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1.
Zoonoses Public Health ; 62(4): 237-53, 2015 Jun.
Article in English | MEDLINE | ID: mdl-24934203

ABSTRACT

Australia is unique as a populated continent in that canine rabies is exotic, with only one likely incursion in 1867. This is despite the presence of a widespread free-ranging dog population, which includes the naturalized dingo, feral domestic dogs and dingo-dog cross-breeds. To Australia's immediate north, rabies has recently spread within the Indonesian archipelago, with outbreaks occurring in historically free islands to the east including Bali, Flores, Ambon and the Tanimbar Islands. Australia depends on strict quarantine protocols to prevent importation of a rabid animal, but the risk of illegal animal movements by fishing and recreational vessels circumventing quarantine remains. Predicting where rabies will enter Australia is important, but understanding dog population dynamics and interactions, including contact rates in and around human populations, is essential for rabies preparedness. The interactions among and between Australia's large populations of wild, free-roaming and restrained domestic dogs require quantification for rabies incursions to be detected and controlled. The imminent risk of rabies breaching Australian borders makes the development of disease spread models that will assist in the deployment of cost-effective surveillance, improve preventive strategies and guide disease management protocols vitally important. Here, we critically review Australia's preparedness for rabies, discuss prevailing assumptions and models, identify knowledge deficits in free-roaming dog ecology relating to rabies maintenance and speculate on the likely consequences of endemic rabies for Australia.


Subject(s)
Communicable Disease Control/methods , Dog Diseases/prevention & control , Dog Diseases/transmission , Rabies , Animals , Animals, Wild , Australia/epidemiology , Behavior, Animal , Bites and Stings/virology , Databases, Factual , Dog Diseases/epidemiology , Dog Diseases/virology , Dogs , Europe/epidemiology , Humans , Rabies/epidemiology , Rabies/prevention & control , Rabies/transmission , Rabies Vaccines , Research , Risk Factors , United States/epidemiology
2.
Arch Dis Child ; 93(11): 982-5, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18653626

ABSTRACT

Despite the fact that infants spend more time asleep than awake, an understanding of the importance and effects of sleep on the pathophysiology of illness in infancy is a relatively recent development, and is commonly overlooked in paediatric training. In this review we describe some of the characteristics of sleep in infancy, with particular reference to normal developmental physiology and its relevance to the signs, symptoms and pathophysiology of illness in this age group.


Subject(s)
Sleep/physiology , Body Temperature Regulation/physiology , Brain/growth & development , Circadian Rhythm/physiology , Endocrine System/physiology , Humans , Infant , Respiration
3.
Arch Dis Child ; 93(9): 778-83, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18450800

ABSTRACT

BACKGROUND: Some victims of sudden infant death syndrome (SIDS) are found with their heads covered with bedclothes, but the significance of this is uncertain. The aim of this review is to describe the prevalence of head covering, the magnitude of the risk and how far the suggested causal mechanisms agree with current epidemiological evidence. METHODS: Systematic review of population-based age-matched controlled studies. RESULTS: Controlled observations of head covering for the final sleep were found in 10 studies. The pooled prevalence in SIDS victims was 24.6% (95% CI 22.3% to 27.1%) compared to 3.2% (95% CI 2.7% to 3.8%) among controls. The pooled univariate odds ratio (OR) was 9.6 (95% CI 7.9 to 11.7) and the pooled adjusted OR from studies mainly conducted after the fall in SIDS rate was 16.9 (95% CI 12.6 to 22.7). The risk varied in strength but was significant across all studies. In a quarter of cases and controls head covering had occurred at least once previously (pooled adjusted OR = 1.1; 95% CI 0.9 to 1.4). The population attributable risk (27.1%; 95% CI 24.7% to 29.4%) suggests avoiding head covering might reduce SIDS deaths by more than a quarter. CONCLUSIONS: The epidemiological evidence does not fully support postulated causal mechanisms such as hypoxia, hypercapnoea and thermal stress, but neither does it support the idea that head covering is part of some terminal struggle. Head covering is a major modifiable risk factor associated with SIDS deaths and parental advice to avoid this situation should be emphasised.


