Skip to main content
Log in

Novel life cycle stages of Colpodella sp. (Apicomplexa) identified using Sam-Yellowe’s trichrome stains and confocal and electron microscopy

  • Original Article
  • Published:
International Microbiology Aims and scope Submit manuscript

Abstract

Colpodella spp. are free-living flagellates closely related to the apicomplexans. Human infections by Colpodella sp. have been reported. A biflagellated trophozoite and cyst stage comprise the known life cycle stages of Colpodella sp. However, the process of encystation and excystation within the life cycle is unclear. Life cycle stages initiating human infections are unknown. We performed a detailed investigation of the life cycle of Colpodella sp. (ATCC 50594) in culture using Sam-Yellowe’s trichrome stains and differential interference contrast (DIC) for light microscopy and fluorescence microscopy of Congo red-stained cells and investigated ultrastructure using transmission electron microscopy (TEM). We report previously undocumented stages of Colpodella sp. Asymmetric and asynchronous division was detected inside cysts by trichrome staining and by TEM. Odd-numbered juveniles and cysts containing more than four juvenile trophozoites were identified. Live imaging of active cultures captured the excystation and egress of juvenile trophozoites and confirmed the presence of multinucleate cysts. The ultrastructure of the multinucleate cyst is reminiscent of apicomplexan schizonts. Insights gained from the life cycle stages observed in culture allowed the construction of the life cycle of Colpodella sp. Knowledge of the life cycle will aid biochemical and molecular characterization of Colpodella sp. and help identify stages in human infections.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

References

  • Boettcher B, Barral Y (2013) The cell biology of open and closed mitosis. Nucleus 4:160–165

    Article  Google Scholar 

  • Brugerolle G (2002) Colpodella vorax: ultrastructure, predation, life-cycle, mitosis, and phylogenetic relationships. Eur J Protistol 38:113–125

    Article  Google Scholar 

  • Cavalier-Smith T, Chao EE (2004) Protalveolate phylogeny and systematics and the origins of Sporozoa and dinoflagellates (phylum Myzozoa nom. Nov.). Eur J Protistol 40:185–212

    Article  Google Scholar 

  • Francia ME, Streipen B (2014) Cell division in apicomplexan parasites. Nat Rev Microbiol 12:125–136

    Article  CAS  Google Scholar 

  • Gubbels M-J, Keroack C, Dangoudoubiyam S, Worliczek HL et al (2020) Fussing about fission: defining variety among mainstream and exotic apicomplexan cell division modes. Front Cell Infect Microbiol 10:269

    Article  CAS  Google Scholar 

  • Jiang J-F, Jiang R-R, Chang Q-C, Zheng Y-C, Jiang B-G, Sun Y, Jia N, Wei R, Bo H-B, Huo Q-B, Wang H, von Fricken ME, Cao W-C (2018) Potential novel tick-borne Colpodella species parasite infection in patient with neurological symptoms. PLoS Negl Trop Dis 12(8):e0006546

    Article  Google Scholar 

  • Kuvardina ON, Leander BS, Aleshin VV, Mylnikov AP, Keeling PJ, Simdyanov TG (2002) The phylogeny of colpodellids (Alveolata) using small subunit rRNA gene sequences suggests they are the free-living sister group to apicomplexans. J Eukaryot Microbiol 49:498–504

    Article  CAS  Google Scholar 

  • Mylnikov AP (2009) Ultrastructure and phylogeny of colpodellids (Colpodellida, Alveolata). Biol Bull 36:582–590

    Article  Google Scholar 

  • Mylnikov AP, Mylnikova ZM (2008) Feeding spectra and pseudoconoid structure in predatory alveolate flagellates. Inland Water Biol 1:210–216

    Article  Google Scholar 

  • Olmo JL, Esteban GF, Finlay BJ (2011) New records of the ectoparasitic flagellate Colpodella gonderi on non-Colpoda ciliates. Int Microbiol 14:207–211

    PubMed  Google Scholar 

  • Sam-Yellowe TY, Yadavalli R (2018) Giemsa staining and antibody characterization of Colpodella sp. (Apicomplexa). J Microbiol Modern Tech 3(1):103

    Google Scholar 

  • Sam-Yellowe TY, Yadavalli R, Fujioka H, Peterson JW, Drazba JA (2019a) RhopH3, rhoptry gene conserved in the free-living alveolate flagellate Colpodella sp. (Apicomplexa). Eur J Protistol 71:125637

    Article  Google Scholar 

  • Sam-Yellowe TY, Addepalli K, Yadavalli R, Peterson JW (2019b) New trichrome stains identify cysts of Colpodella sp. (Apicomplexa) and Bodo caudatus. Int Microbiol 23:303–311

