Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Fungal Phylum Microsporidia01:28

Fungal Phylum Microsporidia

198
Microsporidia are a group of obligate intracellular fungi that were initially classified as protists but were later reclassified based on phylogenetic, molecular, and structural evidence linking them to the Chytridiomycota. These unicellular, non-motile organisms are highly specialized parasites that infect a wide range of animal hosts, including humans. They have evolved extensive genomic and metabolic reductions, making them highly dependent on their hosts for survival.Morphology and Genomic...
198

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Persistence of <i>Sarcocystis neurona</i> and histopathology in horses with equine protozoal myeloencephalitis.

Frontiers in veterinary science·2026
Same author

Pathology and parasitology of free-ranging coyotes from Tennessee and South Carolina.

PloS one·2025
Same author

Trypanosoma cruzi infection in American black bears (Ursus americanus): A case report in a cub from California and serologic survey for exposure in wild black bears from several states.

Veterinary parasitology, regional studies and reports·2024
Same author

RAPID POINT-OF-CARE TESTING FOR DETECTION OF ANTIBODIES TO TOXOPLASMA GONDII IN BLACK VULTURES AND RING-BILLED GULLS FROM PENNSYLVANIA.

The Journal of parasitology·2024
Same author

USE OF A POINT OF CARE TEST TO DETERMINE THE PREVALENCE OF ANTIBODIES TO TOXOPLASMA GONDII IN BLACK BEARS FROM NORTH CAROLINA AND PENNSYLVANIA.

The Journal of parasitology·2023
Same author

Does Denosumab Really Improve Muscle Strength? Current Evidence Is Weak.

Annals of geriatric medicine and research·2023
Same journal

REDESCRIPTION OF PARABENEDENIELLA POSTEROCOLPA (HARGIS, 1955) BRULE AND BULLARD N. GEN. ET N. COMB. (MONOGENOIDEA: CAPSALIDAE: ENTOBDELLINAE) FROM INFECTIONS ON THREE BATOID HOSTS (RHINOPTERIDAE AND MOBULIDAE) WITH PHYLOGENETIC ANALYSIS AND COMMENTS ABOUT CAPSALID HOST SPECIFICITY.

The Journal of parasitology·2026
Same journal

ASSOCIATION BETWEEN MACROCYCLIC LACTONE AND BENZIMIDAZOLE RESISTANCE IN THE DOG HOOKWORM ANCYLOSTOMA CANINUM.

The Journal of parasitology·2026
Same journal

TISSUE-SPECIFIC ORIGIN OF EGGS IN THE DEFINITIVE HOST DRIVES TRANSCRIPTOMIC AND BEHAVIORAL DIFFERENCES IN SCHISTOSOMA MANSONI MIRACIDIA.

The Journal of parasitology·2026
Same journal

DESCRIPTION, REDESCRIPTION, AND LIFE CYCLES OF PARORCHIS LAFFERTYI N. SP. AND PARORCHIS CATOPTROPHORI (TREMATODA: DIGENEA: PHILOPHTHALMIDAE) FROM THE CALIFORNIA HORN SNAIL, CERITHIDEOPSIS CALIFORNICA (GASTROPODA: POTAMIDIDAE).

The Journal of parasitology·2026
Same journal

CONFIRMATION OF SARCOCYSTIS INFECTIONS IN TONGUES OF FLORIDA PANTHERS (PUMA CONCOLOR CORYI).

The Journal of parasitology·2026
Same journal

MOLECULAR CHARACTERIZATION OF SARCOCYSTIS SPOROCYSTS IN INTESTINES OF BOBCAT (LYNX RUFUS) FROM MINNESOTA.

The Journal of parasitology·2026
See all related articles

Related Experiment Video

Updated: Oct 27, 2025

Mass Isolation and In Vitro Cultivation of Intramolluscan Stages of the Human Blood Fluke Schistosoma Mansoni
12:05

Mass Isolation and In Vitro Cultivation of Intramolluscan Stages of the Human Blood Fluke Schistosoma Mansoni

Published on: January 14, 2018

9.4K

GAMOGONY OF SARCOCYSTIS STRIXI IN MAMMALIAN CELL CULTURES.

David S Lindsay1, S K Verma2,3, J P Dubey2

  • 1Department of Biomedical Sciences and Pathobiology, Virginia Maryland College of Veterinary Medicine, Faculty of Health Sciences, 205 Duck Pond Drive, Virginia Tech, Blacksburg, Virginia 24061.

The Journal of Parasitology
|July 20, 2021
PubMed
Summary
This summary is machine-generated.

Developing a laboratory model for Sarcocystis strixi infection in mammals was unsuccessful. Researchers could not produce sporulated oocysts in cell cultures, failing to validate their hypothesis for disease ecology studies.

Keywords:
Sarcocystis strixiStrix variaBarred OwlBradyzoitesCell CulturesMacrogamontsMicrogamontsOocystsSarcocysts

More Related Videos

Trypsinizing and Subculturing Mammalian Cells
05:59

Trypsinizing and Subculturing Mammalian Cells

Published on: June 12, 2008

21.6K
Concomitant Isolation of Primary Astrocytes and Microglia for Protozoa Parasite Infection
09:34

Concomitant Isolation of Primary Astrocytes and Microglia for Protozoa Parasite Infection

Published on: March 18, 2020

7.9K

Related Experiment Videos

Last Updated: Oct 27, 2025

Mass Isolation and In Vitro Cultivation of Intramolluscan Stages of the Human Blood Fluke Schistosoma Mansoni
12:05

Mass Isolation and In Vitro Cultivation of Intramolluscan Stages of the Human Blood Fluke Schistosoma Mansoni

Published on: January 14, 2018

9.4K
Trypsinizing and Subculturing Mammalian Cells
05:59

Trypsinizing and Subculturing Mammalian Cells

Published on: June 12, 2008

21.6K
Concomitant Isolation of Primary Astrocytes and Microglia for Protozoa Parasite Infection
09:34

Concomitant Isolation of Primary Astrocytes and Microglia for Protozoa Parasite Infection

Published on: March 18, 2020

7.9K

Area of Science:

  • Disease ecology
  • Parasitology
  • Mammalian cell culture

Background:

  • Sarcocystis species infect various hosts, including birds of prey.
  • Understanding Sarcocystis infection dynamics is crucial for disease ecology.

Purpose of the Study:

  • To test the hypothesis of developing a laboratory model for Sarcocystis strixi infection in mammals.
  • To utilize gamma interferon gene knockout (KO) mice and mammalian cell cultures for S. strixi propagation.

Main Methods:

  • Sporocysts of S. strixi from infected owls were fed to KO mice.
  • Bradyzoites were isolated from KO mouse muscles via acid-pepsin digestion.
  • Isolated bradyzoites were used to inoculate mammalian cell cultures.

Main Results:

  • Bradyzoites, metrocytes, and an unidentified spherical stage were observed in muscle digests.
  • Macrogamonts and microgamonts were present in cell cultures 24 hours post-inoculation.
  • Sporulated oocysts were not observed in the infected cell cultures.

Conclusions:

  • The hypothesis of developing a laboratory model for S. strixi infection in mammals using the described methods was rejected.
  • Further research is needed to establish a successful laboratory model for S. strixi propagation.