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Featured researches published by Michael R. Sardelis.


Journal of Medical Entomology | 2005

An Update on the Potential of North American Mosquitoes (Diptera: Culicidae) to Transmit West Nile Virus

Michael J. Turell; David J. Dohm; Michael R. Sardelis; Monica L. O’Guinn; Theodore G. Andreadis; Jamie A. Blow

Abstract Since first discovered in the New York City area in 1999, West Nile virus (WNV) has become established over much of the continental United States and has been responsible for >10,000 cases of severe disease and 400 human fatalities, as well as thousands of fatal infections in horses. To develop appropriate surveillance and control strategies, the identification of which mosquito species are competent vectors and how various factors influence their ability to transmit this virus must be determined. Therefore, we evaluated numerous mosquito species for their ability to transmit WNV under laboratory conditions. This report contains data for several mosquito species not reported previously, as well as a summary of transmission data compiled from previously reported studies. Mosquitoes were allowed to feed on chickens infected with WNV isolated from a crow that died during the 1999 outbreak in New York City. These mosquitoes were tested ≈2 wk later to determine infection, dissemination, and transmission rates. All Culex species tested were competent vectors in the laboratory and varied from highly efficient vectors (e.g., Culex tarsalis Coquillett) to moderately efficient ones (e.g., Culex nigripalpus Theobald). Nearly all of the Culex species tested could serve as efficient enzootic or amplifying vectors for WNV. Several container-breeding Aedes and Ochlerotatus species were highly efficient vectors under laboratory conditions, but because of their feeding preferences, would probably not be involved in the maintenance of WNV in nature. However, they would be potential bridge vectors between the avian–Culex cycle and mammalian hosts. In contrast, most of the surface pool-breeding Aedes and Ochlerotatus species tested were relatively inefficient vectors under laboratory conditions and would probably not play a significant role in transmitting WNV in nature. In determining the potential for a mosquito species to become involved in transmitting WNV, it is necessary to consider not only its laboratory vector competence but also its abundance, host-feeding preference, involvement with other viruses with similar transmission cycles, and whether WNV has been isolated from this species under natural conditions.


Annals of the New York Academy of Sciences | 2006

Potential North American Vectors of West Nile Virus

Michael J. Turell; Michael R. Sardelis; David J. Dohm; Monica L. O'Guinn

Abstract: The outbreak of disease in the New York area in 1999 due to West Nile (WN) virus was the first evidence of the occurrence of this virus in the Americas. To determine potential vectors, more than 15 mosquito species (including Culex pipiens, Cx. nigripalpus, Cx. quinquefasciatus, Cx. salinarius, Aedes albopictus, Ae. vexans, Ochlerotatus japonicus, Oc. sollicitans, Oc. taeniorhynchus, and Oc. triseriatus) from the eastern United States were evaluated for their ability to serve as vectors for the virus isolated from birds collected during the 1999 outbreak in New York. Mosquitoes were allowed to feed on one‐ to four‐day old chickens that had been inoculated with WN virus 1‐3 days previously. The mosquitoes were incubated for 12‐15 days at 26°C and then allowed to refeed on susceptible chickens and assayed to determine transmission and infection rates. Several container‐breeding species (e.g., Ae. albopictus, Oc. atropalpus, and Oc. japonicus) were highly efficient laboratory vectors of WN virus. The Culex species were intermediate in their susceptibility. However, if a disseminated infection developed, all species were able to transmit WN virus by bite. Factors such as population density, feeding preference, longevity, and season of activity also need to be considered in determining the role these species could play in the transmission of WN virus.


PLOS ONE | 2007

A new classification system for the actions of IRS chemicals traditionally used for malaria control.

John P. Grieco; Nicole L. Achee; Theeraphap Chareonviriyaphap; Wannapa Suwonkerd; Kamal Chauhan; Michael R. Sardelis; Donald R. Roberts

