Literature DB >> 33985499

Lethal infection caused by Tetratrichomonas gallinarum in black swans (Cygnus atratus).

Shengyong Feng1,2, Han Chang1,2, Yutian Wang3, Fubing Luo4, Qiaoxing Wu5, Shuyi Han1, Hongxuan He6.   

Abstract

BACKGROUND: Tetratrichomonas gallinarum is parasitic protozoa with a wide host range. However, its lethal infection is rare reported. CASE
PRESENTATION: Here, we described the first lethal cases of T. gallinarum infection in black swans in China. Five black swans died within a week in succession without obvious symptoms except mild diarrhea. At necropsy, severe lesions were observed in caeca with thickened caecal walls and hemorrhages in the mucosa. A large number of moving trophozoites were found in the contents of the cecum by microscopic examination. The livers were enlarged with multiple bleeding spots on the surface. Histopathology of the livers showed mononuclear cell infiltration and moderate hyperplasia of fibrous tissue. The histopathology of the cecum showed that the villi of the cecum were edematous. Finally, the presence of T. gallinarum was determined by specific PCR andin-situ hybridization assay. Additionally, common pathogens that can cause similar symptoms were excluded.
CONCLUSIONS: The death of the black swan was caused by T. gallinarum, suggesting that the parasite might be a new threat to the Cygnus birds.

Entities:  

Keywords:  Black swan; Cecum; China; Liver; T. gallinarum

Year:  2021        PMID: 33985499      PMCID: PMC8117575          DOI: 10.1186/s12917-021-02894-x

Source DB:  PubMed          Journal:  BMC Vet Res        ISSN: 1746-6148            Impact factor:   2.741


Background

Tetratrichomonas gallinarum is parasitic protozoa with a wide host range [1]. Owing to sick birds are usually co-infected with other pathogens and artificially infected animals rarely develop symptoms, the pathogenicity of T. gallinarum is controversial [2-4]. Moreover, lesions caused by T. gallinarum in birds were sporadically reported in some countries, such as in chukar partridges, mockingbird, Waldrapp ibis and white pelican from America [5-8], in duck from Germany [9], in red-legged partridges from Great Britain [10], and in Layer chickens from the Netherlands [11]. Here, we described the first fatal case of black swans (Cygnus atratus) associated with T. gallinarum infection in China, and the threat of the protozoa to Cygnus birds must be considered.

Case presentation

In August 2019, five adult black swans from a wetland park of Beijing died within a week in succession. Before they died, no obvious symptoms were observed except mild diarrhea. The fresh carcasses were sent to the National Research Center for Wildlife Borne Diseases for postmortem and histopathological examination. At routinely pathological investigation, the ceca were swollen and the mucosa were hemorrhages and anabrosis (Fig. 1a). A large number of moving trophozoites were observed by microscopic examination. The livers were enlarged and accompanied by the color turned dark red and the edge was blunt (Fig. 1b). No visible lesions were found in other organs. Histopathological examination showed that cecal hemorrhage, intestinal villi edema, disordered arrangement, epithelial cells exfoliated, and many parasites were found in lamina propria (Fig. 2a). Vacuolar degeneration of hepatocytes and interlobular bile duct hyperplasia were observed in the liver tissues. A large number of mononuclear inflammatory cells infiltrated between the liver lobules, and the fibrous tissue proliferated moderately (Fig. 2b).
Fig. 1

Pathological changes of cecum (a) and liver (b)

Fig. 2

Haematoxylin and eosin staining of the caecum (a) and the liver (b) of a dead black swans. ISH revealed the presence of T. gallinarum in the caecum (c) within the localizations as brown-stained cells. The signals of T. gallinarum probe in the liver was negative (d)

Pathological changes of cecum (a) and liver (b) Haematoxylin and eosin staining of the caecum (a) and the liver (b) of a dead black swans. ISH revealed the presence of T. gallinarum in the caecum (c) within the localizations as brown-stained cells. The signals of T. gallinarum probe in the liver was negative (d) Histological sections from the livers and ceca of the birds were further processed for in situ hybridization (ISH) using the described probe specific for T. gallinarum and H. meleagridis [12, 13]. The positive signals with the T. gallinarum probe were found in the caeca (Fig. 2c) but not in the livers (Fig. 2d). The result of ISH in the caeca and livers showed no signal with the H. meleagridis probe. Using two trichomonad primer sets, TFR1/R2 and 18S-F/R, the ITS and 18S rRNA region of the isolates were successfully amplified with specific single band size of approximately 350 bp and 600 bp in the gel [14, 15] (Fig. 3), respectively. Notably, the PCR products were subcloned into T-vectors before sequencing to ensure that the specific sequences be successfully sequenced. Both sequences were clustered with the reference sequences of T. gallinarum download from GenBank database under phylogenetic analyses (Fig. 4a, b).
Fig. 3

Partial sequence amplification based on 18S rRNA gene and ITS1–5.8S rRNA-ITS2 gene. Lane 1–5, PCR products of18S rRNA gene. Lane 7–11, PCR products of ITS1–5.8S rRNA-ITS2 gene. Lane 6 and 12 were negative control. M, marker

Fig. 4

Phylogenetic tree of the trichomonad nucleic acid sequences based on a the partial 18S rRNA and b ITS1–5.8S rRNA-ITS2 loci. The phylogenetic tree was constructed with a Neighbor-Joining method with the Kimura2-parameter model. Bootstrap values > 70% from 1000 replicates are shown on the nodes. The isolates detected in the current study are shown with solid triangle

Partial sequence amplification based on 18S rRNA gene and ITS1–5.8S rRNA-ITS2 gene. Lane 1–5, PCR products of18S rRNA gene. Lane 7–11, PCR products of ITS1–5.8S rRNA-ITS2 gene. Lane 6 and 12 were negative control. M, marker Phylogenetic tree of the trichomonad nucleic acid sequences based on a the partial 18S rRNA and b ITS1–5.8S rRNA-ITS2 loci. The phylogenetic tree was constructed with a Neighbor-Joining method with the Kimura2-parameter model. Bootstrap values > 70% from 1000 replicates are shown on the nodes. The isolates detected in the current study are shown with solid triangle Other potential pathogens, such as Coccidia spp., Blastocystis spp. and hepatitis E virus were negative using the method previously reported [16-18]. Taken together, after eliminating potential pathogens, such as H. meleagridis, Coccidia, Blastocystis spp., hepatitis E virus as well as pathogenic bacteria, the presence of T. gallinarum was eventually confirmed by microscopic examination, histopathology, specific PCR amplification and ISH. Therefore, the death of the black swan was likely to be caused by T. gallinarum.

Discussion and conclusions

Though T. gallinarum is commonly found gallinaceous and anseriform birds, it seldom causes diseases [19]. The maturity of the immune system may be an important reason for the host to suffer from this parasite, as previous studies have found that most of the dead birds were juveniles or subadults [8, 9]. However, all the dead black swans in the present study were adult, thus the heterogeneity between T. gallinarum isolates might also be an important factor result in the differences in pathogenicity among hosts. Studies conducted by Dimasuay and Rivera shown that T. gallinarum can be detected from healthy ducks (Anas platyrhynchos) [20], which suggested that the parasite might be commensal in some duck species. In the present study, some healthy ducks shared activity area with the black swans. Thus the T. gallinarum recovered from the black swans may be spillover from the ducks. In conclusion, we described the first fatal case of black swans associated with T. gallinarum infection in China, suggesting that the protozoan might be a new threat to the Cygnus birds. A comprehensive epidemiological investigation of T. gallinarum in Cygnus birds is urgently needed in the future.
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