Spatial analysis of seroconversion of sentinel cattle to bluetongue viruses in Queensland

Objective To assess quantitatively the spatial distribution of seroconversion of Queensland cattle to bluetongue viruses.
Design A sentinel herd study. Sample population Sixty-nine sentinel herds at 30 locations.
Procedure Spatial clustering of seroconversion to blue-tongue viruses was investigated during the period from 1990 to 1994.
Results Seroconversion to only two bluetongue virus serotypes, 1 and 21, was observed. The 14 herds, in which seroconversion to bluetongue virus serotype 1 was detected, were located only along the eastern coastal and subcoastal region of Queensland, and were significantly (P < 0.05) clustered. Locations at which seroconversion to serotype 21 was detected, were not significantly clustered. The results generally agree with field observations, except for the failure to detect seroconversion to bluetongue viruses in north-western Queensland.
Conclusion Bluetongue infection of cattle in north-western Queensland may be temporally sporadic. The dominance of serotype 1 in the Queensland cattle population may be the result of differential transmission by potential vector species. Long-term surveillance programs are important for defining disease status of animal populations.     

Active circulation of bluetongue vaccine virus serotype-2 among unvaccinated cattle in central Italy

Several seroconversions occurring in 2002 among sentinel cattle during the bluetongue-vaccination campaign in Lazio and Tuscany (central Italy) led to the suspicion of vaccine-virus circulation. Therefore in 2003, 17 seroconverting sentinel herds were investigated for the characteristics of the virus involved. From these farms, 91 unvaccinated animals and 57 Culicoides pools were tested for the presence of the bluetongue vaccine virus (serotype-2) or other strains. The presence of vaccine virus serotype-2 was confirmed by PCR followed by restriction analysis in the whole blood of 17 unvaccinated sentinel cattle and 12 pools of Culicoides imicola or C. obsoletus. Of the 17 herds, five were positive only for vaccine virus serotype-2, four were positive for other strains and two for both the vaccine and other strains; the remaining premises were virologicaly negative. The vaccine virus serotype-2 also was detected in areas not included in the vaccination campaign.     

Effects of altitude, distance and waves of movement on the dispersal in Australia of the arbovirus vector, Culicoides brevitarsis Kieffer (Diptera: Ceratopogonidae)

The dispersal of the biting midge and arbovirus vector Culicoides brevitarsis in the Bellinger, Macleay and Hastings river valleys and up the escarpment of the great dividing range (GDR) of mid-northern coastal New South Wales, Australia, from 1995 to 2003 was studied. The midge moved up these valleys from the endemic coastal plain in at least two waves between October and May, and both waves were modelled. Dispersal time can be explained by direct distance from the coast and the altitude of the sites. Dispersal times due to distance were similar at 18.2 ± 2.2 (S.D.) and 15.9 ± 2.6 weeks per 100 km for first- and second-occurrences at fixed altitude. Time of the first wave was extended 0.48 ± 0.22 weeks for every 100-m rise in altitude and the second by 1.14 ± 0.24 weeks for every 100-m rise for a set distance. Although C. brevitarsis can move up the escarpment of the GDR (and possibly transmit virus), vector dispersal, survival and establishment at and beyond the top of the range are limited. A third model showed that previously described slower movement of C. brevitarsis up the more-southerly Hunter valley relative to movements down the coastal plain also was related to increasing altitude.     

The use of discriminant analysis in predicting the distribution of bluetongue virus in Queensland,Australia

The climatic variables that were most useful in classifying the infection status of Queensland cattle herds with bluetongue virus were assessed using stepwise linear discriminant analysis. A discriminant function that included average annual rainfall and average daily maximum temperature was found to correctly classify 82.6% of uninfected herds and 72.4% of infected herds. Overall, the infection status of 74.1% of herds was correctly classified. The spatial distribution of infected herds was found to parallel that of the suspected vector,Culicoides brevitarsis. This evidence supports the role of this arthropod species as a vector of bluetongue viruses in Queensland.The effect of potential changes in temperature and rainfall (the so-called global warming scenario) on the distribution of bluetongue virus infection of cattle herds in Queensland was then investigated. With an increase in both rainfall and temperature, the area of endemic bluetongue virus infection was predicted to extend a further 150 km inland in southern Queensland. The implications of this for sheep-raising in Queensland are discussed.Abbreviations AGID agar gel immunodiffusion     