  • Simpson AGB, Patterson DJ (1996) Ultrastructure and identification of the predatory flagellate Colpodella pugnax Cienkowski (Apicomplexa) with a description of Colpodella turpis n. sp. and a review of the genus. Syst Parasitol 33:187–198

    Article  Google Scholar 

  • White MW, Suvorova ES (2018) Apicomplexa cell cycles: something old, borrowed, lost, and new. Trends Parasitol 34:759–771

    Article  Google Scholar 

  • Yadavalli R, Sam-Yellowe TY (2017) Developmental stages identified in the trophozoite of the free-living Alveolate flagellate Colpodella sp. (Apicomplexa). Int Microbiol 20:178–183

    CAS  PubMed  Google Scholar 

  • Yang J-C, Blanton RE, King CL, Fujioka H, Aikawa M, Sam-Yellowe TY (1996) Seroprevalence and specificity of human responses to the Plasmodium falciparum rhoptry protein Rhop-3 determined by using a C-terminal recombinant protein. Infect Immun 64:3584–3591

    Article  CAS  Google Scholar 

  • Yuan CL, Keeling PJ, Krause PJ, Horak A, Bent S, Rollend L, Hua XG (2012) Colpodella spp.–like parasite infection in Woman, China. Emerg Infect Dis 18:125–127

    Article  Google Scholar 

Download references

Acknowledgements

We gratefully acknowledge the Cleveland Clinic Lerner Research Institute, Cleveland Clinic NIH that shared instrument grant for Orbitrap Elite LC-MS instrument; Cleveland Clinic NIH grant 1S100D023436-01 for Fusion Lumos instrument; and Cleveland Clinic Lerner Research Institute, Imaging Core, and MR4-BEI Resources for anti-EBA-175 antiserum.

Funding

The study was supported by funds from the Cleveland State University Undergraduate Summer Research Award 2019

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tobili Y. Sam-Yellowe.

Ethics declarations

Conflict of interest

The authors declare no competing interests.

Additional information

Publisher’s note

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

Supplementary information

Supplementary Fig. 1

Volocity movie of Colpodella sp. and B. caudatus in myzocytosis. The tubular tether bridging the two protists can be seen. The nucleus and kinetoplast in B. caudatus is DAPI stained (top). The nucleus of Colpodella sp. (below) also DAPI stained can be seen. DIC image shows morphology of both protists (AVI 52497 kb)

Supplementary Fig. 2

Volocity movie of Colpodella sp. (below) and B. caudatus (top) cysts. DAPI staining shows six nuclei of Colpodella sp. DIC image of cyst morphology is shown. (AVI 66691 kb)

Supplementary Fig. 3

Volocity movie of Colpodella sp. and B. caudatus cysts. DAPI staining shows four nuclei of Colpodella sp. DIC image of cyst morphology is shown. (AVI 12835 kb)

Supplementary Fig. 4

Normal rabbit serum, 1:100 was used as a negative control in IFA. There was no reactivity with proteins of Colpodella sp. and B. caudatus. The merged image shows two separate attachments of Colpodella sp. and B. caudatus trophozoites. B. DAPI staining shows the nucleus of Colpodella sp. and B. caudatus. C. Background reactivity was observed on cells with NRS. D. DIC images show the attachment of Colpodella sp. and the tubular tethers. (PNG 234 kb)

High resolution image (TIF 316 kb)

MP4 video of trophozoites egressing from Colpodella sp. cysts. Four trophozoites egress individually from a cyst (top, at 10-26 s) followed by egress of eight trophozoites (far right, at 34 s to 3 min 34 s). In the second cyst, the first four trophozoites egress individually and swim away followed by two pairs of trophozoites still joined at the anterior ends. Both pairs of trophozoites complete cytokinesis and separate outside the cyst. Bodo caudatus prey with multiple Colpodella sp. attachments can be seen in the video. The predator-prey connections in myzocytosis are not static but move within the culture. (MP4 61073 kb)

Supplementary Fig. 6

Sam-Yellowe’s Trichrome stained smears of Colpodella sp. life cycle stages. Sam-Yellowe’s Trichrome A stain was used to visualize life cycle stages of Colpodella sp. in culture. Black arrows identify demilune cysts of Colpodella sp., black arrowheads identify mature Colpodella sp. cysts and red arrows identify cysts of Bodo caudatus. (PNG 589 kb)

High resolution image (TIF 782 kb)

ESM 1

(DOCX 14 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sam-Yellowe, T.Y., Getty, T.A., Addepalli, K. et al. Novel life cycle stages of Colpodella sp. (Apicomplexa) identified using Sam-Yellowe’s trichrome stains and confocal and electron microscopy. Int Microbiol 25, 669–678 (2022). https://doi.org/10.1007/s10123-021-00175-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10123-021-00175-z

Keywords

Navigation