scholarly journals Diagnosis Challenges and Control Strategies of Transboundary Diseases Presenting with Respiratory Signs in Small Ruminants in Developing Countries: Emphasis on Contagious Caprine Pleuropneumonia and Peste Des Petits Ruminants

2020 ◽  
pp. 12-25
Author(s):  
A. C. Chota ◽  
G. M. Shirima ◽  
L. J. M. Kusiluka
Keyword(s):  
Developing Countries ◽  
Control Strategies ◽  
Clinical Signs ◽  
Small Ruminants ◽  
Definitive Diagnosis ◽  
Peste Des Petits Ruminants ◽  
Contagious Caprine Pleuropneumonia ◽  
Phd Thesis ◽  
And Control ◽  
Bio Engineering

Aims: To review the diagnosis challenges and control strategies of the diseases presenting with respiratory signs. The emphasis being more on two transboundary animal diseases of small ruminants; contagious caprine pleuropneumonia (CCPP) and peste des petits ruminants (PPR). Clinical signs and postmortem lesions associated with the two diseases were also explicated. Study Design: Review. Place and Duration of Study: Department of Global Health, School of Life Science and Bio-Engineering (LiSBE), Nelson Mandela African Institution of Science and Technology (NM-AIST) from December 2017 to June 2020. Methodology: A comprehensive review was carried out following Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. A total of 506 articles, handbooks, Master’s and PhD thesis and conference proceedings were collected and after removal of the duplicates 80.6% (424/526) passed the first stage. Of the remaining search materials, (n=291) were removed including handbooks, master’s and PhD thesis which did not originate from the developing countries, 31.4% (133/424) passed the second. Of the articles that passed the second stage, (n=85) were removed from the study, these included all articles that did not involve field diagnosis such as review papers and those not originating from the developing countries, 36.1% (48/133) passed the third stage. In the fourth stage, (n=5) articles which reported on retrospective cases and archived samples were removed and 43 articles were reviewed. Results: Out of the 526 documents retrieved, 43 were eligible for review as they met all criteria for inclusion. Control strategies were recommended in 44.2% (19/43) of the articles of which most of them 63.2%, 12/19) recommended vaccination as a control strategy. Most of the articles reported definitive diagnosis reached following laboratory involvement as majority of them involved outbreak investigation or research works which is not the case in routine diagnosis. The major clinical signs mentioned in the review articles including fever 60.9% (14/23), oculonasal discharge 87.0% (20/23), respiratory distress 82.6% (19/23), erosive stomatitis 43.5% (10/23), diarrhea 56.5% (13/23) and coughing 30.4% (7/23) have been discussed relating to the definitive diagnosis reached in reporting articles. On the other hand, postmortem lesions including lung consolidation 38.1% (8/21), intestinal hemorrhage 38.1% (8/21), lung congestion 28.6% (6/21), serofibrinous pleurisy 28.6% (6/21), pneumonic lungs 23.8% (5/21) and unilateral lung inflammation 14.3% (3/21), have been discussed in relation to the definitive diagnosis reached.  Conclusion: Despite the similarities in clinical signs and postmortem lesions associated with diseases presenting with respiratory signs, definitive diagnosis of CCPP was reached in cases that involved clinical signs and postmortem lesions confined in the respiratory system whereas, PPR was more diagnosed in cases that presented with clinical signs and postmortem lesions associating the digestive system. However, presence of respiratory signs in the cases the diagnosed PPR may implicate presence of unidentified secondary bacterial infections. Vaccinations being the most advocated approach of control, require a broader look to make sure that polyvalent vaccines are available against the four common diseases. Also, use of treatment to reduce the effect of secondary infecting bacteria may be of help. Furthermore, for effective outcomes of the control strategies, collaborative efforts among countries at risk should be advocated.

scholarly journals Detection of Contagious Caprine Pleuropneumonia and Concurrent Diseases in Outbreaks Presenting with Respiratory Signs in Small Ruminants in Tanzania

2020 ◽  
pp. 70-83
Author(s):  
Andrew Chota ◽  
Gabriel Shirima ◽  
Lughano Kusiluka
Keyword(s):  
Control Strategies ◽  
Clinical Signs ◽  
Small Ruminants ◽  
Conventional Polymerase Chain Reaction ◽  
Ecological Zones ◽  
Pneumonic Pasteurellosis ◽  
Contagious Caprine Pleuropneumonia ◽  
Concurrent Infections ◽  
And Control ◽  
Bio Engineering

