Seroprevalence of, and risk factors for, peste des petits ruminants in sheep and goats in Northern Jordan

2008 ◽  
Vol 85 (1-2) ◽  
pp. 1-8 ◽  
Author(s):  
Ahmad M. Al-Majali ◽  
Nazmi O. Hussain ◽  
Nadim M. Amarin ◽  
Aggrey A. Majok
2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Aziz-ul-Rahman ◽  
Muhammad Abubakar ◽  
Muhammad Hidayat Rasool ◽  
Shumaila Manzoor ◽  
Muhammad Saqalein ◽  
...  

Peste des petits ruminants virus (PPRV) is causing infectious disease with high morbidity and mortality rate in domestic and wild small ruminants of Pakistan with valuable economical losses. The present study was carried out to investigate risk factors of PPRV in domestic small ruminants which were present in the vicinity of wildlife parks. A total of 265 sera samples (27 wild ruminants and 238 domesticated small ruminants) from apparently healthy animals from two different wildlife parks were collected and analysed for PPRV antibodies. Also, 20 nasal swabs from domestic small ruminants showing respiratory signs were collected to check for presence of PPRV antigen. Competitive ELISA revealed highest proportions of anti-PPRV antibodies in domestic small ruminants around the Wildlife Park at Lahore (35%) as compared to Faisalabad (13%), with no existence of PPRV antibodies in tested serum of wild ruminants at these parks. Higher seropositivity was observed in females (25.6%) than in males (5.1%) and in goats (34.5%) compared to sheep (11.2%). The results of N-gene based RT-PCR highlight the absence of PPRV due to lack of current PPR outbreak in the region during study period. Even though grazing was not a significant risk factor, there is still a possibility of wildlife-livestock interactions for feed and water reservoirs, resulting in spillover of PPR to wildlife. Keeping in view the high seropositivity and risk of PPR, vaccination should be adopted to avoid circulation of PPRV among wild and domestic small ruminants (sheep and goats).


2014 ◽  
Vol 1 (2) ◽  
pp. 42 ◽  
Author(s):  
Huyam Salih ◽  
Abdelhamid Elfadil ◽  
Intisar Saeed ◽  
Yahia Ali

2017 ◽  
Vol 7 (1) ◽  
pp. 1368336 ◽  
Author(s):  
Emeli Torsson ◽  
Mikael Berg ◽  
Gerald Misinzo ◽  
Ida Herbe ◽  
Tebogo Kgotlele ◽  
...  

2020 ◽  
Vol 1 (1) ◽  
pp. 22-29
Author(s):  
Waleed Al-Momani ◽  
Mahmoud N. Abo-Shehada

Background. Infectious diseases of the respiratory tract of farm animals are caused by a combination of infectious agents and predisposing factors. Parainfluenza virus type 3 is usually nominated as one of the causes. Seroprevalence and animal risk factors for PI3 infections were investigated in northern Jordan. Methods. The study involved 104 small ruminant flocks (18 sheep, 27 goats, and 59 mixed flocks sampled in northern Jordan. Indirect ELISA was used to test 678 blood samples used in this study. Flocks were identified as infected if at least 1 animal has been detected as positive by the ELISA test. Information regarding production and health management practices was collected in a questionnaire. Statistical analysis was conducted using the Statistical Package for Social Sciences software SPSS 23 (SPSS Inc., Chicago, IL, USA). Results. Flock-level and individual-level seroprevalences were 97%, 37%, and 76%, 11% in sheep and goats respectively. Multivariable logistic regression applied for production and health management practices showed significant risk factors for: Climatic zone (OR= 0.3) was decreasing risk factor for the PI3 seropositivity. Young separated from dams (OR= 4), neonatal deaths (OR= 3), and milking manual (OR= 37.5) were increasing risk factors for the seropositivity of PI3. Conclusions. PI3 virus has a high prevalence in sheep than goats and two risk factors could increase the prevalence of PI3 in both sheep and goats.