Knowledge of how mosquitoes respond to insecticides is of paramount importance in understanding how an insecticide functions to prevent disease transmission. A suite of laboratory assays was used to quantitatively characterize mosquito responses to toxic, contact irritant, and non-contact spatial repellent actions of standard insecticides. Highly replicated tests of these compounds over a range of concentrations proved that all were toxic, some were contact irritants, and even fewer were non-contact repellents. Of many chemicals tested, three were selected for testing in experimental huts to confirm that chemical actions documented in laboratory tests are also expressed in the field. The laboratory tests showed the primary action of DDT is repellent, alphacypermethrin is irritant, and dieldrin is only toxic. These tests were followed with hut studies in Thailand against marked-released populations. DDT exhibited a highly protective level of repellency that kept mosquitoes outside of huts. Alphacypermethrin did not keep mosquitoes out, but its strong irritant action caused them to prematurely exit the treated house. Dieldrin was highly toxic but showed no irritant or repellent action. Based on the combination of laboratory and confirmatory field data, we propose a new paradigm for classifying chemicals used for vector control according to how the chemicals actually function to prevent disease transmission inside houses. The new classification scheme will characterize chemicals on the basis of spatial repellent, contact irritant and toxic actions.


Journal of Medical Entomology | 2002

Experimental vertical transmission of West Nile virus by Culex pipiens (Diptera: Culicidae).

David J. Dohm; Michael R. Sardelis; Michael J. Turell

Abstract Despite the detection of West Nile (WN) virus in overwintering Culex pipiens L. in New York in February 2000, the mechanism by which this virus persists throughout the winter to initiate infections in vertebrate hosts and vectors the following spring remains unknown. After a blood meal, parous mosquitoes generally do not survive until spring and gonotrophic dissociation occurs in only a small percentage of the population. To investigate vertical transmission as a means of viral survival during interepizootics, we intrathoracically inoculated Cx. pipiens and Aedes albopictus (Skuse) with WN virus and subsequently tested their F1 progeny for the presence of virus. Among the Cx. pipiens, we recovered virus from two of 1,417 adult progeny that had been reared at 18°C for a minimal filial infection rate (MFIR) of ≈1.4/1,000 and four of 1,873 adult progeny reared at 26°C (MFIR = 2.1/1,000). The mean titer of the positive pools was 105.6 plaque-forming units (PFU)/ml (=105.9 PFU/mosquito for positive mosquitoes) of virus. Overall, the MFIR was ≈1.8/1,000 for Cx. pipiens. Although reports indicate that Ae. albopictus vertically transmit various viruses in the Japanese encephalitis virus complex, we did not detect WN virus in any of > 13,000 F1 progeny of WN virus-inoculated specimens. Female Cx. pipiens that are vertically infected during the late summer season and then survive the winter could serve as a source of WN virus to initiate an infection cycle the following spring.


Journal of Medical Entomology | 2002

Laboratory transmission of La Crosse virus by Ochlerotatus j. japonicus (Diptera: Culicidae).

Michael R. Sardelis; Michael J. Turell; Richard G. Andre

Abstract Ochlerotatus j. japonicus, a recent introduction to the United States, was studied to determine its capability to serve as a vector of La Crosse (LAC) virus. A field-collected population of Ochlerotatus triseriatus, the primary vector of LAC virus, was similarly tested for comparison. After Oc. j. japonicus ingested virus from hamsters with viremias of 103.6–5.4 plaque-forming units (PFU)/ml of blood, its estimated transmission rates were 35–88%. These rates were slightly lower than, though similar to, those for Oc. triseriatus, 75–100%. Viral titers in Oc. j. japonicus peaked at ≈105.5 PFU/mosquito about 7 d after ingesting a blood meal in which the concentration of LAC virus was 105.4 PFU/ml of blood; virus had disseminated from the midgut in 100% (8/8) of these specimens. These data, combined with the close association between the habitats of Oc. j. japonicus and Oc. triseriatus and the reported expansion of the range of this newly discovered species in the eastern United States, indicate that Oc. j. japonicus could function as an additional vector of LAC virus.


Journal of Medical Entomology | 2001

Aedes (Finlaya) japonicus (Diptera: Culicidae), a Newly Recognized Mosquito in the United States: Analyses of Genetic Variation in the United States and Putative Source Populations

Dina M. Fonseca; Scott R. Campbell; Wayne J. Crans; Motoyoshi Mogi; Ichiro Miyagi; Takako Toma; Mark Bullians; Theodore G. Andreadis; Richard L. Berry; Benedict Pagac; Michael R. Sardelis; Richard C. Wilkerson