Aims: To establish the prevalence and concurrent diseases in outbreaks presenting with respiratory signs, major associated clinical signs and postmortem lesions and proportions of those diseases in clinically and autopsied small ruminants for a proper diagnosis and control strategies. Study Design: Purposive outbreaks investigation. Place and Duration of Study: Department of Global Health, School of Life Science and Bio-Engineering (LiSBE), Nelson Mandela Institution of Science and Technology (NM-AIST) between September 2016 and December 2018. Methodology: We included investigations of outbreaks of diseases presenting with respiratory signs in small ruminants reported from five agro-ecological zones in Tanzania. Small ruminats with clinical signs or postmortem lesions suggestive of respiratory involvement were subjected to clinical or postmortem examination. Samples from all examined animals were tested in the laboratory using conventional polymerase chain reaction (PCR) to confirm the tentative diagnosis. Results: A total of 205 small ruminats were examined and tested, of these 72.2% and 20.8% were goats and sheep respectively. In goats, 79.1% (117/148) and sheep, 28.1% (16/57) were confirmed to have concurrent infections, and pneumonic pasteurellosis and peste des petits ruminants (PPR) for goats, and PPR for sheep being mostly involved diseases. Contagious caprine pleuropneumonia (CCPP) was detected in 16.1% (n=205) of the animals, and was significantly high in goats (p=0.003, OR=7.3) than sheep. Pneumonic mannheimiosis (prevalence = 9.3%) was less likely to affect goats than sheep (p=0.047, OR=0.38). In goats (n=148), detection of all diseases was significantly (p<0.05) low in clinically examined animals except pneumonic pasteurellosis and PPR, (p =0.056, OR=2.1) and (p=0.096, OR=2.15) respectively, though the difference was not significant. In sheep (n=57), CCPP was significantly (p=0.005, OR=0.17) more likely to be detected in clinically examined animals. Conclusion: In investigations of outbreaks presenting with respiratory signs in small ruminants, it is important to consider concurrent infections in the interventions and control strategies to be deployed, which may include development and use of multivalent vaccines.

Recent advances in the laboratory diagnosis of peste des petits ruminants

2021 ◽  
Vol 77 (05) ◽  
pp. 226-231
Author(s):  
WIESŁAW NIEDBALSKI ◽  
ANDRZEJ FITZNER ◽  
KRZYSZTOF BULENGER ◽  
ANDRZEJ KĘSY
Keyword(s):  
Reverse Transcription ◽  
Animal Health ◽  
Clinical Signs ◽  
Small Ruminants ◽  
Clinical Diagnostics ◽  
Molecular Diagnostic ◽  
Molecular Diagnostic Techniques ◽  
Peste Des Petits Ruminants ◽  
Rt Pcr ◽  
Agar Gel

Peste des petits ruminants (PPR) is a highly contagious and economically important, viral disease of small ruminants caused by the peste des petits ruminants virus (PPRV), which belongs to the genus Morbilivirus in the family Paramyxoviridae. PPR control is achieved mostly through vaccination and/or slaughter of susceptible animals coupled with clinical or laboratory-based diagnosis. Since clinical signs of PPR are not disease-specific and clinical diagnostics is not reliable, it should be confirmed by laboratory testing. Laboratory confirmation of clinical suspicions is made by detection of PPRV in blood, swabs or post-mortem tissues through classical virus isolation (VI), agar gel immunodiffusion (AGID)/agar gel precipitation test (AGPT), counter-immunoelectrophoresis (CIE), immunoperoxidase test (IPT) or enzyme-linked immunosorbent (ELISA) assays. However, these conventional methods have been superseded by more rapid, sensitive and accurate molecular diagnostic techniques based on the amplification of parts of either nucleocapsid (N) or fusion (F) protein gene, such as RT-PCR, real-time RT-PCR, reverse transcription loop-mediated isothermal amplification (RT-LAMP), reverse transcription recombinase polymerase amplification (RT-RPA) and Oxford nanopore MinION technology. Although these molecular diagnostic assays are accurate, rapid and sensitive, they have to be performed in laboratory settings, and samples must be transported under appropriate conditions from the field to the laboratory, which can delay the confirmation of PPRV infection. The recently developed immunochromatographic lateral flow device (IC-LFD) assay can be used in the field (“pen-side”) without the need for expensive equipment, so a well-established laboratory is not required. The control and eventual eradication of PPR is now one of the top priorities for the Food and Agriculture Organization (FAO) and the World Organization for Animal Health (OIE). In 2015, the international community agreed on a global strategy for PPR eradication, setting 2030 as a target date for elimination of the disease

scholarly journals Camelids and Cattle Are Dead-End Hosts for Peste-des-Petits-Ruminants Virus