Subject(s)
Asphyxia Neonatorum/etiology , Bedding and Linens/adverse effects , Sudden Infant Death/etiology , Age Factors , Head , Heart Rate/physiology , Humans , Infant, Newborn , Parents/education , Prevalence , Prone Position , Risk Factors
4.
Int J Epidemiol ; 35(6): 1563-9, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17148463

ABSTRACT

OBJECTIVE: To investigate the diurnal occurrence of Sudden Infant Death Syndrome (SIDS) and interaction with established risk factors in the infant sleeping environment. METHODS: A 3 year population-based case-control study, in five English Health Regions. Parentally defined day-time or night-time deaths of 325 SIDS infants and reference sleep of 1300 age-matched controls. RESULTS: The majority of SIDS deaths (83%) occurred during night-time sleep, although this was often after midnight and at least four SIDS deaths occurred during every hour of the day. The length of time from last observed alive until the discovery of death ranged from

Subject(s)
Sudden Infant Death/epidemiology , Age Factors , Bedding and Linens , Case-Control Studies , England/epidemiology , Environment , Humans , Infant , Infant Care , Parenting , Prone Position , Residence Characteristics , Risk Factors , Sleep , Smoking/adverse effects , Time Factors
5.
Arch Dis Child ; 91(2): 101-6, 2006 Feb.
Article in English | MEDLINE | ID: mdl-15914498

ABSTRACT

AIMS: To determine the combined effects of sudden infant death syndrome (SIDS) risk factors in the sleeping environment for infants who were "small at birth" (pre-term (<37 weeks), low birth weight (<2500 g), or both). METHODS: A three year population based, case-control study in five former health regions in England (population 17.7 million) with 325 cases and 1300 controls. Parental interviews were carried out after each death and reference sleep of age matched controls. RESULTS: Of the SIDS infants, 26% were "small at birth" compared to 8% of the controls. The most common sleeping position was supine, for both controls (69%) and those SIDS infants (48%) born at term or > or =2500 g, but for "small at birth" SIDS infants the commonest sleeping position was side (48%). The combined effect of the risk associated with being "small at birth" and factors in the infant sleeping environment remained multiplicative despite controlling for possible confounding in the multivariate model. This effect was more than multiplicative for those infants placed to sleep on their side or who shared the bed with parents who habitually smoked, while for those "small at birth" SIDS who slept in a room separate from the parents, the large combined effect showed evidence of a significant interaction. No excess risk was identified from bed sharing with non-smoking parents for infants born at term or birth weight > or =2500 g. CONCLUSION: The combined effects of SIDS risk factors in the sleeping environment and being pre-term or low birth weight generate high risks for these infants. Their longer postnatal stay allows an opportunity to target parents and staff with risk reduction messages.


Subject(s)
Infant Care/methods , Sleep , Sudden Infant Death/prevention & control , Analysis of Variance , Beds , Case-Control Studies , Humans , Infant , Infant, Low Birth Weight , Infant, Newborn , Infant, Premature , Posture , Prone Position , Risk Factors , Sudden Infant Death/etiology , Supine Position
7.
ISA Trans ; 40(3): 295-305, 2001.
Article in English | MEDLINE | ID: mdl-11515946

ABSTRACT

ISA S88.01 [1] [ISA (ANSI/S88.01.1995), Standard batch control; part 1: models and terminology, Instrument Society of America, 1995] is a standard that provides a methodology for the dissemination of a batch into standard models and provides the terminology for defining the control requirements of batch plants. The nature of S88 is such that it is not only applicable to the development of computer control systems for a batch plant, but also could be utilised within batch management software, i.e. scheduling. This paper presents a method of interpreting multi-purpose/product batch plant into S88 constructs to provide an object oriented framework for the research and development of a batch scheduling Matlab tool-box. Such a framework provides a thorough and efficient method of articulating the model to effectively apply automatic scheduling/optimisation methods.

