Lu Jingrang, Sanchez Susan, Hofacre Charles, Maurer John J, Harmon Barry G, Lee Margie D
Medical Microbiology and Parasitology, College of Veterinary Medicine, The University of Georgia, Athens, Georgia 30602, USA.
Appl Environ Microbiol. 2003 Feb;69(2):901-8. doi: 10.1128/AEM.69.2.901-908.2003.
Very little is known about the microbial composition of animal bedding wastes, including poultry litter, and what is known has been deduced from standard culture methods, by which some fastidious organisms that exist in the environment may not be detected. We evaluated the bacterial composition of poultry litter by using a combination of culture and molecular detection. Total aerobic bacteria in poultry litter were detected by culture at 10(9) CFU/g of material. Enteric bacteria such as Enterococcus spp. and coliforms composed 0.1 and 0.01%, respectively, of the total aerobic cultivatable bacteria in poultry litter; no Salmonella strains were detected by culture. In order to characterize the most abundant bacterial groups, we sequenced 16S ribosomal DNA (rDNA) genes amplified by PCR with microbial community DNA isolated from poultry litter as the template. From the 16S rDNA library, 31 genera were identified. Twelve families or groups were identified with lactobacilli and Salinococcus spp. forming the most abundant groups. In fact, 82% of the total sequences were identified as gram-positive bacteria with 62% of total belonging to low G+C gram-positive groups. In addition to detection of 16S rDNA sequences associated with the expected fecal bacteria present in manure, we detected many bacterial sequences for organisms, such as Globicatella sulfidofaciens, Corynebacterium ammoniagenes, Corynebacterium urealyticum, Clostridium aminovalericum, Arthrobacter sp., and Denitrobacter permanens, that may be involved in the degradation of wood and cycling of nitrogen and sulfur. Several sequences were identified in the library for bacteria associated with disease in humans and poultry such as clostridia, staphylococci, and Bordetella spp. However, specific PCR targeting other human and veterinary pathogens did not detect the presence of Salmonella, pathogenic Escherichia coli, Campylobacter spp., Yersinia spp., Listeria spp., or toxigenic staphylococci. PCR and DNA hybridization revealed the presence of class 1 integrons with gene cassettes that specify resistance to aminoglycosides and chloramphenicol. Only from understanding the microbial community of animal wastes such as poultry litter can we manage animal disease and limit the impact of animal waste on the environment and human and animal health.
关于动物垫料废物(包括家禽粪便)的微生物组成,我们了解得很少,已知的信息是通过标准培养方法推断出来的,而一些存在于环境中的苛求菌可能无法通过这种方法检测到。我们结合培养和分子检测方法评估了家禽粪便的细菌组成。通过培养检测出家禽粪便中的总需氧菌为每克材料10(9) CFU。肠球菌属和大肠菌群等肠道细菌分别占家禽粪便中总需氧可培养细菌的0.1%和0.01%;培养未检测到沙门氏菌菌株。为了表征最丰富的细菌类群,我们以从家禽粪便中分离的微生物群落DNA为模板,对通过PCR扩增的16S核糖体DNA(rDNA)基因进行了测序。从16S rDNA文库中鉴定出31个属。鉴定出12个科或类群,其中乳酸杆菌属和盐球菌属构成最丰富的类群。事实上,总序列的82%被鉴定为革兰氏阳性菌,其中62%属于低G+C革兰氏阳性菌群。除了检测到与粪便中预期存在的粪便细菌相关的16S rDNA序列外,我们还检测到许多生物体的细菌序列,如硫还原地杆菌、产氨棒状杆菌、解脲棒状杆菌、氨基戊酸梭菌、节杆菌属和持久脱硝杆菌,它们可能参与木材降解以及氮和硫的循环。文库中鉴定出几个与人类和家禽疾病相关的细菌序列,如梭菌属、葡萄球菌属和博德特氏菌属。然而,针对其他人类和兽医病原体的特异性PCR未检测到沙门氏菌、致病性大肠杆菌、弯曲杆菌属、耶尔森菌属、李斯特菌属或产毒素葡萄球菌的存在。PCR和DNA杂交揭示了带有指定对氨基糖苷类和氯霉素抗性的基因盒的1类整合子的存在。只有了解家禽粪便等动物废物的微生物群落,我们才能管理动物疾病,并限制动物废物对环境以及人类和动物健康的影响。