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Journal of medical entomology2011; 48(1); 53-60; doi: 10.1603/me10123

Host blood meal identification by multiplex polymerase chain reaction for dispersal evidence of stable flies (Diptera:Muscidae) between livestock facilities.

Abstract: A species-specific multiplex polymerase chain reaction targeting the cytochrome b gene of cattle, horses, humans, and dogs was developed to determine the blood meal sources of stable flies, Stomoxys calcitrans (L.), collected from Florida equine facilities. Of 595 presumptive blood-fed stable flies analyzed, successful host amplification was obtained in 350, for a field host-detection efficiency of 58.8%. The majority of analyzed stable flies had fed on cattle (64.6%), followed by horses (24.3%), humans (9.5%), and dogs (1.6%). A survey of animal-enclosed pastures occurring within 3 km of stable fly collection sites revealed that the nearest cattle were between 0.8 and 1.5 km from the four horse farm sampling sites. Cattle-feeding frequencies were greater on farms where cattle were located at distances of 0.8 km, suggesting that between farm differences in host-feeding frequency is related to the number of and distance from a particular host type. Time course evaluations of previously laboratory-fed stable flies demonstrated that host-detection efficiency with this system was 100, 50, and 0% when flies were evaluated at 16, 24, and 48 h postblood feeding, respectively. The results of this study suggest short-term stable fly dispersal of up to 1.5 km in a 48-h time period. The implications of these findings are discussed.
Publication Date: 2011-02-23 PubMed ID: 21337948DOI: 10.1603/me10123Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.

Summary

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This research article deals with a study where a special type of polymerase chain reaction was used to identify the blood meal sources of stable flies, which are insects that are notorious for spreading diseases. The main aim was to understand stable flies’ dispersal patterns and feeding habits, which could contribute to efforts to control their populations and to limit the spread of diseases between different animal species and humans within livestock facilities.

Study Methodology and Materials

  • The researchers used a multiplex polymerase chain reaction (PCR), which is a method that allows for the simultaneous amplification of multiple target sequences in a single reaction.
  • For this study, the multiplex PCR was designed to specifically target the cytochrome b gene of cattle, horses, humans, and dogs. This gene was targeted because it is found in the mitochondrial DNA and changes in its sequence can be used to differentiate between species.
  • Stable flies, specifically Stomoxys calcitrans, were collected from equine facilities in Florida and their blood meals were analyzed using this method.

Results of the Study

  • Out of 595 stable flies analyzed, successful amplification was achieved in 350 cases, which amounted to a host-detection efficiency of 58.8%. This shows that the multiplex PCR was able to accurately detect the blood meal source of more than half of the tested flies.
  • The majority of the flies had fed on cattle (64.6%), followed by horses (24.3%), humans (9.5%), and dogs (1.6%). This suggests that stable flies show a preference for certain hosts over others.
  • In terms of distances from the host, cattle-feeding frequencies were greater on farms where cattle were located at distances of 0.8 km. This suggests that both the proximity and population density of hosts affect the feeding preferences of stable flies.
  • Time course evaluations revealed that 100% host-detection efficiency was achieved 16 hours post feeding, 50% at 24 hours post feeding, and 0% at 48 hours post feeding. This demonstrates that the ability to trace the blood meal sources of the flies decreases over time.

Implications and Conclusions

  • The study concludes that stable flies have a short-term dispersal distance of up to 1.5 km within a 48-hour timespan.
  • Understanding these dispersal and feeding patterns can be instrumental in controlling fly populations and curbing the spread of diseases in livestock facilities.
  • The hosts’ proximity and abundance play a significant role in influencing the flies’ feeding habits, which could also provide insights into effective pest management strategies.
  • This species-specific multiplex PCR may serve as a significant tool in monitoring and management of stable flies in the perspective of livestock health and human safety.

Cite This Article

APA
Pitzer JB, Kaufman PE, Tenbroeck SH, Maruniak JE. (2011). Host blood meal identification by multiplex polymerase chain reaction for dispersal evidence of stable flies (Diptera:Muscidae) between livestock facilities. J Med Entomol, 48(1), 53-60. https://doi.org/10.1603/me10123

Publication

ISSN: 0022-2585
NlmUniqueID: 0375400
Country: England
Language: English
Volume: 48
Issue: 1
Pages: 53-60

Researcher Affiliations

Pitzer, Jimmy B
  • Entomology and Nematology Department, University of Florida, 970 Natural Area Drive, Gainesville, FL 32611, USA.
Kaufman, Phillip E
    Tenbroeck, Saundra H
      Maruniak, James E

        MeSH Terms

        • Animals
        • Base Sequence
        • Blood Chemical Analysis
        • Cattle / parasitology
        • Dogs
        • Florida
        • Horses / parasitology
        • Host-Parasite Interactions
        • Housing, Animal
        • Humans
        • Molecular Sequence Data
        • Muscidae / chemistry
        • Polymerase Chain Reaction
        • Population Dynamics

        Citations

        This article has been cited 11 times.
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