8.
BMJ ; 322(7290): 822, 2001 Apr 07.
Article in English | MEDLINE | ID: mdl-11290634

ABSTRACT

OBJECTIVES: To investigate whether the accelerated immunisation programme in the United Kingdom is associated, after adjustment for potential confounding, with the sudden infant death syndrome. DESIGN: Population based case-control study, February 1993 to March 1996. Parental interviews were conducted for each death and for four controls matched for age, locality, and time of sleep. Immunisation status was taken from records held by the parents. SETTING: Five regions in England with a combined population of over 17 million. SUBJECTS: Immunisation details were available for 93% (303/325) of infants whose deaths were attributed to the sudden infant death syndrome (SIDS); 90% (65/72) of infants with explained sudden deaths; and 95% (1515/1588) of controls. RESULTS: After all potential confounding factors were controlled for, immunisation uptake was strongly associated with a lower risk of SIDS (odds ratio 0.45 (95% confidence interval 0.24 to 0.85)). This difference became non-significant (0.67 (0.31 to 1.43)) after further adjustment for other factors specific to the infant's sleeping environment. Similar proportions of SIDS deaths and reference sleeps (corresponding to the time of day during which the index baby had died) among the controls occurred within 48 hours of the last vaccination (5% (7/149) v 5% (41/822)) and within two weeks (21% (31/149) v 27% (224/822)). No longer term temporal association with immunisation was found (P=0.78). Of the SIDS infants who died within two weeks of vaccination, 16% (5/31) had signs and symptoms of illness that suggested that medical contact was required, compared with 26% (16/61) of the non-immunised SIDS infants of similar age. The findings for the infants who died suddenly and unexpectedly but of explained causes mirrored those for SIDS infants. CONCLUSIONS: Immunisation does not lead to sudden unexpected death in infancy, and the direction of the relation is towards protection rather than risk.


Subject(s)
Immunization Programs/organization & administration , Sudden Infant Death/etiology , Age Factors , Case-Control Studies , Confounding Factors, Epidemiologic , Humans , Immunization Programs/statistics & numerical data , Infant , Socioeconomic Factors , United Kingdom/epidemiology
9.
Arch Dis Child ; 82(6): 462-9, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10833177

ABSTRACT

AIMS: To investigate patterns of infant growth that may influence the risk of sudden infant death syndrome (SIDS). DESIGN: Three year population based case control study with parental interviews for each death and four age matched controls. Growth was measured from prospective weight observations using the British 1990 Growth Reference. SETTING: Five regions in England (population greater than 17 million, more than 470 000 live births over three years). SUBJECTS: 247 SIDS cases and 1110 controls. RESULTS: The growth rate from birth to the final weight observation was significantly poorer among the SIDS infants despite controlling for potential confounders (SIDS mean change in weight z score (deltazw) = -0.38 (SD 1.40) v controls = +0.22 (SD 1.10), multivariate: p < 0.0001). Weight gain was poorer among SIDS infants with a normal birth weight (above the 16th centile: odds ratio (OR) = 1.75, 95% confidence interval (CI) 1. 48-2.07, p < 0.0001) than for those with lower birth weight (OR = 1. 09, 95% CI 0.61-1.95, p = 0.76). There was no evidence of increased growth retardation before death. CONCLUSIONS: Poor postnatal weight gain was independently associated with an increased risk of SIDS and could be identified at the routine six week assessment.


Subject(s)
Sudden Infant Death/etiology , Weight Gain , Birth Weight/physiology , Case-Control Studies , England/epidemiology , Female , Humans , Infant , Infant, Newborn , Male , Multivariate Analysis , Risk Assessment , Risk Factors , Sudden Infant Death/epidemiology
12.
J Mol Biol ; 299(2): 487-98, 2000 Jun 02.
Article in English | MEDLINE | ID: mdl-10860754

ABSTRACT

We have used the occluded surface algorithm to estimate the packing of both buried and exposed amino acid residues in protein structures. This method works equally well for buried residues and solvent-exposed residues in contrast to the commonly used Voronoi method that works directly only on buried residues. The atomic packing of individual globular proteins may vary significantly from the average packing of a large data set of globular proteins. Here, we demonstrate that these variations in protein packing are due to a complex combination of protein size, secondary structure composition and amino acid composition. Differences in protein packing are conserved in protein families of similar structure despite significant sequence differences. This conclusion indicates that quality assessments of packing in protein structures should include a consideration of various parameters including the packing of known homologous proteins. Also, modeling of protein structures based on homologous templates should take into account the packing of the template protein structure.


