RESUMEN
Chlamydiaceae are a family of obligate intracellular bacterial pathogens that affect both humans and animals. Recently, a new species named Chlamydia (C.) buteonis was isolated from hawks. In this study, we aimed to investigate the prevalence of Chlamydiaceae in 60 falcons that underwent a routine health check at a specialized clinic in Dubai, United Arab Emirates. Using real-time PCR, we analyzed cloacal and tracheal swabs from these birds and found that 39 of them tested positive for Chlamydiaceae. Subsequent real-time PCR assays specific for C. psittaci, C. abortus, C. avium, and C. gallinacea yielded negative results, while testing positive for C. buteonis. Analysis of ompA and MLST sequences indicated a highly conserved group of strains within this set of samples, but with sequences distinct from the C. buteonis RSHA reference strains and other C. buteonis strains isolated from hawks in the United States. Two strains were further isolated by cell culture and sequenced using whole-genome sequencing, confirming the clustering of these falcon strains within the C. buteonis species, but in a separate clade from the previously identified hawk strains. We also developed a SNP-based PCR-HRM assay to distinguish between these different genotypes. Overall, our findings suggest a high prevalence of C. buteonis in falcons in Dubai and highlight the importance of monitoring this pathogen in birds of prey.
Asunto(s)
Chlamydia , Chlamydiaceae , Falconiformes , Humanos , Animales , Tipificación de Secuencias Multilocus/veterinaria , Chlamydia/genética , Aves/microbiología , GenotipoRESUMEN
Burkholderia mallei is the etiologic agent of glanders, an infectious disease of solipeds, with renewed scientific interest due to its increasing incidence in different parts of the world. More rapid, sensitive and specific assays are required by laboratories for confirmatory testing of this disease. A microsphere-based immunoassay consisting of beads coated with B. mallei recombinant proteins (BimA, GroEL, Hcp1, and TssB) has been developed for the serological diagnosis of glanders. The proteins' performance was compared with the OIE reference complement fixation test (CFT) and an indirect enzyme-linked immunosorbent assay (iELISA) on a large panel of sera comprised of uninfected horses (n=198) and clinically confirmed cases of glanders from India and Pakistan (n=99). Using Receiver Operating Characteristics (ROC) analysis and adjusting the cutoff levels, Hcp1 (Se=100%, Sp=99.5%) and GroEL (Se= 97%, Sp=99.5%) antigens exhibited the best specificity and sensitivity. Neither Hcp1 and GroEL proteins, nor iELISA reacted with doubtful and positive CFT samples from glanders free countries which further confirmed the false positive reactions seen in CFT.
Asunto(s)
Burkholderia mallei/inmunología , Muermo/diagnóstico , Animales , Pruebas de Fijación del Complemento , Ensayo de Inmunoadsorción Enzimática , Caballos , Microesferas , Pruebas SerológicasRESUMEN
Middle East respiratory syndrome (MERS) is a zoonotic viral disease identified in both animals and human beings. More than 2,200 laboratory-confirmed cases have been reported in humans from 27 countries, with a crude case fatality rate of 35% since the disease's emergence in the Middle East in 2012. In the coming years, MERS will continue to pose a severe threat to economic development as well as to the elimination of poverty and advances in food security. An important gap in the effort to keep MERS at bay is the lack of surveillance of animals in the Middle East. The authors identify the need for international collaboration to conduct MERS coronavirus (CoV) surveillance in animals in the Middle East, since the emergence of new MERS-CoV variants with the ability to sustain efficient person-to-person transmission is a genuine threat. However, effective surveillance will be very difficult, if not impossible, to achieve. There are multiple obstacles in the region to overcome, including a lack of transparency as governments in the Middle East generally do not disclose detailed information on animal diseases. In addition, there is minimal collaboration between local and international agencies in both the human and animal health sectors and a limited number of readily available qualified laboratories to screen animals for MERS- CoV. Last, but not least, there is a lack of adequate active communication between all relevant laboratories, local and abroad. However, with the support of the Food and Agriculture Organization of the United Nations (FAO), the World Organisation for Animal Health (OIE), and other partners, the responsibility of the Mediterranean Zoonosis Control Centre in Athens, Greece, could be widened to include the countries of the Middle East. This would foster a stronger alliance and far more effective collaboration in the spirit of One Health.
