We examined three virus isolates from birds. Virus strains RI-166 and RI-175 were both isolated from brain tissue of dead pigeons (Columba livia) collected at two localities in Rhode Island in summer 2000, as part of WNV surveillance activities. The two dead pigeons were collected on September 15 and 16 in Barrington, Bristol County (#175), and East Providence, Providence County (#166), respectively. No trauma or obvious gross pathology was noticed in the brain of either bird at necropsy. Brain tissue, including nearly equal portions of cerebrum and cerebellum, was collected and immediately frozen at –80^oC until processed for culture. Frozen tissue was thawed, and a small portion was completely homogenized in 3.0 mL of medium 199 (Sigma, St. Louis, MO). Homogenized brain tissue was centrifuged at 3,500 × g for 20 minutes at 2^oC in a refrigerated centrifuge; then 100 μL of the supernatants was immediately added to 25-mL flasks containing Vero cell monolayers. Tissue cultures were incubated at 37^oC and 5% CO₂ and examined for cytopathic effect (CPE) on days 3–7 postinoculation.

The third virus, designated CT-114, was originally isolated from an unknown wild bird captured in central Connecticut in 1969 by the late Robert B. Wallis, during surveillance for EEEV (6). The original isolation of CT-114 virus was made by intracerebral injection of newborn mice; no other information is available about this isolate.

Antigens for the three virus unknowns were prepared from infected newborn mouse brain by the sucrose-acetone extraction method (7). Hyperimmune mouse ascitic fluids (HMAF) to RI-166 and CT-114 viruses were prepared in adult mice as described (8). The adult mouse immunization schedule was four intraperitoneal injections per week of 10% crude suspensions of infected suckling mouse brain in phosphate-buffered saline mixed with Freund’s adjuvant. To induce ascites formation, sarcoma 180 cells were given intraperitoneally with the final injection.

Of the other rhabdovirus antigens and immune reagents used to characterize the three virus unknowns, some antigens were sucrose-acetone–extracted infected mouse brain, while others were medium from infected Vero cell cultures. The latter viruses, antigens, and HMAF were from the Arbovirus Reference and Reagent Collection maintained at the University of Texas Medical Branch (UTMB).

Complement fixation (CF) tests were performed by a microtechnique (7) with two full units of guinea pig complement. Titers were recorded as the highest dilutions giving 3+ or 4+ fixation of complement on a scale of 0 to 4+.

Indirect immunofluorescent antibody (IFA) tests were done on Vero and mosquito cells grown in eight-chamber Lab Tek tissue culture slides (Nunc, Inc., Naperville, IL). The mosquito cells tested were the C6/36 clone of Aedes albopictus cells (9) and a Culex quinquefasciatus cell line (10). After addition of virus, the Vero and mosquito cells were incubated with appropriate media at 37^oC and 28^oC, respectively. Culture slides with Vero cells were fixed in cold acetone when the cells showed 2+ to 3+ viral CPE; the mosquito cells were fixed after 6 days of incubation. The IFA tests were performed by using HMAF at dilutions of 1:10 and 1:20 and a commercial fluorescein isothiocyanate-conjugated goat antimouse immunoglobulin G (Sigma, St. Louis, MO) (11).

Immediately after removal of the medium, Vero cell monolayers infected with RI-175 and CT-114 viruses were fixed in a mixture of 1.25% formaldehyde and 2.5% glutaraldehyde in 0.05 M cacodylate buffer at pH 7.3, to which 0.03% trinitrophenol and 0.03% CaCl₂ were added, as described (12). After primary fixation, monolayers were washed in cacodylate buffer. Then the cells were scraped off the plastic, pelleted by light centrifugation in buffer, and postfixed in 1% OsO₄ in the same buffer. They were stained en bloc with 1% uranyl acetate in 0.1 M maleate buffer at pH 5.0, dehydrated in ethanol, and embedded in Poly/Bed 812 (Polysciences, Warrington, PA). Ultrathin sections were cut on a Reichert/Leica Ultracut S ultramicrotome (Leica Microsystems, Inc., Bannockburn, IL), stained with 2% aqueous uranyl acetate and 0.4% lead citrate, and examined with Philips 201 or Philips CM-100 electron microscopes at 60 kV (Philips Electron Optics, Eindhoven, the Netherlands).

