Heifers (n = 103) ranging in age from 1d to 2 yr were sampled to determine the coagulase-negative staphylococcal flora of haircoat, nares, vagina, teat skin, and streak canal. A total of 2706 staphylococal strains were identified from 3612 bacterial isolates. Other genera or groups identified included Bacillus, Micrococcus, Corynebacterium, and coliforms. Staphylococci were identified utilizing a simplified biochemical scheme. Staphylococcus xylosus, S. chromogenes, and S. warneri were the predominant species recovered from anatomic sites and streak canal. Staphylococcal strains identified from specific body sites (expressed as percentage of heifers harboring these species) were: nares 74% S. xylosus and 48% S. warneri; haircoat, 70% S. xylosus and 57% S. chromogenes; vagina, 60% S. chromogenes and 54% S. xylosus; teat skin 62% S. chromogenes and 61% S. warneri; streak canal 53% S. chromogenes, and 43% S. warneri. The prevalent staphylococcal strains identified differed from heifers in confined housing compared with heifers on pasture. Differences observed in distribution of Staphylococcus species among body sites, particularly those between teat skin and streak canal, suggest that establishment of staphylococcal microflora depends on the ability of a species to adapt to and colonize anatomic sites as well as on environmental conditions present.

The body sites of 163 heifers, bedding and feedstuff samples, flies, and hands and nares of the research personnel were sampled in order to determine the sources of Staphylococcus aureus in a dairy herd other than the lactating mammary gland. Lesions on the udder of lactating animals and the air in the milking parlor were also sampled. Staphylococci isolated from bedding samples were identified as to species. Staphylococcus aureus was isolated from all sources examined except flies. An enrichment procedure was necessary for isolating S. aureus from two bedding samples although other Staphylococcus species were present in high numbers. The designation "environmental staphylococci" is proposed for Staphylococcus species that were apparently free-living in the environment.

During a 14-mo period, 77 multiparous and 36 primiparous cows were sampled to determine the prevalence of staphylococci during the periparturient period. Distal streak canal swabs were taken at 14 d prepartum, and foremilk was sampled the first 5 consecutive wk of lactation. Staphylococcus aureus was isolated from 7.6% of quarters of primiparous cows but from only .6% of quarters of multiparous cows at parturition. Prevalence in primiparous cows declined to 3.5% by the wk-1 sampling. Quarter prevalence of coagulase-negative Staphylococcus species prepartum, at parturition, and wk 1 to 5 in primiparous cows was 38.9, 27.8, 15.3, 14.6, 13.2, 15.3, and 14.6%, respectively. In multiparous cows, prevalence at these times was 50.3, 12.3, 6.2, 8.1, 10.7, 7.1, and 8.1%. Staphylococcus chromogenes was the predominant species isolated, accounting for over 50% of the staphylococci isolated at each sampling time. Results suggest that high prevalence of staphylococci isolated prepartum is a reflection of natural skin flora and that a higher postpartum prevalence of these organisms was observed in primiparous cows than in multiparous cows. These data suggest also that the peripartum heifer could be a source of Staphylococcus aureus in the lactating herd.

Botrytis-inoculated fruit were treated with three levels of naturally occurring volatile compounds in capped bottles and rated for Botrytis development and evidence of phytotoxicity during 7 days of storage at 2 °C followed by 3−6 more days at 22 °C for strawberry and 7 days at 15 °C for blackberry and grape. Hexanal, 1-hexanol, (E)-2-hexen-1-ol, (Z)-6-nonenal, (E)-3-nonen-2-one, methyl salicylate, and methyl benzoate exhibited potential as postharvest fumigants for control of Botrytis on strawberry at the lowest level tested. Ten compounds were evaluated on blackberry and grape. None caused phytotoxic responses as with strawberry, while nearly all of the compounds inhibited Botrytis at all three test levels. Strawberry, blackberry, and grape metabolized (E)-2-hexenal with reduction of the aldehyde to an alcohol and saturation of the carbon−carbon double bond adjacent to the carbonyl, but strawberry yielded more esters as major products. Keywords: Fragaria × ananassa; Rubus; Vitis vinifera; metabolism; antifungal; (E)-2-hexenal