Le syndrome respiratoire du Moyen-Orient (MERS) est une maladie virale zoonotique qui affecte à la fois l'homme et les animaux. Plus de 2 200 cas humains confirmés au laboratoire ont été notifiés dans 27 pays depuis l'apparition de la maladie au Moyen-Orient en 2012, avec un taux brut de létalité de 35 %. Dans les années à venir, le MERS continuera à représenter une menace aussi bien pour le développement économique que pour la réussite des objectifs d'élimination de la pauvreté et de sécurisation de l'approvisionnement alimentaire. L'un des principaux obstacles empêchant de tenir le MERS en échec est l'absence de surveillance sanitaire exercée sur les populations animales au Moyen-Orient. Les auteurs soulignent la nécessité d'une collaboration internationale en matière de surveillance du coronavirus responsable du MERS (MERS-Cov) chez les animaux au Moyen-Orient, d'autant que l'émergence de nouveaux variants du MERS-CoV qui entretiennent l'infection en favorisant la transmission de personne à personne constitue un véritable danger. Toutefois, il sera extrêmement difficile, voire impossible de mettre en place une surveillance efficace. En effet les obstacles sont nombreux dans la région, en particulier l'absence de transparence puisque les gouvernements du Moyen-Orient ne publient généralement pas d'informations détaillées sur les maladies animales présentes sur leur territoire. En outre, la collaboration entre les agences locales et internationales des secteurs de la santé publique et animale est réduite au minimum et rares sont à ce jour les laboratoires possédant les compétences requises pour procéder au dépistage de l'infection par le MERS-CoV chez les animaux. Dernière difficulté mais non la moindre, les laboratoires compétents dans les pays et à l'étranger ne communiquent pas entre eux de manière proactive. Dans ce contexte, il est envisagé d'élargir la portée du Centre méditerranéen de lutte contre les zoonoses, situé à Athènes (Grèce) afin d'y intégrer les pays du Moyen-Orient, avec le soutien de l'Organisation des Nations Unies pour l'alimentation et l'agriculture (FAO), de l'Organisation mondiale de la santé animale (OIE) et d'autres partenaires. Cette initiative permettrait de renforcer les alliances et de déployer une collaboration bien plus efficace, dans une perspective Une seule santé.
El síndrome respiratorio de Oriente Medio (MERS, por su acrónimo inglés) es una enfermedad viral zoonótica que se ha descrito tanto en animales como en personas. Desde que en 2012 surgió en el Oriente Medio, se han notificado más de 2 200 casos confirmados en laboratorio que afectan a personas de 27 países, con una tasa bruta de letalidad del 35%. En los próximos años, el MERS seguirá constituyendo una grave amenaza para el desarrollo económico y también para el avance hacia la eliminación de la pobreza y la seguridad alimentaria. A la hora de poner coto a la enfermedad, un importante problema es la deficiente vigilancia zoosanitaria en el Oriente Medio. Los autores señalan la necesidad de colaboración internacional para hacer efectiva en la región la vigilancia del coronavirus (CoV) del MERS en los animales, pues la aparición de nuevas variantes de este virus capaces de transmitirse eficaz y sostenidamente entre las personas constituye un verdadero peligro. Sin embargo, resultará difícil, si no imposible, efectuar una vigilancia eficaz, habida cuenta de la multitud de obstáculos que hay que superar en el Oriente Medio, incluida la falta de transparencia de los gobiernos, que no acostumbran a revelar información detallada sobre las enfermedades animales. Además, la colaboración entre instancias locales y organismos internacionales en los sectores de la salud humana y la sanidad animal es mínima, y hay contados laboratorios cualificados para la detección del MERSCoV en animales que estén en condiciones de intervenir con presteza. Por último, pero no menos importante, no hay una adecuada comunicación activa entre todos los laboratorios competentes, ya sean de los propios países o del extranjero. No obstante, con apoyo de la Organización de las Naciones Unidas para la Alimentación y la Agricultura (FAO), la Organización Mundial de Sanidad Animal (OIE) y otros colaboradores, sería posible extender a los países del Oriente Medio el ámbito de responsabilidad y actuación del Centro de Control de Zoonosis del Mediterráneo, sito en Atenas (Grecia), cosa que favorecería alianzas más sólidas y mucho más eficaces, conforme al espíritu de Una sola salud.
