ZFIN ID: ZDB-PUB-170721-8
Comparison of Antemortem and Environmental Samples for Zebrafish Health Monitoring and Quarantine
Crim, M.J., Lawrence, C., Livingston, R.S., Rakitin, A., Hurley, S.J., Riley, L.K.
Date: 2017
Source: Journal of the American Association for Laboratory Animal Science : JAALAS   56: 412-424 (Journal)
Registered Authors: Crim, Marcus J., Lawrence, Christian
Keywords: none
MeSH Terms:
  • Animals
  • Embryo, Nonmammalian/microbiology
  • Embryo, Nonmammalian/parasitology
  • Fish Diseases/microbiology*
  • Fish Diseases/parasitology*
  • Infections/microbiology
  • Infections/parasitology
  • Infections/veterinary*
  • Microsporidia/classification
  • Microsporidia/isolation & purification
  • Mycobacterium/classification
  • Mycobacterium/isolation & purification
  • Nematoda/classification
  • Nematoda/isolation & purification
  • Quarantine/veterinary*
  • Real-Time Polymerase Chain Reaction
  • Zebrafish*
PubMed: 28724491
Molecular diagnostic assays offer both exquisite sensitivity and the ability to test a wide variety of sample types. Various types of environmental sample, such as detritus and concentrated water, might provide a useful adjunct to sentinels in routine zebrafish health monitoring. Similarly, antemortem sampling would be advantageous for expediting zebrafish quarantine, without euthanasia of valuable fish. We evaluated the detection of Mycobacterium chelonae, M. fortuitum, M. peregrinum, Pseudocapillaria tomentosa, and Pseudoloma neurophilia in zebrafish, detritus, pooled feces, and filter membranes after filtration of 1000-, 500-, and 150-mL water samples by real-time PCR analysis. Sensitivity varied according to sample type and pathogen, and environmental sampling was significantly more sensitive than zebrafish sampling for detecting Mycobacterium spp. but not for Pseudocapillaria neurophilia or Pseudoloma tomentosa. The results of these experiments provide strong evidence of the utility of multiple sample types for detecting pathogens according to each pathogen's life cycle and ecological niche within zebrafish systems. In a separate experiment, zebrafish subclinically infected with M. chelonae, M. marinum, Pleistophora hyphessobryconis, Pseudocapillaria tomentosa, or Pseudoloma neurophilia were pair-spawned and individually tested with subsets of embryos from each clutch that received no rinse, a fluidizing rinse, or were surface-disinfected with sodium hypochlorite. Frequently, one or both parents were subclinically infected with pathogen(s) that were not detected in any embryo subset. Therefore, negative results from embryo samples may not reflect the health status of the parent zebrafish.