Subject(s)
Amino Acids/analysis , Amino Acids/metabolism , Proteins/chemistry , Proteins/metabolism , Alcohol Dehydrogenase/chemistry , Alcohol Dehydrogenase/metabolism , Algorithms , Amino Acids/chemistry , Animals , Ascorbate Oxidase/chemistry , Ascorbate Oxidase/metabolism , Crystallography, X-Ray , Humans , Models, Molecular , Molecular Weight , Muramidase/chemistry , Muramidase/metabolism , Protein Structure, Secondary , Proteins/classification , Ribonuclease, Pancreatic/chemistry , Ribonuclease, Pancreatic/metabolism , Solubility , Solvents , Subtilisins/chemistry , Subtilisins/metabolism , Surface Properties , Tetrahydrofolate Dehydrogenase/chemistry , Tetrahydrofolate Dehydrogenase/metabolism
13.
Proc Natl Acad Sci U S A ; 97(11): 5796-801, 2000 May 23.
Article in English | MEDLINE | ID: mdl-10823938

ABSTRACT

Helix packing is important in the folding, stability, and association of membrane proteins. Packing analysis of the helical portions of 7 integral membrane proteins and 37 soluble proteins show that the helices in membrane proteins have higher packing values (0.431) than in soluble proteins (0.405). The highest packing values in integral membrane proteins originate from small hydrophobic (G and A) and small hydroxyl-containing (S and T) amino acids, whereas in soluble proteins large hydrophobic and aromatic residues have the highest packing values. The highest packing values for membrane proteins are found in the transmembrane helix-helix interfaces. Glycine and alanine have the highest occurrence among the buried amino acids in membrane proteins, whereas leucine and alanine are the most common buried residue in soluble proteins. These observations are consistent with a shorter axial separation between helices in membrane proteins. The tight helix packing revealed in this analysis contributes to membrane protein stability and likely compensates for the lack of the hydrophobic effect as a driving force for helix-helix association in membranes.


Subject(s)
Membrane Proteins/chemistry , Protein Folding , Protein Structure, Secondary , Amino Acids/chemistry , Amino Acids/classification , Animals , Protein Structure, Tertiary
14.
Respir Physiol ; 119(2-3): 123-32, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10722855

ABSTRACT

The mechanisms underlying the sudden infant death syndrome (SIDS) appear to have origins in the fetal environment resulting in neural damage which later compromises responses to breathing or blood pressure challenges during sleep. The deficits appear to involve alterations in neurotransmitter receptors within regions involved in chemoreception and cardiovascular control. SIDS risk is enhanced by pre- and postnatal nicotine exposure, and possibly by hypoxic experiences. The prone sleeping position plays a significant role in risk, as do head positions that minimize facial escape from enclosed spaces; elevated body temperature may also be a factor. Compensatory mechanisms, including diminished gasping ability, relative failure to arouse to a safer state, or a failure to recruit respiratory efforts to overcome a blood pressure loss have been the object of recent research efforts. The findings suggest that the fatal event involves a neurally-compromised infant, circumstances that challenge vital physiology, most likely during sleep, at a particular developmental period.


Subject(s)
Homeostasis/physiology , Respiratory Mechanics/physiology , Sleep/physiology , Sudden Infant Death/pathology , Animals , Humans
15.
Arch Dis Child ; 82(2): 98-106, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10648361

ABSTRACT

OBJECTIVES: To compare the clinical characteristics associated with sudden infant death syndrome (SIDS) and explained sudden unexpected deaths in infancy (SUDI). DESIGN: Three year population based, case control study with parental interviews for each death and four age matched controls. SETTING: Five regions in England (population, > 17 million; live births, > 470,000). SUBJECTS: SIDS: 325 infants; explained SUDI: 72 infants; controls: 1,588 infants. RESULTS: In the univariate analysis, all the clinical features and health markers at birth, after discharge from hospital, during life, and shortly before death, significant among the infants with SIDS were in the same direction among the infants who died of explained SUDI. In the multivariate analysis, at least one apparent life threatening event had been experienced by more of the infants who died than in controls (SIDS: 12% v 3% controls; odds ratio (OR) = 2.55; 95% confidence interval (CI), 1.02 to 6.41; explained SUDI: 15% v 4% controls; OR = 16.81; 95% CI, 2.52 to 112.30). Using a retrospective illness scoring system based on "Baby Check", both index groups showed significant markers of illness in the last 24 hours (SIDS: 22% v 8% controls; OR = 4.17; 95% CI, 1.88 to 9.24; explained SUDI: 49% v 8% controls; OR = 31.20; 95% CI, 6.93 to 140.5). CONCLUSIONS: The clinical characteristics of SIDS and explained SUDI are similar. Baby Check might help identify seriously ill babies at risk of sudden death, particularly in high risk infants.


