17
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Co-infection patterns of intestinal parasites in arboreal primates (proboscis monkeys, Nasalis larvatus) in Borneo

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Non-human primates of South-East Asia remain under-studied concerning parasite epidemiology and co-infection patterns. Simultaneously, efforts in conservation demand knowledge of parasite abundance and biodiversity in threatened species. The Endangered proboscis monkey, Nasalis larvatus, a primate flagship species for conservation in Borneo, was investigated in the present study. Habitat loss and fragmentation are among the greatest threats to bachelor and harem groups of this folivorous colobine. Designed as a follow-up study, prevalence and co-infection status of intestinal parasites from N. larvatus in a protected area in Malaysian Borneo were analyzed from fecal samples using a flotation method. For the first time, the intestinal parasite co-infection patterns were examined using quantitative analyses. Overall, 92.3% of fecal samples (N = 652) were positive for helminth eggs. Five helminth groups were detected: (1) trichurids (82.7% prevalence) including Trichuris spp. (82.1%) and Anatrichosoma spp. (1.4%), (2) strongyles (58.9%) including Trichostrongylus spp. (48.5%) and Oesophagostomum/Ternidens spp. (22.8%), (3) Strongyloides fuelleborni (32.7%), (4) Ascaris lumbricoides (8.6%), and (5) Enterobius spp. (5.5%). On average, an individual was co-infected with two different groups. Significant positive associations were found for co-infections of trichurids with strongyles and S. fuelleborni as well as S. fuelleborni with A. lumbricoides and strongyles. This study shows a high prevalence of various gastrointestinal helminths with potential transmission pathways primarily related to soil and with zoonotic relevance in wild proboscis monkeys in their remaining natural habitats. Observed positive associations of trichurids with strongyles and Strongyloides spp. may result from the high prevalence of trichurids. Similarly, positive associations between Strongyloides and Ascaris were found, both of which typically occur predominantly in juvenile hosts. These findings should be considered when proposing conservation actions in altered habitats nearby human settlements and when managing captive populations.

          Graphical abstract

          Highlights

          • First study on interactions of co-infecting helminthes in wild proboscis monkeys.

          • 92% of fecal samples contain potentially zoonotic parasites.

          • Five trichurid and three strongylid morphotypes significantly differ in size.

          • Three reciprocal associations and one directed effect among five helminth orders.

          • Juveniles may act as reservoirs for Strongyloides spp., Ascaris spp., and strongyles.

          Related collections

          Most cited references62

          • Record: found
          • Abstract: found
          • Article: not found

          Emphasizing the ecology in parasite community ecology.

          In natural systems, individuals are often co-infected by many species of parasites. However, the significance of interactions between species and the processes that shape within-host parasite communities remain unclear. Studies of parasite community ecology are often descriptive, focusing on patterns of parasite abundance across host populations rather than on the mechanisms that underlie interactions within a host. These within-host interactions are crucial for determining the fitness and transmissibility of co-infecting parasite species. Here, we highlight how techniques from community ecology can be used to restructure the approaches used to study parasite communities. We discuss insights offered by this mechanistic approach that will be crucial for predicting the impact on wildlife and human health of disease control measures, climate change or novel parasite species introductions.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Pandemic human viruses cause decline of endangered great apes.

            Commercial hunting and habitat loss are major drivers of the rapid decline of great apes [1]. Ecotourism and research have been widely promoted as a means of providing alternative value for apes and their habitats [2]. However, close contact between humans and habituated apes during ape tourism and research has raised concerns that disease transmission risks might outweigh benefits [3-7]. To date only bacterial and parasitic infections of typically low virulence have been shown to move from humans to wild apes [8, 9]. Here, we present the first direct evidence of virus transmission from humans to wild apes. Tissue samples from habituated chimpanzees that died during three respiratory-disease outbreaks at our research site, Côte d'Ivoire, contained two common human paramyxoviruses. Viral strains sampled from chimpanzees were closely related to strains circulating in contemporaneous, worldwide human epidemics. Twenty-four years of mortality data from observed chimpanzees reveal that such respiratory outbreaks could have a long history. In contrast, survey data show that research presence has had a strong positive effect in suppressing poaching around the research site. These observations illustrate the challenge of maximizing the benefit of research and tourism to great apes while minimizing the negative side effects.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Multiparasite communities in animals and humans: frequency, structure and pathogenic significance.

              Individual humans and animals are subject to infection by a variety of parasites (broadly defined to include viruses, bacteria and other non-protozoan microparasites) at any one time. Multiple parasite infections occur frequently in populations of wild animals as well as in humans from developing countries. In some species and regions, hosts with multiple infections are more common than hosts with either no infection or a single infection. Studies, predominantly on animals, show that a wide variety of environmental and host-dependent factors can influence the structure and dynamics of the communities of parasites that make up these multiple infections. In addition, synergistic and competitive interactions can occur between parasite species, which can influence the likelihood of their successful transmission to other hosts and increase or decrease their overall pathogenic impact. This review summarises aspects of our current knowledge on the frequency of multiparasite infections, the factors which influence them, and their pathogenic significance.
                Bookmark

                Author and article information

                Contributors
                Journal
                Int J Parasitol Parasites Wildl
                Int J Parasitol Parasites Wildl
                International Journal for Parasitology: Parasites and Wildlife
                Elsevier
                2213-2244
                20 September 2017
                December 2017
                20 September 2017
                : 6
                : 3
                : 320-329
                Affiliations
                [a ]Institute for Parasitology, University of Veterinary Medicine Hannover, Hannover, Buenteweg 17, 30559 Hannover, Germany
                [b ]Institute of Zoology, University of Veterinary Medicine Hannover, Hannover, Buenteweg 17, 30559 Hannover, Germany
                [c ]Sabah Wildlife Department, 5th Floor, B Block, Wisma MUIS, 88100 Kota Kinabalu, Sabah, Malaysia
                [d ]Organisms and Environment Division, School of Biosciences, Cardiff University, The Sir Martin Evans Building, Museum Avenue, Cardiff CF10 3AX, United Kingdom
                [e ]Danau Girang Field Centre, C/o Sabah Wildlife Department, Kota Kinabalu, Sabah, Malaysia
                [f ]Sustainable Places Research Institute, Cardiff University, 33 Park Pl, Cardiff CF10 3BA, United Kingdom
                Author notes
                []Corresponding author. christina.strube@ 123456tiho-hannover.de
                [1]

                Present address: Zoo Hannover, Adenauerallee 3, 30175 Hannover, Germany.

                Article
                S2213-2244(17)30023-8
                10.1016/j.ijppaw.2017.09.005
                6031963
                29988805
                2a9ce083-c9f4-448b-9656-e44337d82494
                © 2017 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 13 February 2017
                : 28 August 2017
                : 14 September 2017
                Categories
                Regular Paper

                nasalis larvatus,gastrointestinal parasites,co-infection,conservation,south-east asia,malaysia,zoonosis

                Comments

                Comment on this article