Asunto(s)
Infecciones por Coronavirus , Coronavirus del Síndrome Respiratorio de Oriente Medio , Animales , Infecciones por Coronavirus/prevención & control , Humanos , Colaboración Intersectorial , Medio Oriente , Vigilancia de la Población , Zoonosis/prevención & controlRESUMEN
[This corrects the article DOI: 10.1016/j.bdq.2015.10.001.].
RESUMEN
We present the first molecular characterisation based on MLVA and SNP analysis of a strain of Burkholderia mallei isolated from a mule found dead in Brazil in 2016.
Asunto(s)
Burkholderia mallei/clasificación , Burkholderia mallei/genética , Equidae/microbiología , Muermo/epidemiología , Muermo/microbiología , Animales , Brasil/epidemiología , Burkholderia mallei/aislamiento & purificación , Genoma Bacteriano , Genotipo , Tipificación de Secuencias Multilocus , Filogenia , Polimorfismo de Nucleótido Simple , Secuenciación Completa del GenomaRESUMEN
Glanders is the contagious zoonotic disease caused by infection with Burkholderia mallei. It affects primarily horses, donkeys and mules. The disease was eradicated from large areas of the Western world in the early 20th century, but, over the last 10-20 years, has emerged and re-emerged in areas in which it was previously unknown or had been eradicated. Although glanders was previously thought to manifest in only acute or chronic presentations, it now appears that B. mallei can produce latent infections similar to those caused by Burkholderia pseudomallei. These latent infections may or may not be detectable by current diagnostic tests. The diagnostic test currently recommended by the World Organisation for Animal Health (Office International des Epizooties [OIE]) for international trade in equids is the complement fixation test (CFT). This test has been shown to have varying sensitivities and specificities depending on the antigen and methodology used. False positives are problematic for the horse-owner and veterinary authority, whereas false negatives may allow the reintroduction of B. mallei into B. mallei-free areas. These gaps in knowledge of the epidemiology of glanders, and weaknesses in its diagnosis, coupled with the increased movement of equids, indicate that infection with B. mallei remains a major risk in the context of international movement of equids.
Asunto(s)
Muermo/transmisión , Internacionalidad , Transportes , Animales , Caballos , Factores de Riesgo , ZoonosisRESUMEN
The emergence of Middle East respiratory syndrome (MERS) and the discovery of MERS coronavirus (MERS-CoV) in 2012 suggests that another SARS-like epidemic is occurring. Unlike the severe acute respiratory syndrome (SARS) epidemic, which rapidly disappeared in less than one year, MERS has persisted for over three years. More than 1,600 cases of MERS have been reported worldwide, and the disease carries a worryingly high fatality rate of >30%. A total of 182 MERS-CoV genomes have been sequenced, including 94 from humans and 88 from dromedary camels. The 182 genomes all share >99% identity, indicating minimal variation among MERS-CoV genomes. MERS-CoV is a lineage C Betacoronavirus (ßCoV). MERS-CoV genomes can be roughly divided into two clades: clade A, which contains only a few strains, and clade B, to which most strains belong. In contrast to ORF1ab and structural proteins, the putative proteins encoded by ORF3, ORF4a, ORF4b, ORF5 and ORF8b in the MERS-CoV genome do not share homology with any known host or virus protein, other than those of its closely related lineage C ßCoVs. Human and dromedary viral genomes have intermingled, indicating that multiple camel-to-human transmission events have occurred. The multiple origins of MERS-CoV suggest that the virus has been resident in dromedaries for many years. This is consistent with the detection of anti-MERS-CoV antibodies in dromedary camels as early as the 1980s.
