Volume 8, Number 7—July 2002
Prevalence, Distribution, and Host Range of Peste des petits ruminants virus, Turkey
Peste des petits ruminants virus (PPRV, genus Morbillivirus), which causes a severe disease in sheep and goats, has only recently been officially declared to be present in Turkey. We carried out a study to determine the prevalence, distribution, and host range of PPRV in Turkey. A total of 1,607 animals, reared in 18 different locations, were monitored for the presence of antibodies to PPRV and the related virus of large ruminants, Rinderpest virus (RPV). Only two farms had animals that were free of antibody responses to either disease. Prevalence for PPRV infection varied (range 0.87%–82.6%) and was higher in sheep (29.2%) than in goats (20%). The overall antibody responses to PPRV and RPV were 22.4% and 6.28%, respectively. Two PPRVs of lineage 4, which comprises many other PPRVs whose origins are in the Middle East, the Arabian Peninsula, and southern Asia, were isolated from Turkish sheep.
Peste des petits ruminants virus (PPRV) is a morbillivirus that primarily infects sheep and goats. The virus is present in Africa (1–3), the Middle East (4), the Arabian Peninsula (5), and southern Asia (6,7) and is closely related to Rinderpest virus (RPV), Canine distemper virus, and human measles virus (8). Infection with PPRV results in an acute, highly contagious disease characterized by fever, anorexia, necrotic stomatitis, diarrhea, purulent ocular and nasal discharges, and respiratory distress (9,10). Infection rates in sheep and goats rise with age, and the disease, which varies in severity, is rapidly fatal in young animals (10,11). As with other morbillivirus infections, PPRV needs close contact between infected and susceptible animals to spread (10). The two ruminant morbilliviruses, PPRV and RPV, have common antigens demonstrable in a variety of serologic test systems, and they also show a degree of cross-neutralization (12,13). Originally PPRV was considered a variant of RPV adapted to small ruminants; however, the two viruses have separate epizootiologic cycles in nature, and each exists in its own right (14,15).
PPRV infection has only recently been officially reported in Turkey, in September 1999 (16,17), but some reports indicate it was present before then (18,19). The objectives of our research were to determine the seroprevalence of PPRV infection in cattle, sheep, and goats; determine the regional distribution of PPRV in Turkey; isolate and characterize the Turkish virus; and compare its genome sequence with those of other PPRV sequences in the sequence database maintained at the World Reference Laboratory, Pirbright, United Kingdom.
Materials and Methods
Animals Used in the Study
Domestic ruminant species (cattle, sheep, and goats) from throughout Turkey were examined for virus-specific antibodies. The sampling procedure depended on the presence of suspected infection and focused on two groups of animals. The first included 193 sheep that local authorities reported as having clinical signs of PPRV infection. These animals were examined, blood samples were collected, and any animals with signs of disease were sampled by swabbing for virus isolation. Cattle grazing with sheep or goats were also sampled to monitor for antibodies to the two viruses. The second group consisted of 1,414 animals randomly selected for serologic screening for PPRV and RPV antibodies from herds near the flocks of sheep and goats in which PPRV-like infection was reported. The numbers of serum samples collected from sheep, goats, and cattle were 884, 209, and 321, respectively.
Tests for PPRV- and RPV-Specific Antibodies
Competitive enzyme-linked immunosorbent assays were performed as described in the manual of Peste des Petits Ruminants enzyme-linked immunosorbent assay (ELISA) kit (20) and the Office International des Epizooties Manual of Standards (9). Each serum sample, regardless of the species from which it was obtained, was tested for the presence of antibodies to RPV and PPRV.
Virus Isolation Material and Infection of Cell Cultures
A total of 328 field samples, including heparinized blood, organ (lung), and swab specimens, were cultured to obtain virus isolates. The processed samples were spread onto Vero cells seeded in rolling culture tubes. The cells were grown in Dulbecco’s modified Eagle medium enriched with 5% fetal bovine serum as a regular culture medium. The cell culture media were changed every 2 days and the inoculated cells observed for 12–14 days. The positive culture tubes were frozen at -80°C when the cytopathic effect (CPE) was 90%, and virus stocks were prepared from the positive samples.
Detection of PPRV RNA
Detection of PPRV RNA by reverse transcription-polymerase chain reaction (RT-PCR) was performed as described (21). PCR amplification was carried out by with a PPRV-specific primer set (PPRVF1b: 5´AGTACAAAAGATTGCTGATCACAGT and PPRVF2d: 5´GGGTCTCGAAGGCTAGGCCCGAATA) selected from the F protein gene sequence, which is expected to amplify a 448-bp DNA product. RT-PCR products were digested by using EcoRI at 37°C for 1 hour. Samples were then analyzed on 1.7% agarose gels to determine the cleavage patterns of the amplicons. DNA products obtained with PPR F1b and F2d primers were sequenced by using a T7 polymerase-based commercial kit (Pharmacia Diagnostics AB, Uppsala, Sweden) with 35SdATP as the radiolabel.