Viruses ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 1133 ◽  
Author(s):  
Claudia Schulz ◽  
Christine Fast ◽  
Ulrich Wernery ◽  
Jörg Kinne ◽  
Sunitha Joseph ◽  
...  
Keyword(s):  
Small Ruminant ◽  
Clinical Signs ◽  
Small Ruminants ◽  
Tissue Tropism ◽  
Peste Des Petits Ruminants ◽  
Dromedary Camels ◽  
Dead End ◽  
Recent Transmission ◽  
Lineage Iv

Peste-des-petits-ruminants virus (PPRV) causes a severe respiratory disease in small ruminants. The possible impact of different atypical host species in the spread and planed worldwide eradication of PPRV remains to be clarified. Recent transmission trials with the virulent PPRV lineage IV (LIV)-strain Kurdistan/2011 revealed that pigs and wild boar are possible sources of PPRV-infection. We therefore investigated the role of cattle, llamas, alpacas, and dromedary camels in transmission trials using the Kurdistan/2011 strain for intranasal infection and integrated a literature review for a proper evaluation of their host traits and role in PPRV-transmission. Cattle and camelids developed no clinical signs, no viremia, shed no or only low PPRV-RNA loads in swab samples and did not transmit any PPRV to the contact animals. The distribution of PPRV-RNA or antigen in lymphoid organs was similar in cattle and camelids although generally lower compared to suids and small ruminants. In the typical small ruminant hosts, the tissue tropism, pathogenesis and disease expression after PPRV-infection is associated with infection of immune and epithelial cells via SLAM and nectin-4 receptors, respectively. We therefore suggest a different pathogenesis in cattle and camelids and both as dead-end hosts for PPRV.

scholarly journals Clostridioides (Clostridium) Difficile in Food-Producing Animals, Horses and Household Pets: A Comprehensive Review

2019 ◽  
Vol 7 (12) ◽  
pp. 667 ◽  
Author(s):  
Melina Kachrimanidou ◽  
Eleni Tzika ◽  
George Filioussis
Keyword(s):  
Clostridium Difficile ◽  
Control Strategies ◽  
Clinical Signs ◽  
Laboratory Diagnosis ◽  
Human Infection ◽  
Current Evidence ◽  
Public Health Issue ◽  
Food Animals ◽  
Ribotype 078 ◽  
And Control

Clostridioides (Clostridium) difficile is ubiquitous in the environment and is also considered as a bacterium of great importance in diarrhea-associated disease for humans and different animal species. Food animals and household pets are frequently found positive for toxigenic C. difficile without exposing clinical signs of infection. Humans and animals share common C. difficile ribotypes (RTs) suggesting potential zoonotic transmission. However, the role of animals for the development of human infection due to C. difficile remains unclear. One major public health issue is the existence of asymptomatic animals that carry and shed the bacterium to the environment, and infect individuals or populations, directly or through the food chain. C. difficile ribotype 078 is frequently isolated from food animals and household pets as well as from their environment. Nevertheless, direct evidence for the transmission of this particular ribotype from animals to humans has never been established. This review will summarize the current available data on epidemiology, clinical presentations, risk factors and laboratory diagnosis of C. difficile infection in food animals and household pets, outline potential prevention and control strategies, and also describe the current evidence towards a zoonotic potential of C. difficile infection.

scholarly journals A Sequential Study on the Pathology of Peste Des Petits Ruminants and Tissue Distribution of the Virus Following Experimental Infection of Black Bengal Goats

2021 ◽  
Vol 8 ◽  
Author(s):  
Shahana Begum ◽  
Mohammed Nooruzzaman ◽  
Mohammad Rafiqul Islam ◽  
Emdadul Haque Chowdhury
Keyword(s):  
Experimental Infection ◽  
Control Strategies ◽  
Clinical Signs ◽  
Electrolyte Imbalance ◽  
Effective Control ◽  
Peste Des Petits Ruminants ◽  
Virus Shedding ◽  
Liver And Kidney ◽  
Ulcerative Lesions ◽  
Lineage Iv