L'émergence du syndrome respiratoire du Moyen-Orient (SRMO, ou MERS d'après son sigle anglais) et l'identification en 2012 du coronavirus responsable de cette maladie (MERS-CoV) indiquent que nous sommes en présence d'une épidémie semblable à celle du syndrome respiratoire aigu sévère (SRAS). Toutefois, contrairement à l'épidémie du SRAS qui avait rapidement disparu en moins d'un an, le MERS persiste depuis plus de trois ans. Plus de 1 600 cas de MERS ont été notifiés dans le monde ; la maladie présente un taux de létalité particulièrement préoccupant, s'élevant à plus de 30 %. Au total, 182 génomes du MERS-CoV ont été séquencés jusqu'à présent, dont 94 provenaient de virus isolés chez l'homme et 88 chez des dromadaires. Ces 182 génomes ont en commun un pourcentage d'identité de 99 %, dénotant une très faible variabilité des génomes viraux. Le MERS-CoV appartient à la lignée C du genre Betacoronavirus (ßCoV). Les génomes du MERSCoV se répartissent, dans leurs grandes lignes, en deux clades : le clade A, qui ne contient que quelques souches, et le clade B regroupant l'immense majorité des souches. Contrairement à ce qui se produit avec la protéine ORF1ab et les protéines structurales, les protéines potentiellement codées par les gènes ORF3, ORF4a, ORF4b, ORF5 et ORF8b du génome du MERS-CoV ne présentent aucune homologie avec des protéines virales ou de l'hôte autres que celles d'autres bêtacoronavirus de la lignée C, qui lui sont étroitement apparentés. Les génomes des virus affectant l'homme et le dromadaire se sont entremêlés, ce qui montre que le virus a connu de multiples épisodes de transmission des camélidés à l'homme. Les origines multiples du MERS-CoV témoignent d'une présence prolongée du virus (plusieurs années) chez les dromadaires. Ce constat est corroboré par le fait que des anticorps anti-MERS-CoV ont été détectés chez des dromadaires dès le début des années 80.
La aparición del síndrome respiratorio de Oriente Medio (MERS, por sus siglas en inglés) y el descubrimiento del coronavirus que lo causa (MERS-CoV) en 2012 parecen apuntar al advenimiento de una nueva epidemia análoga a la del síndrome respiratorio agudo severo (SRAS). Pero a diferencia de lo ocurrido con la epidemia de SRAS, que en menos de un año había desaparecido, el MERS lleva más de tres años presente. En el mundo se han notificado más de 1.600 casos de MERS, y la enfermedad presenta una tasa de letalidad muy alta y preocupante, superior al 30%. Hasta ahora se han secuenciado un total de 182 genomas del MERS-CoV, 94 de ellos obtenidos a partir de personas y 88 a partir de dromedarios. Estos 182 genomas comparten identidad en más de un 99%, lo que pone de manifiesto un nivel mínimo de variación entre los genomas coronavíricos. El coronavirus del MERS pertenece al linaje C del género Betacoronavirus (ßCoV). Los genomas de este virus pueden ser divididos, a grandes rasgos, en dos clados: el clado A, que agrupa unas pocas cepas; y el clado B, al que pertenecen la gran mayoría de las cepas. A diferencia de lo que ocurre con la proteína ORF1ab y las proteínas estructurales, las proteínas que supuestamente codifican los genes ORF3, ORF4a, ORF4b, ORF5 y ORF8b del genoma del MERS-CoV no comparten homología con ninguna proteína conocida de otros virus o anfitriones, salvo con proteínas de otros betacoronavirus del linaje C estrechamente emparentados con él. Los genomas de los virus que afectan a personas y dromedarios se han entremezclado, lo que indica que se han producido numerosos episodios de transmisión de camélidos a humanos. De los múltiples orígenes del MERS-CoV se deduce que el virus lleva muchos años siendo residente en dromedarios, lo que concuerda con el hecho de que ya en los años ochenta se detectaran anticuerpos anti-MERS-CoV en dromedarios.
Asunto(s)
Infecciones por Coronavirus/virología , Coronavirus del Síndrome Respiratorio de Oriente Medio/genética , Zoonosis/virología , Animales , Enfermedades Transmisibles Emergentes , Infecciones por Coronavirus/epidemiología , Infecciones por Coronavirus/mortalidad , Genoma Viral , HumanosRESUMEN
Beak and feather disease is caused by Circovirus, which affects actively growing beak and feather cells of avian species. The disease affects mainly young birds while older birds may overcome the disease with few lasting effects. Due to lack of treatment, the only way to control the disease is through hygiene and early diagnosis. As a diagnostic tool, we have established a Taqman probe based real-time PCR assay to detect the presence of the viral genome in psittacine birds in UAE and reported the incidence of circovirus in different species of psittacine birds. The sensitivity of our assay was found to be very high with detection limit of up to 3.5 fg of DNA in the sample. The mean prevalence of circovirus was found to be 58.33% in African Grey Parrots, 34.42% in Cockatoos, 31.8% in amazon parrots and 25.53% in Macaws. The Taqman assay is a quick, reliable and sensitive detection method that has been instrumental in identifying this disease that was not previously reported in the region.
