidae, Heterakis sp., Globocephalus sp., Physaloptera sp., and Trichuris muris. The results are shown in Table 1.

Table 1

Site of infection, prevalence (%), MA, MI, and range of intestinal helminth species in each rodent species from Vientiane capital, Lao PDR

Rodents (n)Helminth speciesSite of infectionPrevalence (%)MAMIRange
Bandicota indica (97)*H. nanaSI2.10.0420–2
*Raillietina sp.SI32.982.086.310–81
*H. diminutaSI13.40.5440–17
*E. malayanumSI2.10.031.50–2
*E. ilocanumSI4.10.0820–4
TrichostrongylidaeSI9.270.434.670–11
Heterakis sp.LI2.10.1470–11
T. murisLI3.090.165.330–7
*Angiostrongylus cantonensisL3.10.0930–4
Physaloptera sp.S4.120.3380–2
Bandicota savilei (32)*E. ilocanumSI6.250.2540–3
*E. malayanumSI6.70.0610–1
*H. diminutaSI200.3720–3
*H. nanaSI6.30.1320–2
T. murisLI6.30.1320–2
*Raillietina sp.SI15.61.0970–7
TrichostrongylidaeSI12.51.1390–11
Leopoldamys edwardsi (181)*H. diminutaSI19.884.0120.140–172
*Raillietina sp.SI26.520.692.600–21
TrichostrongylidaeSI13.262.5519.210–112
Heterakis sp.LI9.940.181.830–4
*H. nanaSI2.210.104.50–6
Globocephalus sp.SI1.00.13120–5
Physaloptera sp.S2.210.083.750–4

E. ilocanum =Echinostoma ilocanum; E. malayanum = Echinostoma malayanum; H. diminuta = Hymenolepis diminuta; H. nana = Hymenolepis nana; MA = mean abundance; MI = mean intensity; n = number of rodents examined; L = lung; LI = large intestine; S = stomach; SI = small intestine; * = zoonotic helminth.

DISCUSSION

The present study showed the high overall of prevalence (54.2%) of zoonotic helminth infections in three species of investigated rodents, B. indica, B. savilei, and L. edwardsi. To our knowledge, this is the second study to investigate helminth infections in rodents in Lao PDR. The previous study had constructed in Luang Prabang and Champasak Province.19 Consequently, this is the first report of helminth infections in L. edwardsi in Lao PDR. In this study, we found 6 helminth species that potentially infect humans: H. nana, H. diminuta, E. ilocanum, E. malayanum, A. cantonensis, and Raillietina sp.

Hymenolepis diminuta (rat tapeworm) and H. nana (dwarf tapeworm) have been reported in humans worldwide.29,30 Humans acquire it by accidentally eating food that is contaminated with the cysticercoid-infected arthropods, such as fleas and beetles.31,32 They are particularly common in children.30,33 Generally, light infection with H. diminuta and H. nana is asymptomatic, whereas heavy infection with these species can cause dizziness, anorexia, weakness, pruritus, abdominal distress, and diarrhea.34,35 In addition, H. nana can cause autoinfection because this worm can directly complete its life cycle without development in any intermediate host. Humans become infected by eating egg-contaminated food. Rodent species have been reported as reservoirs of H. diminuta: B. indica, B. savilei, Berylmys berdmorei, L. edwardsi, Maxomys rajah, Mus caroli, Mus cookii, Rattus andamanensis, and Rattus tanezumi,21,36,37 and reservoirs of H. nana: Hapalomys delacouri, B. indica, B. savilei, M. caroli, Mus cervicolor, M. cookii, Niviventer fulvescens, R. andamanensis, Rattus annandalei, Rattus exulans, Rattus norvegicus, R. tanezumi, and Rattus tiomanicus.19,20,37