A study on bluetongue virus infection in Saudi Arabia using sentinel ruminants

Four sentinel herds comprising cattle, sheep and goats were established at various localities in Saudi Arabia. Maternal bluetongue antibodies were detected in all four sentinel herds but disappeared in 4-6 months, immediately followed by seroconversion in all. Serological results indicated that the animals were recently exposed to BT virus serotypes 10, 12, 15 and 20. The epidemiology of the disease in Saudi Arabia is discussed.     

Climatic factors associated with the infection of herds of cattle with bluetongue viruses

The incidence of bluetongue virus infection of 15 cattle herds in Queensland, Australia, was determined by a serum neutralization test. The maximum temperature (°C), minimum temperature (°C) and rainfall (mm) data were obtained from the meteorological recording stations closest to each herd. Using unweighted least-squares regression analysis, the best statistical model explaining the most variability in the herd incidence rate included the ratio between the maximum and minimum temperature recorded at both 1 month and 6 months preceding seroconversion, and rainfall recorded at both 2 months and 6 months preceding seroconversion. More than 90% of the variability in the incidence of bluetongue virus infection in the herds was explained by the model, a considerable improvement on previous models that used prevalence data. The prospective nature of the study also supports a strong causal relationship between climatic factors and the occurrence of infection in cattle herds.Abbreviations SN serum neutralization - R _infa ^sup2 adjusted coefficient of multiple determination - AIC Akaike's information criterion - FPE Akaike's final prediction error - PRESS predicted sum of squares     

Models for the dispersal in Australia of the arbovirus vector, Culicoides brevitarsis Kieffer (Diptera: Ceratopogonidae)

Culicoides brevitarsis is the main biting midge responsible for the transmission of bluetongue and Akabane viruses to livestock in Australia. Models are given for its dispersal after winter from endemic areas at the southern limit of its distribution in New South Wales (NSW); the models might also be applicable elsewhere. Model 1 shows that dispersal can be explained by distance from a key point just outside the endemic area in mid-northern/northern coastal NSW. The model provides probability data for times of first occurrence at sites within regions down the southern coastal plain or up the Hunter Valley towards (but rarely reaching) the western slopes and tablelands. Model 2 shows that the movement depends on temperature and wind speed from northerly and easterly directions. Preliminary data also are given to suggest a relationship between density in the endemic area and the maximum distance that C. brevitarsis can travel in a given year. The models can be linked to other information which in combination can provide probabilities for winter survival outside the endemic area, times of occurrence at sites where it cannot survive winter and times when activity ceases naturally at these sites at the end of the season. This information can be used to predict the potential for virus transmission and indicate zones of seasonal freedom from both vector and virus for the export of livestock.     

Serological studies of Australian and Papua New Guinean cattle and Australian sheep for the presence of antibodies against bluetongue group viruses