RESUMEN
Foot-and-mouth disease viruses are often restricted to specific geographical regions and spread to new areas may lead to significant epidemics. Phylogenetic analysis of sequences of the VP1 genome region of recent outbreak viruses from Libya and Saudi Arabia has revealed a lineage, O-Ind-2001, normally found in the Indian subcontinent. This paper describes the characterization of field viruses collected from these cases and provides information about a new real-time RT-PCR assay that can be used to detect viruses from this lineage and discriminate them from other endemic FMD viruses that are co-circulating in North Africa and western Eurasia.
Asunto(s)
Virus de la Fiebre Aftosa/genética , Fiebre Aftosa/epidemiología , Fiebre Aftosa/virología , Animales , Brotes de Enfermedades , Libia/epidemiología , Filogenia , Arabia Saudita/epidemiologíaRESUMEN
REASONS FOR PERFORMING STUDY: Equine grass sickness (EGS) is of unknown aetiology. Despite some evidence suggesting that it represents a toxico-infection with Clostridium botulinum types C and/or D, the effect of EGS on the functional targets of botulinum neurotoxins, namely the soluble N-ethylmaleimide-sensitive factor attachment receptor (SNARE) proteins, is unknown. Further, while it is commonly stated that, unlike EGS, equine botulism is not associated with autonomic and enteric neurodegeneration, this has not been definitively assessed. OBJECTIVES: To determine: 1) whether botulism causes autonomic and enteric neurodegeneration; and 2) the effect of EGS on the expression of SNARE proteins within cranial cervical ganglion (CCG) and enteric neuronal perikarya. STUDY DESIGN: Descriptive study. METHODS: Light microscopy was used to compare the morphology of neurons in haematoxylin-eosin stained sections of CCG and ileum from 6 EGS horses, 5 botulism horses and 6 control horses. Immunohistochemistry was used to compare the expression of synaptosomal-associated protein-25, synaptobrevin (Syb) and syntaxin within CCG neurons, and of Syb in enteric neurons, from horses with EGS, horses with botulism and control horses. The concentrations of these SNARE proteins in extracts of CCG from EGS and control horses were compared using quantitative fluorescent western blotting. RESULTS: EGS, but not botulism, was associated with autonomic and enteric neurodegeneration and with increased immunoreactivity for SNARE proteins within neuronal perikarya. Quantitative fluorescent western blotting confirmed increased concentrations of synaptosomal-associated protein-25, Syb and syntaxin within CCG extracts from EGS vs. control horses, with the increases in the latter 2 proteins being statistically significant. CONCLUSIONS: The occurrence of autonomic and enteric neurodegeneration, and increased expression of SNARE proteins within neuronal perikarya, in EGS but not botulism, suggests that EGS may not be caused by botulinum neurotoxins. Further investigation of the aetiology of EGS is therefore warranted.
Asunto(s)
Enfermedades del Sistema Nervioso Autónomo/veterinaria , Botulismo/veterinaria , Enfermedades de los Caballos/fisiopatología , Proteínas Sensibles a N-Etilmaleimida/metabolismo , Neuronas/metabolismo , Proteínas SNARE/metabolismo , Animales , Regulación de la Expresión Génica , Caballos , Proteínas Sensibles a N-Etilmaleimida/genética , Proteínas SNARE/genéticaRESUMEN
We tested, using a low starting dilution, sequential serum samples from dromedary camels, sheep and horses collected in Dubai from February/April to October of 2005 and from dromedary camels for export/import testing between Canada and USA in 2000-2001. Using a standard Middle East respiratory syndrome coronavirus (MERS-CoV) neutralization test, serial sera from three sheep and three horses were all negative while sera from 9 of 11 dromedary camels from Dubai were positive for antibodies supported by similar results in a MERS-CoV recombinant partial spike protein antibody ELISA. The two negative Dubai camels were both dromedary calves and remained negative over the 5 months studied. The six dromedary samples from USA and Canada were negative in both tests. These results support the recent findings that infection with MERS-CoV or a closely related virus is not a new occurrence in camels in the Middle East. Therefore, interactions of MERS-CoV at the human-animal interface may have been ongoing for several, perhaps many, years and by inference, a widespread pandemic may be less likely unless significant evolution of the virus allow accelerated infection and spread potential in the human population.