Viruses RI-166 and RI-175 were initially isolated in cultures of Vero cells at the Center for Vector-Borne Disease (CVBD), University of Rhode Island. Media from the positive cultures were tested by immunoassay for WNV, EEEV, Highlands J virus, Jamestown Canyon virus, La Crosse virus, Saint Louis encephalitis virus, and Flanders virus antigens, with specific monoclonal and polyclonal antibodies; results were negative. Both viruses RI-166 and RI-175 were subsequently sent to UTMB for further study and characterization. When added to Vero cell cultures, both viruses produced extensive CPE within 48 hours. Newborn Institute for Cancer Research outbred mice that were injected intracerebrally with both RI-166 and RI-175 viruses became sick and moribund within 96 hours. RI-166 virus was also added to cultures of C6/36 and Cx. quinquefasciatus cells; it did not produce CPE, and no viral antigen could be detected in the mosquito cells when examined by IFA 6 days later.

Virus CT-114 was initially isolated by Robert Wallis at the Department of Epidemiology and Public Health, Yale University School of Medicine, following intracerebral injection of a homogenate of bird tissue into newborn mice. The virus was subsequently transferred to UTMB. Virus CT-114 produced illness and death in newborn mice 24–48 hours after intracerebral injection, as well as massive CPE in Vero cells within 48 hours; however, it did not produce CPE in the mosquito cells. Specific viral antigen was detected by IFA in Cx. quinquefasciatus cells injected with CT-114 virus, but not in C6/36 cells.

Virions of isolate CT-114 were bullet shaped and were found budding mostly into the intracytoplasmic vacuoles, either as single virions into a small vacuole, or as several virions budding into the same large vacuole (Figure, A and B). Virions of CT-114 were 55 nm–60 nm in diameter and 145 nm–150 nm long, with a periodicity of striations of 10.5 nm (Figure, B).

Virions of the isolate RI-175 were seen budding predominantly into the extracellular space from the plasmalemma of the Vero cells (Figure, C and D). The virions were bacilliform, measuring 90 nm–100 nm in diameter, up to 500 nm long, and with a 20- to 25-nm periodicity of striations. In some cross-sections, the spiral packaging of the nucleocapsid could be seen and had the appearance of tubules 9 nm in diameter (Figure, C). Large groups of virions could be observed outside the cells.

On the basis of their rhabdovirus-like morphology, RI-166, RI-175, and CT-114 antigens and HMAFs were examined by CF against 36 rhabdovirus antigens and HMAFs in our reference collection. The 36 agents included Carajas virus; Chandipura virus; Cocal virus; Isfahan virus; Maraba virus; Piry virus; vesicular stomatitis virus, types Alagoas, Indiana, and New Jersey; Vesiculovirus species Boteke, Jurona, Klamath, La Joya, Malpais Spring, Radi, and Yug Bogdanovac; Iriri virus, Flanders virus, Mosqueiro virus, Mossuril virus, Kern Canyon virus, Nkolbisson virus, Le Dantec virus, Connecticut virus, New Minto virus, sawgrass virus, Chaco virus, Timbo virus, Bangoran virus, Inhangapi virus, Joinjakaka virus, Kannamangalam virus, Kotonkan virus, Marco virus, Tibrogargan virus, and Yata virus (13,14).

In addition, RI-166 antigen was also tested against 26 other rhabdovirus HMAFs: Calchaqui, Gray Lodge, Kwatta, Mount Elgon bat, Perinet, Porton, Duvenhage, Lagos bat, Mokola, Rabies, Bahia Grande, Hart Park, Kamese, Keuraliba, Almpiwar, Aruac, Bimbo, Charleville, Coastal Plains, Gossas, Kolongo, Navarro, Obodhiang, Parry Creek, Rio Grande, and Sandjimba. In CF tests, RI-166 (selected as the prototype) and RI-175 viruses were indistinguishable (Table 1); but RI-166 antigen and HMAF did not react with any of the other rhabdovirus antigens or HMAFs listed. Because of the geographic region where they were isolated, we initially suspected that RI-166 and CT-114 might be Connecticut or Flanders viruses. However, no antigenic relationship was shown by CF test (Table 1). The antigen RI 907-36 was prepared from a 1999 isolate of Flanders virus from Rhode Island. Likewise, no relationship could be demonstrated between RI-166, CT-114, Connecticut, or Flanders viruses by IFA test (data not shown). Based on these findings, we conclude that RI-166 is probably a new, unassigned vertebrate rhabdovirus. The name Rhode Island virus is proposed for this virus.

In CF tests, CT-114 HMAF reacted with five vesicular stomatitis serogroup antigens: Chandipura, Isfahan, Maraba, Jurona, and La Joya (Table 2). Antigenically, CT-114 was most closely related to Jurona and La Joya viruses. Both Jurona and La Joya viruses are tentative members of the genus Vesiculovirus (14–16). Based on the morphology and antigenic relationships of CT-114, we conclude that it is also a provisional member of the Vesiculovirus genus. The name Farmington is proposed for this new virus.