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[Human arbovirus infections in Burundi: results of a seroepidemiologic survey, 1980-1982].

A serological survey on 623 human sera was conducted in Burundi in 1980-1982, in order to evaluate the frequency of arboviral antibodies in the inhabitants of the three main areas: lowlands, central plateau and mountainous ridge. The results show a rather high activity of arboviruses, mainly in the lowlands (34.2% of inhabitants with antibodies). Chikungunya virus seems to be the most active arbovirus; the activity of Flavivirus is moderate; no trace of activity of yellow fever or West Nile viruses was found; Bunyavirus antibodies (particularly against Ilesha virus) were also detected.

Alphavirus↗

Serologic survey of domestic animals for zoonotic arbovirus infections in the Lacandón Forest region of Chiapas, Mexico.

A serologic survey in domestic animals (birds and mammals) was conducted in four communities located in the Lacandón Forest region of northeastern Chiapas, Mexico, during June 29 to July 1, 2001, with the objective to identify zoonotic arboviruses circulating in this area. We collected 202 serum samples from healthy domestic chickens, geese, ducks, turkeys, horses and cattle. The samples were tested by plaque-reduction neutralization test for antibodies to selected mosquito-borne flaviviruses (family Flaviviridae), including St. Louis encephalitis (SLE), Rocio (ROC), Ilheus (ILH), Bussuquara (BSQ), and West Nile (WN) viruses, and selected alphaviruses (family Togaviridae), including Western equine encephalitis (WEE), Eastern equine encephalomyelitis (EEE), and Venezuelan equine encephalitis (VEE) viruses. Neutralizing antibodies to SLE virus were detected in two (8%) of 26 turkeys, 15 (23%) of 66 cattle, and three (60%) of five horses. Antibodies to VEE virus were detected in 29 (45%) of 65 cattle. Because some of these animals were as young as 2 months old, we demonstrated recent activity of these two viruses. Sub-typing of the VEE antibody responses indicated that the etiologic agents of these infections belonged to the IE variety of VEE, which has been reported from other regions of Chiapas. WN virus-neutralizing antibodies were detected in a single cattle specimen (PRNT(90) = 1:80) that also circulated SLE virus-neutralizing antibodies (PRNT(90) = 1:20), suggesting that WN virus may have been introduced into the region. We also detected weak neutralizing activity to BSQ virus in four cattle and a chicken specimen, suggesting the presence of this or a closely related virus in Mexico. There was no evidence for transmission of the other viruses (ROC, ILH, EEE, WEE) in the study area.

Animals↗

Postinfection therapy of arbovirus infections in mice.

Most antiviral agents are efficacious prophylactically in vivo, and a few are efficacious for postinfection (p.i.) therapy. To explore possibilities for p.i. therapy of encephalogenic Banzi virus (BZV) and Semliki Forest virus infections in mice, we evaluated candidate antiviral therapies after development of the first clinical signs of infection. The earliest clinical indication of BZV viremia in mice is a rise in core body temperature beginning on day 3 p.i. BZV-infected mice showing elevated core body temperatures (greater than or equal to 37.3 degrees C) on days 3 and 4 p.i. were treated intraperitoneally with the interferon inducer poly(ICLC) (80 micrograms per mouse) and/or specific antiserum. Combined therapy on day 3 of a BZV infection protected over 75% of mice showing clinical evidence of viral disease before treatment. Protection against early brain infection must occur on day 4 p.i., since by that day BZV has started multiplying in the brains of the mice. Significant protection occurred with antiserum alone and increased with poly(ICLC). Similar protection was obtained during Semliki Forest virus viremia, but this infection is so rapid that the first clinical signs are reliably detectable only after viremia.

Animals↗

Arbovirus infections among laboratory personnel in Ibadan, Nigeria.

Laboratory-acquired infections encountered between 1963 and 1977 among personnel of the Virus Research Laboratory, Ibadan, Nigeria, are reported. Two cases of chikungunya infection occurred and one each with Dugbe, Wesselsbron, and dengue viruses. In each case, virus was isolated or development of antibody demonstrated. Among virus and two each to chikungunya and Rift Valley fever viruses, without experiencing any clinically recognized disease.

Adult↗

[Etiology of Karelia fever--a new arbovirus infection].

In August-September 1981, in some areas of Karelia (on the border of northern and middle taiga) there occurred diseases with signs of fever, rash, and arthralgia developing in some patients into a chronic condition. Examinations of paired sera from patients with the acute disease and from convalescents using a set of Toga- and Bunya-viruses showed the etiology of the disease to be associated with a virus from the Togaviridae family, genus Alphavirus, of the antigenic Sindbis complex.