Asunto(s)
Anticuerpos Antivirales/sangre , Camelus/virología , Infecciones por Coronavirus/veterinaria , Coronavirus/aislamiento & purificación , Animales , Coronavirus/inmunología , Infecciones por Coronavirus/epidemiología , Infecciones por Coronavirus/virología , Caballos , Incidencia , Medio Oriente , Pruebas de Neutralización , Ovinos , Síndrome , Emiratos Árabes Unidos/epidemiologíaAsunto(s)
Anticuerpos Antiidiotipos/farmacología , Mieloma Múltiple/radioterapia , Radioinmunoterapia , Anticuerpos de Dominio Único/farmacología , Tomografía Computarizada de Emisión de Fotón Único , Microtomografía por Rayos X , Animales , Anticuerpos Antiidiotipos/administración & dosificación , Modelos Animales de Enfermedad , Humanos , Ratones , Mieloma Múltiple/patología , Radiofármacos , Anticuerpos de Dominio Único/administración & dosificación , TecnecioRESUMEN
Camel brucellosis has been diagnosed in all camel-rearing countries except Australia. In many countries the infection is on the rise in Old World camels (OWCs) due to the uncontrolled trade of live animals. Knowledge of camelid brucellosis has increased over the last decade through field investigations, experimental infection trials and comprehensive laboratory testing. Infection with Brucella melitensis is frequent in OWCs and rare with B. abortus. New World Camels rarely contract brucellosis. In East African countries the seroprevalence of brucellosis can reach 40% (herd level) and depends on the management system. The highest incidence is found when camels are kept together with infected small ruminants. Only a combination of serological methods can detect all serological reactors. Culturing the pathogen is still the preferred test method, although several assays based on polymerase chain reaction have been developed.
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Brucelosis/veterinaria , Animales , Brucelosis/epidemiología , Camelus , Salud Global , Humanos , ZoonosisAsunto(s)
Antílopes , Anticuerpos Antivirales/sangre , Peste de los Pequeños Rumiantes/veterinaria , Virus de la Peste de los Pequeños Rumiantes/inmunología , Vacunas Virales/inmunología , Animales , Femenino , Masculino , Peste de los Pequeños Rumiantes/prevención & control , Vacunas Atenuadas/administración & dosificación , Vacunas Atenuadas/inmunología , Vacunas Virales/administración & dosificaciónRESUMEN
The objectives of the present study were to monitor the microbiological quality and somatic cell count (SCC) of bulk tank milk at the world's first large-scale camel dairy farm for a 2-yr period, to compare the results of 2 methods for the enumeration of SCC, to evaluate correlation among milk quality indicators, and to determine the effect of specific factors (year, season, stage of lactation, and level of production) on milk quality indicators. The study was conducted from January 2008 to January 2010. Total viable count (TVC), coliform count (CC), California Mastitis Test (CMT) score, and SCC were determined from daily bulk milk samples. Somatic cell count was measured by using a direct microscopic method and with an automatic cell counter. In addition, production parameters [total daily milk production (TDM, kg), number of milking camels (NMC), average milk per camel (AMC, kg)] and stage of lactation (average postpartum days, PPD) were recorded for each test day. A strong correlation (r=0.33) was found between the 2 methods for SCC enumeration; however, values derived using the microscopic method were higher. The geometric means of SCC and TVC were 394×10(3) cells/mL and 5,157 cfu/mL during the observation period, respectively. Somatic cell count was >500×10(3) cells/mL on 14.6% (106/725) and TVC was >10×10(3) cfu/mL on 4.0% (30/742) of the test days. Both milk quality indicators had a distinct seasonal pattern. For log SCC, the mean was lowest in summer and highest in autumn. The seasonal pattern of log TVC was slightly different, with the lowest values being recorded during the spring. The monthly mean TVC pattern showed a clear difference between years. Coliform count was <10 cfu/mL in most of the samples (709/742, 95.6%). A positive correlation was found between log SCC and log TVC (r=0.32), between log SCC and CMT score (r=0.26), and between log TVC and CC in yr 1 (r=0.30). All production parameters and stage of lactation showed strong seasonal variation. Log SCC was negatively correlated with TDM (r=-0.35), AMC (r=-0.37), and NMC (r=-0.15) and positively correlated with PPD (r=0.40). Log TVC had a negative correlation with AMC (r=-0.40) but a positive correlation with NMC (r=0.32), TDM (r=0.16), and PPD (r=0.45). The linear mixed model with stepwise variable selection showed that the main sources of log SCC variation were PPD, TDM, PPD × season, and season. For log TVC, the same factors and year contributed to the variation.
