Skip to main content

First report on aberrant Ascaris suum infection in a dog, China


An aberrant Ascaris suum infection in a domestic dog in China in 2019 is described for the first time. This pathogen is a common roundworm of pigs with few reported cases in domestic animals. Our findings suggest a wider infection range with a possible transmission of A. suum to domestic animals that interact with humans.

Letter to the Editor

Roundworms, belonging to the family Ascarididae, are among the most common zooparasitic nematodes and cause ascariasis in all major lineages of vertebrates including domestic animals, wildlife and humans. Ascaris suum is a common roundworm of pigs. Although pig husbandry has become more modernized and industrialized, A. suum is still prevalent on a large number of pig farms across the world and the situation has not changed significantly over the last few decades [1]. It is evident that A. suum is zoonotic and its cross-infection and hybridization with the human roundworm Ascaris lumbricoides has been recently confirmed in areas of human-pig sympatry [2]. Importantly, cases of A. suum-related human infections have been reported [3,4,5], including an outbreak in Maine, USA, in 2010–2013 [6]. In addition, aberrant A. suum infections were also reported in domestic animals, such as cattle [7]. Here we expand the currently recognized infection spectrum by firstly describing A. suum infection in domestic dogs in China.

In April 2019, a two-month-old female German shepherd dog puppy from a pig farm was brought to Veterinary Medical Teaching Hospital (VMTH), Sichuan Agricultural University (Sichuan, China), for post-mortem examination. The puppy died with clinical manifestations of dyspnea, coughing, wheezing and general weakness. This farm kept five German shepherd dogs (a bitch and her four puppies), and all the puppies had shown similar clinical signs for about two weeks. Routine vaccinations were administrated to all of the dogs.

Necropsy of the puppy revealed bilateral lungs with significant emphysema and diffusely firm red parenchyma, and the trachea and bronchi were filled with massive blood-tinged froth. Interstitial pneumonia was diagnosed according to the gross appearance, and viral or bacterial pneumonia was suspected. However, histopathological examination showed a diffuse, severe, hemorrhagic, fibrinous interstitial pneumonia with multiple nematode larvae present in alveolar sacs and bronchi which were partially surrounded by inflammatory cells (macrophages, lymphocytes and eosinophils) (Fig. 1a, b). The larvae measured 68 μm in maximum transverse diameter and had a thin cuticle that formed sharply pointed paired lateral alae. The intestine was centrally located, floated in pseudocoelom and flanked by large paired triangular excretory columns. Four to five muscle cells were observed per quadrant. These morphological characteristics are key for ascaridid nematodes. Examination of gastrointestinal tracts from the puppy recovered three acaridid nematodes. No viral or bacterial etiology was diagnosed from routine bacteriological and molecular diagnostic tests.

Fig. 1

Morphological characterization of Ascaris suum nematode infection in the lung of a dog in China, 2019. a Multiple transverse sections of A. suum larvae observed in lung tissues with severe, hemorrhagic, fibrinous interstitial pneumonia. b The morphological characteristics of the larvae included maximum diameter of 68 μm, thin cuticle (Cu), a centrally located intestine (In), paired lateral alae (Al) and excretory columns (EC). Some scattered macrophages, lymphocytes and eosinophils are also indicated. Hematoxylin and eosin stain. Scale-bars: 100 µm

The three acaridid nematodes were provisionally identified as Toxocara canis based on morphology: the presence of a post-oesophageal bulbus, the length and shape of the alae and the length of the spicules. Toxocara canis is a canine roundworm that is highly prevalent in puppies under three months-old and can adopt “hepato-tracheal” migration to develop into adults. Thus, this parasite can also cause histopathological changes of lungs similar to those identified in this study.

