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1.
J Avian Med Surg ; 33(1): 22-28, 2019 03 01.
Article in English | MEDLINE | ID: mdl-31124608

ABSTRACT

We determined the prevalence of Chlamydia psittaci genotypes in asymptomatic and symptomatic birds in northeast Iran. Samples were collected from 11 species of Psittaciformes and 1 species of Columbiformes from 2015 to 2016. Choanal cleft and cloacal swab samples, fresh fecal samples, and/or tissue samples of 70 symptomatic and 130 asymptomatic birds were collected and tested by molecular detection (nested polymerase chain reaction [PCR] testing specific for C psittaci). Results showed C psittaci was detected in 37 (18.5%) of 200 birds (18/37 symptomatic and 19/37 asymptomatic birds) by nested PCR assay. Of the PCR-positive samples, 14 products were positive for oligonucleotide sets CTU/CTL by a second PCR assay and genotyped by outer membrane protein A (ompA) gene sequencing. Of the 10 samples positive for genotype A (cockatiels [Nymphicus hollandicus, n = 5], ring-necked parakeet [Psittacula krameri, n = 2], African gray parrot [Psittacus erithacus, n = 3]), 6 samples were from asymptomatic and 4 from symptomatic birds. Genotype B was observed in 3 samples from symptomatic birds (P krameri [n = 2], pigeon [Columba livia, n = 1]), and provisional genotype I was detected in one symptomatic cockatiel. These findings revealed the importance of monitoring imported asymptomatic birds in developing countries, especially the Middle East, where there is no systematic monitoring. To the best of our knowledge, this is the first report regarding the detection of C psittaci provisional genotype I in cockatiels.


Subject(s)
Bird Diseases/microbiology , Chlamydophila psittaci/classification , Columbiformes , Genotype , Psittaciformes , Psittacosis/veterinary , Animals , Bacterial Outer Membrane Proteins/genetics , Base Sequence , Bird Diseases/epidemiology , Birds , Chlamydophila psittaci/genetics , Columbiformes/microbiology , Iran/epidemiology , Phylogeny , Polymerase Chain Reaction/veterinary , Psittaciformes/microbiology , Psittacosis/epidemiology , Psittacosis/microbiology
2.
PLoS One ; 13(3): e0194857, 2018.
Article in English | MEDLINE | ID: mdl-29579092

ABSTRACT

Gut bacterial communities have been shown to be influenced by diet, host phylogeny and anatomy, but most of these studies have been done in captive animals. Here we compare the bacterial communities in the digestive tract of wild birds. We characterized the gizzard and intestinal microbiota among 8 wild Neotropical bird species, granivorous or frugivorous species of the orders Columbiformes and Passeriformes. We sequenced the V4 region of the 16S rRNA gene in 94 collected samples from 32 wild birds from 5 localities, and compared bacterial communities by foraging guild, organ, locality and bird taxonomy. 16S rRNA gene-based sequencing data were examined using QIIME with linear discriminant analysis effect size (LEfSe) and metabolic pathways were predicted using PICRUSt algorism. We identified 8 bacterial phyla, dominated by Firmicutes, Actinobacteria and Proteobacteria. Beta diversity analyses indicated significant separation of gut communities by bird orders (Columbiformes vs. Passerifomes) and between bird species (p<0.01). In lower intestine, PICRUSt shows a predominance of carbohydrate metabolism in granivorous birds and xenobiotics biodegradation pathways in frugivorous birds. Gizzard microbiota was significantly richer in granivorous, in relation to frugivorous birds (Chao 1; non-parametric t-test, p<0.05), suggesting a microbial gizzard function, beyond grinding food. The results suggest that the most important factor separating the bacterial community structure was bird taxonomy, followed by foraging guild. However, variation between localities is also likely to be important, but this could not been assessed with our study design.


Subject(s)
Animals, Wild/microbiology , Columbiformes/microbiology , Gastrointestinal Microbiome , Gizzard, Avian/pathology , Passeriformes/microbiology , Stomach Diseases/pathology , Algorithms , Animals , Bacteria/genetics , Bacteria/isolation & purification , Biodiversity , DNA, Bacterial/chemistry , DNA, Bacterial/isolation & purification , DNA, Bacterial/metabolism , Discriminant Analysis , Gizzard, Avian/microbiology , Intestines/microbiology , Principal Component Analysis , RNA, Ribosomal, 16S/genetics , RNA, Ribosomal, 16S/metabolism , Sequence Analysis, DNA , Stomach Diseases/microbiology , Stomach Diseases/veterinary
3.
Ecohealth ; 11(4): 544-63, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24947738

ABSTRACT

The significance of chlamydiosis as a cause of mortality in wild passerines (Order Passeriformes), and the role of these birds as a potential source of zoonotic Chlamydia psittaci infection, is unknown. We reviewed wild bird mortality incidents (2005-2011). Where species composition or post-mortem findings were indicative of chlamydiosis, we examined archived tissues for C. psittaci infection using PCR and ArrayTube Microarray assays. Twenty-one of 40 birds tested positive: 8 dunnocks (Prunella modularis), 7 great tits (Parus major), 3 blue tits (Cyanistes caeruleus), 2 collared doves (Streptopelia decaocto, Order Columbiformes), and 1 robin (Erithacus rubecula). Chlamydia psittaci genotype A was identified in all positive passerines and in a further three dunnocks and three robins diagnosed with chlamydiosis from a previous study. Two collared doves had genotype E. Ten of the 21 C. psittaci-positive birds identified in the current study had histological lesions consistent with chlamydiosis and co-localizing Chlamydia spp. antigens on immunohistochemistry. Our results indicate that chlamydiosis may be a more common disease of British passerines than was previously recognized. Wild passerines may be a source of C. psittaci zoonotic infection, and people should be advised to take appropriate hygiene precautions when handling bird feeders or wild birds.


Subject(s)
Bird Diseases/epidemiology , Chlamydophila psittaci/genetics , Chlamydophila psittaci/isolation & purification , Columbiformes/microbiology , Passeriformes/microbiology , Animals , Genotype , Polymerase Chain Reaction , Retrospective Studies , United Kingdom/epidemiology
4.
Appl Environ Microbiol ; 72(11): 7380-2, 2006 Nov.
Article in English | MEDLINE | ID: mdl-16936045

ABSTRACT

Enterocytozoon bieneusi was detected in 24 of 83 samples from birds of the orders Columbiformes, Passeriformes, and Psittaciformes. It was identical to or closely related to the Peru6 genotype, which was previously found in humans in Peru. Thus, various birds can be a significant source of environmental contamination by potentially human-pathogenic E. bieneusi.


Subject(s)
Bird Diseases/epidemiology , Bird Diseases/microbiology , Birds/microbiology , Enterocytozoon/classification , Enterocytozoon/genetics , Microsporidiosis/veterinary , Animals , Birds/classification , Columbiformes/microbiology , Enterocytozoon/isolation & purification , Enterocytozoon/pathogenicity , Genotype , Microsporidiosis/epidemiology , Microsporidiosis/microbiology , Molecular Sequence Data , Passeriformes/microbiology , Psittaciformes/microbiology , Public Health , Sequence Analysis, DNA
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