Raillietina spp. have been reported in human cases in Thailand, China, and Japan.38,39 Humans are infected by ingesting cysticercoid-contaminated intermediate hosts, such as beetles, ants, and cockroaches. Most cases of human infection are asymptomatic. Rodent species were reported as reservoirs of Raillietina spp.: B. indica, B. savilei, Berylmys bowersi, L. edwardsi, Maxomys surifer, M. caroli, M. cervicolor, M. cookii, Niviventer cremoriventer, N. fulvescens, Rattus losea, R. norvegicus, Rattus rattus, and R. tanezumi.19,20,40

Echinostoma malayanum and E. ilocanum, intestinal flukes, have been found in mammals and birds.41,42 They require two intermediate hosts to complete the life cycle. For E. malayanum, the first intermediate hosts are freshwater snails: Lymnaea, Indoplanorbis, etc., and the second intermediate hosts are aquatic organisms such as tadpoles, frogs, and freshwater snails. For E. ilocanum, the first intermediate hosts are Gyraulus and Hippeutis, and the second intermediate hosts are Lymnaea, Viviparous, Thiara, Planorbis, and Pila. Humans become infectious by eating metacercaria-infected second intermediate host. Clinical symptoms are usually caused by heavy infection.43 Pathology varies depending on infecting species; heavy infection with E. malayanum caused anemia, and intestinal perforation has been reported.43 Rodents that act as reservoir hosts of E. malayanum are Rattus jalorensis, R. exulans, R. norvegicus, R. rattus, and R. rattus diardii,40,44 and B. savilei.45 Rodent species that have been reported as reservoir host of E. ilocanum are Rattus mindanensis mindanensis, R. rattus, and R. norvegicus.40,44,46

Angiostrongylus cantonensis, a rat lungworm, can cause eosinophilic meningitis in humans.47,48 Humans acquire the infection by eating undercooked snails, for example, Achatina fulica, Pila, and Pomacea,49 or slugs, which are infected with larvae of the parasite. This worm has been reported in rat species, R. exulans, R. rattus, and B. indica.50,51

In the present study, non-zoonotic helminths, Trichostrongylidae, Heterakis sp., Globocephalus sp., Physaloptera sp., and T. muris, have been reported elsewhere.19,20

Leopoldamys edwardsi (forest rodent) showed the highest prevalence for helminth infection compared with the other two investigated rodents. Previous studies reported that forest rodents have a higher infection rate than lowland or dryland and settlements.45,52 This may explain that soil moisture in forest enhances survival and the stage development of parasites.53,54 The gastropods, intermediate hosts of echinostomatid flukes, E. malayanum and E. ilocanum, are commonly found in lowlands or irrigated rice fields. This could be related to B. indica and B. savilei (lowland or agricultural rodents) infected with these worms, whereas L. edwardsi was not. This result is similar to that from the study in Cambodia.21 In addition, B. indica also was infected with A. cantonensis, in which its intermediate hosts is also gastropod.55,56 Angiostrongylus cantonensis had been reported in B. indica from the previous study.57

This is the first report of zoonotic helminths in L. edwardsi and the first demonstration of A. cantonensis in B. indica; H. diminuta, H. nana, E. malayanum, and E. ilocanum in B. indica; and B. savilei in Lao PDR. Bandicota indica and B. savilei are now major pests in agricultural rice fields, and L. edwardsi is a forest rodent and can be found in disturbed habitats close to forested areas. Our result showed the potential of reservoir hosts of these three rodents and a high prevalence of zoonotic helminths in this study area. Therefore, the ongoing control efforts by the National Helminth Control Program in Lao PDR or even the leader of the community, in terms of education and hygiene, are needed to prevent the transmission of zoonoses in this area.

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    • Export Citation
  • 52.↑

    Bordes F et al. 2015. Habitat fragmentation alters the properties of a host-parasite network: rodents and their helminths in South-East Asia. J Anim Ecol 84: 1253–1263.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 53.↑

    Appleton CC, Gouws E, 1996. The distribution of common intestinal nematodes along an altitudinal transect in KwaZulu-Natal, South Africa. Ann Trop Med Parasitol 90: 181–188.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 54.↑

    O’Connor LJ, Kahn LP, Walkden-Brown SW, 2007. Moisture requirements for the free-living development of Haemonchus contortus: quantitative and temporal effects under conditions of low evaporation. Vet Parasitol 150: 128–138.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 55.↑