Subject(s)
Health Status Indicators , Sudden Infant Death/etiology , Case-Control Studies , Cause of Death , Humans , Infant , Multivariate Analysis , Retrospective Studies , Risk Factors , Sudden Infant Death/prevention & control
16.
BMJ ; 319(7223): 1457-61, 1999 Dec 04.
Article in English | MEDLINE | ID: mdl-10582925

ABSTRACT

OBJECTIVE: To investigate the risks of the sudden infant death syndrome and factors that may contribute to unsafe sleeping environments. DESIGN: Three year, population based case-control study. Parental interviews were conducted for each sudden infant death and for four controls matched for age, locality, and time of sleep. SETTING: Five regions in England with a total population of over 17 million people. SUBJECTS: 325 babies who died and 1300 control infants. RESULTS: In the multivariate analysis infants who shared their parents' bed and were then put back in their own cot had no increased risk (odds ratio 0.67; 95% confidence interval 0.22 to 2.00). There was an increased risk for infants who shared the bed for the whole sleep or were taken to and found in the parental bed (9.78; 4.02 to 23.83), infants who slept in a separate room from their parents (10.49; 4.26 to 25.81), and infants who shared a sofa (48.99; 5.04 to 475.60). The risk associated with being found in the parental bed was not significant for older infants (>14 weeks) or for infants of parents who did not smoke and became non-significant after adjustment for recent maternal alcohol consumption (>2 units), use of duvets (>4 togs), parental tiredness (infant slept 2 people per room of the house). CONCLUSIONS: There are certain circumstances when bed sharing should be avoided, particularly for infants under four months old. Parents sleeping on a sofa with infants should always be avoided. There is no evidence that bed sharing is hazardous for infants of parents who do not smoke.


Subject(s)
Beds , Sleep , Sudden Infant Death/etiology , Case-Control Studies , Crowding , England/epidemiology , Humans , Infant , Infant, Newborn , Population Surveillance , Risk Factors , Sudden Infant Death/epidemiology
17.
Pediatrics ; 104(4): e43, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10506268

ABSTRACT

OBJECTIVES: To establish whether epidemiologic characteristics for sudden infant death syndrome (SIDS) have changed since the decrease in death rate after the "Back to Sleep" campaign in 1991, and to compare these characteristics with sudden and unexpected deaths in infancy (SUDI) from explained causes. DESIGN: Three-year, population-based, case-control study. Parental interviews were conducted soon after the death and for 4 controls matched for age and date of interview. All sudden unexpected deaths were included in the study and the cause of death was established by a multidisciplinary panel of the relevant health care professionals taking into account past medical and social history of the mother and infant, the circumstances of death, and a full pediatric postmortem examination. Contributory factors and the final classification of death were made using the Avon clinicopathologic system. SETTING: Five regions in England, with a total population of >17 million people, took part in the study. The number of live births within these regions during the particular time each region was involved in the study was 473 000. STUDY PARTICIPANTS: Three hundred twenty-five SIDS infants (91.3% of those available), 72 explained SUDI infants (86.7% of those available), and 1588 matched control infants (100% of total for cases included). RESULTS: Many of the epidemiologic features that characterize SIDS infants and families have remained the same, despite the recent decrease in SIDS incidence in the United Kingdom. These include the same characteristic age distribution, few deaths in the first few weeks of life or after 6 months, with a peak between 4 and 16 weeks, a higher incidence in males, lower birth weight, shorter gestation, and more neonatal problems at delivery. As in previous studies there was a strong correlation with young maternal age and higher parity and the risk increased for infants of single mothers and for multiple births. A small but significant proportion of index mothers had also experienced a previous stillbirth or infant death. The majority of the SIDS deaths (83%) occurred during the night sleep and there was no particular day of the week on which a significantly higher proportion of deaths occurred. Major epidemiologic features to change since the decrease in SIDS rate include a reduction in the previous high winter peaks of death and a shift of SIDS families to the more deprived social grouping. Just more than one quarter of the SIDS deaths (27%) occurred in the 3 winter months (December through February) in the 3 years of this study. In half of the SIDS families (49%), the lone parent or both parents were unemployed compared with less than a fifth of control families (18%). This difference was not explained by an excess of single mothers in the index group. Many of the significant factors relating to the SIDS infants and families that distinguish them from the normal population did not distinguish between SIDS and explained SUDI. In the univariate analysis many of the epidemiologic characteristics significant among the SIDS group were also identified and in the same direction among the infants dying as SUDI attributable to known causes. The explained deaths were similarly characterized by the same infant, maternal, and social factors, 48% of these families received no waged income. Using logistic regression to make a direct comparison between the two index groups there were only three significant differences between the two groups of deaths: 1) a different age distribution, the age distribution of the explained deaths peaked in the first 2 months and was more uniform thereafter; 2) more congenital anomalies were noted at birth (odds ratio [OR] = 3.14; 95% confidence intervals [CI]: 1.52-6. (ABSTRACT TRUNCATED)


