_Intraperitoneal_, _-thoracic_, _-cardiac_, _-ocular_, _-muscular_ injections, and injections into the parenchyma of internal organs are accomplished with the hypodermic needle. In the case of the first two, injury to contained organs should be carefully avoided. Intracardiac injection, or aspiration of the heart to secure blood, requires considerable practice to be successful without causing the death of the animal at once through internal hemorrhage. In _subdural_ injections into the cranial cavity it is necessary to trephine the skull first, while such injections into the spinal canal may be accomplished between the vertebra with needles longer and stronger than the usual hypodermic needle. Occasionally animals are caused to _inhale_ the organisms, or are _fed_ cultures mixed with the feed. SECURING AND TRANSPORTING MATERIAL FROM ANIMALS FOR BACTERIOLOGICAL EXAMINATION. If the site of the lesion is readily accessible from the exterior, material from the _living animal_ should be collected with sterile instruments and kept in sterile utensils until the necessary tests can be made. Testing should be done on material as soon after collection as possible, in all cases, to avoid the effects of “decomposition” bacteria. If the blood is to be investigated it may be aspirated from a peripheral vein with a sterile hypodermic syringe of appropriate size or allowed to flow through a sterile canula into sterile receptacles. The site of the puncture should be shaved and disinfected before the instrument is introduced. Discharges of whatever kind should likewise be collected in sterile receptacles and examined as soon as may be. If internal organs are to be examined it is best to kill a moribund animal than to wait for death, since after death, and in severe infections even sometimes before, the tissues are rapidly invaded by saprophytic bacteria from the alimentary and respiratory tracts which complicate greatly the isolation of the specific organism. Hence the search for specific bacteria in carcasses or organs several hours after death is frequently negative. Animal inoculation with such material is very often followed by sepsis or septicemia in a few hours, so that the specific organism has no opportunity to manifest itself. In securing material for cultures from internal organs it is a good plan to burn the surface of the organ with a gas or alcohol flame, or to sear it with a hot instrument to kill surface organisms, then make the incision or puncture through the burned area and secure material from the interior of the organ. Such punctures made with a stiff platinum needle frequently give pure cultures of the organism sought. Slides may be made from such material and culture media inoculated at once.