Adolescent↗

Surveillance of mosquitoes and arbovirus infection at the Ross River Dam (Stage 1), Australia.

This paper describes the temporal and spatial abundance of the mosquito fauna of the Ross River Dam (Stage 1) in northern Queensland, Australia. Culex annulirostris, Anopheles annulipes s.l., Mansonia uniformis, Mansonia septempunctata, and the nondam breeding Aedes vigilax were the major species collected by dry ice-supplemented light traps set at various distances from the edge of the reservoir. To estimate the level of arbovirus activity in these different zones, sentinel chicken flocks were bled 4 times a year and their antibody conversion rates determined by the hemagglutination-inhibition test. Although mosquito abundance at sites close to the reservoir were 1.5-6.1 times higher than at the more distant sites, arbovirus conversion rates, particularly to the alphaviruses Ross River and Sindbis, varied according to zone and year, suggesting that risk of infection was no greater around the dam than elsewhere.

Aedes↗

Arbovirus infection of vertebrate and insect cell cultures, with special emphasis on Mokola, Obodhiang, and kotonkan viruses of the rabies serogroup.

Multiplication of rabies serogroup viruses, Obodhiang and kotonkan (two presumptive arboviruses), was induced in vertebrate cell cultures with Singh's A. albopictus cell cultures used as "helper cells" in cocultivation experiments. Plaque formation without prior in vitro adaptation was induced in Vero cell cultures with eight rabies serogroup viruses: in all five instances by cocultivation of either infected BHK-21 or A. albopictus cells with Vero cells under agar overlay and in three of eight instances by direct plaque assay of infected mouse brain suspensions. In cross-plaque reduction neutralization tests with cloned viruses that represented human pathogens, rabies, Duvenhage, and Mokola, on the one hand, and the presumptive arboviruses Obodhiang and kotonkan, on the other hand, Mokola virus shared common antigenic components with both the nonarboviruses and the arboviruses. Biologically, Mokola virus was different from the other two human pathogens, rabies and Duvenhage, in that it multiplied in both vertebrate and invertebrate cell cultures. Mokola virus thus appears to be the biologic and serologic bridging agent.

Aedes↗

Serologic evidence of bunyamwera group arbovirus infections in Wisconsin and texas deer.

Sera of 81 white-tailed deer from south Texas and 283 white-tailed deer from Wisconsin were tested for neutralizing and hemagglutination-inhibiting antibodies to arboviruses of the Bunyamwera group. Neutralizing antibodies were detected in 100% of the Texas deer sera and hemagglutination-inhibiting antibodies were detected in 61% of those sera collected in 1969 and 78% of those sera collected in 1963. The prevalence of both neutralizing and hemagglutination-inhibiting antibodies in Wisconsin deer sera varied from 72-100% and 42-79% respectively depending on the geographic area tested in the years 1963 and 1969.

Animals↗

Variation in arbovirus infection rates in species of birds sampled in a serological survey during an encephalitis epidemic in the Murray Valley of South-eastern Australia, February 1974.

There was extensive and exuberant breeding of waterbirds before and during an epidemic of arboviral encephalitis in the Murray Valley of south eastern Australia in 1974. As estimated by haemagglutination inhibition tests on 432 bird sera collected between 4th and 13th February, 1974, infection with Murray Valley encephalitis virus, Kunjin virus and possibly other flaviviruses was concentrated in species of the Order Ciconiiformes (55% positive) and Pelecaniformes (41%), compared with only 5% in Anseriformes. Although Sindbis virus infections were also highest in these 2 Orders (56% and 46%, respectively), the incidence of antibodies was spread more uniformly through other Orders than with the flaviviruses: e.g. Anseriformes, 33%, Podicipitiformes, 27%. As viruses were recovered virtually only from Culex annulirostris mosquitoes, the different patterns of infection seem unrelated to host preference by mosquito species or behavioural response to mosquito attack, and suggest a specific relationship between MVE/KUN and Ciconiiformes and Pelecaniformes. The highest infection rate was 22/25 in mature rufous night herons (formerly nankeen night herons) Nycticorax calendonicus, and here tolerance to mosquito attack was probably a contributing factor. Assays of sera from 13 horses indicated high infection rates both alphaviruses and flaviviruses.

Alphavirus↗