Following isolation of a virus (CSIRO19) from insects in Australia and its identification as bluetongue virus serotype 20 (BTV20), a nationwide survey of antibodies in cattle and sheep sera was undertaken. Initial studies using the serum neutralization (SN) test showed that the distribution of BTV20 antibodies in cattle was confined to the northern part of Australia. Group-reactive antibody tests (agar gel diffusion precipitin, AGDP, and complement-fixation, CF) showed group-reactive cattle sera south of the BTV20 zone (northern Australia), and southwards from Queensland to New South Wales. Very few group-reactive sheep sera (45 out of 16213) were found and these were of doubtful epidemiological significance. Some of these BTV group-reactive, BTV20-negative, sera were tested in SN tests against BTV1 to 17 and Ibaraki (IBA) virus. The results indicated that BTV1, or a closely related orbivirus, was active in cattle in Queensland, northern Western Australia, and New South Wales, and that antibody to BTV15 was present in some of the cattle sera in northern Western Australia and the Northern Territory. Antibody to IBA virus was present in some cattle sera in Queensland, northern Western Australia and New South Wales. SN antibody titres ?60 were also found to a number of other BTV serotypes in cattle sera in northern Western Australia and Queensland (principally, BTV2 and BTV7). Low level reactions were commonly observed against these and a number of other BTV serotypes, often in the same serum samples. Further, 22% of the group-reactive cattle sera did not react with any of the viruses in the SN tests. Such results were difficult to interpret in terms of known Australian BTV or BTV-related isolates.     

A sentinel herd system for the study of arbovirus infections in Australia and Papua-New Guinea

The establishment, and development between 1969 and 1978, of a system of sentinel cattle in herds located in many areas of Australia and in Papua New Guinea is described. Though the system was established for the study of the epidemiology of a variety of viruses infecting cattle, the study has been limited since 1974 to arboviruses. By means of serology, it was established that bovine ephemeral fever virus was present in Australia in subclinical form between major epidemics but was not detected in Papua-New Guinea. The development of antibody to bovine ephemeral fever virus in individual cattle before they developed clinical signs in epidemics was clearly demonstrated. The sentinel technique was used to demonstrate that subclinical Akabane virus infection in cattle occurred at the time that virus was present in its suspected vector,Culicoides brevitarsis which had been collected nearby. The epidemiology of other Simbu group viruses, D'Aguilar virus, and bluetongue virus, (serotype 20) was also studied. A limited programme of arbovirus isolation in tissue cultures produced 0.8% of isolates from 2090 of the blood clots which accompanied sentinel herd serum samples.The most valuable aspect of the sentinel herd scheme has been the accumulation of a well documented representative set of serum samples for retrospective serology by the use of newly isolated or imported antigens.     

The dispersal of Culicoides brevitarsis in eastern New South Wales and associations with the occurrences of arbovirus infections in cattle

Distributions of the vector Culicoides brevitarsis Kieffer (Diptera: Ceratopogonidae) (determined from light trap data) and 2 arboviruses (determined from seroconversions in sentinel cattle) were studied in eastern New South Wales in 1993–94. C brevitarsis was recorded progressively from endemic areas on the north coast, to Nowra on the south coast, and westward to Scone, in the Hunter Valley. C brevitarsis also survived through winter at Paterson, in the Hunter Valley. Its apparently focal reappearance in this marginal area had no obvious effect on the broad pattern of its progression or the dispersal of Akabane and bluetongue viruses. These viruses were first recorded from foci near Coffs Harbour, on the mid-north coast. Their first occurrences at different locations were associated with those of C brevitarsis, but not with each other. The viruses were found only within the recorded limits of the vector's distribution. Delays between the initial occurrence of C brevitarsis and first evidence of virus transmissions at locations ranged from 2 to 7 months. The delays decreased away from the points of focus and were negatively associated with the time of initial occurrence of the vector. Seroconversions to the viruses were related to the presence of C brevitarsis. However, the densities of C brevitarsis had no apparent effect on the initial numbers of cattle seroconverting to either virus. The results support the conclusion that the progressions of C brevitarsis and Akabane and bluetongue viruses were the result of gradual movements by the vector.     

Analysis of the IgG antibody response against Paramphistomidae trematoda in naturally infected cattle. Application to serological surveys

The IgG antibody response to Calicophoron daubneyi (Digenea: Paramphistomidae) excretory/secretory antigens was evaluated in naturally infected cattle from Lugo (Galicia, NW Spain) by using an ELISA procedure. Two studies were conducted, first a survey in 524 cattle separated into three groups according to age, G-1 (0–2 years old), G-2 (3–5 years old) and G-3 (>6 years old). In the second study, three groups of cattle were employed: G-I, naturally infected; G-T, naturally infected and treated with oxyclozanide plus levamisole (Nilzan Plus^®); G-C, cattle maintained in a farm where C. daubneyi has never diagnosed. Variations on egg-output and haematic parameters (erythrocytes, haematocrite, leukocytes and lymphocytes) were also analyzed.