Sequence data were analyzed with the GCG (Genetics Computer Group Inc., Madison, WI) package. The nucleic acid sequences obtained from PCR products were aligned with known sequences from representatives of the Morbillivirus genus, and the phylogenetic tree was generated with the DNADIST and FITCH programs of the PHYLIP 3.73 software (22).
Animals with clinical signs of PPRV were detected in 11 provinces (Table 1). In many cases, inspections of flocks confirmed PPRV-suspect cases reported by local veterinarians or identified symptoms indicative of PPRV infection. Most clinical cases were characterized by excessive oculonasal discharge, mild ulcerative stomatitis, dyspnea, and coughing. Severe mucosal eruptions and intestinal signs were not detected.
Serologic Status of Sampled Animals
A total of 1,607 animals from 18 farms were sampled for antibodies to PPRV and RPV (Figure 1). Only two farms (Cihanbeyli and Amasya) had no animals with antibodies specific to either virus. The overall percentages of antibody response to PPRV and RPV were 22.4% and 6.28%, respectively (Table 2). Prevalences of PPRV infection varied between flocks, ranging from 0.87% to 82.60%; however, these figures may not be accurate because of the small sample sizes. In general, the level of PPRV infection was higher in sheep; however, the highest seroprevalence (82.6%) was found in goats in Sakarya Province, where two PPRV isolates were identified from sheep during this project. Of 1,077 sheep examined, 315 (29.2%) were seropositive for PPRV and 1.2% for RPV. The 10 RPV-seropositive sheep in Bursa Province (in a flock with no clinical PPRV) were reported to have been vaccinated against RPV, while only 1 sheep in Konya was found to have seroconverted, probably following natural infection with RPV before 1999. The overall occurrence of PPRV infection in cattle was 15.57% (a total of 50 animals), and approximately 27% of cattle were antibody positive for RPV, indicating previous exposure to the virus either by natural infection or, most probably, by vaccination, since all cattle in the study were >6 months of age.
The study showed no substantial relationship between the occurrence of PPRV infection and geographic location. Although the main portal of entry of the disease is thought to be in the southeastern part of Anatolia, distribution of the prevalence values did not show a clear pattern across the country, and the disease was detected in varying percentages in almost every region studied (Figure 1).
A total of 328 samples were spread onto Vero (African Green Monkey Kidney) cells. Two nasal swab samples (Sakarya 1 and Sakarya 2), from sheep in Sakarya Province, showed CPE on Vero cells. The CPE was observed on day 3 after inoculation and was initially characterized by the formation of rounded cells; later, syncytia developed. RT-PCR was performed on cell culture supernatants after the first passage on the Vero cells. The expected amplification product of 448 bp was observed by using RNA prepared from culture supernatants from only the two samples (data not shown). Restriction fragment length polymorphism analysis of the RT-PCR products indicated nucleotide substitutions in the EcoRI recognition sequence site in the amplified genome region of the isolates. While the PPR vaccine strain (Nigeria 75/1) produced, as expected, two fragments of 202 bp and 246 bp on cleavage with EcoRI, isolates Sakarya 1 and Sakarya 2 were not digested by this restriction enzyme (data not shown). Partial sequencing of the F protein–coding region of the two PPRV isolates showed them to be identical (GenBank accession number AF384687). The Turkey 2000 sequence was then aligned with the sequences of other PPRV isolates from around the world. Figure 2 shows the inferred phylogenetic relationship between the isolates recovered in this research and other PPRVs. The Turkish isolates belonged to PPRV lineage 4 (7), which originates in the Middle East, Arabia, and southern Asia.
We investigated the prevalence, host range, and distribution of PPRV in small private farms in Turkey. We also demonstrated the presence of the disease by observing animals in the field and by isolating virus from clinical specimens. This wide-ranging survey is the first to be carried out on this disease in Turkey. PPRV infection has only recently been officially declared to be present in Turkey in the Elazig Province in eastern Anatolia (16,17). Our research provided valuable data on the serologic status of the three domestic ruminant species (cattle, sheep, and goats) with respect to PPRV. Infection with PPRV was demonstrated in 16 of 18 farms we sampled (except for Cihanbeyli and Amasya). On a flock basis, the highest virus prevalence (82.6%) was in goats in Sakarya, where two isolates were identified from sheep. The second highest prevalence (80%) was in sheep in Eskisehir, followed by 72% in sheep in Van Province and 66.6% in sheep in Malatya Province. Van and Malatya Provinces are in southeastern Turkey near the Iranian border; the remaining provinces are mainly in central Anatolia (Figure 1). Variation in prevalence is probably related to the intensity of trade of illegally imported small ruminants (23).