Abstract Introduction of potential disease vectors into a new geographic area poses health risks to local human, livestock, and wildlife populations. It is therefore important to gain understanding of the dynamics of these invasions, in particular its sources, modes of spread after the introduction, and vectorial potential. We studied the population genetics of Aedes (Finlaya) japonicus japonicus (Theobald), an Asian mosquito that was recognized for the first time in the United States in 1998. We examined patterns of genetic diversity using random amplified polymorphic DNA and sequences of ND4 of mtDNA by comparing samples from populations spanning the range of this mosquito in Japan (six samples) and the United States (nine samples) as well as specimens intercepted in New Zealand in 1999. We found geographically differentiated populations in Japan, indicating limited gene flow even on small spatial scales. In the United States, we found evidence of significant genetic differentiation between samples from New York, Connecticut, and New Jersey and those from mid-Pennsylvania and Maryland. We were unable to pinpoint the source location(s) in Japan, although some of the U.S. samples are genetically close to samples from south Honshu and western Kyushu. Further studies should include samples from Korean populations. Distinct genetic signatures in U.S. populations undergoing expansion suggest the possibility of local increases in genetic diversity if and where they meet.


Journal of Medical Entomology | 2002

Experimental Transmission of Eastern Equine Encephalitis Virus by Ochlerotatus j. japonicus (Diptera: Culicidae)

Michael R. Sardelis; David J. Dohm; Benedict Pagac; Richard G. Andre; Michael J. Turell

Abstract We evaluated the potential for Ochlerotatus j. japonicus (Theobald), a newly recognized invasive mosquito species in the United States, to transmit eastern equine encephalitis (EEE) virus. Aedes albopictus (Skuse) and Culex pipiens (L.) were similarly tested for comparison. Ochlerotatus j. japonicus and Ae. albopictus became infected and transmitted EEE virus by bite after feeding on young chickens 1 d after they had been inoculated with EEE virus (viremias ranging from 107.0–8.7 plaque-forming units [PFU]/ml of blood). No Cx. pipiens (n = 20) had detectable levels of virus 14 d after feeding on an EEE-virus infected chicken with a viremia of 108.1 PFU per ml of blood. Depending on the viral titer in the donor chicken, infection rates ranged from 55–100% for Oc. j. japonicus and 93–100% for Ae. albopictus. In these two species, dissemination rates were identical to or nearly identical to infection rates. Depending on the viral titer in the blood meal, estimated transmission rates ranged from 15 to 25% for Oc. j. japonicus and 59–63% for Ae. albopictus. Studies of replication of EEE virus in Oc. j. japonicus showed that there was an “eclipse phase” in the first 4 d after an infectious blood meal, that viral titers peak by day 7 at around 105.7 per mosquito, and that virus escaped the mid-gut as soon as 3 d after the infectious blood meal. These data, combined with the opportunistic feeding behavior of Oc. j. japonicus in Asia and the reported expansion of its range in the eastern United States, indicate that it could function as a bridge vector for EEE virus between the enzootic Culiseta melanura (Coquillett)-avian cycle and susceptible mammalian hosts.


Journal of Medical Entomology | 2005

Isolation of Viruses from Mosquitoes (Diptera: Culicidae) Collected in the Amazon Basin Region of Peru

Michael J. Turell; Monica L. O’Guinn; J. W. Jones; Michael R. Sardelis; David J. Dohm; Douglas M. Watts; Roberto Fernandez; A.P.A. Travassos da Rosa; H. Guzman; Robert B. Tesh; C. A. Rossi; George V. Ludwig; J. A. Mangiafico; J. Kondig; L. P. Wasieloski; James E. Pecor; M. Zyzak; G. Schoeler; Christopher N. Mores; Carlos Calampa; John S. Lee; T. A. Klein