We studied the sequential pathology of peste des petits ruminants (PPR) in Black Bengal goats and analyzed virus distribution in tissues and virus shedding following experimental infection with a Bangladeshi isolate of lineage IV PPR virus (PPRV). The early clinical signs like fever, depression, and ocular and nasal discharges first appeared at 4–7 days post-infection (dpi). Three out of eight inoculated goats died at 13, 15, and 18 dpi, and the rest were killed at different time points from 5 to 18 dpi. Initially, the virus multiplied mostly in the lymphoid organs of the pharyngeal region and caused extensive lymphoid destruction and hemorrhages. This was followed by viremia, massive virus replication in the lungs, and pneumonia along with the appearance of the clinical signs. Subsequently, the virus spread to other organs causing necrotic and hemorrhagic lesions, as well as the virus localized in the upper respiratory, oral and intestinal mucosa resulting in catarrhal, erosive, and ulcerative lesions. On hematological and biochemical investigation progressive leukopenia and hypoproteinemia, a gradual increase of serum metabolites and enzymes associated with liver and kidney damage, and electrolyte imbalance were observed. Seroconversion started at 7 dpi and all the surviving animals had serum antibodies at 14 dpi. Virus shedding was observed in nasal and ocular secretions at 4 dpi and in feces and urine at 14 dpi, which gradually increased and continued till the end of the experiment (18 dpi) despite seroconversion. Therefore, the virus shedding of naturally infected seroconverted goats should be monitored for effective control strategies.

scholarly journals ASCARIS LUMBRICOIDES: EPIDEMIOLOGY, DIAGNOSIS, TREATMENT, AND CONTROL

2020 ◽  
pp. 8-11
Author(s):  
KANAAN AL-TAMEEMI ◽  
RAIAAN KABAKLI
Keyword(s):  
Developing Countries ◽  
Ascaris Lumbricoides ◽  
Intestinal Parasite ◽  
Control Strategies ◽  
Mechanisms Of Resistance ◽  
Neglected Disease ◽  
Worldwide Distribution ◽  
Resistance To Infection ◽  
And Control

Although Ascaris lumbricoides is a common intestinal parasite of humans with worldwide distribution causing ascariasis, Ascaris is a neglected disease and still is a burden in developing countries. Furthermore, the parasite’s permanence and prevalence present difficulties in control strategies. Therefore, more research on the mechanisms of resistance to infection is required for reducing prevalence parasite and control of infections.

scholarly journals Resistencia a los antihelmínticos: origen, desarrollo y control.

2003 ◽  
Vol 4 (1) ◽  
pp. 55 ◽  
Author(s):  
Dildo Márquez Lara
Keyword(s):  
Anthelmintic Resistance ◽  
Control Strategies ◽  
Small Ruminants ◽  
Nematode Resistance ◽  
Development Of Resistance ◽  
Helminth Infections ◽  
Wide Range ◽  
And Control

<p>Una variada gama de antihelmínticos modernos, con espectro amplio y alto grado de eficacia, como los benzimidazoles, los agonistas nicotínicos y las lactonas macrocíclicas, se encuentran disponibles comercialmente en el mundo para el control de las infecciones causadas por helmintos en rumiantes. El uso intensivo y la administración inadecuada de antihelmínticos, en épocas y grupos de rumiantes no apropiados, han contribuido al desarrollo de resistencia a estas sustancias, lo que constituye un obstáculo importante para el control de los endoparásitos. La resistencia antihelmíntica se ha reportado principalmente en pequeños rumiantes y es escasa la información relacionada con los nemátodos de bovinos. Se han identificado algunos factores aceleradores del proceso de desarrollo de resistencia, entre ellos factores genéticos, reproductivos y ecológicos de los parásitos, así como factores de orden antrópico, siendo la resistencia una característica heredable. El aumento de la resistencia a los antihelmínticos en la última década, así como los requerimientos de información sobre su ocurrencia e incidencia, han señalado la necesidad de desarrollar y estandarizar técnicas más sensibles para su detección. Hay varias técnicas disponibles <em>in vivo </em>e <em>in vitro </em>útiles para detectar la resistencia antihelmíntica, si bien la prueba de Reducción del Conteo de Huevos Fecales (RCH) es la más usada. La detección temprana de esta condición es un factor esencial para el control estratégico de los endoparásitos a fin de preservar la eficacia de los antihelmínticos. La presente revisión propone diferentes alternativas, químicas y no químicas, para el control de helmintos con el objeto de retardar la aparición de resistencia.</p><p> </p><p><strong>Anthelmintic resistance: origin, development and control</strong></p><p>A wide range of modern anthelmintics, with broad-spectrum and high efficacy to control helminth infections in ruminants, are commercially available, such as benzimidazoles, nicotinic agonist and macrocyclic lactones.The intensive use and inadequated dosages of anthelmintics in ruminants have contributed to develop resistance, becoming the main threat to control endoparasites. Anthelmintic resistance has been reported mainly in small ruminants, but there is scarce information about it in nematodes of cattle. Genetic, reproductive, ecological and anthropic factors have been found to enhance the development of resistance. Because nematode resistance has increased in the last decade, it is necessary to investigate about its occurrence and incidence; so, developing and standarization of improved techniques for detection of the resistance should be carried out. There are several techniques (<em>in vivo </em>and <em>in vitro</em>) available for detection of anthelmintic resistance, being the Faecal Egg Count Reduction Test (FECRT) the most commonly used. Early detection of resistance is an essential factor on parasite control strategies in order to preserve the effectiveness of anthelmintics. Different chemical and non-chemical helminth control strategies have been suggested in order to slow the onset of resistance.</p>

scholarly journals Peste des petits ruminants pathogenesis on experimental infected goats by the Moroccan 2015 isolate