Subject(s)
Sudden Infant Death/epidemiology , Age Distribution , Analysis of Variance , Case-Control Studies , Cause of Death , England/epidemiology , Humans , Infant , Infant Mortality/trends , Infant, Newborn , Logistic Models , Maternal Age , Odds Ratio , Risk Factors , Seasons , Smoking , Socioeconomic Factors , Surveys and Questionnaires
18.
Arch Dis Child ; 81(2): 112-6, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10490514

ABSTRACT

OBJECTIVES: To investigate the relation between pacifier use and sudden infant death syndrome (SIDS). DESIGN: Three year population based, case control study with parental interviews for each death and four age matched controls. SETTING: Five regions in England (population > 17 million). SUBJECTS: 325 infants who had died from SIDS and 1300 control infants. RESULTS: Significantly fewer SIDS infants (40%) than controls (51%) used a pacifier for the last/reference sleep (univariate odds ratio (OR), 0.62; 95% confidence interval (CI), 0.46 to 0.83) and the difference increased when controlled for other factors (multivariate OR, 0.41; 95% CI, 0. 22 to 0.77). However, the proportion of infants who had ever used a pacifier for day (66% SIDS v 66% controls) or night sleeps (61% SIDS v 61% controls) was identical. The association of a risk for SIDS infants who routinely used a pacifier but did not do so for the last sleep became non-significant when controlled for socioeconomic status (bivariate OR, 1.39 (0.93 to 2.07)). CONCLUSIONS: Further epidemiological evidence and physiological studies are needed before pacifier use can be recommended as a measure to reduce the risk of SIDS.


Subject(s)
Infant Care , Sudden Infant Death/etiology , Breast Feeding , Case-Control Studies , Cause of Death , England/epidemiology , Humans , Infant , Infant, Newborn , Odds Ratio , Posture/physiology , Risk Factors , Sleep , Social Class
20.
J Wildl Dis ; 34(4): 738-43, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9813843

ABSTRACT

The sera of 195 hunter-killed feral pigs (Sus scrofa), collected in New South Wales (Australia) from April to November 1995, were screened against a reference panel of 14 Leptospira interrogans serovars using a microscopic agglutination test (MAT). The panel represented those serovars previously isolated from wild and domestic mammals in mainland Australia. Antileptospiral agglutinins were detected in 20% of the sera tested and included nine L. interrogans serovars. The majority of serological reactors (63%) were to L. interrogans serovar pomona. Sera from 26% of immunoreactors cross reacted with antigens from one or more serovars. No differences were noted in the prevalence of L. interrogans antibodies between the sexes, or between pigs from areas of low and high rainfall. The implications of leptospirosis in feral pigs on the transmission of leptospires to wildlife, livestock, and humans are discussed.


Subject(s)
Antibodies, Bacterial/blood , Leptospira interrogans/immunology , Swine Diseases/epidemiology , Weil Disease/veterinary , Agglutination Tests/veterinary , Animals , Animals, Wild , Cross Reactions , Female , Humans , Leptospira interrogans/classification , Male , New South Wales/epidemiology , Seroepidemiologic Studies , Swine , Swine Diseases/microbiology , Weil Disease/epidemiology , Weil Disease/microbiology
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