LABORATORY DIAGNOSTIC TESTS AND HOW TO INTERPRET THEM of EHM development is greater in horses infected
with the neuropathogenic genotype (D752).8 Fur- thermore, detection of a neurotropic EHV-1 strain may influence therapy, especially the use of anti- viral drugs such as valacyclovir, used to decrease viremia and prevent the development of neurolog- ical sequelae.9 Contemporary EIV strains circulating worldwide
all belong to the H3N8 Florida sublineage. Recent EIV surveillance data has shown that Florida sub- lineage viruses from both clade 1 and 2 circulate in Europe, while clade 1 viruses have been primarily reported from North America. With the increased national and international transportation of equids, it is very important to monitor the spread of EIV using timely, fast, and reliable molecular diagnostic platforms. In past years, clade affiliation of EIV strains has been monitored using conventional nu- cleic acid sequencing techniques and more recently pyrosequencing, both of which are time- and labor intensive. Recent advances in genomic analysis have identified various SNPs of the hemagglutinin A1 gene of EIV virus able to determine clade affil- iation of EIV field isolates.10 Quantitative PCR assays are presently offered by individual diag- nostic laboratories in order to determine EIV clade affiliation. The information pertaining to EIV clade affiliation is important not only from an epidemiological standpoint but also to monitor and understand EIV outbreaks and update EIV vaccine strains in order to improve protection against clinical disease.
3. Conclusion
Quantitative PCR has without any doubt improved the accuracy and turnaround time for the detection of respiratory viruses. Novel molecular approaches are presently available to complement the already qualitative reporting of qPCR results for respiratory viruses. These include the use of parallel testing for well- and lesser-characterized respiratory vi- ruses in order to expand viral etiologies associated with IURTD, define the contagious nature of an infected horse by assessing the replicative status of selected viruses, and by defining the genotype of selected viruses in order to determine prognostic outcome (EHV-1 in the context of EHM) and vaccine effectiveness (EIV). However, while all these diag- nostic strategies add to a better interpretation of results, one must always keep in mind the biology of the suspected pathogen to be detected, the disease stage of the animal (acute versus subacute or
chronic), the collection of the most sensitive biolog- ical specimen (nasal versus nasopharyngeal secre- tions) to be used and test to be requested. When interpreting qPCR results, one must remember the factors listed above in order to be able to trouble- shoot and explain why a sample unexpectedly tested negative. In conclusion, novel molecular strategies such as absolute quantitation, detection of viral transcripts and genotyping will expand the possibil- ity to better characterize selected viruses, determine the level of environmental contamination and risk of transmission and monitor treatment response and vaccine effectiveness.
Acknowledgments
Declaration of Ethics The Author has adhered to the Principles of Veter- inary Medical Ethics of the AVMA.
Conflict of Interest The Author has no conflicts of interest.
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