To accurately identify the nematodes in the infected lung, genomic DNA was extracted from formalin-fixed, paraffin-embedded (FFPE) tissues and subjected to genetic analysis by sequencing partial fragments of the nuclear 18S ribosomal DNA (18S rDNA) gene [8] and the mitochondrial 12S ribosomal DNA (12S rDNA) gene [9]. The resulting sequences of 18S rDNA (1729 bp; GenBank: MN558962) and 12S rDNA (488 bp; GenBank: MN567666) were found to be 99.9–100% identical with those of A. suum (GenBank: U94367 and FJ418791, respectively), and both grouped together and were clearly distinct from T. canis in phylogenies inferred from either 18S rDNA or 12S rDNA using maximum likelihood and Bayesian inference methods (Fig. 2a, b). Indeed, further investigations supported pigs as the infection source because c.60% pigs in this farm were serologically detected as A. suum-positive by AsHb ELISA (Y. Zheng et al., unpublished data) [10], and parasitological examination of soil and water around the pig farm indicated a heavy contamination with A. suum eggs. This suggested that the free-range German shepherd dogs were probably exposed to the eggs and became infected.

Fig. 2

Molecular characterization of Ascaris suum nematode infection in the lung of a dog in China, 2019. Phylogenetic trees inferred by using Tamura-Nei model-based maximum likelihood (ML) and GTR+I+G model-based Bayesian inference (BI) analyses based on the partial sequences of the nuclear 18S rDNA gene (a) and the mitochondrial 12S rDNA gene (b) of the isolate from the dog (bold and marked with a solid black circle) and other related species. Loa loa (a) and species of Anisakis and Ortleppascaris (b) were used as outgroups. The numbers along the branches indicate bootstrap values resulting from different analyses in the order ML/BI; values > 70% (ML) and 0.95 (BI) are shown

The pig roundworm A. suum has been suggested as causing a widely distributed zoonosis with human cases in North America, Europe and Asia [2, 3, 6]. Some other animals infected with A. suum have been also recently reported [7]. Our finding shows that this roundworm can infect dogs. This observation expands the previously acknowledged infection range and raises questions about infection success and host affiliation of A. suum in nature that are difficult to address by traditional biological, epidemiological and clinical approaches. Moreover, in consideration of the cultural and agricultural tradition of using pig feces as fertilizer and the feature that A. suum eggs remain viable in farm soil for years as well as the location of pig latrines where dogs easily access, the chance of direct or indirect exposure for dogs is likely. Recommended preventive procedures to reduce transmission of A. suum between pigs and dogs, and probably between pigs and humans, include restraining dogs from pig lactrines, periodically examining farm dogs and pigs for infection, prophylactic and therapeutic treatment of pigs to reduce infection, avoiding use of pig manure as fertilizer, and washing hands when there is contact with pigs, pig waste or soil contaminated with pig waste. In addition, the farm owner should have dedicated equipment for handling or depositing animal waste. Because A. suum eggs can persist in the farm surrounding for extended periods, daily foodstuffs, especially produce and vegetables grown using pig manure should be avoided or fed only after thorough cleaning. Overall, an effective prevention of A. suum infections requires an integrated “One-Health” approach that encourages collaboration between farmers, veterinarians and physicians and enhances their awareness to the risk for aberrant infections of A. suum and its transmission to humans and other domestic animals.

Availability of data and materials

Nucleotide sequences reported in this article are available in the GenBank database under the accession numbers MN558962 (18S) and MN567666 (12S).


  1. 1.

    Wang T. Transcriptomic and proteomic analysis of Ascaris suum larvae during their hepato-tracheal migration. Ghent: Ghent University; 2014.

    Google Scholar 

  2. 2.

    Peng W, Criscione CD. Ascariasis in people and pigs: new inferences from DNA analysis of worm populations. Infect Genet Evol. 2012;12:227–35.

    Article  Google Scholar 

  3. 3.

    Bendall RP, Barlow M, Betson M, Stothard JR, Nejsum P. Zoonotic ascariasis, United Kingdom. Emerg Infect Dis. 2011;17:1964–6.

    Article  Google Scholar 

  4. 4.

