Isolation of Citrobacter murliniae from clinically ill and dead quail, ducks and chickens.
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Biomedical subjects
Publications and source records attributed to M M Henton.
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Actinomycete strains isolated from lesions on equine placentas from two horses in Kentucky and one in South Africa were subjected to a polyphasic taxonomic study. Chemotaxonomic and morphological characteristics indicated that the isolates are members of the genus AMYCOLATOPSIS: On the basis of phylogenetic analysis of 16S rDNA sequences, the isolates are related most closely to Amycolatopsis mediterranei. Physiological characteristics of these strains indicated that they do not belong to A. mediterranei and DNA relatedness determinations confirmed that these strains represent three novel species of the genus Amycolatopsis, for which the names Amycolatopsis kentuckyensis (type strain, NRRL B-24129(T)=LDDC 9447-99(T)=DSM 44652(T)), Amycolatopsis lexingtonensis (type strain, NRRL B-24131(T)=LDDC 12275-99(T)=DSM 44653(T)) and Amycolatopsis pretoriensis (type strain, NRRL B-24133(T)=ARC OV1 0181(T)=DSM 44654(T)) are proposed.
The first recorded isolates of Pasteurella testudinis from South African tortoises kept in captivity is presented. P. testudinis was found in association with respiratory disease in affected animals.
Two trials were carried out to assess the diagnostic sensitivity and practicability of preputial scraping as a method of collecting preputial material from bulls infected with Tritrichomonas foetus. In the 1st trial, preputial material was collected by simultaneous scraping and aspiration from 3 infected and 1 uninfected bull 10 times over a 5-week period. In the 2nd trial, samples from 5 infected bulls were collected by both sheath washing and scraping on 6 occasions, while 8 uninfected animals were sampled 3 times. Samples were cultured using a modified Trichomonas culture medium (Oxoid). In the first trial, 29 of 30 samples from infected bulls were found to be positive. In the second trial, 83 % of samples collected by both methods tested positive. In neither trial were any samples from the control bulls found to be positive. Scraping was found to be quick and safe, and offered advantages over preputial washing in that urine contamination was easily avoided, samples were smaller and more concentrated and contamination was reduced. It may, however, be subject to greater operator variability than sheath washing. It is concluded that preputial scraping is as effective as washing and represents a suitable alternative for the collection of material for direct examination and culture of Tritrichomonas foetus.
The prevalence of virulent Rhodococcus equi in soil isolates from two horse farms in South Africa and nine clinical isolates from six foals, a foal foetus, a dog, and a monkey was investigated. The isolates were tested for the presence of virulence plasmid DNA and 15- to 17-kDa antigens by immunoblotting. Rhodococcus equi was isolated from almost all of the soil samples obtained from the two farms with 5.0 x 10(1) to 3.3 x 10(4) colony forming units per gram of soil. Virulent R. equi was isolated from three soil samples from one of the farms and appeared in 3.8% (three of 80 isolates), but not in any of the 182 isolates from the other farm. Of the three virulent R. equi isolates, one contained an 85-kb type I plasmid and two an 87-kb type I plasmid. Of nine clinical isolates from the foals, foal foetus, dog and monkey, five from the foals were virulent R. equi which expressed the virulence-associated antigens and contained a virulence plasmid 85-kb type I, and were all isolated from cases of pneumonia typical of that induced by R. equi in young foals living in widely separated areas in South Africa. The isolates from the other four foals, the dog and the monkey were avirulent R. equi.
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Two polymerase chain reaction (PCR)-based procedures for typing Clostridium, perfringens, which affects most domestic animals, were compared and evaluated for efficiency as substitute to the guinea-pig intradermal test routinely used in our laboratory, namely a multiplex PCR and a protocol based on the individual amplification of gene sequences specific for each toxin. Reference isolates of C. perfringens types A, B, C and D as well as cultures from clinical specimens were tested. The sensitivity and specificity of the PCR was confirmed on reference isolates. There was similarity in results on 43 of the 46 samples typed by all 3 methods. Clear results were obtained by PCR on 5 clinical samples that showed either equivocal or weak skin reactions in guinea-pigs. The multiplex PCR protocol, in combination with the evaluation of bacterial growth, is a better alternative to in vivo toxin typing, since C. perfringens can only be incriminated as cause of a disease when it is present in large numbers in the intestine.
Intestinal contents were collected from wild-caught African dwarf crocodiles (Osteolaemus tetraspis) in 1993 and 1995 which were slaughtered at urban markets in the Congo Republic. The samples were kept frozen and brought back to Onderstepoort for aerobic culture. Out of 29 specimens, 33 species of bacteria and 20 species of fungi were isolated. The bacteria included three isolates of Salmonella and eight isolates of Escherichia coli, most of the latter being rough strains. The flora of individual specimens contained 1-5 bacterial and 0-5 fungal species. Neither Aeromonas hydrophila nor Edwardsiella tarda were isolated from any of the samples.