The effect of feeding subtherapeutic (27.5 micrograms/g of diet for 85 d) and therapeutic (220 micrograms/g of diet for 14 d, followed by an antibiotic-free diet for 71 d) levels of chlortetracycline (CTC) on the antibiotic resistance of fecal coliforms of pigs from two herds (36 pigs/herd) with different histories of antibiotic exposure when housed in a newly constructed confinement facility was determined. The CTC-resistant coliforms were higher (65 vs 51%) for antibiotic (AB) pigs than for nonantibiotic (NAB) pigs after they had been fed an antibiotic-free diet for 21 d. Percentages of isolates resistant to ampicillin, kanamycin, neomycin and tetracycline and multiple antibiotic resistance were greater (P less than .05) in AB pigs after 21 d. Feeding subtherapeutic CTC resulted in a linear increase in CTC-resistant coliforms with time on experiment (P less than .03, NAB; P less than .06, AB). The CTC-resistant coliforms increased during the 14 d that therapeutic CTC was fed, then they decreased during the 71 d that the antibiotic-free diet was fed, resulting in a quadratic response with time (P less than .03, AB). Feeding subtherapeutic CTC resulted in a greater increase in CTC-resistant coliforms in AB (47%) than in NAB (23%) pigs. The CTC-resistant coliforms decreased after the therapeutic group had been returned to the antibiotic-free diet (P less than .05, NAB). Feeding CTC caused greater changes in the precentages of isolates from NAB pigs that were resistant to selected antibiotics and in multiple antibiotic resistance than in isolates from AB pigs.(ABSTRACT TRUNCATED AT 250 WORDS)

Microbiological data from 1123 uninfected quarters and 216 quarters with preexisting coagulase-negative staphylococci infections were analyzed to determine the influence of infection status on subsequent new infection rate. Overall, prevalence of new infections in uninfected quarters was approximately two times that in quarters already harboring a coagulase-negative Staphylococcus infection. New infections by coagulase-negative staphylococci were greater in uninfected quarters than in quarters with preexisting coagulase-negative staphylococci infections. However, no differences were observed between uninfected and infected quarters in number of new infections by major pathogens (Staphylococcus aureus, streptococci, and coliforms). No differences were observed in uninfected or coagulase-negative Staphylococcus-infected quarters in infections with minor pathogens compared with major pathogens. The influence of individual coagulase-negative Staphylococcus species on new infections was also analyzed. However, numbers of existing infections by Staphylococcus species other than Staphylococcus chromogenes were limited. Therefore, the protective capacity of each coagulase-negative Staphylococcus species was difficult to assess. Overall, a significant restriction of bacterial invasion was observed in quarters with a preexisting infection. These results suggest that quarters harboring a coagulase-negative Staphylococcus infection suppress colonization of the mammary gland by mastitis-causing pathogens.

The API Staph-Ident system was evaluated as a means for identifying the species of bovine strains of staphylococci routinely isolated from quarter-milk samples. The species identity of 314 of 581 (54%) isolates of staphylococci was correctly determined by this method. The API Staph-Ident system was more accurate in correctly identifying Staphylococcus alureus (93.9%) than in correctly MATERIALS AND METHODS Bacterial isolates. During a 20-month period, 581 gram-positive catalase-positive cocci of bovine origin were obtained by our laboratory from several sources. A total of 25 isolates were obtained by swabbing the distal end of the streak canal of 14 cows in the University of Kentucky dairy herd during their dry period. The remaining isolates were obtained from the following sources: 96 were activated from freeze-dried cultures of isolates obtained from quarter foremilk samples from the University of Kentucky dairy herd in 1969 (25, 26), 383 were from quarter foremilk samples obtained from the University of Kentucky dairy herd during the 20-month period of this study, 32 were from two private dairy herds in Kentucky with a high incidence of mastitis (18, herd A; 14, herd B), 37 were from J. W. Pankey, North Louisiana Hill Farm Experiment Station, Homer, La., and 9 were from K.

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