    Sakakibara A, Baba K, Niwa S, Yagi T, Wakayama H, Yoshida K, et al. Visceral larva migrans due to Ascaris suum which presented with eosinophilic pneumonia and multiple intra-hepatic lesions with severe eosinophil infiltration—outbreak in a Japanese area other than Kyushu. Intern Med. 2002;41:574–9.

    Article  Google Scholar 

  5. 5.

    Izumikawa K, Kohno Y, Izumikawa K, Hara K, Hayashi H, Maruyama H, et al. Eosinophilic pneumonia due to visceral larva migrans possibly caused by Ascaris suum: a case report and review of recent literatures. Jpn J Infect Dis. 2011;64:428–32.

    PubMed  Google Scholar 

  6. 6.

    Miller LA, Colby K, Manning SE, Hoenig D, McEvoy E, Montgomery S, et al. Ascariasis in humans and pigs on small-scale farms, Maine, USA, 2010–2013. Emerg Infect Dis. 2015;21:332–4.

    CAS  Article  Google Scholar 

  7. 7.

    Taylor HL, Spagnoli ST, Calcutt MJ, Kim DY. Aberrant Ascaris suum nematode infection in cattle, Missouri, USA. Emerg Infect Dis. 2016;22:339–40.

    CAS  Article  Google Scholar 

  8. 8.

    Nadler SA, Hudspeth DS. Ribosomal DNA and phylogeny of the Ascaridoidea (Nemata: Secernentea): implications for morphological evolution and classification. Mol Phylogenet Evol. 1998;10:221–36.

    CAS  Article  Google Scholar 

  9. 9.

    Wickramasinghe S, Yatawara L, Rajapakse R, Agatsuma T. Toxocara canis and Toxocara vitulorum: molecular characterization, discrimination, and phylogenetic analysis based on mitochondrial (ATP synthase subunit 6 and 12S) and nuclear ribosomal (ITS-2 and 28S) genes. Parasitol Res. 2009;104:1425–30.

    Article  Google Scholar 

  10. 10.

    Vlaminck J, Nejsum P, Vangroenweghe F, Thamsborg SM, Vercruysse J, Geldhof P. Evaluation of a serodiagnostic test using Ascaris suum haemoglobin for the detection of roundworm infections in pig populations. Vet Parasitol. 2012;189:267–73.

    CAS  Article  Google Scholar 

Download references


We thank Dr. Joseph F. Urban, Jr., from USDA-ARS, Beltsville Human Nutrition Research Center, Diet, Genomics and Immunology Laboratory for manuscript review and advice.


This work was supported by the Sichuan International Science and Technology Innovation Cooperation/Hong Kong, Macao and Taiwan Science and Technology Innovation Cooperation Project, Sichuan, China (Grant No. 2019YFH0065) and the High-level Scientific Research Foundation for the Introduction of Talents of Sichuan Agricultural University (No. 03120322). The funders had no role in design, decision to publish, or preparation of the manuscript.

Author information




YX and GYY conceived and designed the experiments. YJL and XBG performed the experiments, including PCR and sequencing. RH, HRG and ZCZ carried out the histopathologic examination. YX, YJL and XBG achieved the data analysis. XZ and PXR contributed reagents/materials/analysis tools. YX and GYY wrote the initial manuscript. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Yue Xie or Guangyou Yang.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the Animal Ethics Committee of Sichuan Agricultural University (China; approval no. SYXK 2014-187), and all procedures including the autopsy were performed in strict accordance with the Guide for the Care and Use of Laboratory Animals (National Research Council, Bethesda, MD, USA) and the recommendations in the ARRIVE guidelines (

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

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

Rights and permissions

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

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Xie, Y., Liu, Y., Gu, X. et al. First report on aberrant Ascaris suum infection in a dog, China. Parasites Vectors 13, 86 (2020).

Download citation


  • Ascariasis
  • Ascaris suum
  • Helminthic zoonosis
  • Host range
  • Dogs