The activities of amylase and a trypsin‐like protease in the gut contents of germ‐free and conventional chickens

1. Proteolytic and amylase activities were assayed in the gut contents of germ‐free and conventional chickens aged 3 and 14 d.

2. The tendency was for the proteolytic activity to be increased and the amylase activity to be decreased in conventional chicks. These differences were statistically significant in the caecum.

3. All of the additional proteolytic activity detectable in the caecum of conventional chicks was inhibited by soyabean trypsin inhibitor. However, the increased activity was not detectable in the small intestine and was, therefore, not due to pancreatic trypsin.

4. Attempts to demonstrate in vitro bacterial production of a trypsin‐like enzyme were unsuccessful.     

Jugular venous emboli of brain tissue induced in sheep by the use of captive bolt guns

Emboli of central nervous tissue were detected in the jugular venous blood of two of 15 sheep stunned with a conventional cartridge-operated captive bolt gun and in two of 15 sheep stunned with a pneumatically activated gun. No emboli were detected in arterial blood from these sheep or in venous blood from sheep stunned electrically. Emboli from an animal with BSE could transmit the disease to people.     

Drosophila RNAi screen reveals CD36 family member required for mycobacterial infection

Certain pathogens, such as Mycobacterium tuberculosis, survive within the hostile intracellular environment of a macrophage. To identify host factors required for mycobacterial entry and survival within macrophages, we performed a genomewide RNA interference screen in Drosophila macrophage-like cells, using Mycobacterium fortuitum. We identified factors required for general phagocytosis, as well as those needed specifically for mycobacterial infection. One specific factor, Peste (Pes), is a CD36 family member required for uptake of mycobacteria, but not Escherichia coli or Staphylococcus aureus. Moreover, mammalian class B scavenger receptors (SRs) conferred uptake of bacteria into nonphagocytic cells, with SR-BI and SR-BII uniquely mediating uptake of M. fortuitum, which suggests a conserved role for class B SRs in pattern recognition and innate immunity.     

Isolation of faecal chlamydia from sheep in Britain andtheir characterization by cultural properties

Faeces samples were taken per rectum from sheep on 26 farms in England and Wales and examined for thepresence of chlamydia by culture McCoy cell monolayers. Thirteen of the fars were known to have had abortion outbreaks associated with Chlamydia psittaci (enzootic abortion) and 13 were free of this infection. The chlamydia isolated were characterized by cultural techniques. Chlamydia were isolated from the faeces of lambs on all 26 farms and the prevalence of infection varied from 5–50% on individual farms. There was no significant difference between the proportion of infected lambs on farms where enzootic abortion was present or absent. Lambs first showed infection when they were 3 months old and the prevalence rate of infection increased up to 9 months old. No chlamydia were isolated from the faeces of 316 adult ewes. The chlamydia were identified as enteric rather than abortion type and thus were C. pecorum rather than C. psittaci.     

Receptor activation alters inner surface potential during phagocytosis

The surface potential of biological membranes varies according to their lipid composition. We devised genetically encoded probes to assess surface potential in intact cells. These probes revealed marked, localized alterations in the charge of the inner surface of the plasma membrane of macrophages during the course of phagocytosis. Hydrolysis of phosphoinositides and displacement of phosphatidylserine accounted for the change in surface potential at the phagosomal cup. Signaling molecules such as K-Ras, Rac1, and c-Src that are targeted to the membrane by electrostatic interactions were rapidly released from membrane subdomains where the surface charge was altered by lipid remodeling during phagocytosis.     

Mercury distribution and speciation in floodplain soils and uptake into native earthworms (Diplocardia spp.)

Historically as part of its national security mission, the U.S. Department of Energy's Y-12 National Security Facility in Oak Ridge, TN acquired a significant fraction of the world's supply of elemental mercury. During the 1950s and 1960s, a large amount of elemental mercury escaped confinement and is still present in the watershed surrounding the Y-12 facility. Earthworms are key components in natural food chains, providing a food source for many small mammals and important food sources for small birds. The objectives of this study were to investigate the current status of mercury distribution and speciation and determination of mercury bioavailability to native earthworms in floodplain soils of East Fork Poplar Creek (EFPC) after decades of U.S. Department of Energy's remediation. The present study clearly shows that the total mercury in a tested floodplain field of EFPC was significantly below the US Department of Energy target 400 mg Hg/kg. The major mercury form in the current floodplain soils of EFPC is mainly the non-cinnabar mercury bound form in soil silicates (4 M HNO₃-extractable residual fraction). The results show strong linear relationships between mercury concentrations in native earthworms (both mature and immature groups) and the non-cinnabar mercury form. Native earthworms may be used as a potential mercury ecological bio-indicator (bio-marker) for demonstrating mercury bioavailability and ecotoxicity in the ecosystem.     

Rapid Determination of Mercury in Contaminated Soil and Plant Samples Using Portable Mercury Direct Analyzer without Sample Preparation, a Comparative Study

The objective of this study was to determine the efficiency of a portable total mercury analyzer (OhioLumex RA-915+) in comparison with traditional analytical methods, such as inductively coupled plasma atomic emission spectrometry and cold vapor atomic absorption. The quick mercury analytical procedure with the direct mercury analyzer without sample pretreatment (such as sample digestion) was optimized for a variety of environmental samples, including contaminated soil and plant samples. The efficiency was evaluated using practical parameters, such as time required for analysis, sample amount, mercury species, accuracy, and precision/reproducibility, as well as using statistical analysis. Our results demonstrate that these three instrumental methods yielded similar mercury concentration values and statistical data, while the mercury direct analyzer had the advantages of not requiring for sample digestion and only requiring a small quantity of samples for distribution of mercury in a single root, a single root hair, and sub-regions of a single leaf of plants. These factors are used to justify use of the portable direct mercury analyzer under field conditions and validation of the results.     

Age, geographic, and temporal distribution of fecal shedding of Cryptosporidium parvum oocysts in cow-calf herds

OBJECTIVE: To evaluate fecal shedding of Cryptosporidium parvum from California cow-calf herds with respect to age, geographic region, temporal effects, and association with watery feces. ANIMALS: Cows and calves from 38 beef cow-calf operations. PROCEDURE: Fecal specimens were collected and examined for C parvum oocysts, using immunofluorescent microscopy. Associations between age, geographic region, month of collection, watery feces, and likelihood of shedding C parvum were evaluated. RESULTS: 3.9% of cattle were shedding C parvum oocysts. Prevalence of shedding among calves ranged from 0 to 13%, and was 0.6% among cattle > or = 12 months old. The odds of shedding C parvum among 2-month-old calves were 41 times greater than among cattle > 4 months old. The odds of shedding C parvum among cattle tested in May were 8.7 times greater than among cattle tested during June, July, or August. The odds of infected individuals having watery feces were 3 to 4 times greater than for noninfected individuals, but the etiologic fraction was only 8 to 9%. CONCLUSIONS AND CLINICAL RELEVANCE: Substantial fecal shedding of C parvum by cow-calf herds was limited to calves 1 to 4 months old, with low prevalence detected in older animals. Risk of contamination of watersheds with C parvum was limited to those periods when young calves were in the herd. Although the odds of having watery feces were greater for animals infected with C parvum than for noninfected animals, the low etiologic fraction suggests that most calves with watery feces were not infected with C parvum.