Mortalities and abortions associated with starvation occurred at Cape Cross, Namibia, in Cape fur seals (Arctocephalus pusillus pusillus). Affected seals showed lethargy and emaciation, and the most common pathological signs were those of a respiratory infection, both in adults and offspring. Streptococcus phocae was isolated from adult seals, a cub and aborted foetuses.
Haemostatic forceps contaminated with Pseudomonas aeruginosa, Staphylococcus aureus, Bacillus cereus and Aspergillus flavus were exposed to formaldehyde gas for up to 48 hours at different temperatures and relative humidities. After 24 hours at 22 to 24 degrees C and a relative humidity of 73 per cent they were sterilised reliably and completely.
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Clinical, virological and serological responses were evaluated in 10 pregnant mares after different challenge exposures to the asinine-94 strain of equine arteritis virus (EAV). The outcome of maternal infection on the progeny was also investigated. Mares were inoculated intranasally (n = 4), intramuscularly (n = 2), intravenously (n = 1), or contract-exposed (n = 3). All inoculated mares developed pyrexia, 5 showed mild clinical signs related to EAV infection and 2 remained asymptomatic. Viraemia was detected in all the inoculated animals and shedding of virus from the respiratory tract occurred in 6. Five mares were re-challenged intranasally 7 and 15 weeks after inoculation. Clinical signs of the disease in these mares were limited to mild conjunctivitis. After re-challenge, virus was recovered from buffy coat cultures of 2 mares 2-6 days after re-infection. EAV was not recovered from colostrum and milk samples during the 1st week post partum. All inoculated mares seroconverted to EAV 8-12 days post inoculation and also seroconverted after re-challenge. No clinical signs of EAV infection were observed in the 3 mares kept in close contact during the post-inoculation and re-challenge periods. Serum neutralising antibody to the virus was detected in 1 in-contact mare only, while a detectable concentration of specific IgG was found by ELISA in the colostrum of 1 of the other in-contact mares. Eight of the mares gave birth to clinically normal foals, although 1 was born prematurely. Shortly after birth, 7 foals developed fever and variable clinical signs; 5 foals became septicaemic and 3 of them died 2-5 days after birth, while the remaining 2 were euthanased at 1 month of age. EAV was not recovered from the placenta, from buffy coat fractions of blood collected from foals immediately after birth and 1-3 days later, or from a range of tissues taken from the 3 foals that died and 2 that were euthanased. Virus was not isolated from tissues collected from 1 mare and her foetus 3 weeks after this mare was re-challenged.
This retrospective study was based on 674 cases of colibacillosis in pigs submitted to the diagnostic bacteriology laboratory of the Onderstepoort Veterinary Institute (OVI) over the 20-year period ranging from 1971-1991. During this time, 28,840 cases from various livestock species were received, of which 4162 (14.4%) were from pigs. The 674 porcine cases selected for this study were included if an E. coli infection had been suspected by the referring veterinarian, and typable E. coli strains were then isolated by this laboratory. Enteritis (45.5%) and septicaemia (46.9%) were the most common syndromes, with agalactiae (1.4%) and abortion (1.1 %) representing a far lower prevalence. Oedema-disease signs were described by the submitting veterinarian in only 12 cases. Samples were received from weaners and sucklers in relatively equal numbers until 1981, but subsequently samples from sucklers declined, while those from weaners remained high. There were 69 different somatic and capsulated (OK) antigen groups associated with E. coli infections in pigs. Escherichia coli O149 was the most common isolate (45.8%), while E. coli O141 was the next most common isolate (18.3%). This was followed by O9 (8.9%), O20 (5.2%) and O8 (3.1%). All other serotypes together accounted for less than 20% of the total number of cases, and were isolated fewer than 20 times each. The fimbrial attachment factor, F4 (K88) was found associated with 46.9% of isolates.
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Melioidosis was diagnosed in an adult Boer goat ewe. The owner initially noticed swelling of one half of the udder. Several firm nodules developed in the affected part of the udder 2 weeks later. At necropsy, abscesses containing a creamy to yellowish-green exudate were found in the mammary gland and one of the kidneys. Pure cultures of Pseudomonas pseudomallei were isolated from the abscesses in the udder and inoculation of male guinea-pigs with the causative bacterium, produced a Shwartzman reaction in the testis and serositis as well as necrotic lesions, in parenchymatous organs. The isolate showed sensitivity to amoxycillin-clavulanate, but resistance to a number of other antimicrobials. This appears to be the first case of melioidosis in a domestic animal in South Africa.