The ELISA procedure showed that 61.2% of the cattle in the first study had been exposed to the trematode, but only 10.1% passed eggs in the feces. Age-association with egg-output was shown but not with the IgG values. In the second experiment, the administration of the anthelmintic reduced significantly the IgG kinetic levels and the C. daubneyi-egg-output was suppressed during 12 weeks in the G-T group. The values of red cells, haematocrite, leukocytes and lymphocytes increased significantly in the treated cattle 5 weeks after chemotherapy; however, new reduction after week 5 was recorded, as results of the challenge of these cattle.

This is the first investigation in which evaluation of the IgG humoral response against C. daubneyi in cattle has been carried out. We proved that a notable IgG response in naturally infected cattle is induced, and can be detected by using an ELISA procedure. The IgG antibodies did not increase after challenge infection. Our results proved an important percentage of cattle were exposed to this trematode in the area of study and suitable measures for preventing this relationship must be considered.     

Frequency of bluetongue and bovine parvovirus infection in cattle in South Carolina dairy herds

A survey of South Carolina diary cattle in 12 commercial herds was conducted, using serologic testing to determine the frequency and impact on reproduction of bluetongue (BT) and bovine parvovirus (BFV) infections. Results of the study of serum antibodies titers and dairy cattle health records indicated that the majority of the cattle surveyed was adequately protected against the major reproductive tract diseases through vaccination programs. The frequency of reproductive dysfunction was common in vaccinated herds, however. Six of the 12 herds in the survey had cattle which were BT serotest reactors, although total numbers of these reactor cattle were relatively small. Further, reproductive performance of reactor cows indicated that BT was of little consequence and was not associated with reproductive problems. All herds contained BPV serotest reactors and the latter comprised 59.7% of the total number of cows surveyed. The BPV seroreactor cows were commonly associated with the group of reproductive problem cows which experienced higher rates of embryonic mortality and more services per conception than did nonreactor cattle. The results of the survey emphasize the need for continued investigation and efforts to control BT, and especially BPV infection, in dairy cattle.     

A longitudinal study of serological patterns of respiratory infections in nine infected Danish swine herds

Sixteen litters of seven pigs from each of nine Danish farrow-to-finish herds were followed to investigate the serological patterns caused by natural infection with Mycoplasma hyopneumoniae, Pasteurella multocida toxin and Actinobacillus pleuropneumoniae serotypes 2, 5–7, 12. In seven of the herds, pigs were followed as two separate cohorts started 4 weeks apart, and in two herds only one cohort was followed.

A total of 999 pigs were included in the study. The pigs were blood sampled at weaning and subsequently every fourth week until slaughter. All pigs were examined for antibodies against M. hyopneumoniae (enzyme-linked immunosorbent assay), P. multocida toxin (enzyme-linked immunosorbent assay) and A. pleuropneumoniae serotypes 2, 5–7, 12 (complement-fixation tests). The most-common pattern (28%) of seroconversion was that of pigs first seroconverting to A. pleuropneumoniae serotype 2, followed by seroconversion to M. hyopneumoniae. Each herd had a dominant serotype of A. pleuropneumoniae to which most pigs seroconverted. Seroconversion to the respiratory pathogens occurred mainly in the growing-to-finishing units (8–24 weeks). The risk of seroconversion to the P. multocida toxin was very low (<20%) and occurred late.

None, four and seven herds tested seropositive to PRRS and to swine influenza virus subtypes H3N2 and H1N1, respectively, when testing 10 pigs per herd (selected randomly among the study pigs) at the age of 20 weeks.     