The prevalence of the disease was as high as 28.5% in sheep and goats reared in small private flocks, and the disease was found in almost every region across Turkey. Occurrence of infection did not vary substantially by geographic locations of the livestock tested. Although the presence of PPRV infection in Turkey has been reported before (18,19), the impact of the disease on production of livestock animals has not previously been investigated. The overall prevalence of PPRV was 22.4% of the ruminant population. These results indicate much lower prevalence than the 88.3% reported by Tatar (19). However, if the overall percentage of PPRV infection takes into account animals reported as having clinical signs, the level increases to 51.6% (Table 1). Another ruminant morbillivirus infection, RPV in cattle, caused great economic losses from the deaths or slaughter of affected (or suspected infected) animals in Turkey in recent years (24). Because PPRV and RPV are antigenically related, the attenuated RPV vaccine has been used to protect small ruminants against PPRV. According to anecdotal reports from the field, veterinarians and animal owners widely used the RPV vaccine to protect small ruminants against PPRV infection in some parts of Turkey before RPV vaccination was stopped in the year 2000. This might be one reason for the lower percentage of PPRV-positive animals found in this study.
Cattle act as dead-end hosts for PPRV and show no clinical signs of infection. Nevertheless, they develop a humoral immune response to PPRV that protects them against natural or experimental challenge with virulent RPV (12). In our study, the percentage of natural PPRV infection in cattle was low (0.9%), and all these were in cattle that had contact with infected sheep flocks. Cattle seropositive for PPRV could cause confusion when monitoring for antibodies to RPV after a vaccination campaign to eradicate RPV. Natural infection of cattle with PPRV might prevent the immune response to the RPV vaccine because the PPRV-specific antibodies could neutralize the live attenuated vaccine virus. The cattle would still be protected from subsequent RPV challenge by heterologous PPRV antibody but would register as seronegative when tested in the RPV competitive ELISA. This false value could lead to a low estimation of herd immunity to RPV or suggest that the vaccination coverage was inadequate (12). This risk is high in mixed breeding systems, such as the small-scale production units common in rural regions of Turkey. On the other hand, 14.6% of the cattle had antibodies to both viruses (PPRV and RPV). This finding may indicate that in some cases no interference occurs. Another possible reason is the cross-reactivity of the PPRV assay for antibodies to RPV, as noted by Anderson et al. (25).
Only two PPRVs were isolated—from nasal swab samples of two sheep from Sakarya Province. The reason for the poor success in isolating virus could be the nature of the samples. In previous studies, virus isolations were made from spleen, mesenteric lymph nodes (7,26), or intestinal epithelial smears (15) collected during necropsy of affected animals by inoculation on to Fetal Lamb Kidney (FLK) (19,26) or Vero (15,19) cells. In our study, however, most samples were taken from surviving animals that may have been past the clinical phase of the disease, when the virus is secreted, and so were not likely to yield virus isolates from swabs. Moreover, owners of many sick animals did not grant permission to euthanize them, so internal organs were not available for gross pathologic analysis in most cases. According to a previous study (19), FLK and Vero cells are equally susceptible to PPRV; thus, the use of Vero cells was probably not a factor in our poor success with virus isolation.
Our use of molecular epidemiologic techniques provided data that suggest cross-border transmission into Turkey of PPRV infection that is actively circulating in neighboring countries. The viruses we isolated are PPRV lineage 4, which includes viruses whose origins are in the Middle East, Arabia, and south Asia (7). Because of its geographic location, Turkey has borders with countries where many economically important infectious diseases are endemic. Thus, one of the neighboring countries in the Middle East region is most likely the source of infection. Since the terrain of eastern and southeastern Anatolia permits uncontrolled animal movement, restricting the spread of infectious diseases into the country has been difficult. Therefore, the importance of PPRV as a threat to livestock should be considered, together with other economically important diseases, and measures taken to prevent the import and subsequent spread of such diseases.
Dr. Özkul is a faculty member in the Virology Department of the Veterinary School at Ankara University. His main research interests are the molecular epidemiology of morbilliviruses and the neuropathology of herpes and morbillivirus infections.
Competitive enzyme-linked immunosorbent assay test kits were provided by the Institute for Animal Health, Pirbright Laboratory.
This research was supported by grants of the British Council (Link Project ANK/992/102) and Research Fund of Ankara University (98.10.00.08).
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Suggested citation: Özkul A, Akca Y, Alkan F, Barrett T, Karaoglu T, Dagalp SB, et al. Prevalence, Distribution, and Host Range of Peste des petits ruminants virus, Turkey. Emerg Infect Dis. [serial on the Internet]. 2002 Jul [date cited]. Available from http://wwwnc.cdc.gov/eid/article/8/7/01-0471.htm
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