    Sri-aroon P, Chusongsang P, Chusongsang Y, Limpanont Y, Surinthwong P, Vongphayloth K, Brey PT, 2015. Malacological investigation of the fully operational Nam Theun 2 hydroelectric dam project in Khammouane province, Central Lao PDR. Southeast Asian J Trop Med Public Health 46: 866–879.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 56.↑

    Rodpai R, Intapan PM, Thanchomnang T, Sanpool O, Sadaow L, Laymanivong S, Aung WP, Phosuk I, Laummaunwai P, Maleewong W, 2016. Angiostrongylus cantonensis and A. malaysiensis broadly overlap in Thailand, Lao PDR, Cambodia and Myanmar: a molecular survey of larvae in land snails. PLoS One 11: e0161128.

    • Search Google Scholar
    • Export Citation
  • 57.↑

    Eamsobhana P, Yong HS, Prasartvit A, Wanachiwanawin D, Boonyong S, 2016. Geographical distribution and incidence of Angiostrongylus lungworms (Nematoda: Angiostrongylidae) and their rodent hosts in Thailand. Trop Biomed 33: 35–44.

    • PubMed
    • Search Google Scholar
    • Export Citation

Author Notes

Address correspondence to Porntip Laummaunwai, Khon Kaen University, 123 Mittraphap Road, 40002 Khon Kaen, Thailand. E-mail: porlau@kku.ac.th

Disclosure: This study was supported in part by the Faculty of Medicine of Khon Kaen University and the Department of Medical Laboratory, Faculty of Medical Technology, University of Health Science, Lao PDR.

Authors’ addresses: Phaviny Sithay, Thaksaporn Thongseesuksai, Thidarut Boonmars, and Porntip Laummaunwai, Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand, E-mails: phavist999@hotmail.com, thaksaporn.t@kkumail.com, bthida@kku.ac.th, and porlau@kku.ac.th. Somphonephet Chanthavong, Onekham Savongsy, and Naly Khaminsou, Department of Medical Laboratory, Faculty of Medical Technology, University of Health Sciences, Vientiane, Lao PDR, E-mails: phet2chanthavong@hotmail.com, onekham9876@gmail.com, and khaminsou@hotmail.com.

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    Bordes F et al. 2015. Habitat fragmentation alters the properties of a host-parasite network: rodents and their helminths in South-East Asia. J Anim Ecol 84: 1253–1263.

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    • Export Citation
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    • Export Citation
  • 54.

    O’Connor LJ, Kahn LP, Walkden-Brown SW, 2007. Moisture requirements for the free-living development of Haemonchus contortus: quantitative and temporal effects under conditions of low evaporation. Vet Parasitol 150: 128–138.

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  • 55.

    Sri-aroon P, Chusongsang P, Chusongsang Y, Limpanont Y, Surinthwong P, Vongphayloth K, Brey PT, 2015. Malacological investigation of the fully operational Nam Theun 2 hydroelectric dam project in Khammouane province, Central Lao PDR. Southeast Asian J Trop Med Public Health 46: 866–879.

    • PubMed
    • Search Google Scholar
    • Export Citation
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    Rodpai R, Intapan PM, Thanchomnang T, Sanpool O, Sadaow L, Laymanivong S, Aung WP, Phosuk I, Laummaunwai P, Maleewong W, 2016. Angiostrongylus cantonensis and A. malaysiensis broadly overlap in Thailand, Lao PDR, Cambodia and Myanmar: a molecular survey of larvae in land snails. PLoS One 11: e0161128.

    • Search Google Scholar
    • Export Citation
  • 57.

    Eamsobhana P, Yong HS, Prasartvit A, Wanachiwanawin D, Boonyong S, 2016. Geographical distribution and incidence of Angiostrongylus lungworms (Nematoda: Angiostrongylidae) and their rodent hosts in Thailand. Trop Biomed 33: 35–44.

    • PubMed
    • Search Google Scholar
    • Export Citation
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