CONGENITAL BOVINE EPIZOOTIC ARTHROGRYPOSIS AND HYDRANENCEPHALY IN AUSTRALIA: Distribution of Antibodies to Akabane Virus in Australian Cattle after the 1974 Epizootic

At the end of the 1974 epizootic of bovine congenital arthrogryposis and hydranencephaly in south-eastern New South Wales, an Australia-wide serological survey (about 4,000 serums) was made to determine the ditribution of cattle possessing serum neutralising antibodies against Akabane virus. Eighty per cent of the serums from cattle in northern Australia (Western Australia, Northern Territory, and Queensland) were positive. A detailed study in the epizootic area in New South Wales (particularly around Bega) showed that 80 to 100% of serums from cows in herds in this area possessed neutralising antibodies. The animals possessing antibodies extended as far south as Genoa in north-eastern Victoria, and as far west as Darlington Point on the Murrumbidgee River. There were no positive herds along the Murray River, where an outbreak of the mosquito-borne disease Murray Valley encephalitis occurred in 1974. Serums tested from cows in the rest of Victoria, South Australia, south-western Western Australia, and Tasmania were negative. Arthrogrypotic calves born in Tasmania and south-western Western Australia were not associated with the presence of Akabane virus. In Papua New Guinea, serums collected from cattle at Boroka, Lae, and Goroka did not possess neutralising antibodies. The distribution of cattle possessing antibodies in Australia would fit a spread of the virus by Culicoides brevitarsis, a biting midge from which Akabane virus had been isolated on three occasions. The possibility of other vectors, as well as C. brevitarsis, was suggested by the presence of cows possessing antibodies at Alice Springs, where this biting midge has not been found. Possibly most cattle in northern Australia become infected early in life. The epizootics in New South Wales could occur when seasonal conditions allow a southerly extension of virus-infected C. brevitarsis which feed on susceptible pregnant animals. C. brevitarsis also bites sheep, and both neutralising antibodies to Akabane virus and congenitally deformed lambs have been observed in the epizootic area. An understanding of the distribtuion of Akabane virus and C. brevitarsis, a possible Australian vector for bluetongue virus, may prove useful if bluetongue should enter Australia.     

Infection of cattle in Queensland with bluetongue viruses: 1. prevalence of antibodies

SUMMARY A survey of nearly 20 000 cattle in Queensland was conducted to describe the prevalence and distribution of infection by serotypes of bluetongue virus. The overall prevalence of serum antibodies to one or more bluetongue viruses was 8.7% (95% confidence interval 8.3 to 9.1). Sera from cattle contained neutralising activity against 2 serotypes, 1 and 21. No evidence was found of infection with other serotypes previously isolated in Australia. The overall prevalence of serotype 1 antibodies was 7.7% (95% CI 7.3 to 8.0) and the prevalence of serotype 21 antibodies was 3.3% (95% CI 3.1 to 3.6). The prevalence of serotype 1 antibodies was significantly (P < 0.05) higher than that of serotype 21 in every region of the State, except in the central highlands and south-west Queensland. Overall, 3 significantly (P < 0.05) different zones of prevalence were found: high prevalence (> 20%) in far north Queensland, moderate (5 to 20%) in north-west, northern and southern coastal Queensland, and low (< 5%) in the central highlands, Darling Downs and south-west Queensland.     

Prevalence and first genetic identification of Cryptosporidium spp. in cattle in central Viet Nam