2019 ◽  
Vol 15 (1) ◽  
Author(s):  
Z. Bamouh ◽  
F. Fakri ◽  
M. Jazouli ◽  
N. Safini ◽  
K. Omari Tadlaoui ◽  
...  
Keyword(s):  
Clinical Signs ◽  
Small Ruminants ◽  
Clinical Score ◽  
Viral Disease ◽  
Infection Model ◽  
Intravenous Route ◽  
Invasive Infection ◽  
Peste Des Petits Ruminants ◽  
Virus Suspension ◽  
Short Period

Abstract Background Peste des petits ruminants (PPR) is a viral disease of major economic importance on small ruminants. Goats are usually known to be more susceptible to the disease. Infection chronology, virus circulation, and the disease early detection need to be better understood. This study evaluates the tissue tropism and pathogenesis of PPR following experimental infection of goats using a lineage IV virus, the most dominant in the world originated from Asia. PPRV infection was experimentally induced in 4 six-month-old goats by intra-nasal and intravenous route of cell virus suspension and from infectious mashed tissue. The clinical signs were observed and goats were euthanized at predetermined clinical score level for post-mortem examinations and PPRV detection by RT-PCR. Clinical signs of infection were present, pyrexia, serous-mucopurulent nasal discharges, coughing, diarrhea and asthenia, for both cell virus suspension and infectious mashed tissue. PPRV genome was highly detected in swabs and tissues with clinical signs dominated by pulmonary attack and digestive symptoms secondary. Results Results of this study indicates that PPRV is an invasive infection in animals that in a short period, less than 10 days, invade all vital organs. On live animals, early diagnostic may be easily done on lacrimal and rectal swabs. Conclusion The experimental PPRV-infection model using the cell virus suspension is suitable for vaccine evaluation as a standard model.

scholarly journals Peste Des Petits Ruminants (PPR) in Dromedary Camels and Small Ruminants in Mandera and Wajir Counties of Kenya

2019 ◽  
Vol 2019 ◽  
pp. 1-6 ◽  
Author(s):  
R. N. Omani ◽  
G. C. Gitao ◽  
J. Gachohi ◽  
P. K. Gathumbi ◽  
B. A. Bwihangane ◽  
...  
Keyword(s):  
Sudden Death ◽  
Clinical Signs ◽  
Small Ruminants ◽  
Ventral Surface ◽  
Sudden Death Syndrome ◽  
Unknown Etiology ◽  
Peste Des Petits Ruminants ◽  
Horn Of Africa ◽  
General Weakness

A study was conducted to determine the presence of Peste des petits ruminants (PPR) in camel population kept together with small ruminants in Isiolo, Mandera, Marsabit, and Wajir counties of Kenya. This was done in the wake of a disease with unknown etiology “Camel Sudden Death Syndrome” camels in the horn of Africa. Thirty-eight (38) samples, 12, 8, 15, and 3 samples, were collected from Mandera, Wajir, Isiolo, and Marsabit, respectively, from 25 camels, 7 goats, and 4 sheep. One camel in Mandera and one goat in Wajir were confirmed positive for PPR virus (PPRV) through reverse Polymerase Chain Reaction. The analysis of sequences revealed closest nucleotide identities of obtained sequences from both goat and camel to the lineage III of PPRV albeit with 60.29% of nucleotide identity. This study establishes that camels in the study area suffer with PPR manifest clinical signs that are mainly characterized by inappetence, loss of body condition, and general weakness terminally leading to diarrhea, conjunctivitis, and ocular nasal discharges preceding death. These clinical signs are similar to those observed in small ruminants with slight variations of manifestations such as keratoconjunctivitis as well as edema of the ventral surface of the abdomen. This shows that camels could be involved in the epidemiology of PPR in the region and that PPRV could be involved in the epidemics of Camel Sudden Death syndrome. There is therefore a need for resources to be dedicated in understanding the role camels play in the epidemiology of PPR and the role of the disease in Camels Sudden death syndrome.

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