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Camelus/metabolismo , Leche/microbiología , Animales , Recuento de Células/veterinaria , Femenino , Microbiología de Alimentos , Calidad de los Alimentos , Mastitis/veterinaria , Leche/citología , Estaciones del AñoRESUMEN
The effect of interspecific egg white on the development of chicken embryos was investigated in a surrogate eggshell culture system. Egg yolks were separated from fertile White Leghorn chicken eggs and cultured in different egg whites from turkey (group TK), guineafowl (group GF), and duck (group DK), and chicken (group CK) was used as control. The viability of chicken embryos in groups CK, TK, GF, and DK after 3 d culture in system II was 98.3, 90.2, 96.1, and 91.1%. The whole contents (egg yolk and surrogate egg white) were further transferred into an eggshell from a 1.5 times heavier chicken egg with air space (system III), and incubated for further 16 d, before moving them to a hatcher. No significant difference between the 4 groups was found in their viabilities, which ranged between 72.9 and 81.3%, until 14 d postincubation (P > 0.05). After 21 d, the viability decreased to 60.4, 57.4, 50.0, and 27.7% in groups CK, TK, GF, and DK. The viability in group DK was significantly lower than in the other groups (P < 0.05). Weight loss in system III was approximately 12% in all the 4 groups without significant difference (P > 0.05). Hatchability of the chicken embryo was 60.4, 55.3, 47.9, and 19.1% in groups CK, TK, GF, and DK, respectively, and that in group DK was significantly lower than in the other groups (P < 0.05). There was no difference between the other groups (P > 0.05). These results show that chicken embryos can develop to hatch in duck, guineafowl, and turkey egg whites. However, the hatchability decreases according to the phylogenetic distance. The present study will provide a tool for manipulation of avian embryos and eventual conservation of endangered wild birds.
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Embrión de Pollo/crecimiento & desarrollo , Clara de Huevo/química , Técnicas de Cultivo de Embriones/veterinaria , Animales , Medios de Cultivo , Patos , Galliformes , Especificidad de la Especie , Factores de TiempoRESUMEN
Tuberculosis is a chronic, contagious, granulomatous disease caused by mycobacterial species belonging to the Mycobacterium tuberculosis complex. Camelids were not considered highly susceptible to tuberculosis, but in recent years increased numbers of cases have been experienced in some countries. In most of the cases, transmission probably occurs through contact with infected cattle or wildlife. None of the ante-mortem tests currently available can consistently provide accurate diagnosis of the infection in live camelids. Recently developed serological assays have the potential for rapid and accurate diagnosis of tuberculosis but still need to be validated.
Asunto(s)
Camélidos del Nuevo Mundo , Camelus , Tuberculosis/veterinaria , Animales , Humanos , Mycobacterium/clasificación , Mycobacterium/aislamiento & purificación , Prueba de Tuberculina/veterinaria , Tuberculosis/diagnóstico , Tuberculosis/epidemiología , Tuberculosis/terapia , Zoonosis/microbiologíaRESUMEN
Foot and mouth disease (FMD) remains the most important animal disease. The FMD virus is highly contagious and occurs almost exclusively among cloven-hoofed animals such as cattle, sheep, goats, Bactrian camels and swine. Old World camels (OWCs) and New World camels (NWCs) inhabit FMD-endemic countries in South America, North and East Africa, and the Middle and Far East. Results of experimental infection of OWCs with the virus, and several clinical observations from the field over a century, confirm that the two closely related camel species of Bactrian and dromedary camels possess noticeably different susceptibilities to FMD. It is now certain that Bactrian camels can contract the disease. In contrast, dromedaries are not susceptible to FMD and do not transmit infection, even when in close contact with susceptible animals. The susceptibility of NWCs to the FMD virus has been demonstrated in the field and in experimental infection trials. However, these animals are not very susceptible and do not represent a serious risk in transmitting FMD to susceptible animal species.