We investigated the prevalence of Cryptosporidium infection in relation to age and clinical status in cattle in the central region of Viet Nam. A total of 266 fecal samples from diarrheic and non-diarrheic cattle were examined by the modified Ziehl-Neelsen staining method. Prevalence of Cryptosporidium parvum type infections, those of the Cryptosporidium andersoni type, and mixed infection of both types was 33.5% (89/266), 5.6% (15/266), and 3.4% (9/266), respectively. The infection rate of 44.3% (35/79) of C. parvum in calves less than 6 months old was significantly higher than that of 28.9% (54/187) in cattle greater than 6 months old (P < 0.01). Although no C. andersoni oocysts were detected in calves less than 3 months old, no significant difference was observed between the age groups in the prevalence of C. andersoni infection and mixed infection. The percentage of diarrheic and non-diarrheic cattle identified to be shedding C. parvum oocysts was 46.5% (74/159) and 14.0% (15/107), respectively (P < 0.0001). The risk of diarrhea was 1.7 times greater in C. parvum-infected calves than in their non-infected counterparts. DNA sequences of 18S rRNA genes of C. parvum type and C. andersoni type indicated that they were C. parvum bovine genotype and C. andersoni, respectively. This is the first genetic identification of C. parvum bovine genotype and C. andersoni from cattle in Viet Nam.     

Herd-level Coxiella burnetii seroprevalence was not associated with herd-level breeding performance in Czech dairy herds

Q fever was studied on a large agricultural farm in northern Moravia, Czech Republic. Antibodies to Coxiella burnetii were ascertained by a complement fixation test. Titre of 8 or higher was considered as positive. The seroprevalences in cows (each cow was examined only once immediately after drying-off during a one-year period) from 14 different herds was between 4 to 19%. No significant correlation between seroprevalence levels and fertility characteristics in the cow herds was found. Of a total of 17 samples of milk from 17 randomly-selected cows with antibody titres of 8 to 32, one strain of Coxiella burnetii was isolated. In heifers (n = 339) and beef bulls (n = 210) no antibodies to C. burnetii were found. In cattle from the farm investigated, latent Q fever did not represent any health problem.     

Prevalence of trypanosomiasis in Zebu cattle at Obudu ranch — a tsetse-free zone in Nigeria

A recent cross-sectional survey of bovine trypanosomiasis at the Obudu Cattle Ranch (OCR), located at an altitude of 1576 m on the Obudu Plateau in Nigeria is presented. Blood samples from 68 adult cattle in three herds and 290 cattle (27 calves and 263 adults) in eight herds were screened for trypanosome infections in August 1989 and February 1990, respectively. Although the plateau is designated as tsetse-free, one (1.5%) (0.015, 95% confidence interval ±0.029) and four (1.4%) (0.014, 95% confidence interval ±0.013) of the ranch's cattle in August and Febraury, respectively, had trypanomome infections. Trypanosoma brucei caused one of the infections while the others were caused by Trypanosoma vivax.     

Seroprevalence of bluetongue serotype 8 in cattle in the Netherlands in spring 2007, and its consequences

A cross-sectional study was carried out in spring 2007, at the end of the first bluetongue outbreak season, to determine the geographical spread of bluetongue virus serotype 8 (btv-8) infection in cattle in the Netherlands and the consequences for some production parameters. Blood samples from cattle submitted to the laboratory of the Dutch Animal Health Service for other voluntary and obligatory health programmes were tested serologically for btv-8. In total, 37,073 samples were tested and 659 (1.78 per cent) were seropositive. The samples came from 5436 herds, of which 45 per cent of herds had only one sample submitted from them. The prevalence was highest in the south of the country, where the outbreak had started, and decreased towards the north. In 340 herds more than 50 per cent of cattle were tested, of which 156 herds were located in infected compartments, and in 37 of these herds (10.9 per cent) at least one positive cow was detected. The average within-herd prevalence in the 37 herds was 39.3 per cent: 2.2 per cent in 11 dairy herds, 68.4 per cent in 20 small-scale herds and 14 per cent in four suckler cow herds. The prevalence differed significantly between herd types but did not show a geographical trend. The average net return for milk production amounted to euro2417/cow/year and it decreased significantly on average by euro48/cow/year in the bluetongue-infected dairy herds during the bluetongue period. On the small-scale farms, the incidence of mortality increased by 3.2 (95 per cent confidence interval [CI] 1.2 to 9.1) times in the infected herds during the bluetongue period, but the voluntary culling rate decreased by a factor of 2.3 (95 per cent CI 1.1 to 4.8).