Abstract As part of a comprehensive study on the ecology of arthropod-borne viruses in the Amazon Basin region of Peru, we assayed 539,694 mosquitoes captured in Loreto Department, Peru, for arboviruses. Mosquitoes were captured either by dry ice-baited miniature light traps or with aspirators while mosquitoes were landing on human collectors, identified to species, and later tested on Vero cells for virus. In total, 164 virus isolations were made and included members of the Alphavirus (eastern equine encephalomyelitis, Trocara, Una, Venezuelan equine encephalomyelitis, and western equine encephalomyelitis viruses), Flavivirus (Ilheus and St. Louis encephalitis), and Orthobunyavirus (Caraparu, Itaqui, Mirim, Murutucu, and Wyeomyia viruses) genera. In addition, several viruses distinct from the above-mentioned genera were identified to the serogroup level. Eastern equine encephalomyelitis virus was associated primarily with Culex pedroi Sirivanakarn & Belkin, whereas Venezuelan equine encephalomyelitis virus was associated primarily with Culex gnomatos Sallum, Huchings & Ferreira. Most isolations of Ilheus virus were made from Psorophora ferox (Von Humboldt). Although species of the Culex subgenus Melanoconion accounted for only 45% of the mosquitoes collected, 85% of the virus isolations were made from this subgenus. Knowledge of the viruses that are being transmitted in the Amazon Basin region of Peru will enable the development of more effective diagnostic assays, more efficient and rapid diagnoses of clinical illnesses caused by these pathogens, risk analysis for military/civilian operations, and development of potential disease control measures.


Journal of The American Mosquito Control Association | 2005

A novel high-throughput screening system to evaluate the behavioral response of adult mosquitoes to chemicals

John P. Grieco; Nicole L. Achee; Michael R. Sardelis; Kamlesh R. Chauhan; Donald R. Roberts

ABSTRACT A modular and novel assay system for rapid mass screening of chemical compounds for contact irritant and spatial repellent actions against adult mosquitoes is described. The responses of Aedes aegypti to various concentrations of 3 topical repellents, deet, Bayrepel®, and SS220, were evaluated. At treatment concentrations ≥25 nmol/cm2 of SS220, mosquitoes exhibited significant contact irritant (escape) and spatial repellent (movement away from the chemical source) responses, whereas, a 10-fold increase in the treatment concentration of deet and Bayrepel was required to produce similar responses. The novel bioassay system detected contact irritancy and spatial repellency activity with reproducible results and provided baseline data for determining minimum effective concentrations for other chemicals. The system is compact in size, easy to decontaminate, and requires only a minute quantity of chemical compound.


Journal of Medical Entomology | 2000

Vector Competence of Peruvian Mosquitoes (Diptera: Culicidae) for Epizootic and Enzootic Strains of Venezuelan Equine Encephalomyelitis Virus

Michael J. Turell; James W. Jones; Michael R. Sardelis; David J. Dohm; Russell E. Coleman; Douglas M. Watts; Roberto Fernandez; Carlos Calampa; Terry A. Klein

Abstract Mosquitoes collected in the Amazon Basin, near Iquitos, Peru, were evaluated for their susceptibility to epizootic (IAB and IC) and enzootic (ID and IE) strains of Venezuelan equine encephalomyelitis (VEE) virus. After feeding on hamsters with a viremia of ≈108 plaque-forming units of virus per milliliter, Culex (Melanoconion) gnomatus Sallum, Huchings, & Ferreira, Culex (Melanoconion) vomerifer Komp, and Aedes fulvus (Wiedemann) were highly susceptible to infection with all four subtypes of VEE virus (infection rates ≥87%). Likewise, Psorophora albigenu (Peryassu) and a combination of Mansonia indubitans Dyar & Shannon and Mansonia titillans (Walker) were moderately susceptible to all four strains of VEE virus (infection rates ≥50%). Although Psorophora cingulata (Fabricius) and Coquillettidia venezuelensis (Theobald) were susceptible to infection with each of the VEE strains, these two species were not efficient transmitters of any of the VEE strains, even after intrathoracic inoculation, indicating the presence of a salivary gland barrier in these species. In contrast to the other species tested, both Culex (Melanoconion) pedroi Sirivanakarn & Belkin and Culex (Culex) coronator Dyar & Knab were nearly refractory to each of the strains of VEE virus tested. Although many of the mosquito species found in this region were competent laboratory vectors of VEE virus, additional studies on biting behavior, mosquito population densities, and vertebrate reservoir hosts of VEE virus are needed to incriminate the principal vector species.

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Michael J. Turell

United States Army Medical Research Institute of Infectious Diseases

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David J. Dohm

United States Army Medical Research Institute of Infectious Diseases

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Terry A. Klein

Walter Reed Army Institute of Research

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Richard G. Andre

Uniformed Services University of the Health Sciences

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John P. Grieco

University of Notre Dame

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Douglas M. Watts

University of Texas at El Paso

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Roberto Fernandez

Naval Medical Research Center

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Carlos Calampa

University of Texas Medical Branch

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James E. Pecor

Walter Reed Army Institute of Research

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