Identification and validation of a commercial cryopreservation medium for the practical preservation of Dirofilaria immitis microfilaria.


Journal

Parasites & vectors
ISSN: 1756-3305
Titre abrégé: Parasit Vectors
Pays: England
ID NLM: 101462774

Informations de publication

Date de publication:
29 Jul 2020
Historique:
received: 16 03 2020
accepted: 21 07 2020
entrez: 31 7 2020
pubmed: 31 7 2020
medline: 17 3 2021
Statut: epublish

Résumé

Dirofilaria immitis is a parasitic nematode transmitted by mosquitoes and the cause of heartworm disease in dogs and dirofilariasis in humans and other mammals. The parasite is endemic worldwide. Vector stage research requires a reliable supply of D. immitis microfilariae (mf). It is believed that cryopreserved mf would retain viability and provide a powerful tool for vector stage research. However, reports on cryopreservation of D. immitis mf are limited. Therefore, this study aimed to validate commercial cryopreservation media to establish a practical, convenient and reproducible storage procedure for D. immitis mf. Six different commercially available cryopreservation media were compared with the traditional polyvinylpyrrolidone-dimethyl sulfoxide (PVP-DMSO) preservation solution. In vitro viability of purified D. immitis mf and mf-infected total blood was analyzed using a motility assay and propidium iodide staining. In vivo infectivity of Aedes aegypti mosquitoes with cryopreserved mf was assessed using a mosquito survival test and quantifying the number of third-stage larvae (L3) after 13 days post-infection. Purified mf cryopreserved in CultureSure showed the best viability when compared to mf cryopreserved in the remaining five commercially available media and PVP-DMSO. Viability of mf in mf-infected total blood cryopreserved in CultureSure varied with the ratio of infected blood to CultureSure. Optimum results were obtained with 200 µl mf-infected blood:800 µl CultureSure. CultureSure was also the optimum medium for cryopreserving mf prior to infectivity of A. aegypti. The number of L3 was approximately the same for CultureSure cryopreserved mf (3× concentrated solution) and non-cryopreserved fresh mf. CultureSure is an optimal commercial cryopreservation solution for the storage of D. immitis purified mf, mf-infected total blood, and mf used for in vivo mosquito experiments. Furthermore, this study describes an easy preservation method for clinical D. immitis-infected blood samples facilitating vector stage studies, as well as the study of macrocyclic lactone resistance in heartworms and the education of veterinarians.

Sections du résumé

BACKGROUND BACKGROUND
Dirofilaria immitis is a parasitic nematode transmitted by mosquitoes and the cause of heartworm disease in dogs and dirofilariasis in humans and other mammals. The parasite is endemic worldwide. Vector stage research requires a reliable supply of D. immitis microfilariae (mf). It is believed that cryopreserved mf would retain viability and provide a powerful tool for vector stage research. However, reports on cryopreservation of D. immitis mf are limited. Therefore, this study aimed to validate commercial cryopreservation media to establish a practical, convenient and reproducible storage procedure for D. immitis mf.
METHODS METHODS
Six different commercially available cryopreservation media were compared with the traditional polyvinylpyrrolidone-dimethyl sulfoxide (PVP-DMSO) preservation solution. In vitro viability of purified D. immitis mf and mf-infected total blood was analyzed using a motility assay and propidium iodide staining. In vivo infectivity of Aedes aegypti mosquitoes with cryopreserved mf was assessed using a mosquito survival test and quantifying the number of third-stage larvae (L3) after 13 days post-infection.
RESULTS RESULTS
Purified mf cryopreserved in CultureSure showed the best viability when compared to mf cryopreserved in the remaining five commercially available media and PVP-DMSO. Viability of mf in mf-infected total blood cryopreserved in CultureSure varied with the ratio of infected blood to CultureSure. Optimum results were obtained with 200 µl mf-infected blood:800 µl CultureSure. CultureSure was also the optimum medium for cryopreserving mf prior to infectivity of A. aegypti. The number of L3 was approximately the same for CultureSure cryopreserved mf (3× concentrated solution) and non-cryopreserved fresh mf.
CONCLUSIONS CONCLUSIONS
CultureSure is an optimal commercial cryopreservation solution for the storage of D. immitis purified mf, mf-infected total blood, and mf used for in vivo mosquito experiments. Furthermore, this study describes an easy preservation method for clinical D. immitis-infected blood samples facilitating vector stage studies, as well as the study of macrocyclic lactone resistance in heartworms and the education of veterinarians.

Identifiants

pubmed: 32727546
doi: 10.1186/s13071-020-04257-1
pii: 10.1186/s13071-020-04257-1
pmc: PMC7391585
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

383

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 19H03121
Organisme : Japan Society for the Promotion of Science
ID : 19KK0175

Références

Afr J Med Med Sci. 1980 Mar-Jun;9(1-2):69-71
pubmed: 6282090
J Helminthol. 1960;34:13-26
pubmed: 13775555
Vet Parasitol. 2005 Oct 24;133(2-3):191-5
pubmed: 16099105
Vet Parasitol. 2008 Aug 17;155(3-4):242-8
pubmed: 18602759
Exp Parasitol. 1956 Jul;5(4):371-5
pubmed: 13344500
Parasit Vectors. 2014 Nov 07;7:494
pubmed: 25376278
Vet Parasitol. 2014 Nov 15;206(1-2):38-42
pubmed: 24594213
Vet Parasitol. 2015 Jun 15;210(3-4):167-78
pubmed: 25936435
Parasitology. 2013 Jul;140(8):959-65
pubmed: 23552564
J Helminthol. 1983 Dec;57(4):319-24
pubmed: 6668419
Am J Hyg. 1947 Jan;45(1):102-21
pubmed: 20279331
Am J Trop Med Hyg. 1983 Jan;32(1):138-45
pubmed: 6824119
Parasit Vectors. 2012 Jul 09;5:138
pubmed: 22776618
Exp Parasitol. 1955 Mar;4(2):143-64
pubmed: 14365779
J Mol Model. 2008 Aug;14(8):689-97
pubmed: 18458968
Adv Parasitol. 2008;66:193-285
pubmed: 18486691
Parasit Vectors. 2014 Jan 13;7:1
pubmed: 24411014
Am J Trop Med Hyg. 2001 Aug;65(2):162-3
pubmed: 11508394
Clin Microbiol Rev. 2012 Jul;25(3):507-44
pubmed: 22763636
BMC Vet Res. 2020 Jan 31;16(1):31
pubmed: 32005240

Auteurs

Takahiro Shirozu (T)

National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido, 080-8555, Japan.

Akira Soga (A)

National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido, 080-8555, Japan.

Shinya Fukumoto (S)

National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido, 080-8555, Japan. fukumoto@obihiro.ac.jp.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice
Animals Tail Swine Behavior, Animal Animal Husbandry

Classifications MeSH