Schnabel E L, Jones A L
Department of Botany and Plant Pathology, Michigan State University, East Lansing, Michigan 48824-1312, USA.
Appl Environ Microbiol. 1999 Nov;65(11):4898-907. doi: 10.1128/AEM.65.11.4898-4907.1999.
The extent and nature of tetracycline resistance in bacterial populations of two apple orchards with no or a limited history of oxytetracycline usage were assessed. Tetracycline-resistant (Tc(r)) bacteria were mostly gram negative and represented from 0 to 47% of the total bacterial population on blossoms and leaves (versus 26 to 84% for streptomycin-resistant bacteria). A total of 87 isolates were screened for the presence of specific Tc(r) determinants. Tc(r) was determined to be due to the presence of Tet B in Pantoea agglomerans and other members of the family Enterobacteriacae and Tet A, Tet C, or Tet G in most Pseudomonas isolates. The cause of Tc(r) was not identified in 16% of the isolates studied. The Tc(r) genes were almost always found on large plasmids which also carried the streptomycin resistance transposon Tn5393. Transposable elements with Tc(r) determinants were detected by entrapment following introduction into Escherichia coli. Tet B was found within Tn10. Two of eighteen Tet B-containing isolates had an insertion sequence within Tn10; one had IS911 located within IS10-R and one had Tn1000 located upstream of Tet B. Tet A was found within a novel variant of Tn1721, named Tn1720, which lacks the left-end orfI of Tn1721. Tet C was located within a 19-kb transposon, Tn1404, with transposition genes similar to those of Tn501, streptomycin (aadA2) and sulfonamide (sulI) resistance genes within an integron, Tet C flanked by direct repeats of IS26, and four open reading frames, one of which may encode a sulfate permease. Two variants of Tet G with 92% sequence identity were detected.
对两个土霉素使用量极少或无使用历史的苹果园细菌群体中四环素抗性的程度和性质进行了评估。耐四环素(Tc(r))细菌大多为革兰氏阴性菌,在花朵和叶片上占细菌总数的0%至47%(而耐链霉素细菌为26%至84%)。总共筛选了87株分离株,以检测特定Tc(r)决定簇的存在。已确定Tc(r)是由于聚团泛菌和肠杆菌科其他成员中存在Tet B,以及大多数假单胞菌分离株中存在Tet A、Tet C或Tet G。在16%的研究分离株中未确定Tc(r)的原因。Tc(r)基因几乎总是存在于大质粒上,这些质粒还携带链霉素抗性转座子Tn5393。将带有Tc(r)决定簇的转座元件导入大肠杆菌后,通过捕获法进行检测。在Tn10中发现了Tet B。18株含Tet B的分离株中有两株在Tn10内有插入序列;一株在IS10-R内有IS911,一株在Tet B上游有Tn1000。在一种名为Tn1720的Tn1721新变体中发现了Tet A,该变体缺少Tn1721的左端orfI。Tet C位于一个19 kb的转座子Tn1404内,其转座基因与Tn501的相似,整合子内有链霉素(aadA2)和磺胺(sulI)抗性基因,Tet C两侧为IS26的直接重复序列,还有四个开放阅读框,其中一个可能编码硫酸盐通透酶。检测到两种序列同一性为92%的Tet G变体。