2021 ◽  
Vol 2 (1) ◽  
pp. 14-20
Author(s):  
Waleed Al-Momani ◽  
Robin R.A.J. Nicholas ◽  
Mahmoud N. Abo-Shehada

During 2002-2003 the seroprevalence of Mycoplasma capricolum subsp. capricolum was studied among 104 small ruminant’s flocks (18 sheep, 27 goat and 59 mixed flocks) in northern Jordan. At least 5 serum samples/flock were tested using iELISA test. The true flock-level seroprevalences of Mycoplasma capricolum subsp. capricolum were 56%, 39%, 28% in small ruminant (sheep and goats), sheep and goats respectively. There was no significant difference (X2 = 2, d.f. =1, p = 0.15) between seroprevalences in sheep and goats at the flock level. A total of 29 variables including production and health management practices were tested as risk factors for seropositive flocks and analyzed using logistic regression analysis. The use of communal grazing was found to be a risk factor for Mycoplasma capricolum subsp. capricolum seropositivity with odds ratio of 5.2 and drinking the animals with spring water was a protective factor with odds ratio of 0.27. More than half of the examined flocks were seropositive to Mycoplasma capricolum subsp. capricolum indicating a role for Mycoplasma capricolum subsp. capricolum in contagious agalactiae in small ruminants. The education of farmers regarding the use of communal grazing and housing the newborn in separate barns is expected to help reducing the Mycoplasma capricolum subsp. capricolum infections in their flocks.


2018 ◽  
Vol 37 (3) ◽  
pp. 961-969 ◽  
Author(s):  
S. TESHALE ◽  
G. MOUMIN ◽  
C. MOUSSA ◽  
M. GEZAHEGNE

Animals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1698
Author(s):  
Daniel Pius Mdetele ◽  
Erick Komba ◽  
Misago Dimson Seth ◽  
Gerald Misinzo ◽  
Richard Kock ◽  
...  

Peste des petits ruminants (PPR) is an important transboundary animal disease of domestic small ruminants, camels, and wild artiodactyls. The disease has significant socio-economic impact on communities that depend on livestock for their livelihood and is a threat to endangered susceptible wild species. The aim of this review was to describe the introduction of PPR to Tanzania and its subsequent spread to different parts of the country. On-line databases were searched for peer-reviewed and grey literature, formal and informal reports were obtained from Tanzanian Zonal Veterinary Investigation Centres and Laboratories, and Veterinary Officers involved with PPR surveillance were contacted. PPR virus (PPRV) was confirmed in northern Tanzania in 2008, although serological data from samples collected in the region in 1998 and 2004, and evidence that the virus was already circulating in Uganda in 2003, suggests that PPRV might have been present earlier than this. It is likely that the virus which became established in Tanzania was introduced from Kenya between 2006–7 through the cross-border movement of small ruminants for trade or grazing resources, and then spread to eastern, central, and southern Tanzania from 2008 to 2010 through movement of small ruminants by pastoralists and traders. There was no evidence of PPRV sero-conversion in wildlife based on sera collected up to 2012, suggesting that they did not play a vectoring or bridging role in the establishment of PPRV in Tanzania. PPRV lineages II, III and IV have been detected, indicating that there have been several virus introductions. PPRV is now considered to be endemic in sheep and goats in Tanzania, but there has been no evidence of PPR clinical disease in wildlife species in Tanzania, although serum samples collected in 2014 from several wild ruminant species were PPRV sero-positive. Similarly, no PPR disease has been observed in cattle and camels. In these atypical hosts, serological evidence indicates exposure to PPRV infection, most likely through spillover from infected sheep and goats. Some of the challenges for PPRV eradication in Tanzania include movements of small ruminants, including transboundary movements, and the capacity of veterinary services for disease surveillance and vaccination. Using wildlife and atypical domestic hosts for PPR surveillance is a useful indicator of endemism and the ongoing circulation of PPRV in livestock, especially during the implementation of vaccination to control or eliminate the disease in sheep and goats. PPR disease has a major socio-economic impact in Tanzania, which justifies the investment in a comprehensive PPRV eradication programme.


Sign in / Sign up

Export Citation Format

Share Document